General Information of Disease (ID: DISTVL0C)

Disease Name Anemia
Synonyms anemia (disease); anemia; anaemia (disease)
Disease Class 3A00-3A9Z: Anemia
Definition
A reduction in the number of red blood cells, the amount of hemoglobin, and/or the volume of packed red blood cells. Clinically, anemia represents a reduction in the oxygen-transporting capacity of a designated volume of blood, resulting from an imbalance between blood loss (through hemorrhage or hemolysis) and blood production. Signs and symptoms of anemia may include pallor of the skin and mucous membranes, shortness of breath, palpitations of the heart, soft systolic murmurs, lethargy, and fatigability.
Disease Hierarchy
DIS9XD9A: Hematologic disease
DISTVL0C: Anemia
ICD Code
ICD-11
ICD-11: 3A00-3A9Z
ICD-10
ICD-10: D50-D64
Disease Identifiers
MONDO ID
MONDO_0002280
MESH ID
D000740
UMLS CUI
C0002871
MedGen ID
1526
HPO ID
HP:0001903
SNOMED CT ID
271737000

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 9 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Calcium levofolinate DMVG98V Approved Small molecular drug [1]
Cyanocobalamin DMYY0AJ Approved NA [1]
Darbepoetin alfa DMMJTYW Approved NA [2]
Epoetin alfa DMKWB73 Approved NA [3]
Hemoglobin glutamer DMPKAWJ Approved NA [1]
Iron proteinsuccinylate DMYDNZ3 Approved NA [1]
Levoleucovorin DMH5LME Approved Small molecular drug [1]
Mecobalamin DM0C63F Approved NA [4]
Siltuximab DMGEATB Approved Antibody [5]
------------------------------------------------------------------------------------
⏷ Show the Full List of 9 Drug(s)
This Disease is Treated as An Indication in 25 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
ACE-536 DMRI15Q Phase 3 NA [6]
Epoetin zeta DM9QPOU Phase 3 NA [7]
ErepoXen DM9YI2C Phase 3 NA [8]
Hematide DMUE843 Phase 3 NA [9]
Hemoglobin raffimer DMMTL7V Phase 2/3 NA [10]
Roledumab DMWZ6DK Phase 2/3 Antibody [11]
5-hydroxymethyl-2-furfural DMPFVJB Phase 2 Small molecular drug [12]
BAY-85-3934 DM7NHLC Phase 2 Small molecular drug [13]
Erythropoietin gene therapy DMG5BDT Phase 2 NA [14]
INCB00928 DMFG8TI Phase 2 Small molecular drug [15]
MK-2578 DM1M57I Phase 2 NA [16]
NOX-H94 DM5HPZU Phase 2 NA [17]
Soluble FePPi DMRORBG Phase 2 NA [18]
SPD602 DMKJ9LU Phase 2 NA [19]
Erythropoietin-transfected autologous cell therapy DMNZ6VA Phase 1/2 NA [20]
PBI-1402 DMC8K91 Phase 1/2 NA [21]
ACE-011 DMJ36YH Phase 1 Small molecular drug [22]
DA-3880 DM5O1LU Phase 1 NA [23]
DS-1093 DM42KZW Phase 1 NA [24]
Ferroportin mab DM13YK0 Phase 1 Antibody [25]
GC-1113 DMK96CE Phase 1 NA [26]
Hepcidin mab DMBFYSR Phase 1 Antibody [27]
Long-acting erythropoietin conjugate DM9OA35 Phase 1 NA [28]
LY2787106 DM9NYHT Phase 1 Antibody [29]
Retroviral MGMT-transduced hematopoietic cells DMJTW0A Phase 1 NA [30]
------------------------------------------------------------------------------------
⏷ Show the Full List of 25 Drug(s)
This Disease is Treated as An Indication in 6 Discontinued Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Inactine DM1DGAE Discontinued in Phase 3 NA [31]
ETRX-101 DMRB23N Discontinued in Phase 2 NA [32]
Rozrolimupab DMNBUS7 Discontinued in Phase 2 Antibody [33]
FC EPO DMEX12T Discontinued in Phase 1 NA [34]
Albupoietin DMXK4CI Terminated NA [35]
RHb1.1 DM7CY0T Terminated NA [36]
------------------------------------------------------------------------------------
⏷ Show the Full List of 6 Drug(s)
This Disease is Treated as An Indication in 23 Investigative Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
AFT-EPO DMED3YX Investigative NA [37]
ALN-HPN DMJDLAF Investigative NA [37]
BBT-009 DM2YTXL Investigative NA [38]
BBT-021 DMLIT84 Investigative NA [38]
BR-05001 DM6CQDR Investigative NA [37]
CKD-406 DMIGMFD Investigative NA [37]
EPO peptide mimetics DMP2QF0 Investigative NA [38]
Erythropoietin DM3R8YL Investigative NA [39]
FG-6874 DMN07VU Investigative NA [37]
GX-E2 DMW40HT Investigative NA [37]
Hemoxin DM9SHZF Investigative NA [37]
Human serum albumin DMWDH1Q Investigative NA [37]
JNJ-42041935 DM08YTN Investigative Small molecular drug [37]
MOD-7023 DMVITGF Investigative NA [37]
Nova-EPO DM82DNL Investigative NA [38]
P-1116 DMQ6TZE Investigative NA [38]
PanCyte DMBIVKT Investigative NA [37]
PEG-EPO DM5GVZJ Investigative NA [38]
PEGylated recombinant EPO DMNVPVN Investigative NA [37]
PT-401 DM736T8 Investigative NA [38]
TBI-304 DM5MHGP Investigative NA [37]
YPEG-EPO DMTSZYU Investigative NA [37]
ZP-EPO DMEWYLE Investigative NA [37]
------------------------------------------------------------------------------------
⏷ Show the Full List of 23 Drug(s)

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 105 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
ABCA1 TTJW1GN Limited Genetic Variation [40]
ACVRL1 TTGYPTC Limited Biomarker [41]
CACNA2D3 TTN7T29 Limited Genetic Variation [42]
CD59 TTBGTEJ Limited Altered Expression [43]
F2 TT6L509 Limited Genetic Variation [44]
FABP3 TT3TGLR Limited Biomarker [45]
HLA-B TTGS10J Limited Biomarker [46]
LCAT TTGZ91P Limited Genetic Variation [47]
PDGFRA TT8FYO9 Limited Biomarker [48]
PRL TTJ2TSA Limited Altered Expression [49]
SLC17A5 TTFSUIA Limited Biomarker [50]
SLC29A1 TTLXAKE Limited Genetic Variation [51]
THRA TTTSEPU Limited Biomarker [52]
ACR TTAHE2N moderate Genetic Variation [53]
ANK1 TTKFPMH moderate Genetic Variation [54]
CALCR TTLWS2O moderate Biomarker [55]
IFNA2 TTSIUJ9 moderate Genetic Variation [56]
MTHFR TTQWOU1 moderate Genetic Variation [57]
PTH TT6F7GZ moderate Altered Expression [58]
SLC40A1 TT6Y1PG moderate Altered Expression [59]
SLC6A8 TTYUHB5 moderate Biomarker [55]
TYMS TTP1UKZ moderate Genetic Variation [60]
ACHE TT1RS9F Strong Biomarker [61]
AGT TT5C0UB Strong Biomarker [62]
ALAD TTJHKYD Strong Biomarker [63]
APOA1 TT5S8DR Strong Biomarker [64]
APOH TT2OUI9 Strong Biomarker [65]
ATG7 TTLVB9Z Strong Biomarker [66]
BACH1 TT2ME4S Strong Altered Expression [67]
BMP6 TT07RIB Strong Biomarker [68]
BRIP1 TTZV7LJ Strong Biomarker [69]
CA5A TT75WPO Strong Biomarker [70]
CAD TT2YT1K Strong Genetic Variation [71]
CASR TTBUYHA Strong Genetic Variation [72]
CCL21 TTLZK1U Strong Altered Expression [73]
CDK6 TTO0FDJ Strong Biomarker [74]
CEACAM5 TTY6DTE Strong Biomarker [75]
CSF3 TT5TQ2W Strong Biomarker [76]
CSNK1A1 TTFQEMX Strong Biomarker [77]
CUBN TT9YLCR Strong Genetic Variation [78]
DYRK3 TTV4EX0 Strong Altered Expression [79]
E2F2 TT5FYX0 Strong Genetic Variation [80]
EGLN1 TT9ISBX Strong Biomarker [81]
EPHB6 TTZEMUY Strong Biomarker [82]
EPOR TTAUX24 Strong Biomarker [83]
F10 TTCIHJA Strong Biomarker [84]
F11 TTDM4ZU Strong Biomarker [85]
FABP1 TTIV96N Strong Altered Expression [86]
FABP2 TTS4YLO Strong Altered Expression [86]
FANCA TTV5HJS Strong Genetic Variation [87]
FCGR2A TTXT21W Strong Biomarker [88]
FECH TTQ6VF4 Strong Genetic Variation [89]
FGF23 TT2IZ4K Strong Biomarker [90]
FUT3 TTUPAD7 Strong Biomarker [91]
G6PD TTKN8W0 Strong Genetic Variation [92]
GBA TT1B5PU Strong Altered Expression [93]
GPX1 TTYAHBP Strong Therapeutic [94]
GSR TTEP6RV Strong Biomarker [95]
HBB TTM6HK1 Strong Biomarker [96]
HP TTLC8E1 Strong Biomarker [97]
IFNAR1 TTSYFMA Strong Biomarker [98]
IFNAR2 TTMQB37 Strong Biomarker [98]
IGF2 TTE8WGO Strong Therapeutic [99]
IL12B TTGW72V Strong Genetic Variation [100]
IL2 TTF89GD Strong Altered Expression [101]
JAK1 TT6DM01 Strong Biomarker [102]
KIT TTX41N9 Strong Altered Expression [103]
KLK4 TT4319X Strong Biomarker [104]
LAIR1 TTSI7A8 Strong Biomarker [105]
LCK TT860QF Strong Biomarker [106]
LTF TTSZDQU Strong Altered Expression [107]
MAOB TTGP7BY Strong Biomarker [108]
MPL TTIHYA4 Strong Genetic Variation [109]
MUC1 TTBHFYQ Strong Altered Expression [110]
NCOA4 TT8OY02 Strong Biomarker [111]
NEK1 TTO5QT2 Strong Genetic Variation [112]
PI4KA TTCUS9F Strong Altered Expression [113]
PKLR TT31N4S Strong Genetic Variation [114]
PNP TTMCF1Y Strong Altered Expression [115]
PPOX TTNFMS9 Strong Genetic Variation [116]
PRCP TTTJZ4M Strong Biomarker [117]
PRKAR1A TTNAHEX Strong Genetic Variation [72]
RHD TTLCKI8 Strong Genetic Variation [118]
SF3B1 TTL2WUI Strong Genetic Variation [119]
SLC11A2 TT2IS7P Strong Genetic Variation [120]
SLC15A1 TT5LF3C Strong Altered Expression [121]
SLC19A2 TT2A1DZ Strong Genetic Variation [122]
SLC28A2 TTVP9IQ Strong Biomarker [123]
SLC9A3 TTFZVPO Strong Biomarker [124]
SLCO1B3 TTU86P0 Strong Genetic Variation [125]
TCL1A TTUKRDV Strong Altered Expression [126]
TEC TT1ZV49 Strong Biomarker [127]
TF TT8WXAV Strong Biomarker [128]
TFRC TT8MG4S Strong Biomarker [129]
TGM2 TT2F4OL Strong Biomarker [130]
THPO TTCG5PE Strong Altered Expression [131]
TNFRSF10A TT5WLRX Strong Biomarker [132]
UGCG TTPHEX3 Strong Biomarker [133]
CD55 TT5Z9WY Definitive Altered Expression [43]
CSF2 TTNYZG2 Definitive Biomarker [134]
EPAS1 TTWPA54 Definitive Genetic Variation [111]
JMJD1C TTBISK4 Definitive Genetic Variation [135]
REN TTB2MXP Definitive Biomarker [62]
SLC46A1 TTY8Z2E Definitive Biomarker [136]
TMPRSS6 TTL9KE7 Definitive Altered Expression [137]
------------------------------------------------------------------------------------
⏷ Show the Full List of 105 DTT(s)
This Disease Is Related to 7 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC28A3 DT4YL5R Limited Biomarker [123]
ATP7A DT0LT17 Strong Biomarker [138]
SLC20A1 DTMULXV Strong Biomarker [139]
SLC25A37 DTLBGTZ Strong Biomarker [140]
SLC25A5 DTL1TRY Strong Biomarker [141]
SLC39A8 DTLPQGT Strong Biomarker [142]
SLC4A1 DTB0Q3P Strong Genetic Variation [143]
------------------------------------------------------------------------------------
⏷ Show the Full List of 7 DTP(s)
This Disease Is Related to 9 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
MARS1 DE0K52I Limited Genetic Variation [144]
ALAS2 DE437BY Disputed Biomarker [145]
ABO DESIA7R Strong Biomarker [146]
AKR1C4 DEAJN47 Strong Genetic Variation [53]
CYP2C8 DES5XRU Strong Genetic Variation [147]
GPT DER5HFI Strong Genetic Variation [148]
PGPEP1 DEVDR46 Strong Biomarker [117]
TPMT DEFQ8VO Strong Biomarker [149]
UBASH3B DE10BJ5 Strong Genetic Variation [150]
------------------------------------------------------------------------------------
⏷ Show the Full List of 9 DME(s)
This Disease Is Related to 147 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ARID2 OTIRJXWM Limited Biomarker [151]
ASPG OT5E2EKR Limited Biomarker [152]
CNOT3 OT4D5Z9L Limited Biomarker [153]
COQ2 OTDAKEY4 Limited Genetic Variation [154]
COX10 OTCYIS0L Limited Altered Expression [155]
FANCB OTMZTXB5 Limited Biomarker [156]
FIP1L1 OTF91GTL Limited Biomarker [48]
H2BC11 OTGM083T Limited Genetic Variation [42]
HBG2 OT4J48JJ Limited Biomarker [157]
KLF1 OT1FK08U Limited Genetic Variation [158]
LRPAP1 OT6DVD2Q Limited Biomarker [159]
MECOM OTP983W8 Limited Biomarker [160]
MPIG6B OTVNKQWA Limited Genetic Variation [161]
SEC61A1 OTLBE3CB Limited Genetic Variation [162]
SMAD4 OTWQWCKG Limited Genetic Variation [163]
STAT5B OTZVPEBT Limited Genetic Variation [164]
TET2 OTKKT03T Limited Genetic Variation [165]
TSPAN33 OTH6C0WU Limited Biomarker [166]
ARL6IP5 OTYZ6BEQ Disputed Genetic Variation [167]
ACAD8 OT3JI5GB moderate Biomarker [168]
AMMECR1 OTWMQ67T moderate Genetic Variation [169]
CHMP2B OTZA7RJB moderate Genetic Variation [120]
CP OTM8JE4Y moderate Altered Expression [170]
DMRT1 OT5PU9U1 moderate Genetic Variation [120]
FUT2 OTLXM6WI moderate Genetic Variation [171]
GLRX5 OTE3L48D moderate Genetic Variation [172]
HBG1 OTVL4NSU moderate Biomarker [157]
IL3 OT0CQ35N moderate Therapeutic [99]
MTX1 OTLSDNZO moderate Biomarker [173]
RARS1 OTHPZ6JN moderate Biomarker [174]
RBM38 OTPO8EXU moderate Genetic Variation [175]
TRNT1 OTD57ILL moderate Altered Expression [176]
ACO1 OT2VUR7L Strong Genetic Variation [177]
ADD2 OTRCPCD2 Strong Biomarker [178]
ADGRE1 OTQQ9Q7G Strong Genetic Variation [179]
ADRM1 OTOU4EY6 Strong Biomarker [104]
AHSP OTTHBSUS Strong Biomarker [180]
AK3 OTM59ZGG Strong Biomarker [85]
ALKBH3 OTS1CD9Z Strong Biomarker [181]
APOA5 OTEVKLVA Strong Genetic Variation [57]
ARHGEF12 OTM2D3LT Strong Biomarker [182]
ASF1A OT4S44GP Strong Biomarker [183]
ATAD1 OTJ02XFL Strong Biomarker [184]
ATG5 OT4T5SMS Strong Biomarker [66]
ATOH8 OT7SY3BN Strong Altered Expression [185]
ATP11C OTKMV2K5 Strong Altered Expression [186]
ATP5F1E OTMPLAIS Strong Genetic Variation [89]
ATP5IF1 OTQFD73H Strong Genetic Variation [89]
B3GLCT OTXH6KOQ Strong Biomarker [187]
BMPER OTBYON4H Strong Genetic Variation [188]
BOC OTXBCY9W Strong Genetic Variation [189]
CAV2 OT1FGRQX Strong Biomarker [70]
CD5L OTPY4WQR Strong Genetic Variation [190]
CLEC11A OT9KBH7C Strong Biomarker [191]
COX4I2 OTB98B21 Strong Genetic Variation [192]
CRPPA OTC85K8Q Strong Genetic Variation [193]
CRYGD OTW29JC4 Strong Biomarker [194]
CUL4A OTTBV70J Strong Biomarker [195]
CYGB OTX153DQ Strong Biomarker [196]
DBI OT884QY9 Strong Biomarker [197]
DHX40 OTOL02QN Strong Biomarker [198]
DIRAS1 OT07F6PE Strong Genetic Variation [199]
DMTN OTDTKPBW Strong Biomarker [200]
DNASE2 OT6RC1BL Strong Biomarker [201]
DNLZ OT48CG1W Strong Biomarker [82]
DUOXA1 OTNG3HH4 Strong Genetic Variation [193]
EBAG9 OTTQLQCP Strong Biomarker [202]
EMB OT67E3Q1 Strong Biomarker [203]
ERFE OTSES1HA Strong Biomarker [82]
ERVW-1 OTWV8DXJ Strong Biomarker [204]
ESAM OTF518AI Strong Genetic Variation [205]
FCGR2C OTNLMNYB Strong Genetic Variation [206]
FLOT2 OTZ0QR5L Strong Biomarker [207]
FTMT OTIUX6XG Strong Biomarker [208]
GATA1 OTX1R7O1 Strong Biomarker [209]
GATA2 OTBP2QQ2 Strong Altered Expression [210]
GDF11 OTOSNMND Strong Biomarker [211]
GIPC1 OTXLVCPJ Strong Genetic Variation [193]
GNLY OTZJKA8C Strong Biomarker [212]
HEPH OTZ2F15Z Strong Genetic Variation [213]
HOXD13 OTWSC8TF Strong Biomarker [214]
IFIH1 OTZA2AHA Strong CausalMutation [215]
IFNA1 OTPMKY0L Strong Biomarker [216]
IFNA8 OTW0PCKU Strong Genetic Variation [56]
IL12RB1 OTM1IJO2 Strong Genetic Variation [217]
INHA OT7HWCO3 Strong Biomarker [218]
INSRR OT3F75WA Strong Genetic Variation [219]
IREB2 OT747D24 Strong Biomarker [177]
ISL1 OTVNVKAX Strong Altered Expression [220]
IVNS1ABP OTYHL4I7 Strong Biomarker [221]
KCNE2 OTUO214Y Strong Biomarker [222]
LHX2 OTK61NP8 Strong Biomarker [220]
LPIN2 OTRRTMXX Strong Altered Expression [223]
LUC7L OT77JDB7 Strong Genetic Variation [224]
MMD OTB5I4OC Strong Altered Expression [225]
MOCOS OT0TL3Q5 Strong Biomarker [226]
MPG OTAHW80B Strong Biomarker [227]
MT1E OTXJKU4Y Strong Biomarker [228]
NCOA5 OTOGWTWB Strong Biomarker [183]
NFE2 OTLM94BI Strong Altered Expression [229]
NR1D2 OT9CVF41 Strong Biomarker [230]
NUP98 OTNT12G2 Strong Biomarker [214]
OAS1 OT8ZLOCY Strong Genetic Variation [231]
OR10A4 OTYYB8SY Strong Genetic Variation [232]
PAEP OTQA0NV4 Strong Biomarker [233]
PDC OT1UUVYY Strong Biomarker [234]
PFN2 OT5SSSA7 Strong Biomarker [235]
PGAM1 OTZ5DB06 Strong Biomarker [236]
PGK1 OT6V1ICH Strong Genetic Variation [237]
PIK3C2A OTFBU4GD Strong Genetic Variation [238]
PMCH OT3D9SA4 Strong Biomarker [239]
POU1F1 OTXT8A5C Strong Biomarker [139]
PRB1 OTV0SYMD Strong Biomarker [240]
PRKAG2 OTHTAM54 Strong Genetic Variation [241]
PROCR OTRHED17 Strong Biomarker [242]
PRSS27 OTC4G4UF Strong Genetic Variation [243]
RHOC OTOLE1FT Strong Biomarker [106]
RPL10A OTDLCJ53 Strong Biomarker [244]
RPS14 OTB90KV5 Strong Biomarker [245]
RPS15 OT0WYZYG Strong Genetic Variation [199]
RPS19 OTBKGP48 Strong Genetic Variation [209]
RPS7 OTIK25WI Strong Genetic Variation [246]
RTN3 OTGZ51QF Strong Genetic Variation [179]
RUNX1T1 OT30DED5 Strong Genetic Variation [53]
SAMD14 OTLDQW51 Strong Biomarker [247]
SAMHD1 OTBCIBC7 Strong Genetic Variation [248]
SEC23B OT2NFSIQ Strong Genetic Variation [249]
SFTPA1 OT87XL1U Strong Biomarker [250]
SHMT2 OT5NCAZN Strong Biomarker [251]
SIGLEC1 OTNWSQA9 Strong Biomarker [252]
SIPA1 OTXY5RXC Strong Biomarker [250]
SMARCA5 OT5GR4Z2 Strong Biomarker [253]
SMCP OTXKY794 Strong Biomarker [226]
SMIM10L2B OT04IG2N Strong Biomarker [254]
SPTA1 OT1YMP65 Strong Genetic Variation [255]
ST13 OTNML6UP Strong Biomarker [256]
STK40 OT4R325X Strong Genetic Variation [257]
TBX1 OTQLBPRA Strong Biomarker [258]
TCL1B OT4CSO39 Strong Altered Expression [126]
THOC5 OTHY50SK Strong Biomarker [259]
TMED3 OTNOPHHC Strong Biomarker [260]
TREX1 OTQG7K12 Strong Genetic Variation [261]
TRIT1 OTCU9FS5 Strong Genetic Variation [262]
TTC7A OTDHLPQM Strong Genetic Variation [263]
IL17RD OTKD9XST Definitive Genetic Variation [264]
IL17RE OTMFTNLS Definitive Genetic Variation [264]
RASA3 OT9C54MN Definitive Genetic Variation [265]
------------------------------------------------------------------------------------
⏷ Show the Full List of 147 DOT(s)

References

1 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
2 Emerging treatments for traumatic brain injury. Expert Opin Emerg Drugs. 2009 Mar;14(1):67-84.
3 FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (BLA) 103951.
4 Clinical pipeline report, company report or official report of Eisai.
5 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: 7396).
6 ClinicalTrials.gov (NCT02268409) ACE-536 Extension Study - Beta Thalassemia. U.S. National Institutes of Health.
7 Comparison of the therapeutic effects of epoetin zeta to epoetin alfa in the maintenance phase of renal anaemia treatment. Curr Med Res Opin. 2008 Mar;24(3):625-37.
8 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800033828)
9 Clinical pipeline report, company report or official report of Takeda.
10 ClinicalTrials.gov (NCT00038454) Phase II Study To Evaluate The Safety and Efficacy of Hemoglobin Raffimer in Patients Undergoing First Time CABG Surgery. U.S. National Institutes of Health.
11 ClinicalTrials.gov (NCT02287896) Pharmacokinetics and Safety of Roledumab, in RhD-negative Pregnant Women Carrying an RhD-positive Foetus. U.S. National Institutes of Health.
12 ClinicalTrials.gov (NCT01987908) Evaluation of Different Dose Regimens of Aes-103 Given for 28 Days to Subjects With Stable Sickle Cell Disease. U.S. National Institutes of Health.
13 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: 8456).
14 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800026354)
15 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.
16 ClinicalTrials.gov (NCT00968617) A Study of MK2578 in Patients With Chronic Kidney Disease Who Are Not on Dialysis (2578-002). U.S. National Institutes of Health.
17 The effects of the anti-hepcidin Spiegelmer NOX-H94 on inflammation-induced anemia in cynomolgus monkeys. Blood. 2013 Mar 21;121(12):2311-5.
18 Clinical pipeline report, company report or official report of Rockwell Medical Inc.
19 ClinicalTrials.gov (NCT01671111) Study for Transfusionally Iron Overloaded Children, Adolescents and Adults Using FBS0701 (SSP-004184). U.S. National Institutes of Health.
20 ClinicalTrials.gov (NCT00542568) Safety and Efficacy of Sustained Erythropoietin Therapy. U.S. National Institutes of Health.
21 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800016000)
22 Clinical pipeline report, company report or official report of Acceleron Pharma (2011).
23 ClinicalTrials.gov (NCT02241200) A Study in Healthy Volunteers to Compare the Profiles of DA-3880 and EU Sourced ARANESP (Amgen). U.S. National Institutes of Health.
24 ClinicalTrials.gov (NCT02299661) Pilot PK/PD Study of DS-1093a in Patients With Chronic Kidney Disease. U.S. National Institutes of Health.
25 ClinicalTrials.gov (NCT01991483) A Study of LY2928057 in Hemodialysis Participants. U.S. National Institutes of Health.
26 ClinicalTrials.gov (NCT01363934) To Evaluate the Safety, Tolerability, and Pharmacokinetics/Pharmacodynamics of Erythropoietin. U.S. National Institutes of Health.
27 ClinicalTrials.gov (NCT01340976) A Phase 1 Study of LY2787106 in Cancer and Anemia. U.S. National Institutes of Health.
28 ClinicalTrials.gov (NCT01030315) A Study of HM10760A (Long-acting Erythropoietin) in Healthy Adult Caucasian and Japanese Subjects. U.S. National Institutes of Health.
29 ClinicalTrials.gov (NCT01340976) A Phase 1 Study of LY2787106 in Cancer and Anemia. U.S. National Institutes of Health.
30 In vivo selection for human and murine hematopoietic cells transduced with a therapeutic MGMT lentiviral vector that inhibits HIV replication. Mol Ther. 2004 Feb;9(2):160-72.
31 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800011182)
32 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800013086)
33 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800025976)
34 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800027346)
35 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800017518)
36 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800008362)
37 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
38 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. (Target id: 1718).
39 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: 4921).
40 Genetic variability in drug transport, metabolism or DNA repair affecting toxicity of chemotherapy in ovarian cancer.BMC Pharmacol Toxicol. 2015 Feb 27;16:2. doi: 10.1186/s40360-015-0001-5.
41 Correcting Smad1/5/8, mTOR, and VEGFR2 treats pathology in hereditary hemorrhagic telangiectasia models.J Clin Invest. 2020 Feb 3;130(2):942-957. doi: 10.1172/JCI127425.
42 Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit.Blood Cells Mol Dis. 2015 Dec;55(4):273-80. doi: 10.1016/j.bcmd.2015.07.008. Epub 2015 Jul 16.
43 Expression pattern of CD55 and CD59 on red blood cells in sickle cell disease.Hematology. 2017 Mar;22(2):105-113. doi: 10.1080/10245332.2016.1231988. Epub 2016 Sep 25.
44 Outcomes during anticoagulation in patients with symptomatic vs. incidental splanchnic vein thrombosis.Thromb Res. 2018 Apr;164:69-74. doi: 10.1016/j.thromres.2018.02.143. Epub 2018 Mar 2.
45 Gender differences in the impact of anemia on subclinical myocardial damage and cardiovascular mortality in the general population: The Yamagata (Takahata) study.Int J Cardiol. 2018 Feb 1;252:207-212. doi: 10.1016/j.ijcard.2017.11.019. Epub 2017 Nov 10.
46 HLA-B*15:02 is associated with anemia in patients with chronic hepatitis C treated with pegylated interferon- and ribavirin.Tissue Antigens. 2012 Nov;80(5):424-30. doi: 10.1111/j.1399-0039.2012.01956.x. Epub 2012 Aug 30.
47 Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.Lipids Health Dis. 2019 Jun 5;18(1):132. doi: 10.1186/s12944-019-1045-0.
48 Response to imatinib mesylate in patients with hypereosinophilic syndrome.Int J Hematol. 2012 Sep;96(3):320-6. doi: 10.1007/s12185-012-1141-7. Epub 2012 Jul 18.
49 Prolactinomas in males: any differences?.Pituitary. 2020 Feb;23(1):52-57. doi: 10.1007/s11102-019-01009-y.
50 Clinical and Laboratory Associations with Persistent Hyperferritinemia in 373 Black Hemochromatosis and Iron Overload Screening Study Participants.Ann Hepatol. 2017 Sep-Oct;16(5):802-811. doi: 10.5604/01.3001.0010.2815.
51 Sustained viral response and treatment-induced cytopenia correlate with SLCs and KLF12 genotypes in interferon/ribavirin-treated Chinese chronic hepatitis C patients.J Gastroenterol Hepatol. 2016 Aug;31(8):1489-97. doi: 10.1111/jgh.13290.
52 Anemia in Patients With Resistance to Thyroid Hormone : A Role for Thyroid Hormone Receptor in Human Erythropoiesis.J Clin Endocrinol Metab. 2017 Sep 1;102(9):3517-3525. doi: 10.1210/jc.2017-00840.
53 Utility of the low-accelerating-dose regimen in 182 liver recipients with recurrent hepatitis C virus.World J Gastroenterol. 2015 May 28;21(20):6236-45. doi: 10.3748/wjg.v21.i20.6236.
54 Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis. Clin Genet. 2016 Jul;90(1):69-78. doi: 10.1111/cge.12749. Epub 2016 Mar 15.
55 Baseline hemoglobin <11.0 g/dL has stronger prognostic value than anemia status in nasopharynx cancers treated with chemoradiotherapy.Int J Biol Markers. 2019 Jun;34(2):139-147. doi: 10.1177/1724600818821688. Epub 2019 Mar 13.
56 Reduced interferon (IFN)- conditioned by IFNA2 (-173) and IFNA8 (-884) haplotypes is associated with enhanced susceptibility to severe malarial anemia and longitudinal all-cause mortality.Hum Genet. 2012 Aug;131(8):1375-91. doi: 10.1007/s00439-012-1175-1. Epub 2012 May 9.
57 The Methylenetetrahydrofolate Reductase C677T (rs1801133) and Apolipoprotein A5-1131T>C (rs662799) Polymorphisms, and Anemia Are Independent Risk Factors for Ischemic Stroke.J Stroke Cerebrovasc Dis. 2018 May;27(5):1357-1362. doi: 10.1016/j.jstrokecerebrovasdis.2017.12.025. Epub 2018 Feb 3.
58 The True Story on Deficiencies After Sleeve Gastrectomy: Results of a Double-Blind RCT.Obes Surg. 2020 Apr;30(4):1280-1290. doi: 10.1007/s11695-019-04252-1.
59 Change in iron transporter expression in human term placenta with different maternal iron status.Eur J Obstet Gynecol Reprod Biol. 2008 Sep;140(1):48-54. doi: 10.1016/j.ejogrb.2008.02.012. Epub 2008 Jun 30.
60 Phase II trial of carboplatin and pemetrexed as first-line chemotherapy for non-squamous non-small cell lung cancer, and correlation between the efficacy/toxicity and genetic polymorphisms associated with pemetrexed metabolism: Hokkaido Lung Cancer Clinical Study Group Trial (HOT) 0902.Cancer Chemother Pharmacol. 2014 Dec;74(6):1149-57. doi: 10.1007/s00280-014-2589-3. Epub 2014 Oct 8.
61 Differentiation of erythroblast requires the dimeric form of acetylcholinesterase: Interference with erythropoietin receptor.Chem Biol Interact. 2019 Aug 1;308:317-322. doi: 10.1016/j.cbi.2019.06.006. Epub 2019 Jun 4.
62 Inhibition of the renin-angiotensin system in the cardiorenal syndrome with anaemia: a double-edged sword.J Hypertens. 2019 Nov;37(11):2145-2153. doi: 10.1097/HJH.0000000000002111.
63 Delta-aminolevulinate dehydratase activity in red blood cells of rats infected with Trypanosoma evansi.Parasitology. 2011 Sep;138(10):1272-7. doi: 10.1017/S0031182011000989.
64 Apolipoprotein A-I Is a Prognosticator of Nasopharyngeal Carcinoma in the Era of Intensity-modulated Radiotherapy.J Cancer. 2018 Jan 11;9(4):702-710. doi: 10.7150/jca.22836. eCollection 2018.
65 Impact of IL28B, APOH and ITPA Polymorphisms on Efficacy and Safety of TVR- or BOC-Based Triple Therapy in Treatment-Experienced HCV-1 Patients with Compensated Cirrhosis from the ANRS CO20-CUPIC Study.PLoS One. 2015 Dec 15;10(12):e0145105. doi: 10.1371/journal.pone.0145105. eCollection 2015.
66 Autophagy limits proliferation and glycolytic metabolism in acute myeloid leukemia.Cell Death Discov. 2015 Aug 17;1:15008-. doi: 10.1038/cddiscovery.2015.8.
67 Nuclear factor erythroid 2-related factors 1 and 2 are able to define the worst prognosis group among high-risk diffuse large B cell lymphomas treated with R-CHOEP.J Clin Pathol. 2019 Apr;72(4):316-321. doi: 10.1136/jclinpath-2018-205584. Epub 2019 Feb 12.
68 Pathways for the regulation of hepcidin expression in anemia of chronic disease and iron deficiency anemia in vivo.Haematologica. 2011 Dec;96(12):1761-9. doi: 10.3324/haematol.2011.048926. Epub 2011 Aug 22.
69 FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability.Mol Cell Biol. 2008 Jun;28(12):4116-28. doi: 10.1128/MCB.02210-07. Epub 2008 Apr 21.
70 Severe neurologic disease and chick mortality in crested screamers (Chauna torquata) infected with a novel Gyrovirus.Virology. 2018 Jul;520:111-115. doi: 10.1016/j.virol.2018.05.014. Epub 2018 May 28.
71 Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.Am J Hematol. 2018 May;93(5):672-682. doi: 10.1002/ajh.25058. Epub 2018 Feb 24.
72 Early and late hematologic toxicity following CD19 CAR-T cells.Bone Marrow Transplant. 2019 Oct;54(10):1643-1650. doi: 10.1038/s41409-019-0487-3. Epub 2019 Feb 26.
73 Splenomegaly induced by anemia impairs T cell movement in the spleen partially via EPO.Mol Immunol. 2019 Aug;112:399-405. doi: 10.1016/j.molimm.2019.06.021. Epub 2019 Jul 9.
74 Cdk6 contributes to cytoskeletal stability in erythroid cells.Haematologica. 2017 Jun;102(6):995-1005. doi: 10.3324/haematol.2016.159947. Epub 2017 Mar 2.
75 Clinical features and treatment of patients with lung adenocarcinoma with bone marrow metastasis.Tumori. 2019 Oct;105(5):388-393. doi: 10.1177/0300891619839864. Epub 2019 Apr 1.
76 Efficacy of granulocyte colony stimulating factor in combination with erythropoiesis stimulating agents for treatment of anemia in patients with lower risk myelodysplastic syndromes: A systematic review.Crit Rev Oncol Hematol. 2019 Apr;136:37-47. doi: 10.1016/j.critrevonc.2019.01.021. Epub 2019 Feb 15.
77 Molecular pathogenesis of myelodysplastic syndromes with deletion 5q.Eur J Haematol. 2019 Mar;102(3):203-209. doi: 10.1111/ejh.13207. Epub 2019 Jan 16.
78 Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells.Sci Rep. 2018 Feb 5;8(1):2351. doi: 10.1038/s41598-018-20731-4.
79 Crystal Structure of Human Dual-Specificity Tyrosine-Regulated Kinase 3 Reveals New Structural Features and Insights into its Auto-phosphorylation.J Mol Biol. 2018 May 11;430(10):1521-1530. doi: 10.1016/j.jmb.2018.04.001. Epub 2018 Apr 7.
80 E2F-2 Promotes Nuclear Condensation and Enucleation of Terminally Differentiated Erythroblasts.Mol Cell Biol. 2016 Dec 19;37(1):e00274-16. doi: 10.1128/MCB.00274-16. Print 2017 Jan 1.
81 Application of in-vitro screening methods on hypoxia inducible factor prolyl hydroxylase inhibitors.Bioorg Med Chem. 2017 Aug 1;25(15):3891-3899. doi: 10.1016/j.bmc.2017.05.026. Epub 2017 May 13.
82 Hepcidin-25/erythroferrone ratio predicts improvement of anaemia in haemodialysis patients treated with ferric citrate hydrate.Nephrology (Carlton). 2019 Aug;24(8):819-826. doi: 10.1111/nep.13495. Epub 2019 Apr 29.
83 Model-based approach for methoxy polyethylene glycol-epoetin beta drug development in paediatric patients with anaemia of chronic kidney disease.Br J Clin Pharmacol. 2020 Apr;86(4):801-811. doi: 10.1111/bcp.14186. Epub 2020 Jan 21.
84 Venous thromboprophylaxis after total hip arthroplasty: aspirin, warfarin, enoxaparin, or factor Xa inhibitors?.Hip Int. 2020 Sep;30(5):564-571. doi: 10.1177/1120700019841600. Epub 2019 Apr 16.
85 Clinical manifestations and management of labor and delivery in women with factor IX deficiency.Haemophilia. 2004 Sep;10(5):483-90. doi: 10.1111/j.1365-2516.2004.00946.x.
86 Severe Anemia Is Associated with Intestinal Injury in Preterm Neonates.Am J Perinatol. 2020 May;37(6):603-606. doi: 10.1055/s-0039-1683982. Epub 2019 Apr 4.
87 HSP90 Shapes the Consequences of Human Genetic Variation.Cell. 2017 Feb 23;168(5):856-866.e12. doi: 10.1016/j.cell.2017.01.023. Epub 2017 Feb 16.
88 Functional haplotypes of Fc gamma (Fc) receptor (FcRIIA and FcRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan children.Hum Genet. 2012 Feb;131(2):289-99. doi: 10.1007/s00439-011-1076-8. Epub 2011 Aug 5.
89 Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts.Nature. 2012 Nov 22;491(7425):608-12. doi: 10.1038/nature11536. Epub 2012 Nov 7.
90 FGF23 at the crossroads of phosphate, iron economy and erythropoiesis.Nat Rev Nephrol. 2020 Jan;16(1):7-19. doi: 10.1038/s41581-019-0189-5. Epub 2019 Sep 13.
91 Lower Esophageal Sphincter-preserving Anastomosis Is an Acceptable Reconstruction Method Following Laparoscopy-assisted Proximal Gastrectomy.Anticancer Res. 2019 Jan;39(1):425-430. doi: 10.21873/anticanres.13129.
92 Glucose-6-phosphate dehydrogenase deficiency and risk of cardiovascular disease: A propensity score-matched study.Atherosclerosis. 2019 Mar;282:148-153. doi: 10.1016/j.atherosclerosis.2019.01.027. Epub 2019 Jan 28.
93 Thrombocytopenia and GBA gene mutation in a patient with adult type 1 Gaucher disease.Platelets. 2017 Dec;28(8):829-831. doi: 10.1080/09537104.2017.1306044. Epub 2017 Jun 5.
94 Haematological and biochemical toxicity induced by methanol in rats: ameliorative effects of Opuntia vulgaris fruit extract.Hum Exp Toxicol. 2011 Dec;30(12):1963-71. doi: 10.1177/0960327111403175. Epub 2011 Mar 21.
95 [Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].Humangenetik. 1966;2(3):287-316. doi: 10.1007/BF00395947.
96 Beta-thalassemia: renal complications and mechanisms: a narrative review.Hematology. 2019 Dec;24(1):426-438. doi: 10.1080/16078454.2019.1599096.
97 Effect of percutaneous paravalvular leak closure on hemolysis.Catheter Cardiovasc Interv. 2019 Mar 1;93(4):713-719. doi: 10.1002/ccd.27917. Epub 2018 Oct 2.
98 Deficiency in interferon type 1 receptor improves definitive erythropoiesis in Klf1 null mice.Cell Death Differ. 2018 Mar;25(3):589-599. doi: 10.1038/s41418-017-0003-5. Epub 2017 Dec 11.
99 Antagonism between interleukin 3 and erythropoietin in mice with azidothymidine-induced anemia and in bone marrow endothelial cells.Cytokine. 2002 Apr 7;18(1):51-60. doi: 10.1006/cyto.2002.1029.
100 Polymorphic variability in the 3' untranslated region (UTR) of IL12B is associated with susceptibility to severe anaemia in Kenyan children with acute Plasmodium falciparum malaria.BMC Genet. 2011 Aug 6;12:69. doi: 10.1186/1471-2156-12-69.
101 Role of Intracystic Cytokines and Nitric Oxide in Ovarian Neoplasms.Scand J Immunol. 2017 Dec;86(6):462-470. doi: 10.1111/sji.12617. Epub 2017 Oct 22.
102 Momelotinib inhibits ACVR1/ALK2, decreases hepcidin production, and ameliorates anemia of chronic disease in rodents.Blood. 2017 Mar 30;129(13):1823-1830. doi: 10.1182/blood-2016-09-740092. Epub 2017 Feb 10.
103 The fraction of CD117/c-KIT-expressing erythroid precursors predicts ESA response in low-risk myelodysplastic syndromes.Cytometry B Clin Cytom. 2019 May;96(3):215-222. doi: 10.1002/cyto.b.21781. Epub 2019 Apr 9.
104 Maternal Characteristics Affect Fetal Growth Response in the Women First Preconception Nutrition Trial.Nutrients. 2019 Oct 21;11(10):2534. doi: 10.3390/nu11102534.
105 Molecular basis of reduced LAIR1 expression in childhood severe malarial anaemia: Implications for leukocyte inhibitory signalling.EBioMedicine. 2019 Jul;45:278-289. doi: 10.1016/j.ebiom.2019.06.040. Epub 2019 Jun 27.
106 Gene expression profiles associated with anaemia and ITPA genotypes in patients with chronic hepatitis C (CH-C).J Viral Hepat. 2012 Jun;19(6):414-22. doi: 10.1111/j.1365-2893.2011.01564.x. Epub 2011 Dec 7.
107 Steady-state plasma lactoferrin levels in relation to infections and complications of sickle cell disease.Hematol J. 2004;5(4):371-2. doi: 10.1038/sj.thj.6200372.
108 Fermented Goat Milk Consumption Enhances Brain Molecular Functions during Iron Deficiency Anemia Recovery.Nutrients. 2019 Oct 7;11(10):2394. doi: 10.3390/nu11102394.
109 Congenital amegakaryocytic thrombocytopenia iPS cells exhibit defective MPL-mediated signaling.J Clin Invest. 2013 Sep;123(9):3802-14. doi: 10.1172/JCI64721. Epub 2013 Aug 1.
110 CA 15-3 predicting breast cancer relapse: beware of vitamin B12 deficiency.Per Med. 2018 May 1;15(3):163-165. doi: 10.2217/pme-2017-0067. Epub 2018 May 10.
111 NCOA4 maintains murine erythropoiesis via cell autonomous and non-autonomous mechanisms.Haematologica. 2019 Jul;104(7):1342-1354. doi: 10.3324/haematol.2018.204123. Epub 2019 Jan 10.
112 NIMA-related kinase 1 (NEK1) regulates meiosis I spindle assembly by altering the balance between -Adducin and Myosin X.PLoS One. 2017 Oct 5;12(10):e0185780. doi: 10.1371/journal.pone.0185780. eCollection 2017.
113 A Forward Genetic Screen Targeting the Endothelium Reveals a Regulatory Role for the Lipid Kinase Pi4ka in Myelo- and Erythropoiesis.Cell Rep. 2018 Jan 30;22(5):1211-1224. doi: 10.1016/j.celrep.2018.01.017.
114 Dyserythropoiesis in a child with pyruvate kinase deficiency and coexistent unilateral multicystic dysplastic kidney.Pediatr Blood Cancer. 2014 Aug;61(8):1463-5. doi: 10.1002/pbc.24953. Epub 2014 Jan 30.
115 Nucleoside-phosphorylase deficiency in a child with severely defective T-cell immunity and normal B-cell immunity.Lancet. 1975 May 3;1(7914):1010-3. doi: 10.1016/s0140-6736(75)91950-9.
116 High-content screening in zebrafish embryos identifies butafenacil as a potent inducer of anemia.PLoS One. 2014 Aug 4;9(8):e104190. doi: 10.1371/journal.pone.0104190. eCollection 2014.
117 A Model to Predict In-Hospital Mortality in HIV/AIDS Patients with Pneumocystis Pneumonia in China: The Clinical Practice in Real World.Biomed Res Int. 2019 Feb 17;2019:6057028. doi: 10.1155/2019/6057028. eCollection 2019.
118 Management of red cell alloimmunisation in pregnancy: the non-invasive monitoring of the disease.Prenat Diagn. 2010 Jul;30(7):668-73. doi: 10.1002/pd.2551.
119 Activin Receptor II Ligand Traps: New Treatment Paradigm for Low-Risk MDS.Curr Hematol Malig Rep. 2019 Aug;14(4):346-351. doi: 10.1007/s11899-019-00517-9.
120 The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease.PLoS One. 2017 Oct 12;12(10):e0185822. doi: 10.1371/journal.pone.0185822. eCollection 2017.
121 Fermented goat milk consumption during anaemia recovery: ergogenic effect and improvement of skeletal muscle homeostasis.Eur J Nutr. 2017 Oct;56(7):2277-2287. doi: 10.1007/s00394-016-1268-z. Epub 2016 Jul 13.
122 Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies.J Inherit Metab Dis. 2019 Jul;42(4):581-597. doi: 10.1002/jimd.12125. Epub 2019 Jun 24.
123 Role of ITPA and SLC28A2 genes in the prediction of anaemia associated with protease inhibitor plus ribavirin and peginterferon in hepatitis C treatment. J Clin Virol. 2015 Jul;68:56-60.
124 Intestinal brush-border Na+/H+ exchanger-3 drives H+-coupled iron absorption in the mouse.Am J Physiol Gastrointest Liver Physiol. 2016 Sep 1;311(3):G423-30. doi: 10.1152/ajpgi.00167.2016. Epub 2016 Jul 7.
125 Pharmacogenetic analysis of advanced non-small-cell lung cancer patients treated with first-line paclitaxel and carboplatin chemotherapy. Pharmacogenet Genomics. 2016 Mar;26(3):116-25.
126 TCL1 expression predicts overall survival in patients with mantle cell lymphoma.Eur J Haematol. 2015 Dec;95(6):583-94. doi: 10.1111/ejh.12539. Epub 2015 Mar 16.
127 Transient erythroblastopenia of childhood associated with human herpesvirus type 6, variant B.Am J Clin Pathol. 1997 Aug;108(2):127-32. doi: 10.1093/ajcp/108.2.127.
128 Identification of protein changes in the blood plasma of lung cancer patients subjected to chemotherapy using a 2D-DIGE approach.PLoS One. 2019 Oct 17;14(10):e0223840. doi: 10.1371/journal.pone.0223840. eCollection 2019.
129 Evaluation of reticulocyte hemoglobin for assessment of anemia in rheumatological disorders.Int J Rheum Dis. 2019 May;22(5):815-825. doi: 10.1111/1756-185X.13567. Epub 2019 Apr 9.
130 HLA-DQ2/DQ8 frequency in adult patients with celiac disease, their first-degree relatives, and normal population in Turkey.Turk J Gastroenterol. 2019 Apr;30(4):321-325. doi: 10.5152/tjg.2019.18255.
131 Anemia and thrombocytosis induced by ribavirin monotherapy in patients with chronic hepatitis C.J Gastroenterol. 2012 Nov;47(11):1228-37. doi: 10.1007/s00535-012-0579-y. Epub 2012 Mar 30.
132 Mapatumumab, an antibody targeting TRAIL-R1, in combination with paclitaxel and carboplatin in patients with advanced solid malignancies: results of a phase I and pharmacokinetic study.J Clin Oncol. 2009 Sep 10;27(26):4413-21. doi: 10.1200/JCO.2008.21.7422. Epub 2009 Aug 3.
133 Risk factors associated with in-hospital mortality in elderly patients admitted to a regional trauma center after sustaining a fall.Aging Clin Exp Res. 2017 Jun;29(3):427-433. doi: 10.1007/s40520-016-0579-5. Epub 2016 May 3.
134 Full-dose CHOP chemotherapy combined with granulocyte colony-stimulating factor for aggressive non-Hodgkin's lymphoma in elderly patients: a prospective study.Ann Hematol. 2001 Oct;80(10):602-6. doi: 10.1007/s002770100358.
135 Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.PLoS One. 2017 Apr 13;12(4):e0175681. doi: 10.1371/journal.pone.0175681. eCollection 2017.
136 A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency.Blood. 2011 May 5;117(18):4895-904. doi: 10.1182/blood-2010-04-279653. Epub 2011 Feb 23.
137 RNAi-mediated reduction of hepatic Tmprss6 diminishes anemia and secondary iron overload in a splenectomized mouse model of -thalassemia intermedia.Am J Hematol. 2018 Jun;93(6):745-750. doi: 10.1002/ajh.25079. Epub 2018 Mar 23.
138 Investigation of iron metabolism in mice expressing a mutant Menke's copper transporting ATPase (Atp7a) protein with diminished activity (Brindled; Mo (Br) (/y) ).PLoS One. 2013 Jun 11;8(6):e66010. doi: 10.1371/journal.pone.0066010. Print 2013.
139 Mice lacking the sodium-dependent phosphate import protein, PiT1 (SLC20A1), have a severe defect in terminal erythroid differentiation and early B cell development.Exp Hematol. 2013 May;41(5):432-43.e7. doi: 10.1016/j.exphem.2013.01.004. Epub 2013 Jan 30.
140 Reduction of mitoferrin results in abnormal development and extended lifespan in Caenorhabditis elegans.PLoS One. 2012;7(1):e29666. doi: 10.1371/journal.pone.0029666. Epub 2012 Jan 11.
141 Mitochondrial ATP transporter Ant2 depletion impairs erythropoiesis and B lymphopoiesis.Cell Death Differ. 2015 Sep;22(9):1437-50. doi: 10.1038/cdd.2014.230. Epub 2015 Jan 23.
142 In utero gene expression in the Slc39a8(neo/neo) knockdown mouse.Sci Rep. 2018 Jul 16;8(1):10703. doi: 10.1038/s41598-018-29109-y.
143 Promoter polymorphism of the anion-exchange protein 1 associated with severe malarial anemia and fatality.J Infect Dis. 2006 Oct 1;194(7):949-57. doi: 10.1086/507430. Epub 2006 Aug 30.
144 Mutations in methionyl-tRNA synthetase gene in a Chinese family with interstitial lung and liver disease, postnatal growth failure and anemia.J Hum Genet. 2017 Jun;62(6):647-651. doi: 10.1038/jhg.2017.10. Epub 2017 Feb 2.
145 A toxicogenomic approach for identifying biomarkers for myelosuppressive anemia in rats.Toxicology. 2011 Apr 11;282(3):139-45. doi: 10.1016/j.tox.2011.01.027. Epub 2011 Feb 4.
146 Increased susceptibility of blood type O individuals to develop anemia in Plasmodium vivax infection.Infect Genet Evol. 2017 Jun;50:87-92. doi: 10.1016/j.meegid.2017.03.001. Epub 2017 Mar 6.
147 SNPs and taxane toxicity in breast cancer patients.Pharmacogenomics. 2014;15(15):1845-58. doi: 10.2217/pgs.14.127.
148 Pralatrexate in Chinese Patients with Relapsed or Refractory Peripheral T-cell Lymphoma: A Single-arm, Multicenter Study.Target Oncol. 2019 Apr;14(2):149-158. doi: 10.1007/s11523-019-00630-y.
149 Expressing thiopurine S-methyltransferase activity as units per litre of whole-blood overcomes misleading high results in patients with anaemia.Ann Clin Biochem. 2010 Sep;47(Pt 5):408-14. doi: 10.1258/acb.2010.010058. Epub 2010 Jul 1.
150 Propensity score matching analysis of a phase II study on simultaneous modulated accelerated radiation therapy using helical tomotherapy for nasopharyngeal carcinomas.BMC Cancer. 2017 Aug 29;17(1):582. doi: 10.1186/s12885-017-3581-1.
151 The chromatin remodeling subunit Baf200 promotes normal hematopoiesis and inhibits leukemogenesis.J Hematol Oncol. 2018 Feb 26;11(1):27. doi: 10.1186/s13045-018-0567-7.
152 The sonographic appearance of cyclophosphamide-induced acute haemorrhagic cystitis.Clin Radiol. 1990 Apr;41(4):289-90. doi: 10.1016/s0009-9260(05)81670-8.
153 Insufficient liver maturation affects murine early postnatal hair cycle.Biochem Biophys Res Commun. 2020 Jan 1;521(1):172-177. doi: 10.1016/j.bbrc.2019.10.099. Epub 2019 Oct 18.
154 Merozoite surface antigen 1 and 2 genotypes and rosetting of Plasmodium falciparum in severe and mild malaria in Lambarn, Gabon.Trans R Soc Trop Med Hyg. 1998 Jan-Feb;92(1):110-4. doi: 10.1016/s0035-9203(98)90979-8.
155 Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.Hum Mol Genet. 2003 Oct 15;12(20):2693-702. doi: 10.1093/hmg/ddg284. Epub 2003 Aug 19.
156 Fas ligand expression in the bone marrow in myelodysplastic syndromes correlates with FAB subtype and anemia, and predicts survival.Leukemia. 1999 Jan;13(1):44-53. doi: 10.1038/sj.leu.2401233.
157 Lentiviral Transfer of -Globin with Fusion Gene NUP98-HOXA10HD Expands Hematopoietic Stem Cells and Ameliorates Murine -Thalassemia.Mol Ther. 2017 Mar 1;25(3):593-605. doi: 10.1016/j.ymthe.2017.01.019. Epub 2017 Feb 9.
158 Novel mutations in KLF1 encoding the In(Lu) phenotype reflect a diversity of clinical presentations.Transfusion. 2018 Jan;58(1):196-199. doi: 10.1111/trf.14378. Epub 2017 Oct 19.
159 Modified activin receptor IIB ligand trap mitigates ineffective erythropoiesis and disease complications in murine -thalassemia.Blood. 2014 Jun 19;123(25):3864-72. doi: 10.1182/blood-2013-06-511238. Epub 2014 May 2.
160 EVI1 Impairs myelopoiesis by deregulation of PU.1 function.Cancer Res. 2009 Feb 15;69(4):1633-42. doi: 10.1158/0008-5472.CAN-08-2562. Epub 2009 Feb 10.
161 Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia.Eur J Haematol. 2017 Mar;98(3):218-227. doi: 10.1111/ejh.12819. Epub 2017 Jan 3.
162 Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia.Am J Hum Genet. 2016 Jul 7;99(1):174-87. doi: 10.1016/j.ajhg.2016.05.028.
163 Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation.J Gastroenterol. 2012 Jul;47(7):795-804. doi: 10.1007/s00535-012-0545-8. Epub 2012 Feb 14.
164 Integrative view on how erythropoietin signaling controls transcription patterns in erythroid cells.Curr Opin Hematol. 2018 May;25(3):189-195. doi: 10.1097/MOH.0000000000000415.
165 A zebrafish model of myelodysplastic syndrome produced through tet2 genomic editing.Mol Cell Biol. 2015 Mar;35(5):789-804. doi: 10.1128/MCB.00971-14. Epub 2014 Dec 15.
166 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.
167 Haptoglobin genotype, anaemia and malaria in Gambian children.Trop Med Int Health. 2008 Jan;13(1):76-82. doi: 10.1111/j.1365-3156.2007.01976.x.
168 Inflammation, but Not the Underlying Disease or Its Location, Predicts Oral Iron Absorption Capacity in Patients With Inflammatory Bowel Disease.J Crohns Colitis. 2020 Mar 13;14(3):316-322. doi: 10.1093/ecco-jcc/jjz149.
169 X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.Gene. 2017 Mar 30;606:47-52. doi: 10.1016/j.gene.2017.01.001. Epub 2017 Jan 9.
170 Clinical relevance of heterozygosis for aceruloplasminemia.Am J Med Genet B Neuropsychiatr Genet. 2019 Jun;180(4):266-271. doi: 10.1002/ajmg.b.32723. Epub 2019 Mar 22.
171 Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant.Biochimie. 2013 May;95(5):995-1001. doi: 10.1016/j.biochi.2013.01.022. Epub 2013 Feb 8.
172 The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. Blood. 2007 Aug 15;110(4):1353-8. doi: 10.1182/blood-2007-02-072520. Epub 2007 May 7.
173 Cytopenias among patients with rheumatic diseases using methotrexate: a meta-analysis of randomized controlled clinical trials.Rheumatology (Oxford). 2020 Apr 1;59(4):709-717. doi: 10.1093/rheumatology/kez343.
174 The role of JAK2 mutations in RARS and other MDS.Hematology Am Soc Hematol Educ Program. 2008:52-9. doi: 10.1182/asheducation-2008.1.52.
175 RNA Binding Protein RBM38 Regulates Expression of the 11-Kilodalton Protein of Parvovirus B19, Which Facilitates Viral DNA Replication.J Virol. 2018 Mar 28;92(8):e02050-17. doi: 10.1128/JVI.02050-17. Print 2018 Apr 15.
176 Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Hum Mol Genet. 2016 Jan 1;25(1):44-56. doi: 10.1093/hmg/ddv446. Epub 2015 Oct 22.
177 Iron-regulatory proteins secure iron availability in cardiomyocytes to prevent heart failure.Eur Heart J. 2017 Feb 1;38(5):362-372. doi: 10.1093/eurheartj/ehw333.
178 Haematological phenotypes in relation to the C1797T beta-adducin polymorphism in a Caucasian population.Clin Sci (Lond). 2003 Apr;104(4):369-76.
179 Association of candidate gene polymorphisms and TGF-beta/IL-10 levels with malaria in three regions of Cameroon: a case-control study.Malar J. 2014 Jun 16;13:236. doi: 10.1186/1475-2875-13-236.
180 Transgenic human alpha-hemoglobin stabilizing protein could partially relieve betaIVS-2-654-thalassemia syndrome in model mice.Hum Gene Ther. 2010 Feb;21(2):149-56. doi: 10.1089/hum.2009.132.
181 Plasma advanced oxidative protein products are associated with anti-oxidative stress pathway genes and malaria in a longitudinal cohort.Malar J. 2014 Apr 3;13:134. doi: 10.1186/1475-2875-13-134.
182 ARHGEF12 regulates erythropoiesis and is involved in erythroid regeneration after chemotherapy in acute lymphoblastic leukemia patients.Haematologica. 2020 Apr;105(4):925-936. doi: 10.3324/haematol.2018.210286. Epub 2019 Aug 29.
183 Synergetic pathogenicity of Newcastle disease vaccines LaSota strain and contaminated chicken infectious anemia virus.Poult Sci. 2019 May 1;98(5):1985-1992. doi: 10.3382/ps/pey555.
184 Genetic linkage of autologous T cell epitopes in a chimeric recombinant construct improves anti-parasite and anti-disease protective effect of a malaria vaccine candidate.Vaccine. 2010 Mar 19;28(14):2580-92. doi: 10.1016/j.vaccine.2010.01.019. Epub 2010 Jan 22.
185 Hepcidin suppression in -thalassemia is associated with the down-regulation of atonal homolog 8.Int J Hematol. 2017 Aug;106(2):196-205. doi: 10.1007/s12185-017-2231-3. Epub 2017 Apr 12.
186 Identification and functional analyses of disease-associated P4-ATPase phospholipid flippase variants in red blood cells.J Biol Chem. 2019 Apr 26;294(17):6809-6821. doi: 10.1074/jbc.RA118.007270. Epub 2019 Mar 8.
187 Molecular predictors for anaemia after kidney transplantation.Nephrol Dial Transplant. 2009 Mar;24(3):1015-23. doi: 10.1093/ndt/gfn683. Epub 2008 Dec 18.
188 Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR.Hepatology. 2011 Feb;53(2):389-95. doi: 10.1002/hep.24068. Epub 2011 Jan 10.
189 Overall safety profile of boceprevir plus peginterferon alfa-2b and ribavirin in patients with chronic hepatitis C genotype 1: a combined analysis of 3 phase 2/3 clinical trials.Liver Int. 2014 May;34(5):707-19. doi: 10.1111/liv.12300. Epub 2013 Oct 9.
190 Association of Anemia and Iron Parameters With Mortality Among Patients Undergoing Prevalent Hemodialysis in Taiwan: The AIM - HD Study.J Am Heart Assoc. 2018 Aug 7;7(15):e009206. doi: 10.1161/JAHA.118.009206.
191 A novel functional variant in the stem cell growth factor promoter protects against severe malarial anemia.Infect Immun. 2010 Jan;78(1):453-60. doi: 10.1128/IAI.00895-09. Epub 2009 Nov 2.
192 Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene.Am J Hum Genet. 2009 Mar;84(3):412-7. doi: 10.1016/j.ajhg.2009.02.006. Epub 2009 Mar 5.
193 Efficacy and safety of Everolimus and Exemestane in hormone-receptor positive (HR+) human-epidermal-growth-factor negative (HER2-) advanced breast cancer patients: New insights beyond clinical trials. The EVA study.Breast. 2017 Oct;35:115-121. doi: 10.1016/j.breast.2017.06.043. Epub 2017 Jul 13.
194 Anti-cyclic citrullinated peptide antibody is highly associated with rheumatoid factor and radiological defects in rheumatoid arthritis patients.Medicine (Baltimore). 2019 Mar;98(12):e14945. doi: 10.1097/MD.0000000000014945.
195 Cul4a promotes zebrafish primitive erythropoiesis via upregulating scl and gata1 expression.Cell Death Dis. 2019 May 17;10(6):388. doi: 10.1038/s41419-019-1629-7.
196 A Clinical scoring model to predict mortality in HIV/TB co-infected patients at end stage of AIDS in China: An observational cohort study.Biosci Trends. 2019 May 12;13(2):136-144. doi: 10.5582/bst.2018.01309. Epub 2019 Mar 29.
197 Dietary Balance Index-07 and the Risk of Anemia in Middle Aged and Elderly People in Southwest China: A Cross Sectional Study.Nutrients. 2018 Jan 31;10(2):162. doi: 10.3390/nu10020162.
198 Anemia in patients with diabetic foot ulcer and its impact on disease outcome among Nigerians: Results from the MEDFUN study.PLoS One. 2019 Dec 17;14(12):e0226226. doi: 10.1371/journal.pone.0226226. eCollection 2019.
199 A phase II/III randomized study to compare the efficacy and safety of rigosertib plus gemcitabine versus gemcitabine alone in patients with previously untreated metastatic pancreatic cancer.Ann Oncol. 2015 Sep;26(9):1923-1929. doi: 10.1093/annonc/mdv264. Epub 2015 Jun 19.
200 Headpiece domain of dematin is required for the stability of the erythrocyte membrane.Proc Natl Acad Sci U S A. 2002 May 14;99(10):6637-42. doi: 10.1073/pnas.052155999.
201 Dnases in health and disease.Dev Biol. 2017 Sep 1;429(1):1-11. doi: 10.1016/j.ydbio.2017.06.028. Epub 2017 Jun 28.
202 A novel mechanism in suppression of erythropoiesis during inflammation: a crucial role of RCAS1.Eur J Haematol. 2005 May;74(5):365-73. doi: 10.1111/j.1600-0609.2004.00389.x.
203 Retrovirus-induced feline pure red blood cell aplasia: pathogenesis and response to suramin.Blood. 1991 Apr 1;77(7):1442-51.
204 A putative cell surface receptor for anemia-inducing feline leukemia virus subgroup C is a member of a transporter superfamily.J Virol. 1999 Aug;73(8):6500-5. doi: 10.1128/JVI.73.8.6500-6505.1999.
205 Endothelial Cell-Selective Adhesion Molecule Contributes to the Development of Definitive Hematopoiesis in the Fetal Liver.Stem Cell Reports. 2019 Dec 10;13(6):992-1005. doi: 10.1016/j.stemcr.2019.11.002.
206 Association of FCgamma receptor IIA (CD32) polymorphism with malarial anemia and high-density parasitemia in infants and young children.Am J Trop Med Hyg. 2006 Apr;74(4):573-7.
207 Trends in anemia care in non-dialysis-dependent chronic kidney disease (CKD) patients in the United States (2006-2015).BMC Nephrol. 2018 Nov 9;19(1):318. doi: 10.1186/s12882-018-1119-7.
208 Aberrant splicing of genes involved in haemoglobin synthesis and impaired terminal erythroid maturation in SF3B1 mutated refractory anaemia with ring sideroblasts.Br J Haematol. 2015 Nov;171(4):478-90. doi: 10.1111/bjh.13610. Epub 2015 Aug 10.
209 Single-cell analyses demonstrate that a heme-GATA1 feedback loop regulates red cell differentiation.Blood. 2019 Jan 31;133(5):457-469. doi: 10.1182/blood-2018-05-850412. Epub 2018 Dec 10.
210 Melanoma-Induced Anemia Could be Rescued by Sca-1(+) Mesenchymal Stromal Cells in Mice.Stem Cells Dev. 2017 Apr 1;26(7):495-502. doi: 10.1089/scd.2016.0139. Epub 2017 Feb 7.
211 GDF11 is increased in patients with aplastic anemia.Hematology. 2019 Dec;24(1):331-336. doi: 10.1080/16078454.2019.1574386.
212 T cell and monocyte/macrophage activation markers associate with adverse outcome, but give limited prognostic value in anemic patients with heart failure: results from RED-HF.Clin Res Cardiol. 2019 Feb;108(2):133-141. doi: 10.1007/s00392-018-1331-2. Epub 2018 Jul 26.
213 Large scale expression and purification of secreted mouse hephaestin.PLoS One. 2017 Sep 7;12(9):e0184366. doi: 10.1371/journal.pone.0184366. eCollection 2017.
214 Analysis of hematopathology and alteration of JAK1/STAT3/STAT5 signaling axis in experimental myelodysplastic syndrome.Chem Biol Interact. 2016 Dec 25;260:176-185. doi: 10.1016/j.cbi.2016.10.010. Epub 2016 Oct 8.
215 An extremely severe case of Aicardi-Goutires syndrome 7 with a novel variant in IFIH1.Eur J Med Genet. 2020 Feb;63(2):103646. doi: 10.1016/j.ejmg.2019.04.003. Epub 2019 Apr 6.
216 Interferon-alpha Treatment for Disease Control in Metastatic Pheochromocytoma/Paraganglioma Patients.Horm Cancer. 2017 Dec;8(5-6):330-337. doi: 10.1007/s12672-017-0303-8. Epub 2017 Jul 26.
217 Polymorphisms in genes of interleukin 12 and its receptors and their association with protection against severe malarial anaemia in children in western Kenya.Malar J. 2010 Mar 29;9:87. doi: 10.1186/1475-2875-9-87.
218 Methylation status of immune response genes promoters in cell-free DNA differs in hemodialyzed patients with diabetic nephropathy according to the intensity of anemia therapy.Blood Purif. 2013;36(3-4):280-6. doi: 10.1159/000356094. Epub 2013 Dec 20.
219 Predictors of Recurrent Hospitalizations and the Importance of These Hospitalizations for Subsequent Mortality After Incident Transient Ischemic Attack.J Stroke Cerebrovasc Dis. 2019 Jan;28(1):167-174. doi: 10.1016/j.jstrokecerebrovasdis.2018.09.028. Epub 2018 Oct 17.
220 Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities.Eur J Endocrinol. 2012 Jul;167(1):85-91. doi: 10.1530/EJE-12-0026. Epub 2012 Apr 24.
221 Canine Parvovirus ns1 gene and Chicken Anemia vp3 gene induce partial oncolysis of Canine Transmissible Venereal Tumor.Sci Rep. 2017 Nov 13;7(1):15419. doi: 10.1038/s41598-017-15734-6.
222 Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia.Exp Hematol. 2014 Dec;42(12):1053-8.e1. doi: 10.1016/j.exphem.2014.07.269. Epub 2014 Aug 12.
223 A conserved serine residue is required for the phosphatidate phosphatase activity but not the transcriptional coactivator functions of lipin-1 and lipin-2.J Biol Chem. 2009 Oct 23;284(43):29968-78. doi: 10.1074/jbc.M109.023663. Epub 2009 Aug 28.
224 Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease.Nat Genet. 2003 Jun;34(2):157-65. doi: 10.1038/ng1157.
225 Excessive folic acid intake and relation to adverse health outcome.Biochimie. 2016 Jul;126:71-8. doi: 10.1016/j.biochi.2016.04.010. Epub 2016 Apr 27.
226 Clinical and equipment-related factors associated with the adequate peripheral blood stem cell collection in autologous transplant at a tertiary cancer center in Kerala - A retrospective cohort study.Transfus Apher Sci. 2019 Aug;58(4):457-463. doi: 10.1016/j.transci.2019.05.007. Epub 2019 Jun 21.
227 Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients.Curr Pharm Biotechnol. 2017;18(4):303-308. doi: 10.2174/1389201018666170127104801.
228 A phase I trial investigating pulsatile erlotinib in combination with gemcitabine and oxaliplatin in advanced biliary tract cancers.Invest New Drugs. 2017 Feb;35(1):95-104. doi: 10.1007/s10637-016-0406-z. Epub 2016 Nov 16.
229 A role of NF-E2 in chronic inflammation and clonal evolution in essential thrombocythemia, polycythemia vera and myelofibrosis?.Leuk Res. 2014 Feb;38(2):263-6. doi: 10.1016/j.leukres.2013.07.002. Epub 2013 Aug 9.
230 Multimorbidity and acute heart failure in internal medicine.Int J Cardiol. 2017 Apr 1;232:208-215. doi: 10.1016/j.ijcard.2017.01.020. Epub 2017 Jan 5.
231 Pharmacogenetics of efficacy and safety of HCV treatment in HCV-HIV coinfected patients: significant associations with IL28B and SOCS3 gene variants.PLoS One. 2012;7(11):e47725. doi: 10.1371/journal.pone.0047725. Epub 2012 Nov 2.
232 Seasonal childhood anaemia in West Africa is associated with the haptoglobin 2-2 genotype.PLoS Med. 2006 May;3(5):e172. doi: 10.1371/journal.pmed.0030172. Epub 2006 May 2.
233 ITPA genetic variants influence efficacy of PEG-IFN/RBV therapy in older patients infected with HCV genotype 1 and favourable IL28B type.J Viral Hepat. 2014 Jul;21(7):466-74. doi: 10.1111/jvh.12171. Epub 2013 Sep 3.
234 Hypoxia-inducible factor stabilizers for treating anemia of chronic kidney disease.Curr Opin Nephrol Hypertens. 2018 Sep;27(5):331-338. doi: 10.1097/MNH.0000000000000431.
235 The actin-binding protein profilin 2 is a novel regulator of iron homeostasis.Blood. 2017 Oct 26;130(17):1934-1945. doi: 10.1182/blood-2016-11-754382. Epub 2017 Aug 3.
236 Phosphoglycerate mutase BB isoenzyme deficiency in a patient with non-spherocytic anemia: familial and metabolic studies.Haematologica. 2005 Feb;90(2):257-9.
237 Therapeutic Benefit of Blood Transfusion in a Patient With Novel PGK1 Mutation (c.461T>C [p.L154P]).J Pediatr Hematol Oncol. 2020 May;42(4):e228-e230. doi: 10.1097/MPH.0000000000001463.
238 A phase Ib study of BGJ398, a pan-FGFR kinase inhibitor in combination with imatinib in patients with advanced gastrointestinal stromal tumor.Invest New Drugs. 2019 Apr;37(2):282-290. doi: 10.1007/s10637-018-0648-z. Epub 2018 Aug 13.
239 Alpha-thalassaemia.Orphanet J Rare Dis. 2010 May 28;5:13. doi: 10.1186/1750-1172-5-13.
240 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.
241 Association mapping reveals candidate loci for resistance and anaemic response to an emerging temperature-driven parasitic disease in a wild salmonid fish.Mol Ecol. 2018 Mar;27(6):1385-1401. doi: 10.1111/mec.14509. Epub 2018 Mar 6.
242 Severe malaria: update on pathophysiology and treatment.Curr Opin Infect Dis. 2019 Oct;32(5):413-418. doi: 10.1097/QCO.0000000000000584.
243 Improvement of the hematologic toxicities of ruxolitinib in patients with MPN-associated myelofibrosis using a combination of thalidomide, stanozolol and prednisone.Hematology. 2019 Dec;24(1):516-520. doi: 10.1080/16078454.2019.1631509.
244 Abnormal development of zebrafish after knockout and knockdown of ribosomal protein L10a.Sci Rep. 2019 Dec 2;9(1):18130. doi: 10.1038/s41598-019-54544-w.
245 The molecular pathogenesis of the myelodysplastic syndromes.Eur J Haematol. 2015 Jul;95(1):3-15. doi: 10.1111/ejh.12515. Epub 2015 Feb 20.
246 Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.PLoS Genet. 2013;9(1):e1003094. doi: 10.1371/journal.pgen.1003094. Epub 2013 Jan 31.
247 GATA Factor-Regulated Samd14 Enhancer Confers Red Blood Cell Regeneration and Survival in Severe Anemia.Dev Cell. 2017 Aug 7;42(3):213-225.e4. doi: 10.1016/j.devcel.2017.07.009.
248 Effects of human SAMHD1 polymorphisms on HIV-1 susceptibility.Virology. 2014 Jul;460-461:34-44. doi: 10.1016/j.virol.2014.04.023. Epub 2014 May 29.
249 The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.Am J Hematol. 2019 Nov;94(11):1227-1235. doi: 10.1002/ajh.25613. Epub 2019 Aug 30.
250 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.
251 Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders.Sci Rep. 2019 Nov 5;9(1):16054. doi: 10.1038/s41598-019-52372-6.
252 A Shift in Myeloid Cell Phenotype via Down Regulation of Siglec-1 in Island Macrophages of Bone Marrow Is Associated With Decreased Late Erythroblasts Seen in Anemia of Critical Illness.Front Med (Lausanne). 2019 Nov 20;6:260. doi: 10.3389/fmed.2019.00260. eCollection 2019.
253 The ISWI ATPase Smarca5 (Snf2h) Is Required for Proliferation and Differentiation of Hematopoietic Stem and Progenitor Cells.Stem Cells. 2017 Jun;35(6):1614-1623. doi: 10.1002/stem.2604. Epub 2017 Apr 15.
254 Ledipasvir/sofosbuvir with or without ribavirin for the treatment of chronic hepatitis C genotype 1: A pairwise meta-analysis.J Gastroenterol Hepatol. 2017 Apr;32(4):749-755. doi: 10.1111/jgh.13620.
255 Three Novel Spectrin Variants in Jaundiced Neonates.Clin Pediatr (Phila). 2018 Jan;57(1):19-26. doi: 10.1177/0009922816687326. Epub 2017 Jan 15.
256 Later puberty onset among chronically undernourished adolescents living in a Karachi slum, Pakistan.Acta Paediatr. 2020 May;109(5):1019-1025. doi: 10.1111/apa.15053. Epub 2019 Oct 30.
257 Deletion of Stk40 impairs definitive erythropoiesis in the mouse fetal liver.Cell Death Dis. 2017 Mar 30;8(3):e2722. doi: 10.1038/cddis.2017.148.
258 Anemia and hematinic deficiencies in anti-gastric parietal cell antibody-positive and -negative recurrent aphthous stomatitis patients with anti-thyroid antibody positivity.J Formos Med Assoc. 2017 Mar;116(3):145-152. doi: 10.1016/j.jfma.2016.10.008. Epub 2016 Nov 5.
259 Colla corii asini might upregulate ZNF471 and THOC5 by KRAB domain-containing zinc-finger protein pathway and THO complex subunit 5 pathway to improve anemia of pregnant women with -thalassemia.Ann Hematol. 2019 Aug;98(8):1813-1826. doi: 10.1007/s00277-019-03710-1. Epub 2019 May 16.
260 Enzyme-linked immunosorbent assay and agar gel immunodiffusion assay for diagnosis of equine infectious anemia employing p26 protein fused to the maltose-binding protein.Arch Virol. 2018 Oct;163(10):2871-2875. doi: 10.1007/s00705-018-3923-6. Epub 2018 Jul 7.
261 TREX1 D18N mice fail to process erythroblast DNA resulting in inflammation and dysfunctional erythropoiesis.Autoimmunity. 2018 Nov;51(7):333-344. doi: 10.1080/08916934.2018.1522305. Epub 2018 Nov 13.
262 Cost-effectiveness of malaria preventive treatment for HIV-infected pregnant women in sub-Saharan Africa.Malar J. 2017 Oct 6;16(1):403. doi: 10.1186/s12936-017-2047-x.
263 The Tetratricopeptide repeat domain 7 gene is mutated in flaky skin mice: a model for psoriasis, autoimmunity, and anemia.Exp Biol Med (Maywood). 2005 Oct;230(9):659-67. doi: 10.1177/153537020523000908.
264 Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon.PLoS One. 2013 Nov 27;8(11):e81071. doi: 10.1371/journal.pone.0081071. eCollection 2013.
265 Increased Reactive Oxygen Species and Cell Cycle Defects Contribute to Anemia in the RASA3 Mutant Mouse Model scat.Front Physiol. 2018 Jun 5;9:689. doi: 10.3389/fphys.2018.00689. eCollection 2018.