General Information of Disease (ID: DISF7HVM)

Disease Name Amyotrophic lateral sclerosis
Synonyms motor neuron disease, bulbar; Lou Gehrig's disease; amyotrophic lateral sclerosis; Charcot disease; ALS; Lou Gehrig disease
Disease Class 8B60: Motor neuron disease
Definition
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.
Disease Hierarchy
DISF6XLX: Anterior horn disorder
DISUHWUI: Motor neurone disease
DISF7HVM: Amyotrophic lateral sclerosis
ICD Code
ICD-11
ICD-11: 8B60.0
ICD-9
ICD-9: 335.2
Expand ICD-11
'8B60.0
Expand ICD-9
335.2
Disease Identifiers
MONDO ID
MONDO_0004976
MESH ID
D000690
UMLS CUI
C0002736
MedGen ID
274
HPO ID
HP:0007354
Orphanet ID
803
SNOMED CT ID
86044005

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 5 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Ibudilast DM4LSPN Approved Small molecular drug [1]
MCI-186 DM8ZHP1 Approved Small molecular drug [2]
Pioglitazone DMKJ485 Approved Small molecular drug [3]
Riluzole DMECBWN Approved Small molecular drug [4]
Tofersen DM0AEDT Approved Antisense oligonucleotide [5]
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This Disease is Treated as An Indication in 41 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
AL-02 DM450I4 Phase 3 NA [6]
ALS 001 DMSXOJL Phase 3 Cell therapy [7]
AQST-117 DMORP5T Phase 3 NA [1]
CK-2017357 DMJ9ZIY Phase 3 Small molecular drug [8]
Donaperminogene seltoplasmid DMH8IT5 Phase 3 Gene therapy [9]
GSK4527223 DMXLD07 Phase 3 Antibody [10]
ION363 DM2J3CX Phase 3 Antisense oligonucleotide [11]
Masitinib DMRSNEU Phase 3 Small molecular drug [8]
NurOwn DMZ9LRY Phase 3 NA [1]
VM-202 DMSW80U Phase 3 NA [8]
AMX0035 DMR32AS Phase 2 NA [1]
AT-1501 DMQIA5K Phase 2 Antibody [12]
BIIB105 DMLMUK6 Phase 2 Antisense oligonucleotide [13]
BLZ-945 DMG1LVA Phase 2 Small molecular drug [14]
CK-2127107 DM9FHV8 Phase 2 NA [1]
CORT113176 DMK6IIN Phase 2 Small molecule [15]
EPI 589 DMZT7EP Phase 2 NA [1]
FLX-787 DMQX5UA Phase 2 NA [1]
GM-602 DM8R4YU Phase 2 NA [1]
GM06 DM32TMS Phase 2 NA [8]
H.P. Acthar Gel DMI6L3B Phase 2 NA [8]
IONIS-C9Rx DM6PDX2 Phase 2 Antisense oligonucleotide [16]
IONIS-SOD111RX DMJY9T5 Phase 2 NA [8]
KPAX002 DMDT5WM Phase 2 NA [1]
Mesenchymal stromal cells secreting neurotrophic factors DMJ9E37 Phase 2 NA [8]
NP001 DMVB5E1 Phase 2 Small molecular drug [17]
NSI-566 DMHHXC9 Phase 2 NA [1]
Procysteine DMF9RB4 Phase 2 Small molecular drug [18]
RNS-60 DMDNRU1 Phase 2 NA [1]
RNS60 DMTHZ2V Phase 2 NA [19]
SAR443820 DMNCP7B Phase 2 Small molecule [20]
Cu(II)ATSM DM5I2CC Phase 1/2 NA [1]
BHV-0223 DMBLM5H Phase 1 NA [1]
BRX-005 DMTDWIE Phase 1 Small molecular drug [21]
CC-100 DM2AYUX Phase 1 Small molecular drug [1]
CC100 DMB867J Phase 1 NA [22]
DNL747 DMNSC0O Phase 1 Small molecular drug [23]
GDC0134 DMSE19U Phase 1 NA [1]
ISIS-SOD1 DMV1BTP Phase 1 Antisense drug [24]
NPT520-34 DMVFDGE Phase 1 Small molecule [25]
RPI-MN DM5OXPZ Phase 1 NA [1]
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⏷ Show the Full List of 41 Drug(s)
This Disease is Treated as An Indication in 3 Discontinued Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Brain derived neurotrophic factor DMREO9B Discontinued in Phase 2 NA [26]
FP0011 DMPU5WD Discontinued in Phase 2 NA [27]
T-588 DM3M5TU Discontinued in Phase 2 Small molecular drug [28]
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This Disease is Treated as An Indication in 1 Preclinical Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
M102 DMUFIO9 Preclinical NA [29]
------------------------------------------------------------------------------------

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 411 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
UBQLN2 OT7VD5NH Supportive Autosomal dominant [30]
VAPB OT9ZTZH0 Supportive Autosomal dominant [31]
VCP OTWIX1JU Supportive Autosomal dominant [30]
A1BG OTFVUGNQ Limited Biomarker [248]
ACAT2 OTZ092ZJ Limited Biomarker [249]
ACTN3 OT9DZ7JQ Limited Biomarker [250]
ACY1 OT9WU7X3 Limited Biomarker [251]
ADAMTS3 OT2U6VF5 Limited Biomarker [35]
ADARB2 OTDJKS39 Limited Altered Expression [252]
AGFG1 OTI8ZKC4 Limited Biomarker [147]
AK4 OTA0T02Q Limited Altered Expression [253]
AMPH OTWPGWZX Limited Genetic Variation [254]
APEX1 OT53OI14 Limited Autosomal dominant [39]
APH1A OT97F1TU Limited Biomarker [255]
AQP4 OTA9MYD5 Limited Biomarker [256]
ARPP21 OTWXZN5I Limited Autosomal dominant [46]
ASAP1 OT4DLRYY Limited Biomarker [257]
ASAP2 OTGEXULW Limited Biomarker [257]
ATG4B OTQ4RNRM Limited Altered Expression [258]
ATL1 OTR2788Y Limited Genetic Variation [259]
ATP5F1A OT3FZDLX Limited Biomarker [260]
ATP6 OTPHOGLX Limited Biomarker [261]
AZIN2 OT8OB7CG Limited Biomarker [262]
BBS2 OTPF9JIB Limited Biomarker [263]
BCL11B OT8KKCVJ Limited Biomarker [264]
BICD2 OTVJ03NZ Limited Genetic Variation [265]
BLZF1 OT5QD8FG Limited Biomarker [266]
BNIP1 OT7USYCY Limited Biomarker [267]
BNIP3L OTJKOMXE Limited Biomarker [268]
BTBD10 OTFPYPZE Limited Biomarker [269]
CABIN1 OT4G5CIK Limited Genetic Variation [270]
CALB2 OTSNMCG9 Limited Biomarker [271]
CAMK1G OT1VEDLV Limited Biomarker [270]
CAMK4 OT47RDGV Limited Biomarker [272]
CAV1 OTEZUR1L Limited Autosomal dominant [46]
CAV2 OT1FGRQX Limited Autosomal dominant [46]
CCL4L2 OTDBSXOU Limited Altered Expression [273]
CD2AP OTC76KQM Limited Biomarker [274]
CDKN2D OT2TTZPZ Limited Biomarker [275]
CEACAM4 OT0C7YUD Limited Biomarker [51]
CEBPD OTNBIPMY Limited Biomarker [276]
CHST2 OTV11IZF Limited Genetic Variation [277]
CLDN5 OTUX60YO Limited Altered Expression [278]
CLEC4C OT8ZOPCE Limited Autosomal dominant [39]
CREB5 OTJDUJPI Limited Altered Expression [279]
CRYM OTRGSR6B Limited Biomarker [280]
CYFIP2 OTCAY35T Limited Biomarker [97]
CYLD OT37FKH0 Limited Autosomal dominant [39]
DBR1 OTLTWLTE Limited Altered Expression [281]
DCX OTISR7K3 Limited Altered Expression [282]
DDX3X OTDO4TRX Limited Altered Expression [53]
DECR1 OTCDIR6X Limited Altered Expression [44]
DNAJB9 OT38EQT6 Limited Altered Expression [168]
DNAJC7 OTQ5AL3F Limited Autosomal dominant [46]
EFNA5 OTOH4DRR Limited Altered Expression [283]
EFNB1 OT7JJW8P Limited Biomarker [284]
ELAVL4 OT3YH6J6 Limited Biomarker [285]
ERGIC1 OT351FKB Limited Genetic Variation [267]
ERLIN1 OTUOOODY Limited Autosomal recessive [46]
FADS3 OT9RVXGE Limited Altered Expression [286]
FAM20C OTW5YZ7X Limited Genetic Variation [287]
FCN3 OTPRENLS Limited Biomarker [288]
FLCN OTVM78XM Limited Biomarker [289]
FLVCR1 OT9XCFOC Limited Biomarker [95]
FTL OTYQA8A6 Limited Altered Expression [61]
FZD2 OT952ML1 Limited Biomarker [290]
GADL1 OTJM4A0R Limited Biomarker [262]
GDF11 OTOSNMND Limited Biomarker [291]
GEMIN6 OTE262KF Limited Biomarker [292]
GGNBP2 OT7K9YZV Limited Genetic Variation [293]
GLT8D1 OTG14TPO Limited Biomarker [294]
GLYAT OT3WWYXD Limited Biomarker [295]
GRIN3B OT7T1OJP Limited Biomarker [296]
HADHA OTO557N2 Limited Biomarker [249]
HLA-DRB5 OTUX5TWM Limited Genetic Variation [297]
HLA-F OT76CM19 Limited Biomarker [298]
HNRNPA3 OT4O4NFS Limited Biomarker [299]
HNRNPK OTNPRM8U Limited Biomarker [300]
HOMER1 OTWFD3SI Limited Genetic Variation [301]
HTRA2 OTC7616F Limited Biomarker [302]
IFRD1 OT4SQMLQ Limited Altered Expression [279]
IFT74 OTZBFEDD Limited Genetic Variation [303]
INA OT1D33T4 Limited Biomarker [304]
INPP5B OT0SC8W5 Limited Genetic Variation [305]
JDP2 OTW35WKX Limited Genetic Variation [306]
JPH3 OTHTJO2I Limited Genetic Variation [307]
JTB OT314JB6 Limited Biomarker [308]
KCNIP1 OTGLGK1R Limited Genetic Variation [309]
KCNJ8 OTZ8G8FE Limited Altered Expression [33]
KIF5B OTT34MT8 Limited Biomarker [310]
L3MBTL1 OT8M52QY Limited Biomarker [78]
LAMC1 OTIG527N Limited Altered Expression [311]
LGALS4 OTKQCG0H Limited Genetic Variation [312]
LGALSL OTC983KJ Limited Unknown [46]
LILRA2 OT1O2K47 Limited Biomarker [276]
LXN OTZQ2M6Y Limited Biomarker [313]
LY6E OTMG16BZ Limited Biomarker [314]
LZTS3 OTFFMOJN Limited Genetic Variation [187]
MAGEE1 OTOQQO2X Limited Biomarker [70]
MAP1B OTVXW089 Limited Biomarker [315]
MCIDAS OTK1JVAH Limited Biomarker [316]
MDH1 OTJEO4E8 Limited Genetic Variation [317]
MED19 OTT9RT5N Limited Genetic Variation [318]
MEF2A OTV2SF6E Limited Biomarker [319]
MEF2C OTZGF1Y5 Limited Biomarker [319]
MGRN1 OTFZC41K Limited Biomarker [320]
MMP28 OTHQZXM1 Limited Biomarker [321]
MNX1 OTXP9FH1 Limited Altered Expression [322]
MRPS30 OTDXIAGG Limited Biomarker [257]
MTPAP OT6HQ02S Limited Biomarker [257]
MYBPH OTQJBPUR Limited Biomarker [323]
MYH6 OT3YNCH1 Limited Genetic Variation [324]
MYO6 OTJQYRC7 Limited Genetic Variation [324]
MYOD1 OTV2S79X Limited Altered Expression [325]
NAP1L1 OTI7WBZV Limited Altered Expression [326]
NEFH OTMSCW5I Limited Autosomal dominant [46]
NEUROG1 OTMJZP9G Limited Biomarker [327]
NFIL3 OTQH9HM3 Limited Altered Expression [328]
NGB OTW0SIUY Limited Biomarker [329]
NLN OTFRITPU Limited Biomarker [330]
NMD3 OTXC5APO Limited Genetic Variation [73]
NOC2L OTNT7R33 Limited Biomarker [331]
NONO OTN36Q6U Limited Biomarker [332]
NOP53 OTA2YKO6 Limited Biomarker [333]
NOX1 OTZPJQCC Limited Genetic Variation [334]
NRF1 OTOXWNV8 Limited Altered Expression [93]
NRGN OTVGE10W Limited Biomarker [335]
NT5C3B OT5WAX2N Limited Genetic Variation [293]
NUDT1 OTZSES3W Limited Altered Expression [336]
NUP107 OTG4RDYS Limited Biomarker [337]
NUP205 OTJKHCY6 Limited Biomarker [337]
OLFM1 OTOYPEWW Limited Genetic Variation [338]
OLIG2 OTMCN6D3 Limited Biomarker [339]
OSBP OT7R0OQQ Limited Biomarker [340]
OSBPL3 OT9G194Y Limited Biomarker [340]
P2RX2 OT0LF34A Limited Biomarker [85]
P2RX6 OT1FNTXA Limited Biomarker [85]
PABPN1 OT3MC5SE Limited Altered Expression [341]
PANX1 OTXPEDOK Limited Biomarker [342]
PAPOLA OTPHD65D Limited Biomarker [257]
PCBP1 OTHN0TD7 Limited Biomarker [343]
PDAP1 OTJSWMOD Limited Biomarker [257]
PDSS1 OTXGVHAB Limited Biomarker [344]
PFN2 OT5SSSA7 Limited Biomarker [345]
PICK1 OT8QE6EU Limited Biomarker [346]
PINK1 OT50NR57 Limited Biomarker [347]
PLCD1 OT6WFVXZ Limited Biomarker [348]
POLDIP3 OTTB5SV7 Limited Genetic Variation [349]
PPARGC1A OTHCDQ22 Limited Biomarker [350]
PPIL2 OTL9Y4IO Limited Biomarker [145]
PPP1R15A OTYG179K Limited Biomarker [351]
PRMT8 OT3MRK62 Limited Genetic Variation [352]
PRPH OT6VUH78 Limited Autosomal dominant [46]
PSAP OTUOEKY7 Limited Biomarker [353]
PSMA7 OTPHI6ST Limited Biomarker [354]
PTPRN OTAP7NOL Limited Biomarker [355]
PURA OT975ELW Limited Biomarker [289]
RAB1A OTKPHRD0 Limited Biomarker [356]
RAB29 OTDZT6LP Limited Biomarker [357]
RAMP3 OTX6XLLM Limited Biomarker [358]
RANGAP1 OTZGD3LJ Limited Biomarker [359]
RAPGEF2 OTZWX2AA Limited Autosomal dominant [39]
REST OTLL92LQ Limited Biomarker [329]
RNF112 OT0Q9OUQ Limited Biomarker [360]
RPS17 OTWHZ2JQ Limited Biomarker [261]
RPS25 OTKLWED2 Limited Biomarker [361]
RPS27A OTIIGGZ2 Limited Biomarker [112]
SAGE1 OT4H6FFA Limited Altered Expression [362]
SCG2 OTXWUQQL Limited Biomarker [363]
SCNN1A OTE2KVZV Limited Genetic Variation [364]
SEL1L OTC0FB7T Limited Altered Expression [168]
SH2D1A OTLU49I5 Limited Biomarker [38]
SMCR8 OT52BQH4 Limited Biomarker [365]
SOD3 OTIOZQAB Limited Biomarker [226]
SPAG8 OTZC5XP9 Limited Genetic Variation [366]
SRCIN1 OTQZNQQ5 Limited Biomarker [367]
SUMO2 OT1Y5IKN Limited Genetic Variation [368]
SUMO3 OTTUJQJ1 Limited Biomarker [368]
SYNJ1 OTTE02XC Limited Genetic Variation [305]
SYNJ2 OTLRHXP1 Limited Genetic Variation [305]
SYT9 OT7S8WU0 Limited Genetic Variation [369]
TAAR6 OTUBUJ2N Limited Biomarker [336]
TAF15 OTNE038N Limited Autosomal dominant [46]
TBCB OTHZGAC4 Limited Biomarker [370]
TIA1 OTGPN3P8 Limited Genetic Variation [371]
TRIM69 OTTEGTRD Limited Biomarker [107]
TSBP1 OT5GE8IO Limited Biomarker [372]
TTBK2 OT90YSM5 Limited Biomarker [111]
ACTA1 OTOVGLPG Disputed Altered Expression [373]
AFF2 OTMF1PZW Disputed Biomarker [374]
CALCOCO2 OTRGX0OV Disputed Biomarker [123]
CHRNG OTXC2UR7 Disputed Altered Expression [117]
CUEDC2 OTWMOLAJ Disputed Biomarker [375]
EIF3K OTGTKVGO Disputed Biomarker [376]
GLCE OTPRSHX5 Disputed Biomarker [377]
GPX7 OTINT9Z4 Disputed Biomarker [378]
IFNGR1 OTCTQBWW Disputed Biomarker [171]
MCU OTQZAYWQ Disputed Altered Expression [379]
OGA OT7ZBWT1 Disputed Biomarker [378]
SPDYA OTYKC1AJ Disputed Biomarker [380]
SUPT4H1 OTB3UCTB Disputed Biomarker [381]
ANG OT3ECS6P Supportive Autosomal dominant [118]
ANXA11 OT8SRY1C Supportive Autosomal dominant [233]
CCNF OTJFVU43 Supportive Autosomal dominant [382]
CFAP410 OTJ94J99 Supportive Autosomal dominant [184]
CHCHD10 OTCDHAM6 Supportive Autosomal dominant [383]
CHMP2B OTZA7RJB Supportive Autosomal dominant [384]
ERBB4 OT9L6C41 Supportive Autosomal dominant [119]
FIG4 OT501PY9 Supportive Autosomal dominant [30]
GLE1 OT0K44H1 Supportive Autosomal dominant [385]
HNRNPA1 OTIRPN6B Supportive Autosomal dominant [120]
MATR3 OTESJ5S7 Supportive Autosomal dominant [386]
OPTN OT2UXWH9 Supportive Autosomal dominant [30]
PFN1 OTHTGA1H Supportive Autosomal dominant [387]
PON1 OTD0Z2XO Supportive Autosomal dominant [244]
PON2 OT55NCTD Supportive Autosomal dominant [244]
PON3 OT80W9TA Supportive Autosomal dominant [244]
SOD1 OT39TA1L Supportive Autosomal dominant [31]
SQSTM1 OTGY5D5J Supportive Autosomal dominant [121]
TARDBP OTVOSFWW Supportive Autosomal dominant [30]
ALPP OTZU4G9W moderate Biomarker [123]
ALS2CL OT8RY7TZ moderate Biomarker [388]
ALYREF OTOF2ADD moderate Biomarker [40]
ANKRD1 OTHJ7JV9 moderate Altered Expression [389]
ANKRD2 OT4UYZ71 moderate Altered Expression [389]
ARHGEF28 OT3F32IU Moderate Autosomal dominant [135]
ARHGEF7 OT9BPJCL moderate Biomarker [390]
ATAD1 OTJ02XFL moderate Genetic Variation [391]
ATP13A2 OTKWBUGK moderate Genetic Variation [392]
ATRNL1 OTY5JUX2 moderate Biomarker [123]
ATXN1 OTQF0HNR moderate Biomarker [393]
CALB1 OTM7IXDG moderate Genetic Variation [394]
CARD16 OT4NUHWB moderate Biomarker [395]
CAST OTBXZZGF moderate Biomarker [50]
CASZ1 OTWJ2OR8 moderate Biomarker [236]
CCDC88A OT3SSYYC moderate Altered Expression [396]
CCL27 OTUZYC61 moderate Biomarker [123]
CELSR3 OT8P6QNJ moderate Biomarker [397]
CFDP1 OTXY7J96 moderate Genetic Variation [398]
CHI3L2 OT26R3HQ moderate Genetic Variation [399]
COL4A2 OTJK1LKN moderate Altered Expression [400]
COP1 OT6J2K12 moderate Biomarker [395]
CST7 OTQWZUVQ moderate Biomarker [401]
CTBS OT135K92 moderate Biomarker [143]
DAO OTZFVRIN Moderate Autosomal dominant [135]
DAPK2 OTWODUQG moderate Genetic Variation [155]
DBNL OTT2OQOV moderate Biomarker [401]
DCTN1 OT5B51FJ Moderate Autosomal dominant [46]
DCUN1D1 OT8UJLZU moderate Biomarker [402]
DDX20 OT6G8YF3 moderate Biomarker [403]
DENR OTXP9HOY moderate Genetic Variation [155]
DERL1 OTJUS74N moderate Biomarker [404]
EIF4G2 OTEO98CR moderate Genetic Variation [398]
EWSR1 OT7SRHV3 Moderate Autosomal dominant [135]
FBXO32 OTUE978R moderate Biomarker [405]
FGGY OTLNEC2X moderate Biomarker [406]
GAL3ST1 OTSFFZRD moderate Biomarker [236]
GARS1 OT5B6R9Y moderate Biomarker [407]
GEMIN2 OT4L6TLL moderate Biomarker [408]
GEMIN4 OTX7402E moderate Genetic Variation [398]
GFRA1 OT3WBVYB moderate Altered Expression [409]
HNRNPA2B1 OTBZKX4P Moderate Autosomal dominant [135]
KCNIP3 OTCQPEM4 moderate Biomarker [410]
LIG4 OT40DNXU moderate Biomarker [411]
LRP4 OTO4M459 moderate Biomarker [412]
LSM2 OTHL77NY moderate Biomarker [413]
MAP2 OT6UYT3X moderate Biomarker [170]
MB OTYWYL2D moderate Biomarker [414]
MFN1 OTCBXQZF moderate Altered Expression [93]
MOK OTQK7M9V moderate Biomarker [415]
MT1B OTUA4FFH moderate Altered Expression [416]
MTHFSD OTB5ZUYF moderate Genetic Variation [187]
NOP56 OTT67SRZ moderate Genetic Variation [417]
PADI1 OT13WAQX moderate Genetic Variation [418]
PDC OT1UUVYY moderate Genetic Variation [419]
PDIA2 OTC2WMXS moderate Genetic Variation [418]
PDLIM3 OTVXQC81 moderate Biomarker [123]
PSMD2 OT6HZHN7 moderate Genetic Variation [398]
PVALB OTZW1WVQ moderate Biomarker [420]
RAB11A OTC4FW0J moderate Biomarker [421]
RAB5A OTFR2KM4 moderate Altered Expression [422]
RANBP2 OTFG5CVF moderate Biomarker [423]
RASGRF1 OTNWJ7EN moderate Biomarker [424]
RHOT1 OTBIRR8Q moderate Altered Expression [425]
RIPK3 OTL1D484 moderate Biomarker [426]
RRAD OTW2O4GD moderate Biomarker [427]
SCFD1 OTN4T7JI moderate Genetic Variation [428]
SIL1 OTDI85I5 moderate Biomarker [429]
SNPH OTL6XBFA moderate Altered Expression [430]
SOS1 OTTCWXC3 moderate Biomarker [424]
SPAG11A OTNQ9UB0 moderate Altered Expression [146]
SPAST OTIF3AJI moderate Genetic Variation [431]
SS18L1 OT9ZEGV7 Moderate Autosomal dominant [135]
STMN2 OT0FUHLH moderate Biomarker [432]
TEAD1 OTK6971C moderate Altered Expression [40]
TFEB OTJUJJQY moderate Biomarker [433]
TFPI2 OTZCRWOR moderate Altered Expression [40]
A1CF OTJBKFA1 Strong Biomarker [103]
AATF OT1QOKLD Strong Biomarker [434]
ACD OTC54EPO Strong Biomarker [435]
ADAR OTQNOHR8 Strong Biomarker [252]
ADARB1 OTGKSZEV Strong Biomarker [436]
ALS2 OT8BAM04 Strong Biomarker [437]
APTX OTPAS5G8 Strong Genetic Variation [438]
ARAP2 OTBXYFRH Strong Genetic Variation [212]
ARHGEF2 OTBQTFRT Strong Genetic Variation [212]
ASPM OTKXQMNA Strong Biomarker [103]
ATF6 OTAFHAVI Strong Altered Expression [439]
ATG14 OTPZDKI0 Strong Biomarker [435]
ATG5 OT4T5SMS Strong Biomarker [373]
BSCL2 OT73V6Y4 Strong Biomarker [440]
C19orf12 OTVSJ1AR Strong Biomarker [237]
CAMTA1 OTAN1S5B Strong Genetic Variation [441]
CASP12 OTY2W6FG Strong Biomarker [164]
CCS OTXHT3QO Strong Biomarker [358]
CENPV OTPQ0KT9 Strong Genetic Variation [188]
CHAF1A OTXSSY4H Strong Genetic Variation [442]
CHGA OTXYX5JH Strong Biomarker [443]
CHI3L1 OT2Z7VJH Strong Biomarker [64]
CLEC10A OTD8HQT6 Strong Altered Expression [444]
CPNE4 OTTAGM5L Strong Genetic Variation [212]
CTR9 OTP151PZ Strong Genetic Variation [442]
CUX1 OTU1LCNJ Strong Biomarker [178]
DCDC2 OTSUFH1H Strong Biomarker [445]
DCTN4 OTM7C943 Strong Genetic Variation [180]
DES OTI09KBW Strong Altered Expression [446]
DNAJB2 OTZHPV5M Strong Genetic Variation [447]
DNM1L OTXK1Q1G Strong Altered Expression [448]
ELP1 OTYEWBF7 Strong Genetic Variation [449]
ELP3 OTT5UKSZ Strong Biomarker [450]
EPG5 OT3P5HQD Strong Biomarker [451]
FIS1 OT2HL10J Strong Biomarker [452]
FNDC3A OTUX3S2I Strong Genetic Variation [453]
GPX3 OT6PK94R Strong Genetic Variation [454]
GRIP1 OT958HK1 Strong Genetic Variation [270]
GTF2H1 OTCRXC6B Strong Genetic Variation [180]
GTPBP1 OTA9KV6C Strong Genetic Variation [455]
HCLS1 OTX7WGYN Strong Biomarker [178]
HNRNPC OT47AK4C Strong Biomarker [456]
HNRNPDL OTB3BFCV Strong Biomarker [456]
HNRNPH1 OTFRWOLM Strong Biomarker [457]
HNRNPH2 OTMGP4J7 Strong Biomarker [457]
ICE1 OTOXTBUH Strong Genetic Variation [455]
KHSRP OTDHZARB Strong Biomarker [178]
KIAA0040 OT27EBY3 Strong Genetic Variation [207]
KIAA0513 OT7AVTFB Strong Genetic Variation [212]
KIF1B OTI1XQTO Strong Genetic Variation [458]
LAMA3 OTFME7HT Strong Genetic Variation [212]
LMLN OTQF0JPY Strong Biomarker [185]
LMNB1 OT100T3P Strong Biomarker [459]
MAK16 OTD546E5 Strong Genetic Variation [197]
MOB3B OTZJQG1D Strong Genetic Variation [460]
MSC OTBRPZL5 Strong Biomarker [235]
MST1 OTOC4UNG Strong Biomarker [185]
ND5 OT45LW1K Strong Genetic Variation [193]
NEFM OT8VCBNF Strong Altered Expression [461]
NRXN1 OTJN1JQA Strong Genetic Variation [207]
NUP62 OTMN63DH Strong Genetic Variation [180]
NUP98 OTNT12G2 Strong Biomarker [436]
OXR1 OTPIDMT3 Strong Biomarker [462]
P4HB OTTYNYPF Strong Genetic Variation [418]
PDIA3 OTHPQ0Q3 Strong Genetic Variation [418]
PIK3R4 OTRL8QP8 Strong Genetic Variation [442]
PNO1 OT010GIS Strong Genetic Variation [197]
PTPA OTRGFOI7 Strong Biomarker [463]
RAB3GAP2 OTQTE0GI Strong Genetic Variation [442]
RAG2 OTG9UYTW Strong Biomarker [464]
RAN OT2TER5M Strong Biomarker [361]
RBM45 OTWTHD77 Strong Biomarker [289]
RBM8A OT5SR6G0 Strong Genetic Variation [465]
RBMS3 OTFSC9MR Strong Genetic Variation [197]
RNF19A OTKWCV80 Strong Biomarker [466]
ROPN1L OTRWZJ68 Strong Biomarker [103]
RREB1 OT62460U Strong Biomarker [467]
SFPQ OTLCIAPJ Strong Biomarker [468]
SIGLEC7 OTNDLURR Strong Biomarker [178]
SNRPN OTQB1ID1 Strong Biomarker [213]
SRRM2 OTSIMMC9 Strong Genetic Variation [197]
ST3GAL3 OTOORKUE Strong Genetic Variation [212]
STUB1 OTSUYI9A Strong Genetic Variation [435]
SUGP1 OT7W0EB8 Strong Biomarker [469]
SUMO1 OTJFD4P5 Strong Biomarker [470]
SUN2 OT2IQJUC Strong Genetic Variation [455]
SUN3 OTL5Z9NC Strong Genetic Variation [471]
SUSD2 OTSJTAZP Strong Genetic Variation [270]
TANK OTZSGFIK Strong Genetic Variation [472]
TFAM OTXXV5V7 Strong Biomarker [473]
TFIP11 OT7NVSWU Strong Biomarker [193]
THY1 OTVONVTB Strong Genetic Variation [321]
TMED9 OTYGAQS0 Strong Biomarker [165]
TMEM106B OTUWA6NW Strong Genetic Variation [474]
TMPRSS13 OTMAOAP3 Strong Biomarker [185]
TNIP1 OTRAOTEW Strong Genetic Variation [160]
TNPO1 OT7W2CM8 Strong Genetic Variation [475]
TPPP OTCFMSUF Strong Biomarker [165]
TSHZ1 OTYQ9ECW Strong Genetic Variation [476]
CAPG OTJ86KI6 Definitive Biomarker [170]
COL19A1 OT7W3Q87 Definitive Biomarker [477]
ERCC6L2 OTWFECWG Definitive Genetic Variation [478]
FUS OTPPNGQO Definitive Autosomal dominant [220]
MLC1 OTCNZLSP Definitive Biomarker [479]
MYH15 OTWZA8IF Definitive Genetic Variation [480]
NGLY1 OTZBQD5Q Definitive Altered Expression [481]
PLEC OTU4XDEG Definitive Biomarker [482]
PLP1 OT8CM9CX Definitive Biomarker [483]
RMDN3 OTKO7AUM Definitive Biomarker [484]
RUBCNL OTMQIDOI Definitive Biomarker [485]
SARM1 OTEP4I5O Definitive Biomarker [486]
SPG11 OTZ7LJX4 Definitive Biomarker [487]
STXBP1 OTRYA8C3 Definitive Biomarker [149]
THEM4 OTSIZU8Y Definitive Altered Expression [488]
------------------------------------------------------------------------------------
⏷ Show the Full List of 411 DOT(s)
This Disease Is Related to 220 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
AAK1 TT0Z32T Limited Altered Expression [32]
ABCC9 TTEF5MJ Limited Genetic Variation [33]
ADA TTLP57V Limited Altered Expression [34]
ADAMTS4 TTYG6BU Limited Biomarker [35]
ADCYAP1R1 TT5OREU Limited Biomarker [36]
AOC1 TTM3B5R Limited Biomarker [37]
APCS TTB7VAT Limited Biomarker [38]
APEX1 TTHGL48 Limited Autosomal dominant [39]
APEX1 TTHGL48 Limited Altered Expression [40]
ATAT1 TTWUHQ1 Limited Biomarker [41]
CACNA1H TTZPWGN Limited Biomarker [42]
CACNA1S TT94HRF Limited Genetic Variation [43]
CARM1 TTIZQFJ Limited Altered Expression [44]
CASP3 TTPF2QI Limited Altered Expression [45]
CAV1 TTXUBN2 Limited Autosomal dominant [46]
CBR1 TTVG0SN Limited Altered Expression [47]
CD40LG TTIJP3Q Limited Therapeutic [48]
CDC7 TTSMTDI Limited Biomarker [49]
CDK5 TTL4Q97 Limited Genetic Variation [50]
CEACAM6 TTIGH2W Limited Biomarker [51]
CLEC4C TT7YT06 Limited Autosomal dominant [39]
CLEC4C TT7YT06 Limited Genetic Variation [52]
CSNK1E TTA8PLI Limited Altered Expression [53]
CYBB TT5T8MR Limited Altered Expression [44]
DGAT1 TT0GV3R Limited Altered Expression [54]
DNAJB1 TTPXAWS Limited Biomarker [55]
ELAVL1 TTPC9D0 Limited Biomarker [56]
ERBB4 TTWALCO Limited Altered Expression [57]
EREG TTYSB89 Limited Biomarker [58]
FGFBP1 TTV1YFT Limited Altered Expression [59]
FPR2 TTOJ1NF Limited Biomarker [60]
FTH1 TT975ZT Limited Altered Expression [61]
GBA TT1B5PU Limited Biomarker [62]
GCLM TTNFESW Limited Biomarker [63]
GFAP TTI6FFX Limited Biomarker [64]
GRIN2A TTKJEMQ Limited Genetic Variation [65]
GRM1 TTVBPDM Limited Altered Expression [66]
GRM3 TT8A9EF Limited Biomarker [67]
GSR TTEP6RV Limited Biomarker [68]
GSTP1 TT40K12 Limited Biomarker [69]
HCAR1 TTVK4ZO Limited Biomarker [70]
HDAC11 TT8K17W Limited Altered Expression [71]
HEXA TTJI5JW Limited Genetic Variation [72]
HNMT TT2B6EV Limited Genetic Variation [73]
HSPA8 TTMQL3K Limited Altered Expression [74]
ID2 TTW8A5N Limited Biomarker [75]
JAG2 TTOJY1B Limited Posttranslational Modification [76]
KCNJ11 TT329V4 Limited Genetic Variation [33]
KCNT1 TTGJFK1 Limited Genetic Variation [77]
KMT5A TTGC95K Limited Altered Expression [78]
LTBR TTFO0PM Limited Altered Expression [79]
MAP4K3 TTI0AHJ Limited Genetic Variation [80]
MC4R TTD0CIQ Limited Genetic Variation [81]
MCOLN1 TT9XBVO Limited Biomarker [82]
MGAM TTXWASR Limited Altered Expression [83]
NEDD8 TTNDC4K Limited Biomarker [84]
P2RX1 TTJW7B3 Limited Biomarker [85]
P2RX3 TT2THBD Limited Biomarker [85]
P2RX7 TT473XN Limited Biomarker [86]
P2RY12 TTZ1DT0 Limited Genetic Variation [87]
PABPC1 TTHC8EF Limited Biomarker [88]
PAH TTGSVH2 Limited Biomarker [89]
PCSK2 TT46F0P Limited Genetic Variation [90]
PKN1 TTSL41O Limited Biomarker [91]
PLA2G4A TTT1JVS Limited Biomarker [92]
PPARGC1B TTKSQ3W Limited Altered Expression [93]
PPID TTNAFOU Limited Altered Expression [94]
PPIF TTRFQTB Limited Altered Expression [94]
PTAFR TTQL5VC Limited Biomarker [95]
PTGER3 TTPNGDE Limited Genetic Variation [96]
RBBP9 TTUA38Z Limited Biomarker [97]
SIRT5 TTH0IOD Limited Altered Expression [98]
SLC11A2 TT2IS7P Limited Genetic Variation [99]
SLC12A4 TTJ8C67 Limited Genetic Variation [100]
SLC12A5 TTH6UZY Limited Altered Expression [100]
SLC33A1 TTL69WB Limited Biomarker [101]
SLC40A1 TT6Y1PG Limited Altered Expression [102]
SLC6A1 TTPRKM0 Limited Biomarker [103]
SLC7A11 TTBZMIO Limited Altered Expression [104]
SORT1 TTRX9AV Limited Genetic Variation [105]
SOX5 TTXHSZK Limited Genetic Variation [106]
TICAM1 TT2GQT6 Limited Biomarker [107]
TNFRSF21 TT8UA0T Limited Biomarker [108]
TNKS TTVUSO7 Limited Biomarker [109]
TPH2 TT3KLDP Limited Genetic Variation [110]
TRIM27 TTTO3QN Limited Biomarker [60]
TTBK1 TTYFAM9 Limited Biomarker [111]
UBC TTBP3XA Limited Biomarker [112]
UGCG TTPHEX3 Limited Genetic Variation [113]
CSNK1D TTH30UI Disputed Posttranslational Modification [114]
CTSC TT4H0V2 Disputed Biomarker [115]
DPYSL2 TTZCW3T Disputed Posttranslational Modification [116]
MUSK TT6SA0X Disputed Biomarker [117]
ANG TTURHFP Supportive Autosomal dominant [118]
ERBB4 TTWALCO Supportive Autosomal dominant [119]
HNRNPA1 TTPJ9XK Supportive Autosomal dominant [120]
SQSTM1 TTOT2RY Supportive Autosomal dominant [121]
TARDBP TT9RZ03 Supportive Autosomal dominant [30]
VCP TTYWTI0 Supportive Autosomal dominant [30]
AKT3 TTO6SGY moderate Altered Expression [122]
ASRGL1 TT4WT91 moderate Biomarker [123]
ATG7 TTLVB9Z moderate Biomarker [124]
CNTFR TTT2F9E moderate Biomarker [125]
CTF1 TTXGTZU moderate Biomarker [126]
DAO TT7Y3EJ moderate Biomarker [127]
EIF2AK2 TTXEZJ4 moderate Altered Expression [128]
EPHA1 TTLFZVU moderate Altered Expression [129]
EPHA3 TTHS2LR moderate Genetic Variation [130]
GDA TTK4JTZ moderate Biomarker [131]
GRIA3 TT82EZV moderate Genetic Variation [132]
GRIA4 TTPJR0G moderate Genetic Variation [132]
GRIK1 TT0MYE2 moderate Genetic Variation [133]
HMOX2 TTWZRL4 moderate Biomarker [134]
HNRNPA2B1 TT8UPW6 Moderate Autosomal dominant [135]
HNRNPA2B1 TT8UPW6 moderate Genetic Variation [136]
ITPR2 TTK9OV3 moderate Biomarker [137]
KITLG TTDJ51N moderate Altered Expression [138]
MAOB TTGP7BY moderate Biomarker [139]
MARCKS TTHRM39 moderate Genetic Variation [140]
NTF4 TTIM2WO moderate Biomarker [141]
NTRK3 TTXABCW moderate Altered Expression [142]
PCYT1B TTUAIKM moderate Biomarker [143]
PHGDH TT8DRCK moderate Biomarker [144]
PPIA TTL2ADK moderate Biomarker [145]
PTGER2 TT1ZAVI moderate Altered Expression [146]
SGCG TTSMT9W moderate Biomarker [147]
SLC1A3 TT8WRDA moderate Genetic Variation [148]
SNAP25 TTYQWA0 moderate Biomarker [149]
SRR TTZFUY6 moderate Altered Expression [150]
TDP1 TT64IHJ moderate Biomarker [151]
TRPM2 TTEBMN7 moderate Genetic Variation [152]
UCHL1 TTX9IFP moderate Biomarker [153]
UCP3 TT12RJK moderate Altered Expression [154]
UTRN TTNO1VA moderate Genetic Variation [155]
ADCYAP1 TTW4LYC Strong Biomarker [156]
AIF1 TT12MEP Strong Biomarker [157]
ANPEP TTPHMWB Strong Altered Expression [158]
APP TTE4KHA Strong Altered Expression [159]
ASPA TT6TLZP Strong Biomarker [103]
ATXN3 TT6A17J Strong Genetic Variation [160]
BCL2L1 TTRE6AX Strong Biomarker [41]
C3 TTJGY7A Strong Biomarker [103]
C5AR1 TTHXFA1 Strong Altered Expression [161]
CAPN2 TTG5QB7 Strong Altered Expression [162]
CASP1 TTCQIBE Strong Biomarker [163]
CASP9 TTB6T7O Strong Biomarker [164]
CDK5R1 TTBYM6V Strong Biomarker [165]
CHIT1 TTDYX6T Strong Biomarker [64]
CNR2 TTMSFAW Strong Genetic Variation [166]
CS TTZA6B3 Strong Biomarker [144]
CX3CR1 TT2T98G Strong Biomarker [167]
ERN1 TTKIAT3 Strong Altered Expression [168]
GAPDH TTUGSWA Strong Altered Expression [54]
GDNF TTF23ML Strong Biomarker [169]
GPNMB TT7315J Strong Biomarker [170]
GRIA1 TTVPQTF Strong Biomarker [171]
GRM5 TTHS256 Strong Altered Expression [172]
HNRNPA1 TTPJ9XK Strong Biomarker [173]
HSF1 TTN6STZ Strong Altered Expression [174]
HSPB8 TTY0OJN Strong Biomarker [175]
IGF1R TTQFBMY Strong ModifyingMutation [176]
IGF2R TTPNE41 Strong Biomarker [177]
IL2RB TT9721Y Strong Biomarker [178]
KCNJ10 TTG140O Strong Biomarker [179]
KEAP1 TT3Z6Y9 Strong Genetic Variation [180]
KHDRBS1 TTAT6C7 Strong Genetic Variation [180]
KIF5A TTCJPAH Strong Genetic Variation [181]
LGALS1 TTO3NYT Strong Genetic Variation [182]
MAP2K5 TTV3O87 Strong Biomarker [183]
MAPT TTS87KH Strong Biomarker [123]
MOBP TTYUK4F Strong Genetic Variation [184]
MSMB TTYH1ZK Strong Biomarker [185]
MSTN TTM8I2X Strong Biomarker [186]
NEK1 TTO5QT2 Strong Genetic Variation [187]
NME9 TTHSVK0 Strong Genetic Variation [188]
NPEPPS TT371QC Strong Genetic Variation [189]
NRG1 TTEH395 Strong Biomarker [190]
NTF3 TTZHKV9 Strong Biomarker [191]
P2RX4 TT1NLOA Strong Biomarker [192]
PIGL TTQA8DT Strong Genetic Variation [188]
PLCB1 TTLPGU7 Strong Genetic Variation [193]
PNPLA6 TTWAQU2 Strong Biomarker [194]
PRMT1 TTVOJAI Strong Biomarker [195]
PRNP TTY5F9C Strong Biomarker [196]
PSIP1 TTH9LDP Strong Biomarker [178]
PTBP1 TTWMX0U Strong Genetic Variation [197]
PTGS2 TTVKILB Strong Biomarker [47]
PTPRZ1 TT4SEA8 Strong Therapeutic [198]
RARA TTW38KT Strong Biomarker [199]
RIPK1 TTVJHX8 Strong Biomarker [200]
RNASEL TT7V0K4 Strong Genetic Variation [201]
RRM1 TTWP0NS Strong Biomarker [202]
RRM2 TT1S4LJ Strong Biomarker [203]
RTN4 TT7GXMU Strong Altered Expression [204]
S100A6 TT716MY Strong Biomarker [205]
SCGB1A1 TTONPVW Strong Altered Expression [206]
SCN8A TT54ERL Strong Genetic Variation [207]
SEMA3A TTVKD3S Strong Altered Expression [208]
SIGMAR1 TT5TPI6 Strong Biomarker [209]
SIRT2 TTLKF5M Strong Biomarker [210]
SLC1A1 TTG2A6F Strong Biomarker [211]
STK36 TTX5KEQ Strong Genetic Variation [212]
STMN1 TT7W5OT Strong Biomarker [213]
TBK1 TTMP03S Strong Biomarker [214]
TCF3 TTULOD8 Strong Biomarker [178]
TGM2 TT2F4OL Strong Genetic Variation [215]
TIAM1 TTNU6I5 Strong Genetic Variation [216]
TNFRSF1B TT63WSF Strong Biomarker [178]
TUSC2 TTJ8O14 Strong Genetic Variation [217]
UNC13B TT948FC Strong Genetic Variation [218]
VDAC1 TTAMKGB Strong Biomarker [219]
FUS TTKGYZ9 Definitive Autosomal dominant [220]
GJD2 TTOZAFI Definitive Biomarker [221]
ITPR1 TT5HWAT Definitive Genetic Variation [222]
ITPR3 TTH1769 Definitive Genetic Variation [222]
LANCL1 TTZW8NS Definitive Biomarker [223]
MAP4K4 TT6NI13 Definitive Biomarker [224]
PSEN1 TTZ3S8C Definitive Genetic Variation [225]
SOD2 TT9O4C5 Definitive Biomarker [226]
UCP1 TTI12YJ Definitive Biomarker [227]
------------------------------------------------------------------------------------
⏷ Show the Full List of 220 DTT(s)
This Disease Is Related to 11 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
ANXA11 DTGQ2CF Limited Genetic Variation [228]
ATP7A DT0LT17 Limited Genetic Variation [229]
KCNK2 DTENHUP Limited Biomarker [230]
SLC12A2 DTHKL3Q Limited Genetic Variation [100]
SLC30A6 DTKPRIL Limited Genetic Variation [231]
SLC8A3 DTYFRQT Limited Biomarker [232]
ANXA11 DTGQ2CF Supportive Autosomal dominant [233]
SLC17A6 DT5LHCR moderate Biomarker [234]
SLC25A37 DTLBGTZ moderate Biomarker [235]
SLC35A1 DTVZIRG moderate Biomarker [236]
SLC52A3 DTBVQIO moderate Biomarker [237]
------------------------------------------------------------------------------------
⏷ Show the Full List of 11 DTP(s)
This Disease Is Related to 20 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
ADH5 DEIOH6A Limited Biomarker [238]
ALDH1A2 DEKN1H4 Limited Altered Expression [239]
EGLN3 DEMQTKH Limited Altered Expression [240]
FMO3 DEP76YL Limited Altered Expression [241]
MT1A DE5ME8A Limited Altered Expression [242]
SI DE5EO4Y Limited Altered Expression [83]
TGM6 DEUWCVD Limited Biomarker [243]
PON1 DESDN74 Supportive Autosomal dominant [244]
PON2 DEHJU7E Supportive Autosomal dominant [244]
PON3 DETXQZ1 Supportive Autosomal dominant [244]
SOD1 DEUTDON Supportive Autosomal dominant [31]
CRMP1 DE0EUXB moderate Genetic Variation [155]
DAO DERZQ2Y Moderate Autosomal dominant [135]
FMO1 DEJ73Q9 moderate Altered Expression [241]
NAT10 DEZV4AP moderate Biomarker [123]
CYP27A1 DEBS639 Strong Biomarker [245]
FXN DEXVHDB Strong Biomarker [246]
GLS DE3E0VT Strong Biomarker [247]
PON2 DEHJU7E Strong GermlineCausalMutation [118]
PON3 DETXQZ1 Strong GermlineCausalMutation [118]
------------------------------------------------------------------------------------
⏷ Show the Full List of 20 DME(s)

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12 ClinicalTrials.gov (NCT04322149) A Phase 2a Open-Label, Multi-Center Study to Evaluate the Safety and Tolerability of Multiple Doses of AT-1501 in Adults With ALS. U.S.National Institutes of Health.
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20 ClinicalTrials.gov (NCT05237284) A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of SAR443820 in Adult Participants With Amyotrophic Lateral Sclerosis, Followed by an Open-label Extension. U.S.National Institutes of Health.
21 Bimoclomol: a nontoxic, hydroxylamine derivative with stress protein-inducing activity and cytoprotective effects. Nat Med. 1997 Oct;3(10):1150-4.
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33 K(ATP) Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis.Mol Neurobiol. 2018 Oct;55(10):7962-7972. doi: 10.1007/s12035-018-0970-7. Epub 2018 Feb 28.
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35 ADAMTS-4 in central nervous system pathologies.J Neurosci Res. 2017 Sep;95(9):1703-1711. doi: 10.1002/jnr.24021. Epub 2017 Jan 13.
36 PACAP and PAC1R are differentially expressed in motor cortex of amyotrophic lateral sclerosis patients and support survival of iPSC-derived motor neurons.J Cell Physiol. 2018 Apr;233(4):3343-3351. doi: 10.1002/jcp.26182. Epub 2017 Oct 20.
37 The motor unit number index (MUNIX) profile of patients with adult spinal muscular atrophy.Clin Neurophysiol. 2018 Nov;129(11):2333-2340. doi: 10.1016/j.clinph.2018.08.025. Epub 2018 Sep 13.
38 Phrenic long-term facilitation following intrapleural CTB-SAP-induced respiratory motor neuron death.Respir Physiol Neurobiol. 2018 Oct;256:43-49. doi: 10.1016/j.resp.2017.08.003. Epub 2017 Aug 16.
39 Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.
40 Drosophila Ref1/ALYREF regulates transcription and toxicity associated with ALS/FTD disease etiologies.Acta Neuropathol Commun. 2019 Apr 29;7(1):65. doi: 10.1186/s40478-019-0710-x.
41 The BH4 domain of Bcl-X(L) rescues astrocyte degeneration in amyotrophic lateral sclerosis by modulating intracellular calcium signals.Hum Mol Genet. 2012 Feb 15;21(4):826-40. doi: 10.1093/hmg/ddr513. Epub 2011 Nov 9.
42 CACNA1H missense mutations associated with amyotrophic lateral sclerosis alter Cav3.2 T-type calcium channel activity and reticular thalamic neuron firing.Channels (Austin). 2016 Nov;10(6):466-77. doi: 10.1080/19336950.2016.1204497. Epub 2016 Jun 22.
43 Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.Muscle Nerve. 2008 Jan;37(1):120-4. doi: 10.1002/mus.20825.
44 A C9orf72-CARM1 axis regulates lipid metabolism under glucose starvation-induced nutrient stress.Genes Dev. 2018 Nov 1;32(21-22):1380-1397. doi: 10.1101/gad.315564.118. Epub 2018 Oct 26.
45 Extracellular TDP-43 aggregates target MAPK/MAK/MRK overlapping kinase (MOK) and trigger caspase-3/IL-18 signaling in microglia.FASEB J. 2017 Jul;31(7):2797-2816. doi: 10.1096/fj.201601163R. Epub 2017 Mar 23.
46 Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.
47 Increased Expression of 15-Hydroxyprostaglandin Dehydrogenase in Spinal Astrocytes During Disease Progression in a Model of Amyotrophic Lateral Sclerosis.Cell Mol Neurobiol. 2017 Apr;37(3):445-452. doi: 10.1007/s10571-016-0377-9. Epub 2016 May 2.
48 From transcriptome analysis to therapeutic anti-CD40L treatment in the SOD1 model of amyotrophic lateral sclerosis.Nat Genet. 2010 May;42(5):392-9. doi: 10.1038/ng.557. Epub 2010 Mar 28.
49 CDC7 inhibition blocks pathological TDP-43 phosphorylation and neurodegeneration.Ann Neurol. 2013 Jul;74(1):39-52. doi: 10.1002/ana.23870. Epub 2013 Jul 8.
50 Calpastatin inhibits motor neuron death and increases survival of hSOD1(G93A) mice.J Neurochem. 2016 Apr;137(2):253-65. doi: 10.1111/jnc.13536. Epub 2016 Mar 23.
51 Visual encoding, consolidation, and retrieval in amyotrophic lateral sclerosis: executive function as a mediator, and predictor of performance.Amyotroph Lateral Scler Frontotemporal Degener. 2017 May;18(3-4):193-201. doi: 10.1080/21678421.2016.1272615. Epub 2017 Jan 13.
52 CLEC4C p.K210del variant causes impaired cell surface transport in plasmacytoid dendritic cells of amyotrophic lateral sclerosis.Oncotarget. 2016 May 3;7(18):24942-9. doi: 10.18632/oncotarget.7886.
53 DDX3 binding with CK1 was closely related to motor neuron degeneration of ALS by affecting neurite outgrowth.Am J Transl Res. 2017 Oct 15;9(10):4627-4639. eCollection 2017.
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189 No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.Hum Mol Genet. 2014 Apr 1;23(7):1916-22. doi: 10.1093/hmg/ddt574. Epub 2013 Nov 13.
190 Neuregulin 1 Reduces Motoneuron Cell Death and Promotes Neurite Growth in an in Vitro Model of Motoneuron Degeneration.Front Cell Neurosci. 2018 Jan 9;11:431. doi: 10.3389/fncel.2017.00431. eCollection 2017.
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200 Multitasking Kinase RIPK1 Regulates Cell Death and Inflammation.Cold Spring Harb Perspect Biol. 2020 Mar 2;12(3):a036368. doi: 10.1101/cshperspect.a036368.
201 Insights into the role of ribonuclease 4 polymorphisms in amyotrophic lateral sclerosis.J Biomol Struct Dyn. 2019 Jan;37(1):116-130. doi: 10.1080/07391102.2017.1419147. Epub 2018 Jan 7.
202 Virus-mediated delivery of antibody targeting TAR DNA-binding protein-43 mitigates associated neuropathology.J Clin Invest. 2019 Feb 25;129(4):1581-1595. doi: 10.1172/JCI123931. eCollection 2019 Feb 25.
203 Small Molecule Targeting TDP-43's RNA Recognition Motifs Reduces Locomotor Defects in a Drosophila Model of Amyotrophic Lateral Sclerosis (ALS).ACS Chem Biol. 2019 Sep 20;14(9):2006-2013. doi: 10.1021/acschembio.9b00481. Epub 2019 Aug 27.
204 Conditional Overexpression of rtn4al in Muscle of Adult Zebrafish Displays Defects Similar to Human Amyotrophic Lateral Sclerosis.Mar Biotechnol (NY). 2019 Feb;21(1):52-64. doi: 10.1007/s10126-018-9857-x. Epub 2018 Nov 15.
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206 Plasma level of club-cell (CC-16) predicts outcome in amyotrophic lateral sclerosis.Acta Neurol Scand. 2018 Feb;137(2):233-237. doi: 10.1111/ane.12851. Epub 2017 Oct 1.
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208 ALS-related human cortical and motor neurons survival is differentially affected by Sema3A.Cell Death Dis. 2018 Feb 15;9(3):256. doi: 10.1038/s41419-018-0294-6.
209 Sigma-1 receptor is a key genetic modulator in amyotrophic lateral sclerosis.Hum Mol Genet. 2020 Mar 13;29(4):529-540. doi: 10.1093/hmg/ddz267.
210 Review of the anti-inflammatory effect of SIRT1 and SIRT2 modulators on neurodegenerative diseases.Eur J Pharmacol. 2020 Jan 15;867:172847. doi: 10.1016/j.ejphar.2019.172847. Epub 2019 Dec 5.
211 Edaravone suppresses retinal ganglion cell death in a mouse model of normal tension glaucoma.Cell Death Dis. 2017 Jul 13;8(7):e2934. doi: 10.1038/cddis.2017.341.
212 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.Neurobiol Aging. 2013 Jan;34(1):357.e7-19. doi: 10.1016/j.neurobiolaging.2012.07.017. Epub 2012 Sep 5.
213 The Actin Cytoskeleton in SMA and ALS: How Does It Contribute to Motoneuron Degeneration?.Neuroscientist. 2018 Feb;24(1):54-72. doi: 10.1177/1073858417705059. Epub 2017 May 1.
214 Retinoic acid worsens ATG10-dependent autophagy impairment in TBK1-mutant hiPSC-derived motoneurons through SQSTM1/p62 accumulation.Autophagy. 2019 Oct;15(10):1719-1737. doi: 10.1080/15548627.2019.1589257. Epub 2019 Apr 2.
215 New insight into transglutaminase 2 and link to neurodegenerative diseases.BMB Rep. 2018 Jan;51(1):5-13. doi: 10.5483/bmbrep.2018.51.1.227.
216 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.Lancet Neurol. 2010 Oct;9(10):978-85. doi: 10.1016/S1474-4422(10)70184-8.
217 Vascular regression precedes motor neuron loss in the FUS (1-359) ALS mouse model.Dis Model Mech. 2019 Aug 13;12(8):dmm040238. doi: 10.1242/dmm.040238.
218 Molecular Mechanisms Linking ALS/FTD and Psychiatric Disorders, the Potential Effects of Lithium.Front Cell Neurosci. 2019 Oct 4;13:450. doi: 10.3389/fncel.2019.00450. eCollection 2019.
219 A VDAC1-Derived N-Terminal Peptide Inhibits Mutant SOD1-VDAC1 Interactions and Toxicity in the SOD1 Model of ALS.Front Cell Neurosci. 2019 Aug 14;13:346. doi: 10.3389/fncel.2019.00346. eCollection 2019.
220 De novo FUS mutations in 2 Korean patients with sporadic amyotrophic lateral sclerosis. Neurobiol Aging. 2015 Mar;36(3):1604.e17-9. doi: 10.1016/j.neurobiolaging.2014.10.002. Epub 2014 Oct 13.
221 A potential role for neuronal connexin 36 in the pathogenesis of amyotrophic lateral sclerosis.Neurosci Lett. 2018 Feb 14;666:1-4. doi: 10.1016/j.neulet.2017.12.027. Epub 2017 Dec 12.
222 Genetic analyses uncover pleiotropic compensatory roles for Drosophila Nucleobindin-1 in inositol trisphosphate-mediated intracellular calcium homeostasis.Genome. 2020 Feb;63(2):61-90. doi: 10.1139/gen-2019-0113. Epub 2019 Sep 26.
223 LanCL1 promotes motor neuron survival and extends the lifespan of amyotrophic lateral sclerosis mice.Cell Death Differ. 2020 Apr;27(4):1369-1382. doi: 10.1038/s41418-019-0422-6. Epub 2019 Sep 30.
224 MAP4K4 Activation Mediates Motor Neuron Degeneration in Amyotrophic Lateral Sclerosis.Cell Rep. 2019 Jan 29;26(5):1143-1156.e5. doi: 10.1016/j.celrep.2019.01.019.
225 Mutation analysis of patients with neurodegenerative disorders using NeuroX array.Neurobiol Aging. 2015 Jan;36(1):545.e9-14. doi: 10.1016/j.neurobiolaging.2014.07.038. Epub 2014 Aug 1.
226 Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.Mov Disord. 2008 Dec 15;23(16):2344-8. doi: 10.1002/mds.22262.
227 Histone deacetylase 4 protects from denervation and skeletal muscle atrophy in a murine model of amyotrophic lateral sclerosis.EBioMedicine. 2019 Feb;40:717-732. doi: 10.1016/j.ebiom.2019.01.038. Epub 2019 Feb 1.
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229 Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy.Hum Mol Genet. 2012 Apr 15;21(8):1794-807. doi: 10.1093/hmg/ddr612. Epub 2011 Dec 30.
230 Endothelial TWIK-related potassium channel-1 (TREK1) regulates immune-cell trafficking into the CNS.Nat Med. 2013 Sep;19(9):1161-5. doi: 10.1038/nm.3303. Epub 2013 Aug 11.
231 Zinc transporters ZnT3 and ZnT6 are downregulated in the spinal cords of patients with sporadic amyotrophic lateral sclerosis.J Neurosci Res. 2015 Feb;93(2):370-9. doi: 10.1002/jnr.23491. Epub 2014 Oct 3.
232 Preconditioning, induced by sub-toxic dose of the neurotoxin L-BMAA, delays ALS progression in mice and prevents Na(+)/Ca(2+) exchanger 3 downregulation.Cell Death Dis. 2018 Feb 12;9(2):206. doi: 10.1038/s41419-017-0227-9.
233 Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis. Sci Transl Med. 2017 May 3;9(388):eaad9157. doi: 10.1126/scitranslmed.aad9157.
234 Differential involvement of vesicular and glial glutamate transporters around spinal -motoneurons in the pathogenesis of SOD1(G93A) mouse model of amyotrophic lateral sclerosis.Neuroscience. 2017 Jul 25;356:114-124. doi: 10.1016/j.neuroscience.2017.05.014. Epub 2017 May 17.
235 Reduced sirtuin 1/adenosine monophosphate-activated protein kinase in amyotrophic lateral sclerosis patient-derived mesenchymal stem cells can be restored by resveratrol.J Tissue Eng Regen Med. 2019 Jan;13(1):110-115. doi: 10.1002/term.2776. Epub 2018 Dec 10.
236 The same cortico-efferent tract involvement in progressive bulbar palsy and in 'classical' ALS: A tract of interest-based MRI study.Neuroimage Clin. 2019;24:101979. doi: 10.1016/j.nicl.2019.101979. Epub 2019 Aug 9.
237 Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients.Neurobiol Aging. 2019 Mar;75:225.e9-225.e14. doi: 10.1016/j.neurobiolaging.2018.11.003. Epub 2018 Nov 16.
238 nNOS/GSNOR interaction contributes to skeletal muscle differentiation and homeostasis.Cell Death Dis. 2019 May 1;10(5):354. doi: 10.1038/s41419-019-1584-3.
239 Aldehyde Dehydrogenases 1A2 Expression and Distribution are Potentially Associated with Neuron Death in Spinal Cord of Tg(SOD1*G93A)1Gur Mice.Int J Biol Sci. 2017 Apr 10;13(5):574-587. doi: 10.7150/ijbs.19150. eCollection 2017.
240 Impaired hypoxic sensor Siah-1, PHD3, and FIH system in spinal motor neurons of an amyotrophic lateral sclerosis mouse model.J Neurosci Res. 2013 Feb;91(2):285-91. doi: 10.1002/jnr.23129. Epub 2012 Nov 14.
241 Flavin-containing monooxygenase mRNA levels are up-regulated in als brain areas in SOD1-mutant mice.Neurotox Res. 2011 Aug;20(2):150-8. doi: 10.1007/s12640-010-9230-y. Epub 2010 Nov 17.
242 Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1.Hum Mol Genet. 2014 Mar 1;23(5):1271-85. doi: 10.1093/hmg/ddt517. Epub 2013 Oct 24.
243 Transglutaminase 6 Antibodies in the Serum of Patients With Amyotrophic Lateral Sclerosis.JAMA Neurol. 2015 Jun;72(6):676-81. doi: 10.1001/jamaneurol.2015.48.
244 Paraoxonase gene mutations in amyotrophic lateral sclerosis. Ann Neurol. 2010 Jul;68(1):102-7. doi: 10.1002/ana.21993.
245 Cholesterol, oxysterol, triglyceride, and coenzyme Q homeostasis in ALS. Evidence against the hypothesis that elevated 27-hydroxycholesterol is a pathogenic factor.PLoS One. 2014 Nov 21;9(11):e113619. doi: 10.1371/journal.pone.0113619. eCollection 2014.
246 Diagnostics and Treatments of Iron-Related CNS Diseases.Adv Exp Med Biol. 2019;1173:179-194. doi: 10.1007/978-981-13-9589-5_10.
247 Serial deletion reveals structural basis and stability for the core enzyme activity of human glutaminase 1 isoforms: relevance to excitotoxic neurodegeneration.Transl Neurodegener. 2017 Apr 20;6:10. doi: 10.1186/s40035-017-0080-x. eCollection 2017.
248 GAB(A) receptors present higher affinity and modified subunit composition in spinal motor neurons from a genetic model of amyotrophic lateral sclerosis.Eur J Neurosci. 2008 Oct;28(7):1275-85. doi: 10.1111/j.1460-9568.2008.06436.x.
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250 Differential gene expression in patients with amyotrophic lateral sclerosis.Amyotroph Lateral Scler. 2011 Jul;12(4):250-6. doi: 10.3109/17482968.2011.560946. Epub 2011 Mar 4.
251 Characterization of Parkinson's disease using blood-based biomarkers: A multicohort proteomic analysis.PLoS Med. 2019 Oct 11;16(10):e1002931. doi: 10.1371/journal.pmed.1002931. eCollection 2019 Oct.
252 Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons.Neurobiol Dis. 2012 Mar;45(3):1121-8. doi: 10.1016/j.nbd.2011.12.033. Epub 2011 Dec 28.
253 Enzymatically inactive adenylate kinase 4 interacts with mitochondrial ADP/ATP translocase.Int J Biochem Cell Biol. 2009 Jun;41(6):1371-80. doi: 10.1016/j.biocel.2008.12.002. Epub 2008 Dec 14.
254 Exocytosis regulates trafficking of GABA and glycine heterotransporters in spinal cord glutamatergic synapses: a mechanism for the excessive heterotransporter-induced release of glutamate in experimental amyotrophic lateral sclerosis.Neurobiol Dis. 2015 Feb;74:314-24. doi: 10.1016/j.nbd.2014.12.004. Epub 2014 Dec 10.
255 Cytoplasmic mislocalization of RNA splicing factors and aberrant neuronal gene splicing in TDP-43 transgenic pig brain.Mol Neurodegener. 2015 Sep 3;10:42. doi: 10.1186/s13024-015-0036-5.
256 The potential roles of aquaporin 4 in amyotrophic lateral sclerosis.Neurol Sci. 2019 Aug;40(8):1541-1549. doi: 10.1007/s10072-019-03877-5. Epub 2019 Apr 13.
257 Associative Increases in Amyotrophic Lateral Sclerosis Survival Duration With Non-invasive Ventilation Initiation and Usage Protocols.Front Neurol. 2018 Jul 12;9:578. doi: 10.3389/fneur.2018.00578. eCollection 2018.
258 Cryptic exon splicing function of TARDBP interacts with autophagy in nervous tissue.Autophagy. 2018;14(8):1398-1403. doi: 10.1080/15548627.2018.1474311. Epub 2018 Jul 28.
259 Complex phenotype in an Italian family with a novel mutation in SPG3A.J Neurol. 2010 Mar;257(3):328-31. doi: 10.1007/s00415-009-5311-3. Epub 2009 Sep 19.
260 C9ORF72-ALS/FTD-associated poly(GR) binds Atp5a1 and compromises mitochondrial function in vivo.Nat Neurosci. 2019 Jun;22(6):851-862. doi: 10.1038/s41593-019-0397-0. Epub 2019 May 13.
261 Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis.PLoS One. 2017 Mar 22;12(3):e0174317. doi: 10.1371/journal.pone.0174317. eCollection 2017.
262 Ultra-High Field Diffusion MRI Reveals Early Axonal Pathology in Spinal Cord of ALS mice.Transl Neurodegener. 2018 Aug 8;7:20. doi: 10.1186/s40035-018-0122-z. eCollection 2018.
263 Mutant SOD1 Increases APP Expression and Phosphorylation in Cellular and Animal Models of ALS.PLoS One. 2015 Nov 24;10(11):e0143420. doi: 10.1371/journal.pone.0143420. eCollection 2015.
264 Bcl11b: A New Piece to the Complex Puzzle of Amyotrophic Lateral Sclerosis Neuropathogenesis?.Neurotox Res. 2016 Feb;29(2):201-7. doi: 10.1007/s12640-015-9573-5. Epub 2015 Nov 12.
265 A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice.Hum Mol Genet. 2008 Sep 15;17(18):2849-62. doi: 10.1093/hmg/ddn182. Epub 2008 Jun 25.
266 Developmentally Regulated RNA-binding Protein 1 (Drb1)/RNA-binding Motif Protein 45 (RBM45), a Nuclear-Cytoplasmic Trafficking Protein, Forms TAR DNA-binding Protein 43 (TDP-43)-mediated Cytoplasmic Aggregates.J Biol Chem. 2016 Jul 15;291(29):14996-5007. doi: 10.1074/jbc.M115.712232. Epub 2016 May 12.
267 Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.JAMA Neurol. 2018 Jul 1;75(7):860-875. doi: 10.1001/jamaneurol.2018.0372.
268 The Bcl-2 Homology-3 Domain (BH3)-Only Proteins, Bid, DP5/Hrk, and BNip3L, Are Upregulated in Reactive Astrocytes of End-Stage Mutant SOD1 Mouse Spinal Cord.Front Cell Neurosci. 2018 Jan 30;12:15. doi: 10.3389/fncel.2018.00015. eCollection 2018.
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270 Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis.Nat Genet. 2013 Jun;45(6):697-700. doi: 10.1038/ng.2627. Epub 2013 Apr 28.
271 Calretinin and Neuropeptide Y interneurons are differentially altered in the motor cortex of the SOD1(G93A) mouse model of ALS.Sci Rep. 2017 Mar 15;7:44461. doi: 10.1038/srep44461.
272 Calpain activation and CaMKIV reduction in spinal cords from hSOD1G93A mouse model.Mol Cell Neurosci. 2014 Jul;61:219-25. doi: 10.1016/j.mcn.2014.07.002. Epub 2014 Jul 22.
273 Increased cerebrospinal fluid levels of cytokines monocyte chemoattractant protein-1 (MCP-1) and macrophage inflammatory protein-1 (MIP-1) in patients with amyotrophic lateral sclerosis.Neurologia (Engl Ed). 2020 Apr;35(3):165-169. doi: 10.1016/j.nrl.2017.07.020. Epub 2017 Oct 11.
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275 Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons.Hum Mol Genet. 2008 Jan 1;17(1):130-49. doi: 10.1093/hmg/ddm290. Epub 2007 Oct 4.
276 A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis.Acta Neuropathol Commun. 2017 Mar 16;5(1):23. doi: 10.1186/s40478-017-0424-x.
277 Ablation of keratan sulfate accelerates early phase pathogenesis of ALS.PLoS One. 2013 Jun 25;8(6):e66969. doi: 10.1371/journal.pone.0066969. Print 2013.
278 ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration.Nat Neurosci. 2008 Apr;11(4):420-2. doi: 10.1038/nn2073. Epub 2008 Mar 16.
279 ALS blood expression profiling identifies new biomarkers, patient subgroups, and evidence for neutrophilia and hypoxia.J Transl Med. 2019 May 22;17(1):170. doi: 10.1186/s12967-019-1909-0.
280 Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.Arch Neurol. 2011 May;68(5):587-93. doi: 10.1001/archneurol.2010.351. Epub 2011 Jan 10.
281 Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models.Nat Genet. 2012 Dec;44(12):1302-9. doi: 10.1038/ng.2434. Epub 2012 Oct 28.
282 The TGF- System As a Potential Pathogenic Player in Disease Modulation of Amyotrophic Lateral Sclerosis.Front Neurol. 2017 Dec 15;8:669. doi: 10.3389/fneur.2017.00669. eCollection 2017.
283 Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis.Acta Neuropathol Commun. 2019 Jul 12;7(1):114. doi: 10.1186/s40478-019-0759-6.
284 A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models.Nat Commun. 2017 Oct 27;8(1):1164. doi: 10.1038/s41467-017-01283-z.
285 Mutant FUS and ELAVL4 (HuD) Aberrant Crosstalk in Amyotrophic Lateral Sclerosis.Cell Rep. 2019 Jun 25;27(13):3818-3831.e5. doi: 10.1016/j.celrep.2019.05.085.
286 Systemic down-regulation of delta-9 desaturase promotes muscle oxidative metabolism and accelerates muscle function recovery following nerve injury.PLoS One. 2013 Jun 13;8(6):e64525. doi: 10.1371/journal.pone.0064525. Print 2013.
287 Repetitive Nerve Stimulation in Amyotrophic Lateral Sclerosis.Chin Med J (Engl). 2018 Sep 20;131(18):2146-2151. doi: 10.4103/0366-6999.240798.
288 Amyotrophic lateral sclerosis: The complement and inflammatory hypothesis.Mol Immunol. 2018 Oct;102:14-25. doi: 10.1016/j.molimm.2018.06.007. Epub 2018 Jun 20.
289 The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.Autophagy. 2017;13(12):2115-2162. doi: 10.1080/15548627.2017.1384889. Epub 2017 Dec 17.
290 Expression of Wnt5a and its receptor Fzd2 is changed in the spinal cord of adult amyotrophic lateral sclerosis transgenic mice.Int J Clin Exp Pathol. 2013 Jun 15;6(7):1245-60. Print 2013.
291 Cerebrospinal fluid from patients with amyotrophic lateral sclerosis inhibits sonic hedgehog function.PLoS One. 2017 Feb 7;12(2):e0171668. doi: 10.1371/journal.pone.0171668. eCollection 2017.
292 Sporadic amyotrophic lateral sclerosis: is SMN-Gemins protein complex of importance for the relative resistance of oculomotor nucleus motoneurons to degeneration?.Folia Neuropathol. 2018;56(4):308-320. doi: 10.5114/fn.2018.80864.
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296 Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele.Neurology. 2008 Feb 26;70(9):666-76. doi: 10.1212/01.wnl.0000271078.51280.17. Epub 2007 Aug 8.
297 HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort.J Neurol Sci. 2017 Feb 15;373:124-128. doi: 10.1016/j.jns.2016.12.055. Epub 2016 Dec 28.
298 Major histocompatibility complex class I molecules protect motor neurons from astrocyte-induced toxicity in amyotrophic lateral sclerosis.Nat Med. 2016 Apr;22(4):397-403. doi: 10.1038/nm.4052. Epub 2016 Feb 29.
299 Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.Neurodegener Dis. 2017;17(6):304-312. doi: 10.1159/000481258. Epub 2017 Nov 11.
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310 Dexpramipexole as an oral steroid-sparing agent in hypereosinophilic syndromes.Blood. 2018 Aug 2;132(5):501-509. doi: 10.1182/blood-2018-02-835330. Epub 2018 May 8.
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342 Downregulated Glia Interplay and Increased miRNA-155 as Promising Markers to Track ALS at anEarly Stage.Mol Neurobiol. 2018 May;55(5):4207-4224. doi: 10.1007/s12035-017-0631-2. Epub 2017 Jun 13.
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346 Protein interacting with C kinase and neurological disorders.Synapse. 2013 Aug;67(8):532-40. doi: 10.1002/syn.21657. Epub 2013 Mar 20.
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352 Protein arginine methyltransferase 1 and 8 interact with FUS to modify its sub-cellular distribution and toxicity in vitro and in vivo.PLoS One. 2013 Apr 19;8(4):e61576. doi: 10.1371/journal.pone.0061576. Print 2013.
353 Co-localization of cystatin C and prosaposin in cultured neurons and in anterior horn neurons with amyotrophic lateral sclerosis.J Neurol Sci. 2018 Jan 15;384:67-74. doi: 10.1016/j.jns.2017.11.023. Epub 2017 Nov 20.
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360 Znf179 E3 ligase-mediated TDP-43 polyubiquitination is involved in TDP-43- ubiquitinated inclusions (UBI) (+)-related neurodegenerative pathology.J Biomed Sci. 2018 Nov 8;25(1):76. doi: 10.1186/s12929-018-0479-4.
361 RPS25 is required for efficient RAN translation of C9orf72 and other neurodegenerative disease-associated nucleotide repeats.Nat Neurosci. 2019 Sep;22(9):1383-1388. doi: 10.1038/s41593-019-0455-7. Epub 2019 Jul 29.
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367 Diagnostic and prognostic power of CSF Tau in amyotrophic lateral sclerosis.J Neurol. 2018 Oct;265(10):2353-2362. doi: 10.1007/s00415-018-9008-3. Epub 2018 Aug 16.
368 SUMO3 modification accelerates the aggregation of ALS-linked SOD1 mutants.PLoS One. 2014 Jun 27;9(6):e101080. doi: 10.1371/journal.pone.0101080. eCollection 2014.
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371 Genetic analysis of TIA1 gene in Chinese patients with amyotrophic lateral sclerosis.Neurobiol Aging. 2018 Jul;67:201.e9-201.e10. doi: 10.1016/j.neurobiolaging.2018.03.020. Epub 2018 Mar 23.
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386 Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nat Neurosci. 2014 May;17(5):664-666. doi: 10.1038/nn.3688. Epub 2014 Mar 30.
387 Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature. 2012 Aug 23;488(7412):499-503. doi: 10.1038/nature11280.
388 ALS2CL, the novel protein highly homologous to the carboxy-terminal half of ALS2, binds to Rab5 and modulates endosome dynamics.FEBS Lett. 2004 Sep 24;575(1-3):64-70. doi: 10.1016/j.febslet.2004.07.092.
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