General Information of Disease (ID: DISYHNUI)

Disease Name Myelodysplastic syndrome
Synonyms
myelodysplastic syndrome, susceptibility to; myelodysplasia; myelodysplastic syndromes; MDS; smoldering leukemia; myelodysplastic syndrome/neoplasm; smouldering leukaemia; preleukemia; myelodysplastic syndrome; oligoblastic leukemia; myelodysplastic syndrome, unclassifiable; myelodysplastic neoplasm; MDS-U; MDS, unclassifiable; oligoblastic leukaemia; Myelodysplastic Syndromes; myelodysplastic syndrome, somatic; dysmyelopoietic syndrome; hematopoeitic - myelodysplastic syndrome (MDS)
Disease Class 2A37: Myelodysplastic syndrome
Definition
A clonal hematopoietic disorder characterized by dysplasia and ineffective hematopoiesis in one or more of the hematopoietic cell lines. The dysplasia may be accompanied by an increase in myeloblasts, but the number is less than 20%, which, according to the WHO guidelines, is the requisite threshold for the diagnosis of acute myeloid leukemia. It may occur de novo or as a result of exposure to alkylating agents and/or radiotherapy. (WHO, 2001)
Disease Hierarchy
DIS9RZ96: Neoplastic syndrome
DIS9E81G: Myeloid hemopathy
DISYHNUI: Myelodysplastic syndrome
ICD Code
ICD-11
ICD-11: 2A37
ICD-9
ICD-9: 238.7
Expand ICD-11
'2A3Z
Expand ICD-10
'D46; 'D46.7; 'D46.9
Expand ICD-9
238.7
Disease Identifiers
MONDO ID
MONDO_0018881
MESH ID
D009190
UMLS CUI
C3463824
OMIM ID
614286
MedGen ID
483005
Orphanet ID
52688
SNOMED CT ID
109995007

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 11 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Atezolizumab DMMF8U0 Approved Monoclonal antibody [1]
Azacitidine DMTA5OE Approved Small molecular drug [2]
Clofarabine DMCVJ86 Approved Small molecular drug [3]
Decitabine DMQL8XJ Approved Small molecular drug [4]
Etelcalcetide DMHP9BL Approved Small molecular drug [5]
Lonafarnib DMGM2Z6 Approved Small molecular drug [6]
Luspatercept DM715KM Approved NA [7]
Motixafortide DMW34B1 Approved Peptide [1]
Olutasidenib DMPH916 Approved NA [1]
Romiplostim DM3U7SZ Approved Small molecular drug [8]
Sorafenib DMS8IFC Approved Small molecular drug [9]
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⏷ Show the Full List of 11 Drug(s)
This Disease is Treated as An Indication in 89 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
COL-003 DMNVWY0 Preregistration NA [10]
ACE-536 DMRI15Q Phase 3 NA [1]
ASTX727 DM4HK8Z Phase 3 NA [1]
ATIR101 DMRV7T7 Phase 3 Cell therapy [11]
CC-486 DMTNQB0 Phase 3 Small molecular drug [12]
CPI-613 DM5XUQL Phase 3 Small molecular drug [7]
CPX-351 DM7BMAL Phase 3 NA [1]
Guadecitabine DM9Y3EG Phase 3 NA [1]
Hu5F9-G4 DMBER0Q Phase 3 NA [13]
Magrolimab DMVXUR0 Phase 3 Antibody [14]
MBG453 DMBPY9Z Phase 3 NA [15]
MLN4924 DMP36KD Phase 3 Small molecular drug [1]
NiCord DMTSURO Phase 3 NA [7]
Pracinostat DMTD7AB Phase 3 Small molecular drug [16]
Rigosertib DMOSTXF Phase 3 Small molecular drug [1]
Sapacitabine DM704AN Phase 3 Small molecular drug [7]
V114 DMDEYLO Phase 3 Vaccine [17]
Vadastuximab talirine DM9LH10 Phase 3 NA [18]
Zarnestra DMF30HL Phase 3 Small molecular drug [1]
Imetelstat DMONWJ4 Phase 2/3 Small molecular drug [7]
Rivo-cel DMXLS6K Phase 2/3 Cell therapy [19]
Actimab-MDS DMP8EEX Phase 2 Radiotherapy [20]
AEB1102 DMB5CKZ Phase 2 NA [1]
ALRN-6924 DMLBWT1 Phase 2 NA [1]
APR-246 DMNFADH Phase 2 Small molecular drug [1]
AR-67 DM8A71F Phase 2 Small molecular drug [21]
Bemcentinib DM0YCPL Phase 2 Small molecular drug [22]
BGB-324 DMDI43Y Phase 2 siRNA drug [1]
BI-836858 DMUVMY9 Phase 2 Antibody [1]
BP-100-1-01 DMKDGI8 Phase 2 NA [23]
CHR-2797 DMULZ4W Phase 2 Small molecular drug [1]
CX-01 DMI9MLT Phase 2 NA [1]
Ezatiostat DM2L9CO Phase 2 Small molecular drug [24]
Flotetuzumab DMVR6OM Phase 2 NA [18]
H3B-8800 DML2VSZ Phase 2 NA [25]
HemaMax DMF1MS0 Phase 2 NA [26]
Ifabotuzumab DMGWNCJ Phase 2 NA [18]
IMG-7289 DML9AVG Phase 2 NA [1]
INCB00928 DMFG8TI Phase 2 Small molecular drug [27]
JNJ-74494550 DM3ICO6 Phase 2 Antibody [28]
K-NK002 DMDUS54 Phase 2 Cell therapy [29]
Lirilumab DMNGT89 Phase 2 Monoclonal antibody [18]
ML-04 DMQSO4L Phase 2 NA [30]
Nerofe DMVVBY8 Phase 2 Peptide [31]
OPN-305 DM1IBRT Phase 2 Antibody [32]
SNS-301 DMR5SHK Phase 2 Vaccine [33]
Sotatercept DMXPV7V Phase 2 NA [7]
TEW-7197 DM2LBC3 Phase 2 NA [1]
ALX148 DMGQX0U Phase 1/2 Protein [34]
ASP7517 DMW8OOC Phase 1/2 Cell therapy [35]
CART-123 cells DM0MCTJ Phase 1/2 CAR T Cell Therapy [36]
CNDO-109 DMQ5E8L Phase 1/2 NA [1]
Eltanexor oral DM7CLEZ Phase 1/2 NA [1]
FF-10501-01 DM0HSJK Phase 1/2 NA [1]
GTB-3550 DMK2RIB Phase 1/2 Recombinant protein [37]
IGF-MTX DMXQEAA Phase 1/2 NA [1]
NEXI-001 DMLQTC9 Phase 1/2 Cell therapy [38]
ONO-7475 DMV6GX7 Phase 1/2 Small molecular drug [39]
OTX-015 DMI8RG1 Phase 1/2 Small molecular drug [40]
AB-110 DM0F520 Phase 1 Cell therapy [41]
APVO436 DMUAMZY Phase 1 Antibody [42]
BB-MPI-03 DM0PII2 Phase 1 NA [43]
BGB-11417 DM7QTIC Phase 1 Small molecular drug [44]
BPX-701 DMYERSD Phase 1 NA [18]
CART-117 cells DMAKZTW Phase 1 CAR T Cell Therapy [36]
CART-33 cells DMBHCSL Phase 1 CAR T Cell Therapy [36]
CART-34 cells DMRNIB9 Phase 1 CAR T Cell Therapy [36]
CART-38 cells DMKN8XD Phase 1 CAR T Cell Therapy [36]
CART-56 cells DMQTOBF Phase 1 CAR T Cell Therapy [36]
CART-Muc1 cells DMOJEXG Phase 1 CAR T Cell Therapy [36]
CB-5339 DMOXDIY Phase 1 Small molecular drug [45]
CC-90002 DMK0QDO Phase 1 Antibody [18]
CD123-CD33 Ccar DMUJF9T Phase 1 CAR T Cell Therapy [46]
CM-CS1 T-cell DMY5V4U Phase 1 CAR T Cell Therapy [47]
CYAD-02 DM6EPP8 Phase 1 CAR T Cell Therapy [48]
CYC140 DMC6PKJ Phase 1 Small molecular drug [49]
IBI188 DMXUJ1P Phase 1 Antibody [50]
JNJ-64619178 DMDBW2N Phase 1 Small molecular drug [51]
JNJ-67571244 DMQOHRA Phase 1 Antibody [52]
LP-108 DMYIXQZ Phase 1 NA [53]
M012 DME6UNO Phase 1 Small molecular drug [54]
NKR-2 CAR-T Cells DMDLJM1 Phase 1 CAR T Cell Therapy [55]
NKX101 DMHJ1Y0 Phase 1 CAR T Cell Therapy [56]
OTSSP167 DMF5KNO Phase 1 Small molecular drug [1]
PRGN-3006 DMNAB57 Phase 1 CAR-T cell therapy [57]
SEA-CD70 DMX94YF Phase 1 Antibody [58]
SEL120 DMHCUZV Phase 1 Small molecular drug [59]
SX-682 DMHMG6X Phase 1 Small molecular drug [60]
SY-1425 DMH8UF0 Phase 1 NA [1]
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⏷ Show the Full List of 89 Drug(s)
This Disease is Treated as An Indication in 1 Discontinued Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
ARRY-614 DMXD93K Discontinued in Phase 1 Small molecular drug [61]
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Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 149 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
ABAT TTT2LD9 Limited Posttranslational Modification [62]
CFLAR TTJZQYH Limited Altered Expression [63]
CLEC12A TT70N8V Limited Biomarker [64]
CSF1R TT7MRDV Limited Biomarker [65]
CTAG1A TTE5ITK Limited Biomarker [66]
DCK TTJOCE4 Limited Biomarker [67]
ELANE TTPLTSQ Limited Genetic Variation [68]
GOT1 TTU507L Limited Genetic Variation [69]
IDH1 TTV2A1R Limited Biomarker [70]
IRF1 TT4TU3L Limited Altered Expression [71]
MYB TT8V13P Limited Genetic Variation [72]
NRAS TTW2R9X Limited Genetic Variation [73]
PPM1D TTENJAB Limited Genetic Variation [74]
SCN4A TT84DRB Limited Biomarker [75]
SPN TTOZAX0 Limited Altered Expression [76]
STK4 TTCPLVN Limited Altered Expression [77]
TIE1 TTT4236 Limited Altered Expression [78]
TK1 TTP3QRF Limited Biomarker [79]
CRBN TTDKGTC Disputed Biomarker [80]
FECH TTQ6VF4 Disputed Genetic Variation [81]
HBA2 TTQO71U Disputed Genetic Variation [82]
IL3RA TTENHJ0 Disputed Altered Expression [83]
PRAME TTPH7T0 Disputed Altered Expression [84]
PTPN11 TT7WUAV Disputed Genetic Variation [85]
CALCA TTVSFJW moderate Genetic Variation [86]
CALR TTUZ7OA moderate Genetic Variation [87]
CD36 TTPJMCU moderate Altered Expression [88]
CD55 TT5Z9WY moderate Biomarker [89]
CSNK1A1 TTFQEMX moderate Genetic Variation [90]
CXXC5 TTVS4C3 moderate Biomarker [91]
DICER1 TTTEOPU moderate Altered Expression [92]
HDAC1 TT6R7JZ moderate Altered Expression [93]
MGMT TTJ8DV7 moderate Genetic Variation [94]
PLCG1 TT6T4JI moderate Biomarker [95]
PTPRC TTUS45N moderate Biomarker [96]
RAD51 TTC0G1L moderate Biomarker [97]
SPARC TTBQFM7 moderate Biomarker [98]
ABL1 TT6B75U Strong Genetic Variation [99]
ACVR2A TTX2DRI Strong Biomarker [100]
AIMP2 TTXWHGF Strong Biomarker [101]
ALPI TTHYMUV Strong Biomarker [102]
AMACR TTLN1AP Strong Genetic Variation [103]
ANPEP TTPHMWB Strong Altered Expression [104]
ATG7 TTLVB9Z Strong Biomarker [105]
ATRAID TTFLIKM Strong Biomarker [106]
AURKB TT9RTBL Strong Altered Expression [107]
AZGP1 TTUPYLV Strong Biomarker [108]
BMI1 TTIPNSR Strong Altered Expression [109]
BRCA2 TTUARD6 Strong Biomarker [97]
BRIP1 TTZV7LJ Strong Biomarker [97]
CASP5 TTWR48J Strong Genetic Variation [110]
CBL TT7QT13 Strong Biomarker [111]
CD14 TT6I7DC Strong Altered Expression [112]
CD22 TTM6QSK Strong Biomarker [113]
CD274 TT8ZLTI Strong Biomarker [114]
CD33 TTJVYO3 Strong Biomarker [115]
CD38 TTPURFN Strong Biomarker [116]
CD52 TTQT5S9 Strong Altered Expression [117]
CD6 TTMF6KC Strong Genetic Variation [118]
CD69 TTPQE9F Strong Altered Expression [119]
CDA TTQ12RK Strong Biomarker [120]
CDC20 TTBKFDV Strong Biomarker [121]
CDC25C TTESBNC Strong Biomarker [122]
CDKN1C TTBSUAR Strong Altered Expression [123]
CDKN2C TTBRUGA Strong Biomarker [106]
CHRM4 TTQ3JTF Strong Biomarker [124]
CRLF1 TT6YF5K Strong Biomarker [125]
CRTC1 TT4GO0F Strong Biomarker [126]
CSF1 TT0IQER Strong Biomarker [127]
DAPK3 TTERVQN Strong Genetic Variation [128]
DEK TT1NMGV Strong Genetic Variation [129]
DLK1 TTF4AVB Strong Biomarker [130]
DLL1 TT9CFQD Strong Altered Expression [131]
E2F1 TTASI04 Strong Altered Expression [132]
EED TTFNJ4R Strong Biomarker [133]
ENPEP TT9PBIL Strong Genetic Variation [134]
EPOR TTAUX24 Strong Biomarker [135]
FANCA TTV5HJS Strong Biomarker [97]
FANCF TTNZKFJ Strong Biomarker [97]
FCGR3A TTIFOC0 Strong Biomarker [136]
FUT4 TTNV1KZ Strong Altered Expression [137]
GLIPR1 TTEQF1O Strong Altered Expression [138]
GP6 TTTJUVZ Strong Biomarker [139]
GRB2 TTEYRJ9 Strong Biomarker [140]
GSK3A TTQWAU1 Strong Biomarker [141]
GZMB TTKEPHX Strong Biomarker [142]
HCK TT42OGM Strong Biomarker [143]
HDAC8 TTT6LFV Strong Genetic Variation [144]
HOXA11 TTEX4ZA Strong Biomarker [145]
HOXA13 TTN26OM Strong Biomarker [145]
HSPA9 TTMTPG3 Strong Altered Expression [146]
HTR1B TTK8CXU Strong Biomarker [147]
INPP5D TTTP2Z1 Strong Altered Expression [148]
IRAK4 TTILUKB Strong Biomarker [149]
ITGB3 TTJA1ZO Strong Biomarker [150]
KDM6B TTDIJUQ Strong Altered Expression [151]
KIR2DL1 TT4UXPE Strong Biomarker [152]
KIR2DL3 TTEX3SI Strong Biomarker [152]
KIT TTX41N9 Strong Biomarker [153]
KITLG TTDJ51N Strong Altered Expression [154]
KRAS TTM8FR7 Strong Biomarker [155]
MARCKS TTHRM39 Strong Biomarker [156]
MPL TTIHYA4 Strong Genetic Variation [87]
MVD TTE5J6X Strong Biomarker [157]
MYC TTNQ5ZP Strong Altered Expression [114]
NAAA TTMN4HY Strong Biomarker [158]
NCAM1 TTVXPHT Strong Biomarker [159]
NEDD8 TTNDC4K Strong Biomarker [160]
NOP2 TTBLG3H Strong Biomarker [161]
NR0B2 TT25A9Q Strong Posttranslational Modification [162]
NSD1 TTTSJ3H Strong Genetic Variation [163]
PDCD1LG2 TTW14O3 Strong Altered Expression [164]
PIM2 TT69J2Z Strong Biomarker [165]
PKMYT1 TTB4PAZ Strong Biomarker [106]
PLK2 TT976FS Strong Posttranslational Modification [166]
PLK4 TTGPNZQ Strong Biomarker [167]
PPP3CA TTA4LDE Strong Biomarker [168]
PRSS1 TT2WR1T Strong Biomarker [169]
PSMB6 TT8EPLT Strong Genetic Variation [170]
PTPN13 TT405FP Strong Biomarker [171]
PTPN6 TT369M5 Strong Biomarker [172]
RUNX1 TTWIN3H Strong Genetic Variation [173]
S100A8 TT4AF6N Strong Biomarker [174]
S100A9 TT0TMQG Strong Altered Expression [114]
SCT TTOBVIN Strong Biomarker [175]
SH2B3 TT36N7Z Strong Altered Expression [176]
SLC29A1 TTLXAKE Strong Altered Expression [67]
SPAG6 TTDAKTW Strong Biomarker [177]
SPHK1 TTOHFIY Strong Biomarker [178]
SYVN1 TT8XKYM Strong Genetic Variation [179]
TCL1A TTUKRDV Strong Biomarker [180]
TDG TTEXRQD Strong Genetic Variation [94]
TEC TT1ZV49 Strong Genetic Variation [181]
TERT TTQY2EJ Strong Altered Expression [182]
TFRC TT8MG4S Strong Biomarker [183]
TLR2 TTY7ZHS Strong Altered Expression [93]
TLR6 TTWRI8V Strong Altered Expression [184]
TOR1A TTF85KW Strong Genetic Variation [185]
TPO TT52XDZ Strong Altered Expression [186]
TRPC1 TTA76X0 Strong Biomarker [169]
UBE2T TT0A1R8 Strong Biomarker [97]
WAS TTE8T73 Strong Genetic Variation [187]
WT1 TTZ8UT4 Strong Biomarker [84]
CCR7 TT2GIDQ Definitive Altered Expression [188]
CSF3R TTC70AJ Definitive Genetic Variation [189]
HIPK2 TTOB49C Definitive Genetic Variation [190]
MSI2 TTTXQF6 Definitive Biomarker [191]
OPRK1 TTQW87Y Definitive Biomarker [192]
PLA2R1 TTHKW7D Definitive Posttranslational Modification [193]
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⏷ Show the Full List of 149 DTT(s)
This Disease Is Related to 5 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC25A37 DTLBGTZ Limited Genetic Variation [194]
ABCB7 DT2IMBW Strong Altered Expression [195]
SLC22A5 DT3HUVD Strong Biomarker [196]
SLC29A2 DTW78DQ Strong Biomarker [197]
SLCO6A1 DTIFXNS Strong Biomarker [198]
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This Disease Is Related to 7 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
G6PC3 DEE1B8O Disputed Genetic Variation [199]
ALAS2 DE437BY Strong Biomarker [200]
BAAT DERA3OF Strong Altered Expression [201]
DIO3 DET89OV Strong Genetic Variation [130]
TPMT DEFQ8VO Strong Genetic Variation [202]
UBASH3B DE10BJ5 Strong Biomarker [111]
UCK1 DE478BP Strong Altered Expression [203]
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⏷ Show the Full List of 7 DME(s)
This Disease Is Related to 303 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ACSL5 OT3L9XO3 Limited Genetic Variation [204]
ACSL6 OT0TT8P8 Limited Genetic Variation [204]
ATAD1 OTJ02XFL Limited Posttranslational Modification [205]
ATRX OT77RSQW Limited Genetic Variation [206]
BLVRB OTHCFN2C Limited Genetic Variation [207]
CTAG1B OTIQGW6U Limited Biomarker [66]
DDX10 OTH48438 Limited Altered Expression [208]
DDX41 OT6KEIHP Limited Genetic Variation [209]
ENDOG OT5IM7B3 Limited Biomarker [210]
FTMT OTIUX6XG Limited Biomarker [211]
GFI1 OT9HB9H8 Limited Genetic Variation [212]
HBG1 OTVL4NSU Limited Biomarker [213]
HBG2 OT4J48JJ Limited Biomarker [213]
HLA-DPB1 OTW8JHU2 Limited Genetic Variation [214]
HPSE2 OTGEPP8V Limited Genetic Variation [205]
IDH2 OTTQA4PB Limited Biomarker [215]
ISG20 OTCWRJJW Limited Altered Expression [216]
JARID2 OT14UM8H Limited Biomarker [217]
LIG4 OT40DNXU Limited Biomarker [218]
MLLT11 OTG5RVHC Limited Altered Expression [219]
PCM1 OTFM133C Limited Biomarker [220]
PDCD6 OT2YA5M8 Limited Genetic Variation [221]
PDLIM4 OT23LZYY Limited Posttranslational Modification [222]
PIGA OT51UWUR Limited Altered Expression [223]
PLCE1 OTJISZOX Limited Genetic Variation [224]
RPL23 OTXI1YLM Limited Altered Expression [225]
RPS14 OTB90KV5 Limited Biomarker [226]
TM9SF4 OT85D4H9 Limited Altered Expression [227]
TSPAN33 OTH6C0WU Limited Genetic Variation [228]
CHST9 OT1DEZRM Disputed Biomarker [229]
HBA1 OTW2BQF4 Disputed Genetic Variation [82]
IKBKG OTNWJWSD Disputed Biomarker [230]
IKZF1 OTCW1FKL Disputed Biomarker [231]
RUNX1T1 OT30DED5 Disputed Biomarker [232]
SRSF2 OTVDHO6U Disputed Genetic Variation [133]
DCC OT2C1SHW moderate Biomarker [233]
FANCM OTNJG99Z moderate Biomarker [97]
GDF11 OTOSNMND moderate Genetic Variation [234]
GP9 OTA19OKO moderate Biomarker [235]
IL3 OT0CQ35N moderate Altered Expression [236]
ITGA2B OT4Y17PY moderate Biomarker [237]
MLF1 OTC5BKHU moderate Genetic Variation [238]
PSMG2 OTEMF20S moderate Biomarker [239]
RAD51C OTUD6SY5 moderate Biomarker [97]
RPS19 OTBKGP48 moderate Genetic Variation [240]
A2ML1 OTWNUXIS Strong Biomarker [241]
AADAC OT8VACT2 Strong Biomarker [242]
AGFG2 OTXQZHCR Strong Biomarker [243]
AHSA1 OTC7AFHT Strong Biomarker [101]
AKAP12 OTCVRDDX Strong Altered Expression [244]
AKAP13 OTOZAR14 Strong Biomarker [245]
ANKRD26 OT2ENKKV Strong Genetic Variation [240]
ANKRD28 OTRBREQ9 Strong Biomarker [246]
AP5M1 OTDLWEBL Strong Biomarker [247]
ARHGAP24 OTCQCEZS Strong Posttranslational Modification [248]
ARSH OTG0X9UQ Strong Biomarker [140]
ASXL2 OTNG4E2M Strong Genetic Variation [249]
ATF7IP OTU6ZA7F Strong Genetic Variation [250]
ATG3 OT28VBVK Strong Altered Expression [251]
BBX OTNQ3QUC Strong Genetic Variation [252]
BCL2L10 OTYXQJ3I Strong Biomarker [253]
BCOR OTG013AX Strong Biomarker [254]
BCORL1 OTPTFQN5 Strong Genetic Variation [255]
BDH1 OT62RL5P Strong Biomarker [256]
BIK OTTH1T3D Strong Altered Expression [257]
BLM OTEJOAJX Strong Biomarker [97]
BNIP3L OTJKOMXE Strong Biomarker [258]
BRCA1 OT5BN6VH Strong Biomarker [97]
BRCC3 OTK0ZN7Y Strong Genetic Variation [259]
CABIN1 OT4G5CIK Strong Biomarker [260]
CAST OTBXZZGF Strong Biomarker [231]
CBFB OTIAC6W4 Strong Altered Expression [261]
CCDC54 OTW5WCX9 Strong Altered Expression [262]
CCL28 OTY6XNQ7 Strong Biomarker [263]
CCNH OTKDU3SR Strong Genetic Variation [94]
CD177 OTS79FNF Strong Altered Expression [264]
CD247 OT45FGUX Strong Altered Expression [265]
CD48 OT83ZNPP Strong Genetic Variation [266]
CD99 OTPUZ5DE Strong Biomarker [267]
CDC40 OTOYUNHN Strong Biomarker [268]
CDKL3 OTJ0TQ9T Strong Biomarker [269]
CDKN2D OT2TTZPZ Strong Biomarker [270]
CEACAM8 OTLL9WWO Strong Biomarker [271]
CEBPE OTKZA25M Strong Genetic Variation [272]
CFC1 OT5DHGI8 Strong Biomarker [273]
CFL1 OTT6D5MH Strong Biomarker [106]
CHFR OTRAD2TT Strong Biomarker [274]
CIB2 OT9ZJX1I Strong Genetic Variation [275]
CLEC5A OT19WV30 Strong Biomarker [276]
CNTNAP1 OT5Y03EU Strong Genetic Variation [277]
COL4A2 OTJK1LKN Strong Altered Expression [278]
COLEC10 OTMBADGZ Strong Altered Expression [279]
CTBP1 OTVYH2DH Strong Altered Expression [280]
CTC1 OTRJY7QD Strong Genetic Variation [281]
CTNNA1 OTFC725Z Strong Posttranslational Modification [282]
CUX1 OTU1LCNJ Strong Altered Expression [283]
CYBA OT16N9ZO Strong Posttranslational Modification [271]
DAP OT5YLL7E Strong Altered Expression [284]
DCDC2 OTSUFH1H Strong Biomarker [117]
DERL1 OTJUS74N Strong Biomarker [285]
DIAPH1 OTZBYPLH Strong Biomarker [286]
DIDO1 OT9PB547 Strong Biomarker [287]
DLX4 OTLWVCN4 Strong Biomarker [288]
DNAI1 OTF6C65Q Strong Biomarker [289]
DOCK4 OTH3XY8B Strong Biomarker [172]
DROSHA OTCE68KZ Strong Biomarker [290]
EBF1 OTZ61YYH Strong Genetic Variation [291]
ECI2 OT2TP4IX Strong Biomarker [292]
EEF1E1 OTRA6XOB Strong Biomarker [106]
EOMES OTB9VQFA Strong Biomarker [142]
ERCC6 OT2QZKSF Strong Genetic Variation [94]
ERFE OTSES1HA Strong Genetic Variation [293]
ESPL1 OTMGEVOK Strong Altered Expression [294]
ETFA OTXX61VZ Strong Genetic Variation [295]
ETV1 OT6PMJIK Strong Biomarker [296]
ETV6 OTCZMG61 Strong Genetic Variation [240]
EVPL OTZIAFEK Strong Biomarker [297]
FANCC OTTIDM3P Strong Biomarker [298]
FANCD2 OTVEB5LF Strong Biomarker [97]
FANCE OTKRPBW1 Strong Biomarker [97]
FANCG OT7MC8TZ Strong Biomarker [97]
FANCI OTW8E3SC Strong Biomarker [97]
FANCL OTJC7QPQ Strong Biomarker [97]
FBXL5 OT93D50X Strong Altered Expression [299]
FBXW4 OTEGSZOX Strong Biomarker [242]
FCGR3B OTSLSPZG Strong Biomarker [136]
FGD4 OTYXJQCW Strong Biomarker [300]
FGF3 OT9PK2SI Strong Genetic Variation [301]
FLII OT7G9JG6 Strong Altered Expression [302]
FLT3LG OTU0YGC4 Strong Genetic Variation [303]
FRYL OTBN3XHN Strong Altered Expression [304]
FRZB OTTO3DPY Strong Biomarker [305]
FZD9 OTTZ9MKK Strong Posttranslational Modification [306]
GAB2 OTBFN705 Strong Biomarker [307]
GATA2 OTBP2QQ2 Strong Autosomal dominant [308]
GFI1B OTRDW8YO Strong Biomarker [309]
GFM1 OTUN4V3N Strong Biomarker [310]
GLIS2 OTOUUV1X Strong Biomarker [311]
GPR68 OT1NXSMN Strong Altered Expression [312]
GRAP2 OTS5NIZ3 Strong Biomarker [101]
GSTK1 OTDNGWAF Strong Biomarker [198]
GYPA OTABU4YV Strong Biomarker [313]
GYPB OTESHUIX Strong Biomarker [314]
GYPE OTBHAG6A Strong Biomarker [314]
GYS1 OTJZJRWK Strong Altered Expression [315]
HAS2 OTTD3PAL Strong Altered Expression [316]
HAVCR2 OTOL603T Strong Biomarker [142]
HJV OT4235J2 Strong Posttranslational Modification [317]
HLA-E OTX1CTFB Strong Altered Expression [318]
HLTF OTRX2OSF Strong Genetic Variation [319]
HNRNPD OT5UO1FA Strong Biomarker [200]
HOXA9 OTKNK5H0 Strong Biomarker [276]
HOXD13 OTWSC8TF Strong Biomarker [320]
ID4 OTPMJ39I Strong Posttranslational Modification [321]
IER3 OTZJI5FZ Strong Altered Expression [322]
IFIT1 OTXOQDSG Strong Altered Expression [323]
ILDR1 OTQK8XLK Strong Altered Expression [324]
INTS1 OT7TY1M1 Strong Biomarker [325]
INTS2 OT2N5TCK Strong Genetic Variation [301]
ITIH4 OT460OO1 Strong Biomarker [326]
KDM2B OTDMCVW7 Strong Altered Expression [327]
KDM6A OTZM3MJJ Strong Biomarker [328]
KLF11 OTKVQDJD Strong Genetic Variation [329]
KMT2C OTC59BCO Strong Biomarker [330]
L3MBTL1 OT8M52QY Strong Genetic Variation [331]
LAMTOR1 OTIBJBW9 Strong Biomarker [106]
LEF1 OTWS5I5H Strong Genetic Variation [332]
LGALS9 OT7MF91K Strong Biomarker [142]
LUC7L2 OTOP9Q1V Strong Genetic Variation [133]
LYL1 OTCNOV1M Strong Altered Expression [333]
MAD2L1 OTXNGZCG Strong Biomarker [107]
MAD2L2 OT24ZO59 Strong Biomarker [97]
MAFK OTZJUE4P Strong Biomarker [106]
MAML2 OT1TSVAR Strong Biomarker [126]
MAP3K12 OT5HODDD Strong Genetic Variation [128]
MARCHF1 OTI2EYO6 Strong Biomarker [334]
MBD2 OTUQPP0R Strong Posttranslational Modification [328]
MCM2 OTGGORIQ Strong Altered Expression [335]
MCM3AP OT895FEC Strong Biomarker [336]
MECOM OTP983W8 Strong Biomarker [337]
MEIS1 OTH9DKAD Strong Altered Expression [304]
MFF OTEVIXOM Strong Biomarker [338]
MLKL OTDSLC81 Strong Biomarker [339]
MLLT1 OT41UZU5 Strong Biomarker [340]
MLLT3 OTXH4DDG Strong Altered Expression [341]
MNDA OTCTKR47 Strong Altered Expression [342]
MPPE1 OTINBJVE Strong Biomarker [343]
MPV17 OT579DMU Strong Genetic Variation [344]
MRPL28 OT4LUTZU Strong Posttranslational Modification [345]
MT1E OTXJKU4Y Strong Biomarker [346]
MXI1 OTUQ9E0D Strong Biomarker [107]
MYBL2 OTZ3JX8Q Strong Biomarker [347]
MYH11 OTVNVWY3 Strong Altered Expression [261]
MYOM2 OTD2UOXW Strong Biomarker [348]
MYSM1 OTO73N00 Strong Genetic Variation [349]
MYT1 OTC3660I Strong Biomarker [106]
NANS OTMQ2FUH Strong Biomarker [350]
NME4 OT2JTT42 Strong Altered Expression [351]
NSD3 OT3677ZG Strong Genetic Variation [352]
NUP214 OTWEA19O Strong Genetic Variation [129]
NUP98 OTNT12G2 Strong Altered Expression [353]
NXT1 OT0VO6AY Strong Posttranslational Modification [345]
ORC5 OTFPW8DE Strong Genetic Variation [354]
PAFAH1B1 OT9T2TCJ Strong Genetic Variation [355]
PALB2 OT6DNDBG Strong Biomarker [97]
PANK2 OTFBW889 Strong Biomarker [211]
PDIK1L OTISF4KG Strong Genetic Variation [90]
PHF6 OT8DXI40 Strong Genetic Variation [356]
PIAS2 OTJLSC3V Strong Biomarker [225]
PIAS4 OTB7SVMZ Strong Altered Expression [357]
PIGN OTHHTJKX Strong Altered Expression [223]
PIP4K2A OTO9JO9U Strong Altered Expression [358]
POGLUT1 OTDX7GZD Strong Biomarker [359]
POLDIP2 OT8SZSJ6 Strong Biomarker [101]
POMP OTMPM1P5 Strong Biomarker [336]
PPP1R11 OTSHYPPW Strong Biomarker [360]
PRB1 OTV0SYMD Strong Biomarker [234]
PRC1 OTHD0XS0 Strong Biomarker [361]
PRIMA1 OT9ITT3P Strong Genetic Variation [362]
PRPF8 OTU39JZI Strong Biomarker [200]
PSMA7 OTPHI6ST Strong Biomarker [363]
PURB OTCDDKYB Strong Biomarker [364]
QRSL1 OTJDU2UG Strong Biomarker [365]
RAB40B OTCA9ZF5 Strong Genetic Variation [366]
RAD52 OT0OTDHI Strong Biomarker [367]
RAG1 OTV131E4 Strong Genetic Variation [368]
RALGAPB OTY8CGA3 Strong Biomarker [241]
RANBP2 OTFG5CVF Strong Biomarker [169]
RAP1B OTHEIIMM Strong Genetic Variation [369]
RARS1 OTHPZ6JN Strong Biomarker [370]
RBMY1A1 OTM2F25H Strong Biomarker [371]
RGPD2 OTMUZ0HX Strong Biomarker [243]
RIN2 OTCY73U9 Strong Biomarker [156]
RING1 OTCWTAX0 Strong Altered Expression [361]
RNF19A OTKWCV80 Strong Biomarker [101]
ROBO2 OTFJ9FQW Strong Genetic Variation [372]
RPA3 OT8JAQGL Strong Biomarker [373]
RPL22 OTVCN8K0 Strong Genetic Variation [134]
RPL27A OTQQHPL0 Strong Biomarker [374]
RRM2B OTE8GBUR Strong Altered Expression [375]
SAGE1 OT4H6FFA Strong Altered Expression [125]
SALL4 OTC08PR5 Strong Biomarker [376]
SAMD9 OTDG48P0 Strong Genetic Variation [377]
SAMD9L OTKEJUCI Strong Biomarker [378]
SBDS OTHDCCIB Strong Biomarker [97]
SEC61A1 OTLBE3CB Strong Biomarker [379]
SEPTIN2 OT3G33TM Strong Genetic Variation [380]
SEPTIN9 OT1VMRFQ Strong Biomarker [381]
SETBP1 OTKGCOSR Strong Genetic Variation [382]
SF3B2 OTNW2U4Y Strong Genetic Variation [383]
SFRP5 OTLCVVSH Strong Biomarker [384]
SFTPA1 OT87XL1U Strong Biomarker [385]
SGCE OT9F17JB Strong Genetic Variation [185]
SGCZ OTVGTEOD Strong Genetic Variation [386]
SIN3A OTM8OZWV Strong Genetic Variation [387]
SIPA1 OTXY5RXC Strong Biomarker [385]
SKI OT4KJ8F6 Strong Biomarker [388]
SLU7 OTZUUICN Strong Genetic Variation [389]
SLX4 OTF6236I Strong Biomarker [97]
SMAD5 OTQNSVCQ Strong Genetic Variation [390]
SMPD3 OTHQBETH Strong Biomarker [178]
SOX7 OTOZOFAG Strong Posttranslational Modification [391]
SP7 OT07ETZT Strong Altered Expression [392]
SPA17 OT8J7T7U Strong Altered Expression [262]
SRL OT7IEBWZ Strong Biomarker [393]
SRP72 OTPV73W7 Strong Genetic Variation [240]
SRSF11 OTZSV6CZ Strong Biomarker [394]
STAG2 OTR6X1Q7 Strong Biomarker [155]
STUB1 OTSUYI9A Strong Biomarker [395]
STX11 OTHFRSFP Strong Genetic Variation [396]
SUB1 OTK71JYU Strong Posttranslational Modification [345]
TBC1D9 OTSSCTB5 Strong Genetic Variation [397]
TBCC OTBF0X8R Strong Biomarker [398]
TCIM OTARUXQF Strong Genetic Variation [399]
TFR2 OTMYCCEO Strong Altered Expression [400]
THY1 OTVONVTB Strong Biomarker [401]
TIA1 OTGPN3P8 Strong Altered Expression [402]
TIFAB OTBX12V9 Strong Biomarker [403]
TK2 OTS1V4XB Strong Altered Expression [404]
TNFRSF10C OTVHOL9B Strong Altered Expression [405]
TPPP2 OTI3WA6X Strong Biomarker [106]
TRIB3 OTG5OS7X Strong Biomarker [406]
TRIM33 OT0KS4J7 Strong Biomarker [407]
TSHZ2 OTZWBXXY Strong Genetic Variation [408]
TSPAN31 OT8WQ83R Strong Biomarker [350]
CHGB OT7SAQT2 Definitive Biomarker [409]
DAPK1 OTNCNUCO Definitive Altered Expression [125]
DERL3 OTRZRT6Q Definitive Genetic Variation [179]
FUT1 OTODG57A Definitive Altered Expression [165]
GATA1 OTX1R7O1 Definitive Biomarker [212]
GPX3 OT6PK94R Definitive Posttranslational Modification [410]
MXD1 OTS5CTHX Definitive Altered Expression [411]
NUMB OTMB586Q Definitive Biomarker [191]
PDIA3 OTHPQ0Q3 Definitive Biomarker [412]
PLCB4 OTPA0QHW Definitive Biomarker [412]
PMAIP1 OTXEE550 Definitive Biomarker [362]
PRDM16 OT0BGA27 Definitive Biomarker [413]
PRPF40B OTBPUXVD Definitive Biomarker [414]
PURA OT975ELW Definitive Genetic Variation [415]
RAP1GAP OTC31ONQ Definitive Biomarker [416]
SAA2 OTYAVJWG Definitive Biomarker [417]
SEMG1 OT6Z4BPQ Definitive Biomarker [409]
SF3A1 OTI733D7 Definitive Biomarker [414]
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⏷ Show the Full List of 303 DOT(s)

References

1 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
2 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6796).
3 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6802).
4 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6805).
5 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800031284)
6 ClinicalTrials.gov (NCT00109538) Study of Lonafarnib Versus Placebo in Subjects With Either Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML) (Study P02978AM3)(TERMINATED). U.S. National Institutes of Health.
7 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
8 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6974).
9 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 5711).
10 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800026615)
11 ClinicalTrials.gov (NCT02999854) Safety and Efficacy of ATIR101 as Adjunctive Treatment to Blood Stem Cell Transplantation From a Haploidentical Family Donor Compared to Post-transplant Cyclophosphamide in Patients With Blood Cancer (HATCY). U.S. National Institutes of Health.
12 J Clin Oncol 33, 2015 (suppl, abstr TPS7097).
13 ClinicalTrials.gov (NCT04313881) Magrolimab + Azacitidine Versus Azacitidine + Placebo in Untreated Participants With Myelodysplastic Syndrome (MDS) (ENHANCE). U.S. National Institutes of Health.
14 ClinicalTrials.gov (NCT04313881) Magrolimab + Azacitidine Versus Azacitidine + Placebo in Untreated Participants With Myelodysplastic Syndrome (MDS) (ENHANCE). U.S. National Institutes of Health.
15 ClinicalTrials.gov (NCT04266301) Study of Efficacy and Safety of MBG453 in Combination With Azacitidine in Subjects With Intermediate, High or Very High Risk Myelodysplastic Syndrome (MDS) as Per IPSS-R, or Chronic Myelomonocytic Leukemia-2 (CMML-2) (STIMULUS-MDS2). U.S. National Institutes of Health.
16 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 8365).
17 ClinicalTrials.gov (NCT01215188) A Study of Pneumococcal Conjugate Vaccine (V114) Compared to a Marketed Vaccine (V114-003 AM2). U.S. National Institutes of Health.
18 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
19 ClinicalTrials.gov (NCT03699475) Study of Haplo-HSCT + Rivogenlecleucel vs Haplo-HSCT + Post Transplant Cyclophosphamide in Patients With AML or MDS (THRIVE). U.S. National Institutes of Health.
20 Clinical pipeline report, company report or official report of Actinium Pharmaceuticals
21 ClinicalTrials.gov (NCT01124539) Study of AR-67 in Adult Patients With Recurrence of Glioblastoma Multiforme (GBM) or Gliosarcoma. U.S. National Institutes of Health.
22 ClinicalTrials.gov (NCT03824080) Evaluating the Efficacy and Safety of Bemcentinib in Patients With Myelodysplastic Syndromes. U.S. National Institutes of Health.
23 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800032443)
24 ClinicalTrials.gov (NCT01422486) Phase 2 Study of Telintra in Deletion 5q Myelodysplastic Syndrome. U.S. National Institutes of Health.
25 Targeting mRNA processing as an anticancer strategy. Nat Rev Drug Discov. 2020 Feb;19(2):112-129.
26 ClinicalTrials.gov (NCT02343133) Safety Study of HemaMax (rHuIL-12) to Treat Acute Radiation Syndrome. U.S. National Institutes of Health.
27 ClinicalTrials.gov (NCT04582539) To Assess the Safety and Tolerability of INCB000928 in Participants With Myelodysplastic Syndromes or Multiple Myeloma.. U.S. National Institutes of Health.
28 ClinicalTrials.gov (NCT04264806) A Study of Cusatuzumab in Combination With Azacitidine Compared With Azacitidine Alone in Patients With Higher-risk Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML) and Who Are Not Candidates for Hematopoietic Stem Cell Transplantation (HSCT). U.S. National Institutes of Health.
29 ClinicalTrials.gov (NCT04395092) Haplo-identical Natural Killer (NK) Cells to Prevent Post-Transplant Relapse in AML and MDS (NK-REALM). U.S. National Institutes of Health.
30 ClinicalTrials.gov (NCT00044226) A 20-Week Study of a New Treatment for Men With Benign Prostatic Hyperplasia (BPH).. U.S. National Institutes of Health.
31 ClinicalTrials.gov (NCT03059615) A Phase 2a, Open-Label, Two Stage Study of Nerofe or Nerofe With Doxorubicin in Subjects With AML or MDS. U.S. National Institutes of Health.
32 ClinicalTrials.gov (NCT01794663) Placebo-Controlled Study to Evaluate the Safety and Efficacy of OPN-305 in Preventing Delayed Renal Graft Function. U.S. National Institutes of Health.
33 ClinicalTrials.gov (NCT04217720) SNS-301 Monotherapy in High Risk MDS and CMML. U.S. National Institutes of Health.
34 ClinicalTrials.gov (NCT04417517) A Study of ALX148 With Azacitidine for Higher Risk Myelodysplastic Syndrome (ASPEN-02). U.S. National Institutes of Health.
35 ClinicalTrials.gov (NCT04079296) A Study Investigating the Safety, Tolerability and Efficacy of ASP7517 in Subjects With Relapsed/Refractory Acute Myeloid Leukemia (AML) and Relapsed/Refractory Higher Risk Myelodysplastic Syndrome (MDS). U.S. National Institutes of Health.
36 ClinicalTrials.gov (NCT03291444) CAR-T Cells Combined With Peptide Specific Dendritic Cell in Relapsed/Refractory Leukemia/MDS
37 ClinicalTrials.gov (NCT03214666) GTB-3550 (CD16/IL-15/CD33) Tri-Specific Killer Engager (TriKE) for High Risk Heme Malignancies. U.S. National Institutes of Health.
38 ClinicalTrials.gov (NCT04284228) Antigen-specific T Cell Therapy for AML or MDS Patients With Relapsed Disease After Allo-HCT. U.S. National Institutes of Health.
39 ClinicalTrials.gov (NCT03176277) A Study of ONO-7475 in Patients With Acute Leukemias. U.S. National Institutes of Health.
40 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 8359).
41 ClinicalTrials.gov (NCT03483324) Trial of AB-110 in Adults With Hematologic Malignancies Undergoing Cord Blood Transplantation. U.S. National Institutes of Health.
42 ClinicalTrials.gov (NCT03647800) Study of APVO436 in Patients With AML or MDS. U.S. National Institutes of Health.
43 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
44 ClinicalTrials.gov (NCT04771130) A Study of BGB-11417 in Participants With Myeloid Malignancies. U.S. National Institutes of Health.
45 ClinicalTrials.gov (NCT04402541) Study of CB-5339 in Acute Myeloid Leukemia or Myelodysplastic Syndrome. U.S. National Institutes of Health.
46 ClinicalTrials.gov (NCT04156256) CD123-CD33 cCAR in Patients With Relapsed and/or Refractory, High Risk Hematologic Malignancies. U.S. National Institutes of Health.
47 ClinicalTrials.gov (NCT02203825) Safety Study of Chimeric Antigen Receptor Modified T-cells Targeting NKG2D-Ligands
48 ClinicalTrials.gov (NCT04167696) Study in Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome Patients to Determine the Recommended Dose of CYAD-02 (CYCLE-1). U.S. National Institutes of Health.
49 ClinicalTrials.gov (NCT03884829) A Phase I Study of CYC140, a PLK-1 Inhibitor, in Advanced Leukemias or MDS. U.S. National Institutes of Health.
50 ClinicalTrials.gov (NCT04511975) A Study Evaluating the Safety and Efficacy of IBI188 in Combination With AZA in Subjects With Newly Diagnosed MDS. U.S. National Institutes of Health.
51 ClinicalTrials.gov (NCT03573310) A Study of JNJ-64619178, an Inhibitor of PRMT5 in Participants With Advanced Solid Tumors, NHL, and Lower Risk MDS. U.S. National Institutes of Health.
52 ClinicalTrials.gov (NCT03915379) A Study of JNJ-67571244 in Participants With Relapsed or Refractory Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS). U.S. National Institutes of Health.
53 ClinicalTrials.gov (NCT04139434) Dose-escalation Study of Oral Administration of LP-108 in Patients With Relapsed or Refractory Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML), or Acute Myeloid Leukemia (AML). U.S. National Institutes of Health.
54 Targeting iron metabolism in drug discovery and delivery. Nat Rev Drug Discov. 2017 Jun;16(6):400-423.
55 ClinicalTrials.gov (NCT03612739) EPITHINK: Epigenetic Drug Treatment and Therapeutic Immunotherapy With NKR-2
56 ClinicalTrials.gov (NCT04623944) NKX101, Intravenous Allogeneic Engineered Natural Killer Cells, in Adults With AML or MDS. U.S. National Institutes of Health.
57 ClinicalTrials.gov (NCT03927261) A Phase 1/1b Safety Study of PRGN-3006 Adoptive Cellular Therapy in Patients With CD33-Positive Relapsed or Refractory Acute Myeloid Leukemia, Minimal Residual Disease Positive Acute Myeloid Leukemia, and Higher Risk Myelodysplastic Syndrome. U.S.National Institutes of Health.
58 ClinicalTrials.gov (NCT04227847) A Safety Study of SEA-CD70 in Patients With Myeloid Malignancies. U.S. National Institutes of Health.
59 ClinicalTrials.gov (NCT04021368) SEL120 in Patients With Acute Myeloid Leukemia or High-risk Myelodysplastic Syndrome. U.S. National Institutes of Health.
60 ClinicalTrials.gov (NCT04245397) SX-682 Treatment in Subjects With Myelodysplastic Syndrome Who Had Disease Progression or Are Intolerant to Prior Therapy. U.S. National Institutes of Health.
61 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800026289)
62 High methylation of the 4-aminobutyrate aminotransferase gene predicts a poor prognosis in patients with myelodysplastic syndrome.Int J Oncol. 2019 Feb;54(2):491-504. doi: 10.3892/ijo.2018.4652. Epub 2018 Dec 4.
63 Reduced expression of FLIP SHORT in bone marrow of low risk myelodysplastic syndrome.Leuk Res. 2007 Jun;31(6):853-7. doi: 10.1016/j.leukres.2006.11.017. Epub 2007 Jan 31.
64 Unravelling the relevance of CLEC12A as a cancer stem cell marker in myelodysplastic syndrome.Br J Haematol. 2016 Nov;175(3):393-401. doi: 10.1111/bjh.14270. Epub 2016 Sep 9.
65 Comparative analysis of G-CSFR and GM-CSFR expressions on CD34+ cells in patients with aplastic anemia and myelodysplastic syndrome.Int J Lab Hematol. 2009 Dec;31(6):597-602. doi: 10.1111/j.1751-553X.2008.01083.x. Epub 2008 Jul 14.
66 NY-ESO-1 Vaccination in Combination with Decitabine Induces Antigen-Specific T-lymphocyte Responses in Patients with Myelodysplastic Syndrome.Clin Cancer Res. 2018 Mar 1;24(5):1019-1029. doi: 10.1158/1078-0432.CCR-17-1792. Epub 2017 Sep 25.
67 High expression of the human equilibrative nucleoside transporter 1 gene predicts a good response to decitabine in patients with myelodysplastic syndrome.J Transl Med. 2016 Mar 5;14:66. doi: 10.1186/s12967-016-0817-9.
68 Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia.Blood. 2006 Oct 1;108(7):2182-9. doi: 10.1182/blood-2006-01-010249. Epub 2006 Jun 27.
69 ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.Haematologica. 2008 Mar;93(3):467-8. doi: 10.3324/haematol.11988.
70 The Molecular Pathology of Myelodysplastic Syndrome.Pathobiology. 2019;86(1):24-29. doi: 10.1159/000488712. Epub 2018 May 23.
71 Increase of IRF-1 gene expression and impairment of T regulatory cells suppression activity on patients with myelodysplastic syndrome: A longitudinal one-year study.Leuk Res. 2017 Apr;55:6-17. doi: 10.1016/j.leukres.2017.01.008. Epub 2017 Jan 5.
72 Mutation analysis of therapy-related myeloid neoplasms.Cancer Genet. 2018 Apr;222-223:38-45. doi: 10.1016/j.cancergen.2018.02.006. Epub 2018 Mar 8.
73 Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.Blood Adv. 2019 Nov 26;3(22):3579-3589. doi: 10.1182/bloodadvances.2019000922.
74 PPM1D Mutations Drive Clonal Hematopoiesis in Response to Cytotoxic Chemotherapy.Cell Stem Cell. 2018 Nov 1;23(5):700-713.e6. doi: 10.1016/j.stem.2018.10.004.
75 Correlation between IL-7 genomic protein methylation level and acute myeloid leukemia.Eur Rev Med Pharmacol Sci. 2019 Feb;23(3):1196-1202. doi: 10.26355/eurrev_201902_17012.
76 Patient-derived antibody recognizes a unique CD43 epitope expressed on all AML and has antileukemia activity in mice.Blood Adv. 2017 Aug 18;1(19):1551-1564. doi: 10.1182/bloodadvances.2017008342. eCollection 2017 Aug 22.
77 Hippo kinase loss contributes to del(20q) hematologic malignancies through chronic innate immune activation.Blood. 2019 Nov 14;134(20):1730-1744. doi: 10.1182/blood.2019000170.
78 High expression of the receptor tyrosine kinase Tie-1 in acute myeloid leukemia and myelodysplastic syndrome.Leuk Lymphoma. 2001 Jul;42(3):511-6. doi: 10.3109/10428190109064609.
79 Internal tandem duplication of the FLT3 gene is preferentially seen in acute myeloid leukemia and myelodysplastic syndrome among various hematological malignancies. A study on a large series of patients and cell lines.Leukemia. 1997 Oct;11(10):1605-9. doi: 10.1038/sj.leu.2400812.
80 Crbn (I391V) is sufficient to confer in vivo sensitivity to thalidomide and its derivatives in mice.Blood. 2018 Oct 4;132(14):1535-1544. doi: 10.1182/blood-2018-05-852798. Epub 2018 Jul 31.
81 Case of late-onset erythropoietic protoporphyria with myelodysplastic syndrome who has homozygous IVS3-48C polymorphism in the ferrochelatase gene.J Dermatol. 2017 Jun;44(6):651-655. doi: 10.1111/1346-8138.13709. Epub 2016 Dec 27.
82 Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.Blood. 2004 Feb 15;103(4):1518-20. doi: 10.1182/blood-2003-09-3222. Epub 2003 Oct 23.
83 CD123 CAR T cells for the treatment of myelodysplastic syndrome.Exp Hematol. 2019 Jun;74:52-63.e3. doi: 10.1016/j.exphem.2019.05.002. Epub 2019 May 25.
84 Overexpression of WT1 and PRAME predicts poor outcomes of patients with myelodysplastic syndromes with thrombocytopenia.Blood Adv. 2019 Nov 12;3(21):3406-3418. doi: 10.1182/bloodadvances.2019000564.
85 Plasmacytoid dendritic cell proliferations and neoplasms involving the bone marrow : Summary of the workshop cases submitted to the 18th Meeting of the European Association for Haematopathology (EAHP) organized by the European Bone Marrow Working Group, Basel 2016.Ann Hematol. 2017 May;96(5):765-777. doi: 10.1007/s00277-017-2947-4. Epub 2017 Feb 12.
86 Aberrant methylation in pediatric myelodysplastic syndrome.Leuk Res. 2007 Feb;31(2):175-81. doi: 10.1016/j.leukres.2006.06.013. Epub 2006 Aug 4.
87 Progress in elucidation of molecular pathophysiology of myeloproliferative neoplasms and its application to therapeutic decisions.Int J Hematol. 2020 Feb;111(2):182-191. doi: 10.1007/s12185-019-02778-9. Epub 2019 Nov 18.
88 Immunophenotypic analysis of erythroid dysplasia in myelodysplastic syndromes. A report from the IMDSFlow working group.Haematologica. 2017 Feb;102(2):308-319. doi: 10.3324/haematol.2016.147835. Epub 2016 Oct 6.
89 Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure.Br J Haematol. 2009 Oct;147(1):102-12. doi: 10.1111/j.1365-2141.2009.07822.x. Epub 2009 Jul 28.
90 Tumor-derived CK1 mutations enhance MDMX inhibition of p53.Oncogene. 2020 Jan;39(1):176-186. doi: 10.1038/s41388-019-0979-z. Epub 2019 Aug 28.
91 RINF (CXXC5) is overexpressed in solid tumors and is an unfavorable prognostic factor in breast cancer.Ann Oncol. 2011 Oct;22(10):2208-15. doi: 10.1093/annonc/mdq737. Epub 2011 Feb 16.
92 DICER1 gene and miRNA dysregulation in mesenchymal stem cells of patients with myelodysplastic syndrome and acute myeloblastic leukemia.Leuk Res. 2017 Dec;63:62-71. doi: 10.1016/j.leukres.2017.10.006. Epub 2017 Oct 31.
93 Effects of arsenic disulfide on apoptosis, histone acetylation, toll like receptor 2 activation, and erythropoiesis in bone marrow mononuclear cells of myelodysplastic syndromes patients in vitro. Leuk Res. 2017 Nov;62:4-11. doi: 10.1016/j.leukres.2017.09.010. Epub 2017 Sep 19.
94 Genetic Variant Screening of DNA Repair Genes in Myelodysplastic Syndrome Identifies a Novel Mutation in the XRCC2 Gene.Oncol Res Treat. 2019;42(5):263-268. doi: 10.1159/000497209. Epub 2019 Mar 12.
95 Reduced PLCG1 expression is associated with inferior survival for myelodysplastic syndromes.Cancer Med. 2020 Jan;9(2):460-468. doi: 10.1002/cam4.2717. Epub 2019 Nov 21.
96 Yttrium-90-labeled anti-CD45 antibody followed by a reduced-intensity hematopoietic cell transplantation for patients with relapsed/refractory leukemia or myelodysplasia.Haematologica. 2020 Jun;105(6):1731-1737. doi: 10.3324/haematol.2019.229492. Epub 2019 Oct 3.
97 Germline Genetic Predisposition to Hematologic Malignancy.J Clin Oncol. 2017 Mar 20;35(9):1018-1028. doi: 10.1200/JCO.2016.70.8644. Epub 2017 Feb 13.
98 Gene expression profiling in myelodysplastic syndrome after SPARC overexpression associated with Ara-C.Oncol Rep. 2015 Oct;34(4):2072-82. doi: 10.3892/or.2015.4139. Epub 2015 Jul 20.
99 Activating CBL mutations are associated with a distinct MDS/MPN phenotype.Ann Hematol. 2012 Nov;91(11):1713-20. doi: 10.1007/s00277-012-1521-3. Epub 2012 Aug 10.
100 Transforming growth factor (TGF)- pathway as a therapeutic target in lower risk myelodysplastic syndromes.Leukemia. 2019 Jun;33(6):1303-1312. doi: 10.1038/s41375-019-0448-2. Epub 2019 Apr 8.
101 Iron overload may promote alteration of NK cells and hematopoietic stem/progenitor cells by JNK and P38 pathway in myelodysplastic syndromes.Int J Hematol. 2017 Aug;106(2):248-257. doi: 10.1007/s12185-017-2237-x. Epub 2017 Apr 12.
102 Expression of IAP family proteins in myelodysplastic syndromes transforming to overt leukemia.Leuk Res. 2004 Nov;28(11):1203-11. doi: 10.1016/j.leukres.2004.03.020.
103 A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.Genes Chromosomes Cancer. 2002 Sep;35(1):11-9. doi: 10.1002/gcc.10090.
104 Enhanced myeloid specificity of CD117 compared with CD13 and CD33.Leuk Res. 1999 Apr;23(4):341-7. doi: 10.1016/s0145-2126(98)00185-4.
105 Rapamycin and bafilomycin A1 alter autophagy and megakaryopoiesis.Platelets. 2017 Jan;28(1):82-89. doi: 10.1080/09537104.2016.1204436. Epub 2016 Aug 18.
106 Hematopathological alterations of major tumor suppressor cascade, vital cell cycle inhibitors and hematopoietic niche components in experimental myelodysplasia.Chem Biol Interact. 2017 Aug 1;273:1-10. doi: 10.1016/j.cbi.2017.05.014. Epub 2017 May 23.
107 Prognostic importance of Aurora Kinases and mitotic spindle genes transcript levels in Myelodysplastic syndrome.Leuk Res. 2018 Jan;64:61-70. doi: 10.1016/j.leukres.2017.11.013. Epub 2017 Nov 28.
108 Mapping of the human Zn-alpha 2-glycoprotein gene (AZGP1) to chromosome 7q22 by in situ hybridization.Cytogenet Cell Genet. 1994;66(4):263-6. doi: 10.1159/000133708.
109 BMI1 reprogrammes histone acetylation and enhances c-fos pathway via directly binding to Zmym3 in malignant myeloid progression. J Cell Mol Med. 2014 Jun;18(6):1004-17. doi: 10.1111/jcmm.12246. Epub 2014 Feb 27.
110 Repeated sequences in CASPASE-5 and FANCD2 but not NF1 are targets for mutation in microsatellite-unstable acute leukemia/myelodysplastic syndrome.Mol Cancer Res. 2005 May;3(5):251-60. doi: 10.1158/1541-7786.MCR-04-0182.
111 UBASH3B/Sts-1-CBL axis regulates myeloid proliferation in human preleukemia induced by AML1-ETO.Leukemia. 2016 Mar;30(3):728-39. doi: 10.1038/leu.2015.275. Epub 2015 Oct 9.
112 Aberrant overexpression of CD14 on granulocytes sensitizes the innate immune response in mDia1 heterozygous del(5q) MDS.Blood. 2014 Jul 31;124(5):780-90. doi: 10.1182/blood-2014-01-552463. Epub 2014 Jun 2.
113 Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8.Ann Hematol. 1997 Jan;74(1):37-40. doi: 10.1007/s002770050253.
114 S100A9-induced overexpression of PD-1/PD-L1 contributes to ineffective hematopoiesis in myelodysplastic syndromes.Leukemia. 2019 Aug;33(8):2034-2046. doi: 10.1038/s41375-019-0397-9. Epub 2019 Feb 8.
115 Management of myelodysplastic syndromes after failure of response to hypomethylating agents.Ther Adv Hematol. 2019 May 9;10:2040620719847059. doi: 10.1177/2040620719847059. eCollection 2019.
116 SF3B1 mutant MDS-initiating cells may arise from the haematopoietic stem cell compartment.Nat Commun. 2015 Dec 8;6:10004. doi: 10.1038/ncomms10004.
117 Identification of campath-1 (CD52) as novel drug target in neoplastic stem cells in 5q-patients with MDS and AML.Clin Cancer Res. 2014 Jul 1;20(13):3589-602. doi: 10.1158/1078-0432.CCR-13-2811. Epub 2014 May 5.
118 Activin A contributes to the definition of a pro-oncogenic bone marrow microenvironment in t(12;21) preleukemia.Exp Hematol. 2019 May;73:7-12.e4. doi: 10.1016/j.exphem.2019.02.006. Epub 2019 Feb 28.
119 Erythropoietin administration is associated with improved T-cell properties in patients with myelodysplastic syndromes.Leuk Res. 2017 Jan;52:20-27. doi: 10.1016/j.leukres.2016.11.002. Epub 2016 Nov 2.
120 An oral fixed-dose combination of decitabine and cedazuridine in myelodysplastic syndromes: a multicentre, open-label, dose-escalation, phase 1 study.Lancet Haematol. 2019 Apr;6(4):e194-e203. doi: 10.1016/S2352-3026(19)30030-4.
121 Proteins of the mitotic checkpoint and spindle are related to chromosomal instability and unfavourable prognosis in patients with myelodysplastic syndrome.J Clin Pathol. 2015 May;68(5):381-7. doi: 10.1136/jclinpath-2014-202728. Epub 2015 Jan 30.
122 A critical role for phosphatase haplodeficiency in the selective suppression of deletion 5q MDS by lenalidomide.Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12974-9. doi: 10.1073/pnas.0811267106. Epub 2009 May 26.
123 Expression of CDKN1C in the bone marrow of patients with myelodysplastic syndrome and secondary acute myeloid leukemia is associated with poor survival after conventional chemotherapy.Int J Cancer. 2016 Sep 15;139(6):1402-13. doi: 10.1002/ijc.30181. Epub 2016 Jun 3.
124 Muscarinic acetylcholine receptor regulates self-renewal of early erythroid progenitors.Sci Transl Med. 2019 Sep 25;11(511):eaaw3781. doi: 10.1126/scitranslmed.aaw3781.
125 Despite differential gene expression profiles pediatric MDS derived mesenchymal stromal cells display functionality in vitro.Stem Cell Res. 2015 Mar;14(2):198-210. doi: 10.1016/j.scr.2015.01.006. Epub 2015 Jan 28.
126 Identification of a novel fusion gene MLL-MAML2 in secondary acute myelogenous leukemia and myelodysplastic syndrome with inv(11)(q21q23).Genes Chromosomes Cancer. 2007 Sep;46(9):813-9. doi: 10.1002/gcc.20467.
127 Expression and genomic configuration of GM-CSF, IL-3, M-CSF receptor (C-FMS), early growth response gene-1 (EGR-1) and M-CSF genes in primary myelodysplastic syndromes.Leuk Lymphoma. 1994 Sep;15(1-2):135-41. doi: 10.3109/10428199409051688.
128 Identification of myelodysplastic syndrome-specific genes by DNA microarray analysis with purified hematopoietic stem cell fraction.Blood. 2001 Jul 15;98(2):422-7. doi: 10.1182/blood.v98.2.422.
129 Clinicopathologic and molecular characterization of myeloid neoplasms with isolated t(6;9)(p23;q34).Int J Lab Hematol. 2017 Aug;39(4):409-417. doi: 10.1111/ijlh.12641. Epub 2017 Mar 20.
130 Relationship between Altered miRNA Expression and DNA Methylation of the DLK1-DIO3 Region in Azacitidine-Treated Patients with Myelodysplastic Syndromes and Acute Myeloid Leukemia with Myelodysplasia-Related Changes.Cells. 2018 Sep 14;7(9):138. doi: 10.3390/cells7090138.
131 Identification of microRNA-regulated pathways using an integration of microRNA-mRNA microarray and bioinformatics analysis in CD34+ cells of myelodysplastic syndromes.Sci Rep. 2016 Aug 30;6:32232. doi: 10.1038/srep32232.
132 Expression analysis of mir-17-5p, mir-20a and let-7a microRNAs and their target proteins in CD34+ bone marrow cells of patients with myelodysplastic syndromes.Leuk Res. 2013 Mar;37(3):251-8. doi: 10.1016/j.leukres.2012.11.011. Epub 2012 Dec 14.
133 Distinct and convergent consequences of splice factor mutations in myelodysplastic syndromes.Am J Hematol. 2020 Feb;95(2):133-143. doi: 10.1002/ajh.25673. Epub 2019 Nov 18.
134 Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations.Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):4004-8. doi: 10.1073/pnas.91.9.4004.
135 Erythropoietin receptor in myelodysplastic syndrome and leukemia.Leuk Lymphoma. 2002 Feb;43(2):261-4. doi: 10.1080/10428190290006026.
136 161533 TriKE stimulates NK-cell function to overcome myeloid-derived suppressor cells in MDS.Blood Adv. 2018 Jun 26;2(12):1459-1469. doi: 10.1182/bloodadvances.2017012369.
137 Clinical implications of immunophenotypic abnormalities of bone marrow myeloid cell compartment in myelodysplastic syndromes.J BUON. 2010 Oct-Dec;15(4):746-52.
138 Endoplasmic reticulum protein GliPR1 regulates G protein signaling and the cell cycle and is overexpressed in AML.Oncol Rep. 2013 Nov;30(5):2254-62. doi: 10.3892/or.2013.2716. Epub 2013 Sep 4.
139 Platelet glycoprotein expression in patients with myelodysplastic syndrome.Thromb Res. 2000 Oct 1;100(1):27-34. doi: 10.1016/s0049-3848(00)00302-9.
140 Meeting report: myelodysplastic syndromes at ASH 2007.Leukemia. 2008 May;22(5):893-7. doi: 10.1038/leu.2008.45. Epub 2008 Mar 6.
141 GSK3 Deficiencies in Hematopoietic Stem Cells Initiate Pre-neoplastic State that Is Predictive of Clinical Outcomes of Human Acute Leukemia.Cancer Cell. 2016 Jan 11;29(1):61-74. doi: 10.1016/j.ccell.2015.11.012.
142 CD8(+) T cells exhaustion induced by myeloid-derived suppressor cells in myelodysplastic syndromes patients might be through TIM3/Gal-9 pathway.J Cell Mol Med. 2020 Jan;24(1):1046-1058. doi: 10.1111/jcmm.14825. Epub 2019 Nov 22.
143 Hematopoietic cell kinase (HCK) is a potential therapeutic target for dysplastic and leukemic cells due to integration of erythropoietin/PI3K pathway and regulation of erythropoiesis: HCK in erythropoietin/PI3K pathway.Biochim Biophys Acta Mol Basis Dis. 2017 Feb;1863(2):450-461. doi: 10.1016/j.bbadis.2016.11.013. Epub 2016 Nov 11.
144 Cloning and characterization of human histone deacetylase 8.FEBS Lett. 2000 Jul 28;478(1-2):77-83. doi: 10.1016/s0014-5793(00)01813-5.
145 Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 in myeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocation t(7;11)(p15;p15).Blood. 2002 Feb 15;99(4):1428-33. doi: 10.1182/blood.v99.4.1428.
146 Knockdown of HSPA9 induces TP53-dependent apoptosis in human hematopoietic progenitor cells.PLoS One. 2017 Feb 8;12(2):e0170470. doi: 10.1371/journal.pone.0170470. eCollection 2017.
147 Serotonin receptor type 1B constitutes a therapeutic target for MDS and CMML.Sci Rep. 2018 Sep 17;8(1):13883. doi: 10.1038/s41598-018-32306-4.
148 Loss of SHIP-1 protein expression in high-risk myelodysplastic syndromes is associated with miR-210 and miR-155.Oncogene. 2012 Sep 13;31(37):4085-94. doi: 10.1038/onc.2011.579. Epub 2012 Jan 16.
149 U2AF1 mutations induce oncogenic IRAK4 isoforms and activate innate immune pathways in myeloid malignancies.Nat Cell Biol. 2019 May;21(5):640-650. doi: 10.1038/s41556-019-0314-5. Epub 2019 Apr 22.
150 Vitamin K antagonism impairs the bone marrow microenvironment and hematopoiesis.Blood. 2019 Jul 18;134(3):227-238. doi: 10.1182/blood.2018874214. Epub 2019 Apr 19.
151 KDM6B overexpression activates innate immune signaling and impairs hematopoiesis in mice.Blood Adv. 2018 Oct 9;2(19):2491-2504. doi: 10.1182/bloodadvances.2018024166.
152 Abnormal populations and functions of natural killer cells in patients with myelodysplastic syndromes.Oncol Lett. 2018 Apr;15(4):5497-5504. doi: 10.3892/ol.2018.8062. Epub 2018 Feb 15.
153 Anti-CD117 antibody depletes normal and myelodysplastic syndrome human hematopoietic stem cells in xenografted mice.Blood. 2019 May 9;133(19):2069-2078. doi: 10.1182/blood-2018-06-858159. Epub 2019 Feb 11.
154 Insufficient stromal support in MDS results from molecular and functional deficits of mesenchymal stromal cells.Leukemia. 2013 Sep;27(9):1841-51. doi: 10.1038/leu.2013.193. Epub 2013 Mar 29.
155 Dynamics of clonal evolution in myelodysplastic syndromes.Nat Genet. 2017 Feb;49(2):204-212. doi: 10.1038/ng.3742. Epub 2016 Dec 19.
156 Alteration of c-mpl-mediated signal transduction in CD34(+) cells from patients with myelodysplastic syndromes.Exp Hematol. 2000 Oct;28(10):1158-63. doi: 10.1016/s0301-472x(00)00527-0.
157 Recent advances in the pathogenesis and treatment of juvenile myelomonocytic leukaemia.Br J Haematol. 2011 Mar;152(6):677-87. doi: 10.1111/j.1365-2141.2010.08525.x.
158 Prognostic Significance of Platelet Recovery in Myelodysplastic Syndromes With Severe Thrombocytopenia.Clin Appl Thromb Hemost. 2018 Dec;24(9_suppl):217S-222S. doi: 10.1177/1076029618802363. Epub 2018 Oct 8.
159 Multicentric study underlining the interest of adding CD5, CD7 and CD56 expression assessment to the flow cytometric Ogata score in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms.Haematologica. 2015 Apr;100(4):472-8. doi: 10.3324/haematol.2014.112755. Epub 2015 Jan 30.
160 Assessment of Drug Sensitivity in Hematopoietic Stem and Progenitor Cells from Acute Myelogenous Leukemia and Myelodysplastic Syndrome Ex Vivo.Stem Cells Transl Med. 2017 Mar;6(3):840-850. doi: 10.5966/sctm.2016-0034. Epub 2016 Nov 7.
161 RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia.Nat Commun. 2018 Mar 21;9(1):1163. doi: 10.1038/s41467-018-03513-4.
162 Hypermethylation of SHP-1 promoter in patient with high-risk myelodysplastic syndrome and it predicts poor prognosis.Med Oncol. 2012 Dec;29(4):2359-63. doi: 10.1007/s12032-012-0163-6. Epub 2012 Jan 19.
163 Acute Myeloid Leukemia With Myelodysplasia-Related Changes.Am J Clin Pathol. 2015 Jul;144(1):29-43. doi: 10.1309/AJCP58RSMFRHLHHH.
164 Myeloid maturation potentiates STAT3-mediated atypical IFN- signaling and upregulation of PD-1 ligands in AML and MDS.Sci Rep. 2019 Aug 12;9(1):11697. doi: 10.1038/s41598-019-48256-4.
165 High expression of PIM2 induces HSC proliferation in myelodysplastic syndromes via the IDH1/HIF1- signaling pathway.Oncol Lett. 2019 Jun;17(6):5395-5402. doi: 10.3892/ol.2019.10256. Epub 2019 Apr 16.
166 Polo-like kinase 2 (SNK/PLK2) is a novel epigenetically regulated gene in acute myeloid leukemia and myelodysplastic syndromes: genetic and epigenetic interactions.Ann Hematol. 2011 Sep;90(9):1037-45. doi: 10.1007/s00277-011-1193-4. Epub 2011 Feb 22.
167 The deregulated promoter methylation of the Polo-like kinases as a potential biomarker in hematological malignancies.Leuk Lymphoma. 2015 Jul;56(7):2123-33. doi: 10.3109/10428194.2014.971407. Epub 2015 Jan 24.
168 Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing.Genes Chromosomes Cancer. 2013 Dec;52(12):1167-77. doi: 10.1002/gcc.22112. Epub 2013 Oct 7.
169 Chromosome abnormalities in bone marrow of Fanconi anemia patients.Cancer Genet Cytogenet. 1993 Jan;65(1):47-50. doi: 10.1016/0165-4608(93)90057-s.
170 Immunoglobulin and T-cell receptor delta gene rearrangements are rarely found in myelodysplastic syndromes in chronic phase.Leuk Res. 1994 May;18(5):365-71. doi: 10.1016/0145-2126(94)90020-5.
171 Spontaneous down-regulation of Fas-associated phosphatase-1 may contribute to excessive apoptosis in myelodysplastic marrows.Int J Hematol. 1999 Aug;70(2):83-90.
172 Loss of Function of DOCK4 in Myelodysplastic Syndromes Stem Cells is Restored by Inhibitors of DOCK4 Signaling Networks.Clin Cancer Res. 2019 Sep 15;25(18):5638-5649. doi: 10.1158/1078-0432.CCR-19-0924. Epub 2019 Jul 15.
173 RUNX1 mutation in a patient with myelodysplastic syndrome and decreased erythrocyte expression of blood group A antigen.Transfusion. 2020 Jan;60(1):184-196. doi: 10.1111/trf.15628. Epub 2019 Dec 16.
174 Circulating S100A8 and S100A9 protein levels in plasma of patients with acquired aplastic anemia and myelodysplastic syndromes.Cytokine. 2019 Jan;113:462-465. doi: 10.1016/j.cyto.2018.06.025. Epub 2018 Jun 27.
175 Combination Lenalidomide and Azacitidine: A Novel Salvage Therapy in Patients Who Relapse After Allogeneic Stem-Cell Transplantation for Acute Myeloid Leukemia.J Clin Oncol. 2019 Mar 1;37(7):580-588. doi: 10.1200/JCO.18.00889. Epub 2019 Jan 17.
176 Genetic alterations in 47 patients with a novel myelodysplastic syndrome diagnosis at a single center.Oncol Lett. 2019 Nov;18(5):5077-5084. doi: 10.3892/ol.2019.10853. Epub 2019 Sep 12.
177 SPAG6 silencing induces apoptosis in the myelodysplastic syndrome cell line SKM? via the PTEN/PI3K/AKT signaling pathway in vitro and in vivo.Int J Oncol. 2018 Jul;53(1):297-306. doi: 10.3892/ijo.2018.4390. Epub 2018 May 2.
178 Implications of sphingosine kinase 1 expression level for the cellular sphingolipid rheostat: relevance as a marker for daunorubicin sensitivity of leukemia cells.Int J Hematol. 2008 Apr;87(3):266-75. doi: 10.1007/s12185-008-0052-0. Epub 2008 Feb 20.
179 der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.Cancer Genet Cytogenet. 1991 Jul 1;54(1):129-31. doi: 10.1016/0165-4608(91)90041-r.
180 Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients.Am J Clin Pathol. 1996 Nov;106(5):680-8. doi: 10.1093/ajcp/106.5.680.
181 Molecular cloning and analysis of the human Tec protein-tyrosine kinase.Leukemia. 1994 Oct;8(10):1663-72.
182 Naive T-cells in myelodysplastic syndrome display intrinsic human telomerase reverse transcriptase (hTERT) deficiency.Leukemia. 2013 Apr;27(4):897-906. doi: 10.1038/leu.2012.300. Epub 2012 Oct 17.
183 Uncoupling of CD71 shedding with mitochondrial clearance in reticulocytes in a subset of myelodysplastic syndromes.Leukemia. 2019 Jan;33(1):217-229. doi: 10.1038/s41375-018-0204-z. Epub 2018 Jul 26.
184 Toll-like receptor alterations in myelodysplastic syndrome.Leukemia. 2013 Sep;27(9):1832-40. doi: 10.1038/leu.2013.180. Epub 2013 Jun 14.
185 Deep brain stimulation for myoclonus-dystonia syndrome with double mutations in DYT1 and DYT11.Sci Rep. 2017 Jan 19;7:41042. doi: 10.1038/srep41042.
186 Thrombocytopenia in MDS: epidemiology, mechanisms, clinical consequences and novel therapeutic strategies.Leukemia. 2016 Mar;30(3):536-44. doi: 10.1038/leu.2015.297. Epub 2015 Oct 26.
187 Wiskott-Aldrich syndrome gene mutations modulate cancer susceptibility in the p53() murine model.Oncoimmunology. 2018 Jul 30;7(9):e1468954. doi: 10.1080/2162402X.2018.1468954. eCollection 2018.
188 3q26/EVI1 rearrangement in myelodysplastic/myeloproliferative neoplasms: An early event associated with a poor prognosis.Leuk Res. 2018 Feb;65:25-28. doi: 10.1016/j.leukres.2017.12.004. Epub 2017 Dec 23.
189 Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia.Front Immunol. 2019 Feb 28;10:116. doi: 10.3389/fimmu.2019.00116. eCollection 2019.
190 Functional impairment of the HIPK2 small ubiquitin-like modifier (SUMO)-interacting motif in acute myeloid leukemia.Am J Cancer Res. 2019 Jan 1;9(1):94-107. eCollection 2019.
191 Distinct expression profiles of MSI2 and NUMB genes in myelodysplastic syndromes and acute myeloid leukemia patients.Leuk Res. 2012 Oct;36(10):1300-3. doi: 10.1016/j.leukres.2012.06.010. Epub 2012 Jul 9.
192 A novel monoclonal antibody, KOR-SA3544 which reacts to Philadelphia chromosome-positive acute lymphoblastic leukemia cells with high sensitivity.Leukemia. 1995 Jul;9(7):1233-9.
193 Aberrant methylation of the M-type phospholipase A(2) receptor gene in leukemic cells.BMC Cancer. 2012 Dec 5;12:576. doi: 10.1186/1471-2407-12-576.
194 Distinct iron architecture in SF3B1-mutant myelodysplastic syndrome patients is linked to an SLC25A37 splice variant with a retained intron.Leukemia. 2015 Jan;29(1):188-95. doi: 10.1038/leu.2014.170. Epub 2014 May 23.
195 Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1-mutant myelodysplastic syndromes.Leukemia. 2016 Dec;30(12):2322-2331. doi: 10.1038/leu.2016.149. Epub 2016 May 23.
196 Downregulation of carnitine acyltransferases and organic cation transporter OCTN2 in mononuclear cells in healthy elderly and patients with myelodysplastic syndromes.J Mol Med (Berl). 2003 Jul;81(7):435-42. doi: 10.1007/s00109-003-0447-6. Epub 2003 Jun 12.
197 Spectrum of complex chromosomal aberrations in a myelodysplastic syndrome and a brief review.J Cancer Res Ther. 2016 Jul-Sep;12(3):1203-1206. doi: 10.4103/0973-1482.197563.
198 Applying a Weight-of-Evidence Approach to Evaluate Relevance of Molecular Landscapes in the Exposure-Disease Paradigm.Biomed Res Int. 2015;2015:515798. doi: 10.1155/2015/515798. Epub 2015 Aug 3.
199 Genetic analysis and clinical picture of severe congenital neutropenia in Israel.Pediatr Blood Cancer. 2015 Jan;62(1):103-8. doi: 10.1002/pbc.25251. Epub 2014 Oct 4.
200 Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells.Leukemia. 2015 May;29(5):1092-103. doi: 10.1038/leu.2014.331. Epub 2014 Nov 27.
201 Methylation and expression of mismatch repair gene human mutS homolog 2 in myelodysplastic syndromes.Exp Ther Med. 2018 Jan;15(1):500-505. doi: 10.3892/etm.2017.5402. Epub 2017 Oct 30.
202 Treatment-related myelodysplastic syndrome in a child with acute myeloid leukemia and TPMT heterozygosity.J Pediatr Hematol Oncol. 2015 May;37(4):e242-4. doi: 10.1097/MPH.0000000000000211.
203 Expression of nucleoside-metabolizing enzymes in myelodysplastic syndromes and modulation of response to azacitidine.Leukemia. 2014 Mar;28(3):621-8. doi: 10.1038/leu.2013.330. Epub 2013 Nov 6.
204 Fusion of TEL/ETV6 to a novel ACS2 in myelodysplastic syndrome and acute myelogenous leukemia with t(5;12)(q31;p13).Genes Chromosomes Cancer. 1999 Nov;26(3):192-202. doi: 10.1002/(sici)1098-2264(199911)26:3<192::aid-gcc2>3.0.co;2-e.
205 Semi-quantitative study of calcitonin gene methylation in myelodysplastic syndrome.Chin Med J (Engl). 1998 Aug;111(8):690-3.
206 A diagnosis of discernment: Identifying a novel ATRX mutation in myelodysplastic syndrome with acquired -thalassemia.Cancer Genet. 2019 Feb;231-232:36-40. doi: 10.1016/j.cancergen.2019.01.002. Epub 2019 Jan 9.
207 Mutations within the FLR exon of NF1 are rare in myelodysplastic syndromes and acute myelocytic leukemias.Leukemia. 1993 Jul;7(7):1058-60.
208 Clonal evolution with inv(11)(p15q22) and NUP98/DDX10 fusion gene in imatinib-resistant chronic myelogenous leukemia.Cancer Genet Cytogenet. 2005 Mar;157(2):104-8. doi: 10.1016/j.cancergencyto.2004.06.014.
209 DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high-risk disease.Am J Hematol. 2019 Jul;94(7):757-766. doi: 10.1002/ajh.25486. Epub 2019 May 7.
210 Inhibition of NEMO, the regulatory subunit of the IKK complex, induces apoptosis in high-risk myelodysplastic syndrome and acute myeloid leukemia.Oncogene. 2007 Apr 5;26(16):2299-307. doi: 10.1038/sj.onc.1210043. Epub 2006 Oct 16.
211 Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.Genet Test Mol Biomarkers. 2010 Dec;14(6):793-6. doi: 10.1089/gtmb.2010.0076. Epub 2010 Oct 12.
212 LSD1-mediated repression of GFI1 super-enhancer plays an essential role in erythroleukemia.Leukemia. 2020 Mar;34(3):746-758. doi: 10.1038/s41375-019-0614-6. Epub 2019 Nov 1.
213 In vivo effects of decitabine in myelodysplasia and acute myeloid leukemia: review of cytogenetic and molecular studies.Ann Hematol. 2005 Dec;84 Suppl 1:32-8. doi: 10.1007/s00277-005-0004-1.
214 Functional distance between recipient and donor HLA-DPB1 determines nonpermissive mismatches in unrelated HCT.Blood. 2016 Jul 7;128(1):120-9. doi: 10.1182/blood-2015-12-686238. Epub 2016 May 9.
215 Isocitrate dehydrogenase 2 mutations correlate with leukemic transformation and are predicted by 2-hydroxyglutarate in myelodysplastic syndromes.J Cancer Res Clin Oncol. 2018 Jun;144(6):1037-1047. doi: 10.1007/s00432-018-2627-3. Epub 2018 Mar 16.
216 Abnormal CD25 expression on hematopoietic cells in myelodysplastic syndromes.Leuk Res. 2018 Apr;67:12-16. doi: 10.1016/j.leukres.2017.11.010. Epub 2017 Dec 15.
217 JARID2 Functions as a Tumor Suppressor in Myeloid Neoplasms by Repressing Self-Renewal in Hematopoietic Progenitor Cells.Cancer Cell. 2018 Nov 12;34(5):741-756.e8. doi: 10.1016/j.ccell.2018.10.008.
218 Can synthetic lethality approach be used with DNA repair genes for primary and secondary MDS?.Med Oncol. 2019 Oct 30;36(12):99. doi: 10.1007/s12032-019-1324-7.
219 Elevated AF1q expression is a poor prognostic marker for adult acute myeloid leukemia patients with normal cytogenetics.Am J Hematol. 2009 May;84(5):308-9. doi: 10.1002/ajh.21396.
220 Myeloid neoplasms with eosinophilia.Blood. 2017 Feb 9;129(6):704-714. doi: 10.1182/blood-2016-10-695973. Epub 2016 Dec 27.
221 RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia.PLoS One. 2018 Apr 19;13(4):e0196181. doi: 10.1371/journal.pone.0196181. eCollection 2018.
222 RIL, a LIM gene on 5q31, is silenced by methylation in cancer and sensitizes cancer cells to apoptosis.Cancer Res. 2007 Mar 1;67(5):1997-2005. doi: 10.1158/0008-5472.CAN-06-3093.
223 PIGN gene expression aberration is associated with genomic instability and leukemic progression in acute myeloid leukemia with myelodysplastic features.Oncotarget. 2017 May 2;8(18):29887-29905. doi: 10.18632/oncotarget.15136.
224 Phosphoinositide-phospholipase C beta1 mono-allelic deletion is associated with myelodysplastic syndromes evolution into acute myeloid leukemia.J Clin Oncol. 2009 Feb 10;27(5):782-90. doi: 10.1200/JCO.2008.19.3748. Epub 2008 Dec 29.
225 Ribosomal protein L23 negatively regulates cellular apoptosis via the RPL23/Miz-1/c-Myc circuit in higher-risk myelodysplastic syndrome.Sci Rep. 2017 May 24;7(1):2323. doi: 10.1038/s41598-017-02403-x.
226 MMP9 inhibition increases erythropoiesis in RPS14-deficient del(5q) MDS models through suppression of TGF- pathways.Blood Adv. 2019 Sep 24;3(18):2751-2763. doi: 10.1182/bloodadvances.2019000537.
227 Human TM9SF4 Is a New Gene Down-Regulated by Hypoxia and Involved in Cell Adhesion of Leukemic Cells.PLoS One. 2015 May 11;10(5):e0126968. doi: 10.1371/journal.pone.0126968. eCollection 2015.
228 Penumbra encodes a novel tetraspanin that is highly expressed in erythroid progenitors and promotes effective erythropoiesis.Blood. 2007 Apr 15;109(8):3244-52. doi: 10.1182/blood-2006-09-046672. Epub 2006 Dec 7.
229 Examination of copy number variations of CHST9 in multiple types of hematologic malignancies.Cancer Genet Cytogenet. 2010 Dec;203(2):176-9. doi: 10.1016/j.cancergencyto.2010.07.132.
230 ATM mediates constitutive NF-kappaB activation in high-risk myelodysplastic syndrome and acute myeloid leukemia.Oncogene. 2009 Feb 26;28(8):1099-109. doi: 10.1038/onc.2008.457. Epub 2008 Dec 15.
231 A calcium- and calpain-dependent pathway determines the response to lenalidomide in myelodysplastic syndromes.Nat Med. 2016 Jul;22(7):727-34. doi: 10.1038/nm.4127. Epub 2016 Jun 13.
232 FLT3 mutation and AML/ETO in a case of Myelodysplastic syndrome in transformation corroborates the two hit model of leukemogenesis.Leuk Res. 2007 Jul;31(7):1015-8. doi: 10.1016/j.leukres.2006.09.018. Epub 2006 Oct 31.
233 Alterations in the colorectal carcinoma gene and protein in a novel human myeloid leukemia cell line with trisomy 18 established from overt leukemia after myelodysplastic syndrome.Int J Hematol. 1998 Feb;67(2):153-64. doi: 10.1016/s0925-5710(97)00106-0.
234 Luspatercept for the treatment of anemia in myelodysplastic syndromes and primary myelofibrosis.Blood. 2019 Feb 21;133(8):790-794. doi: 10.1182/blood-2018-11-876888. Epub 2019 Jan 2.
235 Altered immunophenotypic features of peripheral blood platelets in myelodysplastic syndromes.Haematologica. 2012 Jun;97(6):895-902. doi: 10.3324/haematol.2011.057158. Epub 2012 Jan 22.
236 The interleukin-3 receptor CD123 targeted SL-401 mediates potent cytotoxic activity against CD34(+)CD123(+) cells from acute myeloid leukemia/myelodysplastic syndrome patients and healthy donors.Haematologica. 2018 Aug;103(8):1288-1297. doi: 10.3324/haematol.2018.188193. Epub 2018 May 17.
237 CD41 immune staining of micromegakaryocytes improves the diagnosis of myelodysplastic syndrome and differentiation from pancytopenia.Leuk Res. 2018 Mar;66:15-19. doi: 10.1016/j.leukres.2017.10.004. Epub 2017 Oct 18.
238 Detection of t(3;5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature.Cancer Genet Cytogenet. 2010 Jun;199(2):101-9. doi: 10.1016/j.cancergencyto.2010.02.009.
239 Short- and long-term benefits of lenalidomide treatment in patients with lower-risk del(5q) myelodysplastic syndromes.Ann Oncol. 2016 Jan;27(1):62-8. doi: 10.1093/annonc/mdv488. Epub 2015 Oct 26.
240 Hereditary myeloid malignancies.Best Pract Res Clin Haematol. 2019 Jun;32(2):163-176. doi: 10.1016/j.beha.2019.05.001. Epub 2019 May 3.
241 High expression of the multidrug resistance P-glycoprotein in high-risk myelodysplasia is associated with immature phenotype.Leukemia. 1993 Jul;7(7):963-9.
242 Establishment and molecular characterization of decitabine-resistant K562 cells.J Cell Mol Med. 2019 May;23(5):3317-3324. doi: 10.1111/jcmm.14221. Epub 2019 Feb 22.
243 Loss of p53 accelerates the complications of myelodysplastic syndrome in a NUP98-HOXD13-driven mouse model.Blood. 2012 Oct 11;120(15):3089-97. doi: 10.1182/blood-2012-01-405332. Epub 2012 Aug 27.
244 Downregulation of microRNA-144 inhibits proliferation and promotes the apoptosis of myelodysplastic syndrome cells through the activation of the AKAP12-dependent ERK1/2 signaling pathway.Cell Signal. 2020 Apr;68:109493. doi: 10.1016/j.cellsig.2019.109493. Epub 2019 Dec 3.
245 Ludwig Boltzmann Cluster Oncology (LBC ONC): first 10years and future perspectives.Wien Klin Wochenschr. 2018 Sep;130(17-18):517-529. doi: 10.1007/s00508-018-1355-7. Epub 2018 Jul 13.
246 A novel gene, ANKRD28 on 3p25, is fused with NUP98 on 11p15 in a cryptic 3-way translocation of t(3;5;11)(p25;q35;p15) in an adult patient with myelodysplastic syndrome/acute myelogenous leukemia.Int J Hematol. 2007 Oct;86(3):238-45. doi: 10.1532/IJH97.07054.
247 Related transplantation with HLA-1 Ag mismatch in the GVH direction and HLA-8/8 allele-matched unrelated transplantation: a nationwide retrospective study.Blood. 2012 Mar 8;119(10):2409-16. doi: 10.1182/blood-2011-08-372573. Epub 2011 Oct 31.
248 Methylation of the p73 gene in patients with myelodysplastic syndromes: correlations with apoptosis and prognosis.Tumour Biol. 2013 Feb;34(1):165-72. doi: 10.1007/s13277-012-0524-y. Epub 2012 Sep 28.
249 Loss of Asxl2 leads to myeloid malignancies in mice.Nat Commun. 2017 Jun 8;8:15456. doi: 10.1038/ncomms15456.
250 Induction of a hematological and cytogenetic remission in a patient with a myelodysplastic syndrome secondary to Fanconi's anemia employing the S-HAM regimen.Ann Hematol. 1997 Jun;74(6):275-7. doi: 10.1007/s002770050299.
251 Atg3 Overexpression Enhances Bortezomib-Induced Cell Death in SKM-1 Cell.PLoS One. 2016 Jul 8;11(7):e0158761. doi: 10.1371/journal.pone.0158761. eCollection 2016.
252 Durable long-term responses in patients with myelodysplastic syndromes treated with lenalidomide.Clin Lymphoma Myeloma. 2009 Jun;9(3):E10-3. doi: 10.3816/CLM.2009.n.053.
253 Clinical Outcomes of Decitabine Treatment for Patients With Lower-Risk Myelodysplastic Syndrome on the Basis of the International Prognostic Scoring System.Clin Lymphoma Myeloma Leuk. 2019 Oct;19(10):656-664. doi: 10.1016/j.clml.2019.06.003. Epub 2019 Jun 27.
254 Concurrent mutations in other epigenetic modulators portend better prognosis in BCOR-mutated myelodysplastic syndrome.J Clin Pathol. 2020 Apr;73(4):209-212. doi: 10.1136/jclinpath-2019-206132. Epub 2019 Nov 26.
255 C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies.Int J Hematol. 2018 Dec;108(6):652-657. doi: 10.1007/s12185-018-2514-3. Epub 2018 Aug 6.
256 Use of a Blast Dominance-Hematogone Index for the Flow Cytometric Evaluation of Myelodysplastic Syndrome (MDS).Am J Clin Pathol. 2019 May 3;151(6):584-592. doi: 10.1093/ajcp/aqz004.
257 Apoptosis-Related Gene Expression Profiling in Hematopoietic Cell Fractions of MDS Patients.PLoS One. 2016 Nov 30;11(11):e0165582. doi: 10.1371/journal.pone.0165582. eCollection 2016.
258 Impaired Mitophagy of Nucleated Erythroid Cells Leads to Anemia in Patients with Myelodysplastic Syndromes.Oxid Med Cell Longev. 2018 Jun 3;2018:6328051. doi: 10.1155/2018/6328051. eCollection 2018.
259 Functional characterization of BRCC3 mutations in acute myeloid leukemia with t(8;21)(q22;q22.1).Leukemia. 2020 Feb;34(2):404-415. doi: 10.1038/s41375-019-0578-6. Epub 2019 Oct 1.
260 Ex Vivo CD34(+)-Selected T Cell-Depleted Peripheral Blood Stem Cell Grafts for Allogeneic Hematopoietic Stem Cell Transplantation in Acute Leukemia and Myelodysplastic Syndrome Is Associated with Low Incidence of Acute and Chronic Graft-versus-Host Disease and High Treatment Response.Biol Blood Marrow Transplant. 2017 Mar;23(3):452-458. doi: 10.1016/j.bbmt.2016.12.633. Epub 2016 Dec 23.
261 Preleukemia and Leukemia-Initiating Cell Activity in inv(16) Acute Myeloid Leukemia.Front Oncol. 2018 Apr 26;8:129. doi: 10.3389/fonc.2018.00129. eCollection 2018.
262 Decitabine treatment sensitizes tumor cells to T-cell-mediated cytotoxicity in patients with myelodysplastic syndromes.Am J Transl Res. 2017 Feb 15;9(2):454-465. eCollection 2017.
263 Mitoxantrone, etoposide, and cytarabine with or without valspodar in patients with relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome: a phase III trial (E2995).J Clin Oncol. 2004 Mar 15;22(6):1078-86. doi: 10.1200/JCO.2004.07.048.
264 Overexpression of the polycythemia rubra vera-1 gene in essential thrombocythemia.J Clin Oncol. 2002 Oct 15;20(20):4249-54. doi: 10.1200/JCO.2002.11.507.
265 Impaired expression of the CD3-zeta chain in peripheral blood T cells of patients with chronic myeloid leukaemia results in an increased susceptibility to apoptosis.Br J Haematol. 2000 Dec;111(3):817-25.
266 High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome.Leukemia. 2006 Apr;20(4):627-34. doi: 10.1038/sj.leu.2404135.
267 Do preclinical studies suggest that CD99 is a potential therapeutic target in acute myeloid leukemia and the myelodysplastic syndromes?.Expert Opin Ther Targets. 2018 May;22(5):381-383. doi: 10.1080/14728222.2018.1464140. Epub 2018 Apr 20.
268 miR-378 inhibits cell growth and enhances apoptosis in human myelodysplastic syndromes.Int J Oncol. 2016 Nov;49(5):1921-1930. doi: 10.3892/ijo.2016.3689. Epub 2016 Sep 13.
269 Identification of NKIAMRE, the human homologue to the mitogen-activated protein kinase-/cyclin-dependent kinase-related protein kinase NKIATRE, and its loss in leukemic blasts with chromosome arm 5q deletion.Cancer Res. 1999 Aug 15;59(16):4069-74.
270 Molecular analysis of the cyclin-dependent kinase inhibitor genes, p15, p16, p18 and p19 in the myelodysplastic syndromes.Leuk Res. 1997 Mar;21(3):235-40. doi: 10.1016/s0145-2126(96)00115-4.
271 Reduced expression of flavocytochrome b558, a component of the NADPH oxidase complex, in neutrophils from patients with myelodysplasia.Exp Hematol. 2003 Sep;31(9):752-9. doi: 10.1016/s0301-472x(03)00188-7.
272 C/EBP-epsilon: chromosomal mapping and mutational analysis of the gene in leukemia and preleukemia.Leuk Res. 1997 Sep;21(9):833-9. doi: 10.1016/s0145-2126(97)00072-6.
273 Genome-wide DNA-mapping of CD34+ cells from patients with myelodysplastic syndrome using 500K SNP arrays identifies significant regions of deletion and uniparental disomy.Exp Hematol. 2009 Feb;37(2):215-224. doi: 10.1016/j.exphem.2008.10.012.
274 Methylation-independent CHFR expression is a potential biomarker affecting prognosis in acute myeloid leukemia.J Cell Physiol. 2018 Jun;233(6):4707-4714. doi: 10.1002/jcp.26253. Epub 2018 Jan 15.
275 Aberrant DNA methylation of p57(KIP2) gene in the promoter region in lymphoid malignancies of B-cell phenotype.Blood. 2002 Oct 1;100(7):2572-7. doi: 10.1182/blood-2001-11-0026.
276 Myelodysplastic syndromes are induced by histone methylationaltering ASXL1 mutations.J Clin Invest. 2013 Nov;123(11):4627-40. doi: 10.1172/JCI70739.
277 Progression from myelodysplastic syndrome to acute lymphoblastic leukaemia with Philadelphia chromosome and p190 BCR-ABL transcript.Br J Haematol. 1996 May;93(2):389-91. doi: 10.1046/j.1365-2141.1996.4931034.x.
278 Prognostic Impact of Immunohistochemical p53 Expression in Bone Marrow Biopsy in Higher Risk MDS: a Pilot Study.Mediterr J Hematol Infect Dis. 2019 Mar 1;11(1):e2019015. doi: 10.4084/MJHID.2019.015. eCollection 2019.
279 C-type lectin-like molecule-1: a novel myeloid cell surface marker associated with acute myeloid leukemia.Cancer Res. 2004 Nov 15;64(22):8443-50. doi: 10.1158/0008-5472.CAN-04-1659.
280 AML1-FOG2 fusion protein in myelodysplasia.Blood. 2005 Jun 1;105(11):4523-6. doi: 10.1182/blood-2004-07-2762. Epub 2005 Feb 10.
281 Impact of germline CTC1 alterations on telomere length in acquired bone marrow failure.Br J Haematol. 2019 Jun;185(5):935-939. doi: 10.1111/bjh.15862. Epub 2019 Mar 19.
282 Aberrant hypermethylation of CTNNA1 gene is associated with higher IPSS risk in patients with myelodysplastic syndrome.Clin Chem Lab Med. 2014 Dec;52(12):1859-65. doi: 10.1515/cclm-2014-0446.
283 Distinct clinical and biological implications of CUX1 in myeloid neoplasms.Blood Adv. 2019 Jul 23;3(14):2164-2178. doi: 10.1182/bloodadvances.2018028423.
284 Aberrant methylation of DAP-kinase in therapy-related acute myeloid leukemia and myelodysplastic syndromes.Blood. 2004 Jan 15;103(2):698-700. doi: 10.1182/blood-2003-07-2249. Epub 2003 Sep 22.
285 Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.Cancer Genet Cytogenet. 2010 Jan 1;196(1):89-92. doi: 10.1016/j.cancergencyto.2009.07.003.
286 5q- myelodysplastic syndromes: chromosome 5q genes direct a tumor-suppression network sensing actin dynamics.Oncogene. 2009 Oct 1;28(39):3429-41. doi: 10.1038/onc.2009.207. Epub 2009 Jul 13.
287 Dido gene expression alterations are implicated in the induction of hematological myeloid neoplasms.J Clin Invest. 2005 Sep;115(9):2351-62. doi: 10.1172/JCI24177. Epub 2005 Aug 25.
288 Hypermethylation of DLX4 predicts poor clinical outcome in patients with myelodysplastic syndrome.Clin Chem Lab Med. 2016 May;54(5):865-71. doi: 10.1515/cclm-2015-0536.
289 Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization.Cancer Genet Cytogenet. 1998 Nov;107(1):65-8. doi: 10.1016/s0165-4608(98)00055-7.
290 Impaired expression of DICER, DROSHA, SBDS and some microRNAs in mesenchymal stromal cells from myelodysplastic syndrome patients.Haematologica. 2012 Aug;97(8):1218-24. doi: 10.3324/haematol.2011.054437. Epub 2012 Feb 27.
291 Retracted: EBF1 gene promotes the proliferation and inhibits the apoptosis of bone marrow CD34+ cells in patients with myelodysplastic syndrome through negative regulation of mitogen-activated protein kinase axis.J Cell Biochem. 2019 Feb;120(2):1407-1419. doi: 10.1002/jcb.27177. Epub 2018 Oct 18.
292 Diazepam-binding inhibitor-related protein 1: a candidate autoantigen in acquired aplastic anemia patients harboring a minor population of paroxysmal nocturnal hemoglobinuria-type cells.Blood. 2004 Oct 15;104(8):2425-31. doi: 10.1182/blood-2004-05-1839. Epub 2004 Jun 24.
293 A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome.Sci Transl Med. 2019 Jul 10;11(500):eaav5467. doi: 10.1126/scitranslmed.aav5467.
294 Increased separase activity and occurrence of centrosome aberrations concur with transformation of MDS.PLoS One. 2018 Jan 25;13(1):e0191734. doi: 10.1371/journal.pone.0191734. eCollection 2018.
295 Epoetin alfa for the treatment of myelodysplastic syndrome-related anemia: A review of clinical data, clinical guidelines, and treatment protocols.Leuk Res. 2019 Jun;81:35-42. doi: 10.1016/j.leukres.2019.03.006. Epub 2019 Mar 27.
296 Gene expression profiling of the bone marrow mononuclear cells from patients with myelodysplastic syndrome.Oncol Rep. 2005 Nov;14(5):1189-97.
297 Late-appearing Philadelphia chromosome in a patient with acute nonlymphocytic leukaemia derived from myelodysplastic syndrome: detection of P210- and P190-type bcr/abl fusion gene transcripts at the leukaemic stage.Br J Haematol. 1994 May;87(1):51-6. doi: 10.1111/j.1365-2141.1994.tb04869.x.
298 Discussing and managing hematologic germ line variants.Blood. 2016 Nov 24;128(21):2497-2503. doi: 10.1182/blood-2016-06-716704.
299 Essential role of FBXL5-mediated cellular iron homeostasis in maintenance of hematopoietic stem cells.Nat Commun. 2017 Jul 17;8:16114. doi: 10.1038/ncomms16114.
300 Mechanisms of Impaired Neutrophil Migration by MicroRNAs in Myelodysplastic Syndromes.J Immunol. 2017 Mar 1;198(5):1887-1899. doi: 10.4049/jimmunol.1600622. Epub 2017 Jan 27.
301 MDS shows a higher expression of hTERT and alternative splice variants in unactivated T-cells.Oncotarget. 2016 Nov 1;7(44):71904-71914. doi: 10.18632/oncotarget.12115.
302 Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q- syndrome.Blood. 2011 Oct 27;118(17):4666-73. doi: 10.1182/blood-2010-12-324715. Epub 2011 Aug 26.
303 Haematopoietic and immune defects associated with GATA2 mutation.Br J Haematol. 2015 Apr;169(2):173-87. doi: 10.1111/bjh.13317. Epub 2015 Feb 23.
304 Prospective tracing of MLL-FRYL clone with low MEIS1 expression from emergence during neuroblastoma treatment to diagnosis of myelodysplastic syndrome.Blood. 2008 Apr 1;111(7):3802-12. doi: 10.1182/blood-2007-07-096065. Epub 2008 Jan 14.
305 Epigenetically Aberrant Stroma in MDS Propagates Disease via Wnt/-Catenin Activation.Cancer Res. 2017 Sep 15;77(18):4846-4857. doi: 10.1158/0008-5472.CAN-17-0282. Epub 2017 Jul 6.
306 Aberrant DNA methylation is a dominant mechanism in MDS progression to AML.Blood. 2009 Feb 5;113(6):1315-25. doi: 10.1182/blood-2008-06-163246. Epub 2008 Oct 2.
307 GAB2 is a novel target of 11q amplification in AML/MDS.Genes Chromosomes Cancer. 2006 Sep;45(9):798-807. doi: 10.1002/gcc.20344.
308 The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.
309 Gfi1b: a key player in the genesis and maintenance of acute myeloid leukemia and myelodysplastic syndrome.Haematologica. 2018 Apr;103(4):614-625. doi: 10.3324/haematol.2017.167288. Epub 2018 Jan 11.
310 Treatment of myelodysplastic syndromes with excess of blasts by bevacizumab is well tolerated and is associated with a decrease of VEGF plasma level.Ann Hematol. 2012 Jan;91(1):39-46. doi: 10.1007/s00277-011-1242-z. Epub 2011 May 7.
311 NKL homeobox gene activities in normal and malignant myeloid cells.PLoS One. 2019 Dec 11;14(12):e0226212. doi: 10.1371/journal.pone.0226212. eCollection 2019.
312 GPR68: An Emerging Drug Target in Cancer.Int J Mol Sci. 2019 Jan 28;20(3):559. doi: 10.3390/ijms20030559.
313 Purification of Bone Marrow Clonal Cells from Patients with Myelodysplastic Syndrome via IGF-IR.PLoS One. 2015 Oct 15;10(10):e0140372. doi: 10.1371/journal.pone.0140372. eCollection 2015.
314 Detection of hematopoietic maturation abnormalities by flow cytometry in myelodysplastic syndromes and its utility for the differential diagnosis with non-clonal disorders.Leuk Res. 2007 Feb;31(2):147-55. doi: 10.1016/j.leukres.2006.04.010. Epub 2006 Jun 5.
315 Overexpression of GYS1, MIF, and MYC is associated with adverse outcome and poor response to azacitidine in myelodysplastic syndromes and acute myeloid leukemia.Clin Lymphoma Myeloma Leuk. 2015 Apr;15(4):236-44. doi: 10.1016/j.clml.2014.10.003. Epub 2014 Oct 23.
316 Clinical significance of hyaluronan levels and its pro-osteogenic effect on mesenchymal stromal cells in myelodysplastic syndromes.J Transl Med. 2018 Aug 24;16(1):234. doi: 10.1186/s12967-018-1614-4.
317 Decitabine treatment could ameliorate primary iron-overload in myelodysplastic syndrome patients.Cancer Invest. 2015 Apr;33(4):98-106. doi: 10.3109/07357907.2014.1001895. Epub 2015 Feb 20.
318 Natural killer expansion, human leukocyte antigens-E expression and CD14(+) CD56(+) monocytes in a myelodysplastic syndrome patient.Eur J Haematol. 2013 Sep;91(3):265-269. doi: 10.1111/ejh.12152. Epub 2013 Jun 28.
319 A germline HLTF mutation in familial MDS induces DNA damage accumulation through impaired PCNA polyubiquitination.Leukemia. 2019 Jul;33(7):1773-1782. doi: 10.1038/s41375-019-0385-0. Epub 2019 Jan 29.
320 Leptin-deficient obesity prolongs survival in a murine model of myelodysplastic syndrome.Haematologica. 2018 Apr;103(4):597-606. doi: 10.3324/haematol.2017.181958. Epub 2018 Jan 25.
321 Clinical implications of the quantitative detection of ID4 gene methylation in myelodysplastic syndrome.Eur J Med Res. 2015 Feb 20;20(1):16. doi: 10.1186/s40001-015-0092-x.
322 Simultaneous analysis of the expression of 14 genes with individual prognostic value in myelodysplastic syndrome patients at diagnosis: WT1 detection in peripheral blood adversely affects survival.Ann Hematol. 2012 Dec;91(12):1887-95. doi: 10.1007/s00277-012-1538-7. Epub 2012 Aug 9.
323 Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.Blood. 2006 Jul 1;108(1):337-45. doi: 10.1182/blood-2005-12-4769. Epub 2006 Mar 9.
324 A new recurrent chromosomal translocation t(3;11)(q13;q14) in myelodysplastic syndromes associated with overexpression of the ILDR1 gene.Leuk Res. 2012 Jul;36(7):852-6. doi: 10.1016/j.leukres.2012.01.026. Epub 2012 Feb 25.
325 Health-related quality of life in lower-risk MDS patients compared with age- and sex-matched reference populations: a European LeukemiaNet study.Leukemia. 2018 Jun;32(6):1380-1392. doi: 10.1038/s41375-018-0089-x. Epub 2018 Mar 6.
326 Identification of disease- and therapy-associated proteome changes in the sera of patients with myelodysplastic syndromes and del(5q).Leukemia. 2010 Nov;24(11):1875-84. doi: 10.1038/leu.2010.182. Epub 2010 Aug 26.
327 The KDM2B- let-7b -EZH2 axis in myelodysplastic syndromes as a target for combined epigenetic therapy.PLoS One. 2014 Sep 16;9(9):e107817. doi: 10.1371/journal.pone.0107817. eCollection 2014.
328 Epigenetic drug library screening identified an LSD1 inhibitor to target UTX-deficient cells for differentiation therapy.Signal Transduct Target Ther. 2019 Apr 26;4:11. doi: 10.1038/s41392-019-0040-2. eCollection 2019.
329 Epigenetic inactivation of tumour suppressor gene KLF11 in myelodysplastic syndromes*.Eur J Haematol. 2010 Apr;84(4):298-303. doi: 10.1111/j.1600-0609.2009.01389.x. Epub 2009 Nov 28.
330 Loss of Mll3 Catalytic Function Promotes Aberrant Myelopoiesis.PLoS One. 2016 Sep 9;11(9):e0162515. doi: 10.1371/journal.pone.0162515. eCollection 2016.
331 Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells.Genes Chromosomes Cancer. 2004 Nov;41(3):203-13. doi: 10.1002/gcc.20087.
332 The lower risk MDS patient at risk of rapid progression.Leuk Res. 2010 Dec;34(12):1551-5. doi: 10.1016/j.leukres.2010.05.023. Epub 2010 Jun 22.
333 Oncogenic potential of the transcription factor LYL1 in acute myeloblastic leukemia. Leukemia. 2005 Nov;19(11):1941-7. doi: 10.1038/sj.leu.2403836.
334 Association between anti-thymocyte globulin exposure and survival outcomes in adult unrelated haemopoietic cell transplantation: a multicentre, retrospective, pharmacodynamic cohort analysis.Lancet Haematol. 2017 Apr;4(4):e183-e191. doi: 10.1016/S2352-3026(17)30029-7. Epub 2017 Mar 16.
335 Overexpression of MCM2 in myelodysplastic syndromes: association with bone marrow cell apoptosis and peripheral cytopenia.Exp Mol Pathol. 2012 Feb;92(1):160-6. doi: 10.1016/j.yexmp.2011.11.003. Epub 2011 Nov 15.
336 MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.Hum Mutat. 2016 Mar;37(3):257-68. doi: 10.1002/humu.22939. Epub 2015 Dec 30.
337 A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.Blood. 2018 Feb 15;131(7):717-732. doi: 10.1182/blood-2017-09-806489. Epub 2017 Nov 16.
338 Iron overload promotes mitochondrial fragmentation in mesenchymal stromal cells from myelodysplastic syndrome patients through activation of the AMPK/MFF/Drp1 pathway.Cell Death Dis. 2018 May 1;9(5):515. doi: 10.1038/s41419-018-0552-7.
339 Transcriptomic analysis implicates necroptosis in disease progression and prognosis in myelodysplastic syndromes.Leukemia. 2020 Mar;34(3):872-881. doi: 10.1038/s41375-019-0623-5. Epub 2019 Nov 12.
340 Clinical outcome and monitoring of minimal residual disease in patients with acute lymphoblastic leukemia expressing the MLL/ENL fusion gene.Am J Hematol. 2011 Dec;86(12):993-7. doi: 10.1002/ajh.22161. Epub 2011 Sep 22.
341 MicroRNA?43 increases cell apoptosis in myelodysplastic syndrome through the Fas/FasL pathway both invitro and invivo.Int J Oncol. 2018 Nov;53(5):2191-2199. doi: 10.3892/ijo.2018.4534. Epub 2018 Aug 22.
342 Dysregulated human myeloid nuclear differentiation antigen expression in myelodysplastic syndromes: evidence for a role in apoptosis.Cancer Res. 2006 May 1;66(9):4645-51. doi: 10.1158/0008-5472.CAN-06-0229.
343 Costimulatory Molecules and Immune Checkpoints Are Differentially Expressed on Different Subsets of Dendritic Cells.Front Immunol. 2019 Jun 11;10:1325. doi: 10.3389/fimmu.2019.01325. eCollection 2019.
344 Hepatocerebral form of mitochondrial DNA depletion syndrome due to mutation in MPV17 gene.Saudi J Gastroenterol. 2012 Jul-Aug;18(4):285-9. doi: 10.4103/1319-3767.98439.
345 Prognostic impact of p15 gene aberrations in acute leukemia.Leuk Lymphoma. 2017 Feb;58(2):257-265. doi: 10.1080/10428194.2016.1201574. Epub 2016 Jul 12.
346 Phase Ib Study of Glasdegib, a Hedgehog Pathway Inhibitor, in Combination with Standard Chemotherapy in Patients with AML or High-Risk MDS.Clin Cancer Res. 2018 May 15;24(10):2294-2303. doi: 10.1158/1078-0432.CCR-17-2824. Epub 2018 Feb 20.
347 MYBL2 Supports DNA Double Strand Break Repair in Hematopoietic Stem Cells.Cancer Res. 2018 Oct 15;78(20):5767-5779. doi: 10.1158/0008-5472.CAN-18-0273. Epub 2018 Aug 6.
348 The presence of monoclonal gammopathy in Ph-negative myeloproliferative neoplasms is associated with a detrimental effect on outcomes.Leuk Lymphoma. 2017 Nov;58(11):2582-2587. doi: 10.1080/10428194.2017.1312380. Epub 2017 May 9.
349 Neutrophilic Panniculitis in a child with MYSM1 deficiency.Pediatr Dermatol. 2019 Mar;36(2):258-259. doi: 10.1111/pde.13757. Epub 2019 Feb 12.
350 Association between mitochondrial DNA haplogroup and myelodysplastic syndromes.Genes Chromosomes Cancer. 2016 Sep;55(9):688-93. doi: 10.1002/gcc.22370. Epub 2016 Jun 21.
351 High expression of ERCC1, FLT1, NME4 and PCNA associated with poor prognosis and advanced stages in myelodysplastic syndrome.Leuk Lymphoma. 2008 Jul;49(7):1297-305. doi: 10.1080/10428190802129918.
352 NUP98-NSD3 fusion gene in radiation-associated myelodysplastic syndrome with t(8;11)(p11;p15) and expression pattern of NSD family genes.Cancer Genet Cytogenet. 2009 Apr 15;190(2):108-12. doi: 10.1016/j.cancergencyto.2008.12.008.
353 The NUP98-HOXD13 fusion oncogene induces thymocyte self-renewal via Lmo2/Lyl1.Leukemia. 2019 Aug;33(8):1868-1880. doi: 10.1038/s41375-018-0361-0. Epub 2019 Jan 30.
354 Mutation analysis of the origin recognition complex subunit 5 (ORC5L) gene in adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22.Hum Genet. 2001 Apr;108(4):304-9. doi: 10.1007/s004390100498.
355 Clinical Benefit-Risk Profile of Lenalidomide in Patients With Lower-risk Myelodysplastic Syndromes Without del(5q): Results of a PhaseIIITrial.Clin Lymphoma Myeloma Leuk. 2019 Apr;19(4):213-219.e4. doi: 10.1016/j.clml.2018.12.012. Epub 2018 Dec 21.
356 Glycogen synthase kinase-3 and alternative splicing.Wiley Interdiscip Rev RNA. 2018 Nov;9(6):e1501. doi: 10.1002/wrna.1501. Epub 2018 Aug 17.
357 DNA microarray analysis of stage progression mechanism in myelodysplastic syndrome.Br J Haematol. 2003 Oct;123(2):288-96. doi: 10.1046/j.1365-2141.2003.04601.x.
358 Differential profile of PIP4K2A expression in hematological malignancies.Blood Cells Mol Dis. 2015 Oct;55(3):228-35. doi: 10.1016/j.bcmd.2015.06.014. Epub 2015 Jun 30.
359 Overexpression of human CAP10-like protein 46 KD in T-acute lymphoblastic leukemia and acute myelogenous leukemia.Genet Test Mol Biomarkers. 2010 Feb;14(1):127-33. doi: 10.1089/gtmb.2009.0145.
360 Antileukemic Efficacy in Vitro of Talazoparib and APE1 Inhibitor III Combined with Decitabine in Myeloid Malignancies.Cancers (Basel). 2019 Oct 3;11(10):1493. doi: 10.3390/cancers11101493.
361 Polycomb protein RING1A limits hematopoietic differentiation in myelodysplastic syndromes.Oncotarget. 2017 Dec 1;8(70):115002-115017. doi: 10.18632/oncotarget.22839. eCollection 2017 Dec 29.
362 Synergistic effects of PRIMA-1(Met) (APR-246) and 5-azacitidine in TP53-mutated myelodysplastic syndromes and acute myeloid leukemia.Haematologica. 2020 Jun;105(6):1539-1551. doi: 10.3324/haematol.2019.218453. Epub 2019 Sep 5.
363 Bone marrow MSCs in MDS: contribution towards dysfunctional hematopoiesis and potential targets for disease response to hypomethylating therapy.Leukemia. 2019 Jun;33(6):1487-1500. doi: 10.1038/s41375-018-0310-y. Epub 2018 Dec 21.
364 Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia.Leukemia. 2001 Jun;15(6):954-62. doi: 10.1038/sj.leu.2402108.
365 Pediatric MDS: GATA screen the germline.Blood. 2016 Mar 17;127(11):1377-8. doi: 10.1182/blood-2016-01-690016.
366 A prognostic model of therapy-related myelodysplastic syndrome for predicting survival and transformation to acute myeloid leukemia.Clin Lymphoma Myeloma Leuk. 2014 Oct;14(5):401-10. doi: 10.1016/j.clml.2014.03.001. Epub 2014 May 6.
367 DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population.J Hematol Oncol. 2013 Jan 22;6:9. doi: 10.1186/1756-8722-6-9.
368 A rare case of acquired immunodeficiency associated with myelodysplastic syndrome.Mol Genet Genomic Med. 2019 Nov;7(11):e923. doi: 10.1002/mgg3.923. Epub 2019 Sep 10.
369 Mutation in RAP1 is a rare event in myelodysplastic syndromes.Leukemia. 2005 Sep;19(9):1678-80. doi: 10.1038/sj.leu.2403882.
370 Predictors of survival in refractory anemia with ring sideroblasts and thrombocytosis (RARS-T) and the role of next-generation sequencing.Am J Hematol. 2016 May;91(5):492-8. doi: 10.1002/ajh.24332. Epub 2016 Apr 4.
371 "Bone marrow aspirate automated counts on hematology analyzers: formulating a scoring system based on hematology parameters, to discriminate reactive versus myelodysplastic syndrome-related bone marrows".Int J Lab Hematol. 2019 Aug;41(4):542-549. doi: 10.1111/ijlh.13049. Epub 2019 May 18.
372 Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes.Nat Commun. 2015 Nov 26;6:8806. doi: 10.1038/ncomms9806.
373 Differential expression of homologous recombination DNA repair genes in the early and advanced stages of myelodysplastic syndrome.Eur J Haematol. 2017 Oct;99(4):323-331. doi: 10.1111/ejh.12920. Epub 2017 Jul 24.
374 RPL27A is a target of miR-595 and may contribute to the myelodysplastic phenotype through ribosomal dysgenesis.Oncotarget. 2016 Jul 26;7(30):47875-47890. doi: 10.18632/oncotarget.10293.
375 p53-inducible ribonucleotide reductase (p53R2/RRM2B) is a DNA hypomethylation-independent decitabine gene target that correlates with clinical response in myelodysplastic syndrome/acute myelogenous leukemia. Cancer Res. 2008 Nov 15;68(22):9358-66. doi: 10.1158/0008-5472.CAN-08-1860.
376 Leukemic survival factor SALL4 contributes to defective DNA damage repair.Oncogene. 2016 Nov 24;35(47):6087-6095. doi: 10.1038/onc.2016.146. Epub 2016 May 2.
377 Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.Pediatr Blood Cancer. 2019 Apr;66(4):e27589. doi: 10.1002/pbc.27589. Epub 2018 Dec 19.
378 Outcomes of Hematopoietic Cell Transplantation in Patients with Germline SAMD9/SAMD9L Mutations.Biol Blood Marrow Transplant. 2019 Nov;25(11):2186-2196. doi: 10.1016/j.bbmt.2019.07.007. Epub 2019 Jul 12.
379 Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.Blood Cells Mol Dis. 2016 Jul;59:52-7. doi: 10.1016/j.bcmd.2016.04.005. Epub 2016 Apr 13.
380 A novel MLL-SEPT2 fusion variant in therapy-related myelodysplastic syndrome.Cancer Genet Cytogenet. 2008 Aug;185(1):62-4. doi: 10.1016/j.cancergencyto.2008.05.002.
381 An MLL-SEPT9 fusion and t(11;17)(q23;q25) associated with de novo myelodysplastic syndrome.Leuk Res. 2007 Aug;31(8):1145-8. doi: 10.1016/j.leukres.2006.12.006. Epub 2007 Jan 23.
382 SETBP1 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome.Pathol Res Pract. 2018 May;214(5):706-712. doi: 10.1016/j.prp.2018.03.010. Epub 2018 Mar 7.
383 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.Nat Biotechnol. 2016 Feb;34(2):155-63. doi: 10.1038/nbt.3391. Epub 2015 Nov 30.
384 Methylation of Wnt antagonist genes: a useful prognostic marker for myelodysplastic syndrome.Ann Hematol. 2013 Jan;92(2):199-209. doi: 10.1007/s00277-012-1595-y. Epub 2012 Oct 24.
385 Myeloproliferative stem cell disorders by deregulated Rap1 activation in SPA-1-deficient mice.Cancer Cell. 2003 Jul;4(1):55-65. doi: 10.1016/s1535-6108(03)00163-6.
386 SGCZ mutations are unlikely to be associated with myoclonus dystonia.Neuroscience. 2014 Jul 11;272:88-91. doi: 10.1016/j.neuroscience.2014.04.034. Epub 2014 Apr 30.
387 t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.Mol Cancer. 2015 Dec 16;14:211. doi: 10.1186/s12943-015-0484-0.
388 SKI controls MDS-associated chronic TGF- signaling, aberrant splicing, and stem cell fitness.Blood. 2018 Nov 22;132(21):e24-e34. doi: 10.1182/blood-2018-06-860890. Epub 2018 Sep 24.
389 Mutations in Splicing Factor Genes in Myeloid Malignancies: Significance and Impact on Clinical Features.Cancers (Basel). 2019 Nov 22;11(12):1844. doi: 10.3390/cancers11121844.
390 Differential expression of a novel C-terminally truncated splice form of SMAD5 in hematopoietic stem cells and leukemia.Blood. 2000 Jun 15;95(12):3945-50.
391 SOX7 methylation is an independent prognostic factor in myelodysplastic syndromes.Pathol Res Pract. 2019 Feb;215(2):322-328. doi: 10.1016/j.prp.2018.12.003. Epub 2018 Dec 6.
392 Phenotype of mesenchymal stem cells from patients with myelodyplastic syndrome maybe partly modulated by decitabine.Oncol Lett. 2019 Nov;18(5):4457-4466. doi: 10.3892/ol.2019.10788. Epub 2019 Sep 3.
393 In Vitro and in Vivo Evaluation of Fully Substituted (5-(3-Ethoxy-3-oxopropynyl)-4-(ethoxycarbonyl)-1,2,3-triazolyl-glycosides as Original Nucleoside Analogues to Circumvent Resistance in Myeloid Malignancies.J Med Chem. 2017 Feb 23;60(4):1523-1533. doi: 10.1021/acs.jmedchem.6b01803. Epub 2017 Feb 2.
394 Discovering transcription and splicing networks in myelodysplastic syndromes.PLoS One. 2013 Nov 14;8(11):e79118. doi: 10.1371/journal.pone.0079118. eCollection 2013.
395 ICUS, IDUS, CHIP and CCUS: Diagnostic Criteria, Separation from MDS and Clinical Implications.Pathobiology. 2019;86(1):30-38. doi: 10.1159/000489042. Epub 2018 Jun 1.
396 Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.J Med Genet. 2006 Apr;43(4):e14. doi: 10.1136/jmg.2005.035253.
397 MDR-1 and GST polymorphisms are involved in myelodysplasia progression.Leuk Res. 2013 Aug;37(8):970-3. doi: 10.1016/j.leukres.2013.04.024. Epub 2013 May 17.
398 Reduction in multi-lineage and erythroid progenitors distinguishes myelodysplastic syndromes from non-malignant cytopenias.Leuk Res. 2009 Dec;33(12):1636-42. doi: 10.1016/j.leukres.2009.03.019. Epub 2009 May 2.
399 Investigation of copy-number variations of C8orf4 in hematological malignancies.Med Oncol. 2011 Dec;28 Suppl 1:S647-52. doi: 10.1007/s12032-010-9698-6. Epub 2010 Sep 29.
400 Expression of transferrin receptor 2 in normal and neoplastic hematopoietic cells.Blood. 2001 Nov 1;98(9):2714-9. doi: 10.1182/blood.v98.9.2714.
401 Perturbed hematopoietic stem and progenitor cell hierarchy in myelodysplastic syndromes patients with monosomy 7 as the sole cytogenetic abnormality.Oncotarget. 2016 Nov 8;7(45):72685-72698. doi: 10.18632/oncotarget.12234.
402 Apoptotic cells and clonally expanded cytotoxic T cells in bone marrow trephines of patients with myelodysplastic syndrome.Histopathology. 2012 Aug;61(2):200-11. doi: 10.1111/j.1365-2559.2012.04209.x. Epub 2012 Jun 13.
403 Epistasis between TIFAB and miR-146a: neighboring genes in del(5q) myelodysplastic syndrome.Leukemia. 2017 Jul;31(7):1659. doi: 10.1038/leu.2017.95. Epub 2017 Apr 7.
404 Reversion of mtDNA depletion in a patient with TK2 deficiency.Neurology. 2003 Apr 8;60(7):1203-5. doi: 10.1212/01.wnl.0000055928.58122.47.
405 Expression of tumor necrosis factor-related apoptosis-inducing ligand, Apo2L, and its receptors in myelodysplastic syndrome: effects on in vitro hemopoiesis.Blood. 2001 Nov 15;98(10):3058-65. doi: 10.1182/blood.v98.10.3058.
406 From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype.Genes Chromosomes Cancer. 2012 May;51(5):419-28. doi: 10.1002/gcc.21927. Epub 2012 Jan 17.
407 Anti-TIF1gamma Antibody-Positive Dermatomyositis Associated with Myelodysplastic Syndrome: Response to Treatment.Cureus. 2019 Sep 26;11(9):e5775. doi: 10.7759/cureus.5775.
408 ASXL1 gene alterations in patients with isolated 20q deletion.Neoplasma. 2019 Jul 23;66(4):627-630. doi: 10.4149/neo_2018_181010N754.
409 Guadecitabine (SGI-110): an investigational drug for the treatment of myelodysplastic syndrome and acute myeloid leukemia.Expert Opin Investig Drugs. 2019 Oct;28(10):835-849. doi: 10.1080/13543784.2019.1667331. Epub 2019 Sep 19.
410 GPX3 methylation in bone marrow predicts adverse prognosis and leukemia transformation in myelodysplastic syndrome.Cancer Med. 2017 Jan;6(1):267-274. doi: 10.1002/cam4.984. Epub 2016 Nov 28.
411 Telomere length, c-myc and mad-1 expression could represent prognosis markers of myelodysplastic syndrome.Leuk Res. 2013 Nov;37(11):1538-44. doi: 10.1016/j.leukres.2013.07.022. Epub 2013 Oct 3.
412 Nuclear phospholipase C in biological control and cancer.Crit Rev Eukaryot Gene Expr. 2011;21(3):291-301. doi: 10.1615/critreveukargeneexpr.v21.i3.50.
413 PRDM16 isoforms differentially regulate normal and leukemic hematopoiesis and inflammatory gene signature.J Clin Invest. 2018 Aug 1;128(8):3250-3264. doi: 10.1172/JCI99862. Epub 2018 Jul 23.
414 The changing mutational landscape of acute myeloid leukemia and myelodysplastic syndrome.Mol Cancer Res. 2013 Aug;11(8):815-27. doi: 10.1158/1541-7786.MCR-12-0695. Epub 2013 May 3.
415 PURA, the gene encoding Pur-alpha, member of an ancient nucleic acid-binding protein family with mammalian neurological functions.Gene. 2018 Feb 15;643:133-143. doi: 10.1016/j.gene.2017.12.004. Epub 2017 Dec 6.
416 Methylation level of Rap1GAP and the clinical significance in MDS.Oncol Lett. 2018 Dec;16(6):7287-7294. doi: 10.3892/ol.2018.9503. Epub 2018 Sep 26.
417 T-cell receptor Vbeta CDR3 oligoclonality frequently occurs in childhood refractory cytopenia (MDS-RC) and severe aplastic anemia.Leukemia. 2008 Jun;22(6):1170-4. doi: 10.1038/leu.2008.23. Epub 2008 Mar 6.