Entry |
|
Name |
Amyotrophic lateral sclerosis - Homo sapiens (human)
|
Description |
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by a progressive degeneration of motor neurons in the brain and spinal cord. In 90% of patients, ALS is sporadic, with no clear genetic linkage. On the other hand, the remaining 10% of cases show familial inheritance, with mutations in SOD1, TDP43(TARDBP), FUS, or C9orf72 genes being the most frequent causes. In spite of such difference, familial ALS and sporadic ALS have similarities in their pathological features. Proposed disease mechanisms contributing to motor neuron degeneration in ALS are: impaired proteostasis, aberrant RNA processing, mitochondrial disfunction and oxidative stress, microglia activation, and axonal dysfunction.
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Class |
Human Diseases; Neurodegenerative disease
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Pathway map |

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Network |
|
Element |
N01135 | Mutation-caused aberrant SOD1 to intrinsic apoptotic pathway |
N01136 | Mutation-caused aberrant TDP43 to electron transfer in Complex I |
N01138 | Mutation-inactivated OPTN to PINK-Parkin-mediated autophagosome formation |
N01139 | Mutation-inactivated p62 to PINK-Parkin-mediated autophagosome formation |
N01141 | Mutation-inactivated TBK1 to TBK1-mediated autophagosome formation |
N01143 | Mutation-inactivated C9orf72 to C9orf72-mediated autophagy initiation |
N01144 | Mutation-caused aberrant SOD1 to 26S proteasome-mediated protein degradation |
N01145 | Mutation-inactivated VCP to 26S proteasome-mediated protein degradation |
N01146 | Mutation-inactivated UBQLN2 to 26S proteasome-mediated protein degradation |
N01147 | Mutation-caused aberrant SOD1 to ATF6-mediated transcription |
N01148 | Mutation-caused aberrant SOD1 to IRE1a-XBP1 signaling pathway |
N01149 | Mutation-caused aberrant SOD1 to PERK-ATF4 signaling pathway |
N01150 | Mutation-inactivated VAPB to ATF6-mediated transcription |
N01151 | Mutation-inactivated SIGMAR1 to Ca2+ -apoptotic pathway |
N01153 | Mutation-caused aberrant GLE1 to nuclear export of mRNA |
N01155 | Mutation-caused aberrant TDP43 to TDP-43-regulated splicing |
N01157 | Mutation-caused aberrant FUS to FUS-regulated splicing |
N01158 | Mutation-caused aberrant DCTN1 to retrograde axonal transport |
N01159 | Mutation-caused aberrant TUBA4A to retrograde axonal transport |
N01160 | Mutation-caused aberrant SOD1 to retrograde axonal transport |
N01162 | Mutation-caused aberrant PFN1 to actin polymerization |
N01164 | Mutation-inactivated ERBB4 to NRG-ERBB4-PI3K signaling pathway |
|
Disease |
H00058 | Amyotrophic lateral sclerosis (ALS) |
|
Drug |
D11811 | Tofersen (JAN/USAN/INN) |
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Organism |
Homo sapiens (human) [GN: hsa]
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Gene |
637 | BID; BH3 interacting domain death agonist [KO:K04726] |
596 | BCL2; BCL2 apoptosis regulator [KO:K02161] |
581 | BAX; BCL2 associated X, apoptosis regulator [KO:K02159] |
572 | BAD; BCL2 associated agonist of cell death [KO:K02158] |
317 | APAF1; apoptotic peptidase activating factor 1 [KO:K02084] |
4731 | NDUFV3; NADH:ubiquinone oxidoreductase subunit V3 [KO:K03944] |
4694 | NDUFA1; NADH:ubiquinone oxidoreductase subunit A1 [KO:K03945] |
4695 | NDUFA2; NADH:ubiquinone oxidoreductase subunit A2 [KO:K03946] |
4696 | NDUFA3; NADH:ubiquinone oxidoreductase subunit A3 [KO:K03947] |
4697 | NDUFA4; NDUFA4 mitochondrial complex associated [KO:K03948] |
56901 | NDUFA4L2; NDUFA4 mitochondrial complex associated like 2 [KO:K03948] |
4698 | NDUFA5; NADH:ubiquinone oxidoreductase subunit A5 [KO:K03949] |
4700 | NDUFA6; NADH:ubiquinone oxidoreductase subunit A6 [KO:K03950] |
4701 | NDUFA7; NADH:ubiquinone oxidoreductase subunit A7 [KO:K03951] |
4702 | NDUFA8; NADH:ubiquinone oxidoreductase subunit A8 [KO:K03952] |
4704 | NDUFA9; NADH:ubiquinone oxidoreductase subunit A9 [KO:K03953] |
4705 | NDUFA10; NADH:ubiquinone oxidoreductase subunit A10 [KO:K03954] |
4706 | NDUFAB1; NADH:ubiquinone oxidoreductase subunit AB1 [KO:K03955] |
126328 | NDUFA11; NADH:ubiquinone oxidoreductase subunit A11 [KO:K03956] |
55967 | NDUFA12; NADH:ubiquinone oxidoreductase subunit A12 [KO:K11352] |
51079 | NDUFA13; NADH:ubiquinone oxidoreductase subunit A13 [KO:K11353] |
4707 | NDUFB1; NADH:ubiquinone oxidoreductase subunit B1 [KO:K03957] |
4708 | NDUFB2; NADH:ubiquinone oxidoreductase subunit B2 [KO:K03958] |
4709 | NDUFB3; NADH:ubiquinone oxidoreductase subunit B3 [KO:K03959] |
4710 | NDUFB4; NADH:ubiquinone oxidoreductase subunit B4 [KO:K03960] |
4711 | NDUFB5; NADH:ubiquinone oxidoreductase subunit B5 [KO:K03961] |
4712 | NDUFB6; NADH:ubiquinone oxidoreductase subunit B6 [KO:K03962] |
4713 | NDUFB7; NADH:ubiquinone oxidoreductase subunit B7 [KO:K03963] |
4714 | NDUFB8; NADH:ubiquinone oxidoreductase subunit B8 [KO:K03964] |
4715 | NDUFB9; NADH:ubiquinone oxidoreductase subunit B9 [KO:K03965] |
4716 | NDUFB10; NADH:ubiquinone oxidoreductase subunit B10 [KO:K03966] |
54539 | NDUFB11; NADH:ubiquinone oxidoreductase subunit B11 [KO:K11351] |
4724 | NDUFS4; NADH:ubiquinone oxidoreductase subunit S4 [KO:K03937] |
4725 | NDUFS5; NADH:ubiquinone oxidoreductase subunit S5 [KO:K03938] |
4726 | NDUFS6; NADH:ubiquinone oxidoreductase subunit S6 [KO:K03939] |
4717 | NDUFC1; NADH:ubiquinone oxidoreductase subunit C1 [KO:K03967] |
4718 | NDUFC2; NADH:ubiquinone oxidoreductase subunit C2 [KO:K03968] |
6389 | SDHA; succinate dehydrogenase complex flavoprotein subunit A [KO:K00234] [EC:1.3.5.1] |
6390 | SDHB; succinate dehydrogenase complex iron sulfur subunit B [KO:K00235] [EC:1.3.5.1] |
6391 | SDHC; succinate dehydrogenase complex subunit C [KO:K00236] |
6392 | SDHD; succinate dehydrogenase complex subunit D [KO:K00237] |
7386 | UQCRFS1; ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 [KO:K00411] [EC:7.1.1.8] |
7384 | UQCRC1; ubiquinol-cytochrome c reductase core protein 1 [KO:K00414] |
7385 | UQCRC2; ubiquinol-cytochrome c reductase core protein 2 [KO:K00415] |
7388 | UQCRH; ubiquinol-cytochrome c reductase hinge protein [KO:K00416] |
440567 | UQCRHL; ubiquinol-cytochrome c reductase hinge protein like [KO:K00416] |
7381 | UQCRB; ubiquinol-cytochrome c reductase binding protein [KO:K00417] |
27089 | UQCRQ; ubiquinol-cytochrome c reductase complex III subunit VII [KO:K00418] |
29796 | UQCR10; ubiquinol-cytochrome c reductase, complex III subunit X [KO:K00419] |
10975 | UQCR11; ubiquinol-cytochrome c reductase, complex III subunit XI [KO:K00420] |
4514 | COX3; cytochrome c oxidase subunit III [KO:K02262] |
4513 | COX2; cytochrome c oxidase subunit II [KO:K02261] |
84701 | COX4I2; cytochrome c oxidase subunit 4I2 [KO:K02263] |
1327 | COX4I1; cytochrome c oxidase subunit 4I1 [KO:K02263] |
9377 | COX5A; cytochrome c oxidase subunit 5A [KO:K02264] |
1329 | COX5B; cytochrome c oxidase subunit 5B [KO:K02265] |
1337 | COX6A1; cytochrome c oxidase subunit 6A1 [KO:K02266] |
1339 | COX6A2; cytochrome c oxidase subunit 6A2 [KO:K02266] |
1340 | COX6B1; cytochrome c oxidase subunit 6B1 [KO:K02267] |
1345 | COX6C; cytochrome c oxidase subunit 6C [KO:K02268] |
1346 | COX7A1; cytochrome c oxidase subunit 7A1 [KO:K02270] |
1347 | COX7A2; cytochrome c oxidase subunit 7A2 [KO:K02270] |
9167 | COX7A2L; cytochrome c oxidase subunit 7A2 like [KO:K02270] |
1349 | COX7B; cytochrome c oxidase subunit 7B [KO:K02271] |
1350 | COX7C; cytochrome c oxidase subunit 7C [KO:K02272] |
1351 | COX8A; cytochrome c oxidase subunit 8A [KO:K02273] |
498 | ATP5F1A; ATP synthase F1 subunit alpha [KO:K02132] |
509 | ATP5F1C; ATP synthase F1 subunit gamma [KO:K02136] |
513 | ATP5F1D; ATP synthase F1 subunit delta [KO:K02134] |
514 | ATP5F1E; ATP synthase F1 subunit epsilon [KO:K02135] |
515 | ATP5PB; ATP synthase peripheral stalk-membrane subunit b [KO:K02127] |
516 | ATP5MC1; ATP synthase membrane subunit c locus 1 [KO:K02128] |
517 | ATP5MC2; ATP synthase membrane subunit c locus 2 [KO:K02128] |
518 | ATP5MC3; ATP synthase membrane subunit c locus 3 [KO:K02128] |
10476 | ATP5PD; ATP synthase peripheral stalk subunit d [KO:K02138] |
539 | ATP5PO; ATP synthase peripheral stalk subunit OSCP [KO:K02137] |
522 | ATP5PF; ATP synthase peripheral stalk subunit F6 [KO:K02131] |
7416 | VDAC1; voltage dependent anion channel 1 [KO:K05862] |
10452 | TOMM40; translocase of outer mitochondrial membrane 40 [KO:K11518] |
84134 | TOMM40L; translocase of outer mitochondrial membrane 40 like [KO:K11518] |
11337 | GABARAP; GABA type A receptor-associated protein [KO:K08341] |
23710 | GABARAPL1; GABA type A receptor associated protein like 1 [KO:K08341] |
11345 | GABARAPL2; GABA type A receptor associated protein like 2 [KO:K08341] |
10010 | TANK; TRAF family member associated NFKB activator [KO:K12650] |
4218 | RAB8A; RAB8A, member RAS oncogene family [KO:K07901] |
116442 | RAB39B; RAB39B, member RAS oncogene family [KO:K07925] |
5861 | RAB1A; RAB1A, member RAS oncogene family [KO:K07874] |
9821 | RB1CC1; RB1 inducible coiled-coil 1 [KO:K17589] |
55626 | AMBRA1; autophagy and beclin 1 regulator 1 [KO:K17985] |
29982 | NRBF2; nuclear receptor binding factor 2 [KO:K21246] |
26100 | WIPI2; WD repeat domain, phosphoinositide interacting 2 [KO:K17908] |
55062 | WIPI1; WD repeat domain, phosphoinositide interacting 1 [KO:K17908] |
57679 | ALS2; alsin Rho guanine nucleotide exchange factor ALS2 [KO:K04575] |
5868 | RAB5A; RAB5A, member RAS oncogene family [KO:K07887] |
25978 | CHMP2B; charged multivesicular body protein 2B [KO:K12192] |
9896 | FIG4; FIG4 phosphoinositide 5-phosphatase [KO:K22913] [EC:3.1.3.-] |
80208 | SPG11; SPG11 vesicle trafficking associated, spatacsin [KO:K19026] |
5534 | PPP3R1; protein phosphatase 3 regulatory subunit B, alpha [KO:K06268] |
5535 | PPP3R2; protein phosphatase 3 regulatory subunit B, beta [KO:K06268] |
5701 | PSMC2; proteasome 26S subunit, ATPase 2 [KO:K03061] |
5700 | PSMC1; proteasome 26S subunit, ATPase 1 [KO:K03062] |
5704 | PSMC4; proteasome 26S subunit, ATPase 4 [KO:K03063] |
5706 | PSMC6; proteasome 26S subunit, ATPase 6 [KO:K03064] |
5702 | PSMC3; proteasome 26S subunit, ATPase 3 [KO:K03065] |
5705 | PSMC5; proteasome 26S subunit, ATPase 5 [KO:K03066] |
5708 | PSMD2; proteasome 26S subunit, non-ATPase 2 [KO:K03028] |
5707 | PSMD1; proteasome 26S subunit, non-ATPase 1 [KO:K03032] |
5709 | PSMD3; proteasome 26S subunit, non-ATPase 3 [KO:K03033] |
5715 | PSMD9; proteasome 26S subunit, non-ATPase 9 [KO:K06693] |
5718 | PSMD12; proteasome 26S subunit, non-ATPase 12 [KO:K03035] |
5717 | PSMD11; proteasome 26S subunit, non-ATPase 11 [KO:K03036] |
9861 | PSMD6; proteasome 26S subunit, non-ATPase 6 [KO:K03037] |
5713 | PSMD7; proteasome 26S subunit, non-ATPase 7 [KO:K03038] |
5719 | PSMD13; proteasome 26S subunit, non-ATPase 13 [KO:K03039] |
5710 | PSMD4; proteasome 26S subunit, non-ATPase 4 [KO:K03029] |
10213 | PSMD14; proteasome 26S subunit, non-ATPase 14 [KO:K03030] |
5714 | PSMD8; proteasome 26S subunit, non-ATPase 8 [KO:K03031] |
11047 | ADRM1; adhesion regulating molecule 1 [KO:K06691] |
7979 | SEM1; SEM1 26S proteasome complex subunit [KO:K10881] |
220988 | HNRNPA3; heterogeneous nuclear ribonucleoprotein A3 [KO:K12741] |
3178 | HNRNPA1; heterogeneous nuclear ribonucleoprotein A1 [KO:K12741] |
144983 | HNRNPA1L2; heterogeneous nuclear ribonucleoprotein A1 like 2 [KO:K12741] |
3181 | HNRNPA2B1; heterogeneous nuclear ribonucleoprotein A2/B1 [KO:K13158] |
283 | ANG; angiogenin [KO:K16631] [EC:3.1.27.-] |
4686 | NCBP1; nuclear cap binding protein subunit 1 [KO:K12882] |
6428 | SRSF3; serine and arginine rich splicing factor 3 [KO:K12892] |
6432 | SRSF7; serine and arginine rich splicing factor 7 [KO:K12896] |
29107 | NXT1; nuclear transport factor 2 like export factor 1 [KO:K14285] |
55916 | NXT2; nuclear transport factor 2 like export factor 2 [KO:K14285] |
7175 | TPR; translocated promoter region, nuclear basket protein [KO:K09291] |
4928 | NUP98; nucleoporin 98 and 96 precursor [KO:K14297] |
6396 | SEC13; SEC13 homolog, nuclear pore and COPII coat complex component [KO:K14004] |
9883 | POM121; POM121 transmembrane nucleoporin [KO:K14316] |
94026 | POM121L2; POM121 transmembrane nucleoporin like 2 [KO:K14316] |
5903 | RANBP2; RAN binding protein 2 [KO:K12172] [EC:2.3.2.-] |
400916 | CHCHD10; coiled-coil-helix-coiled-coil-helix domain containing 10 [KO:K22759] |
9217 | VAPB; VAMP associated protein B and C [KO:K10707] |
22926 | ATF6; activating transcription factor 6 [KO:K09054] |
1649 | DDIT3; DNA damage inducible transcript 3 [KO:K04452] |
2081 | ERN1; endoplasmic reticulum to nucleus signaling 1 [KO:K08852] [EC:2.7.11.1 3.1.26.-] |
9451 | EIF2AK3; eukaryotic translation initiation factor 2 alpha kinase 3 [KO:K08860] [EC:2.7.11.1] |
1965 | EIF2S1; eukaryotic translation initiation factor 2 subunit alpha [KO:K03237] |
468 | ATF4; activating transcription factor 4 [KO:K04374] |
3710 | ITPR3; inositol 1,4,5-trisphosphate receptor type 3 [KO:K04960] |
10280 | SIGMAR1; sigma non-opioid intracellular receptor 1 [KO:K20719] |
7132 | TNFRSF1A; TNF receptor superfamily member 1A [KO:K03158] |
7133 | TNFRSF1B; TNF receptor superfamily member 1B [KO:K05141] |
1616 | DAXX; death domain associated protein [KO:K02308] |
9973 | CCS; copper chaperone for superoxide dismutase [KO:K04569] |
7280 | TUBB2A; tubulin beta 2A class IIa [KO:K07375] |
9001 | HAP1; huntingtin associated protein 1 [KO:K04647] |
1767 | DNAH5; dynein axonemal heavy chain 5 [KO:K10408] |
1768 | DNAH6; dynein axonemal heavy chain 6 [KO:K10408] |
1770 | DNAH9; dynein axonemal heavy chain 9 [KO:K10408] |
8701 | DNAH11; dynein axonemal heavy chain 11 [KO:K10408] |
1769 | DNAH8; dynein axonemal heavy chain 8 [KO:K10408] |
8632 | DNAH17; dynein axonemal heavy chain 17 [KO:K10408] |
7802 | DNALI1; dynein axonemal light intermediate chain 1 [KO:K10410] |
27019 | DNAI1; dynein axonemal intermediate chain 1 [KO:K10409] |
64446 | DNAI2; dynein axonemal intermediate chain 2 [KO:K11143] |
6506 | SLC1A2; solute carrier family 1 member 2 [KO:K05613] |
2890 | GRIA1; glutamate ionotropic receptor AMPA type subunit 1 [KO:K05197] |
2891 | GRIA2; glutamate ionotropic receptor AMPA type subunit 2 [KO:K05198] |
2902 | GRIN1; glutamate ionotropic receptor NMDA type subunit 1 [KO:K05208] |
2903 | GRIN2A; glutamate ionotropic receptor NMDA type subunit 2A [KO:K05209] |
2904 | GRIN2B; glutamate ionotropic receptor NMDA type subunit 2B [KO:K05210] |
2905 | GRIN2C; glutamate ionotropic receptor NMDA type subunit 2C [KO:K05211] |
2906 | GRIN2D; glutamate ionotropic receptor NMDA type subunit 2D [KO:K05212] |
|
Compound |
C04549 | 1-Phosphatidyl-1D-myo-inositol 3-phosphate |
|
Reference |
|
Authors |
Brown RH, Al-Chalabi A |
Title |
Amyotrophic Lateral Sclerosis. |
Journal |
|
Reference |
|
Authors |
Webster CP, Smith EF, Shaw PJ, De Vos KJ |
Title |
Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities? |
Journal |
|
Reference |
|
Authors |
Valko K, Ciesla L |
Title |
Amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL |
Title |
Genetics of amyotrophic lateral sclerosis: A review. |
Journal |
|
Reference |
|
Authors |
Turner MR, Hardiman O, Benatar M, Brooks BR, Chio A, de Carvalho M, Ince PG, Lin C, Miller RG, Mitsumoto H, Nicholson G, Ravits J, Shaw PJ, Swash M, Talbot K, Traynor BJ, Van den Berg LH, Veldink JH, Vucic S, Kiernan MC |
Title |
Controversies and priorities in amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Pasinelli P, Brown RH |
Title |
Molecular biology of amyotrophic lateral sclerosis: insights from genetics. |
Journal |
|
Reference |
|
Authors |
Goodall EF, Morrison KE |
Title |
Amyotrophic lateral sclerosis (motor neuron disease): proposed mechanisms and pathways to treatment. |
Journal |
|
Reference |
|
Authors |
Smith EF, Shaw PJ, De Vos KJ |
Title |
The role of mitochondria in amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Kodavati M, Wang H, Hegde ML |
Title |
Altered Mitochondrial Dynamics in Motor Neuron Disease: An Emerging Perspective. |
Journal |
|
Reference |
|
Authors |
Hervias I, Beal MF, Manfredi G |
Title |
Mitochondrial dysfunction and amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Bacman SR, Bradley WG, Moraes CT |
Title |
Mitochondrial involvement in amyotrophic lateral sclerosis: trigger or target? |
Journal |
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Reference |
|
Authors |
Lin MT, Beal MF |
Title |
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. |
Journal |
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Reference |
|
Authors |
Bendotti C, Bao Cutrona M, Cheroni C, Grignaschi G, Lo Coco D, Peviani M, Tortarolo M, Veglianese P, Zennaro E |
Title |
Inter- and intracellular signaling in amyotrophic lateral sclerosis: role of p38 mitogen-activated protein kinase. |
Journal |
|
Reference |
|
Authors |
Simpson EP, Yen AA, Appel SH |
Title |
Oxidative Stress: a common denominator in the pathogenesis of amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Bendotti C, Carri MT |
Title |
Lessons from models of SOD1-linked familial ALS. |
Journal |
|
Reference |
|
Authors |
Robertson J, Kriz J, Nguyen MD, Julien JP |
Title |
Pathways to motor neuron degeneration in transgenic mouse models. |
Journal |
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Reference |
|
Authors |
Eve DJ, Dennis JS, Citron BA |
Title |
Transcription factor p53 in degenerating spinal cords. |
Journal |
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Reference |
|
Authors |
Bahar E, Kim H, Yoon H |
Title |
ER Stress-Mediated Signaling: Action Potential and Ca(2+) as Key Players. |
Journal |
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Reference |
|
Authors |
Bezprozvanny I |
Title |
Calcium signaling and neurodegenerative diseases. |
Journal |
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Reference |
|
Authors |
von Lewinski F, Keller BU |
Title |
Ca2+, mitochondria and selective motoneuron vulnerability: implications for ALS. |
Journal |
|
Reference |
|
Authors |
Julien JP. |
Title |
Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded. |
Journal |
|
Reference |
|
Authors |
Hand CK, Rouleau GA |
Title |
Familial amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Barber SC, Mead RJ, Shaw PJ |
Title |
Oxidative stress in ALS: a mechanism of neurodegeneration and a therapeutic target. |
Journal |
|
Reference |
|
Authors |
Prasad A, Bharathi V, Sivalingam V, Girdhar A, Patel BK |
Title |
Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis. |
Journal |
|
Reference |
|
Authors |
Nguyen DKH, Thombre R, Wang J |
Title |
Autophagy as a common pathway in amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Lee JK, Shin JH, Lee JE, Choi EJ |
Title |
Role of autophagy in the pathogenesis of amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Oakes JA, Davies MC, Collins MO |
Title |
TBK1: a new player in ALS linking autophagy and neuroinflammation. |
Journal |
|
Reference |
|
Authors |
Ramesh N, Pandey UB |
Title |
Autophagy Dysregulation in ALS: When Protein Aggregates Get Out of Hand. |
Journal |
|
Reference |
|
Authors |
Kunita R, Otomo A, Mizumura H, Suzuki-Utsunomiya K, Hadano S, Ikeda JE |
Title |
The Rab5 activator ALS2/alsin acts as a novel Rac1 effector through Rac1-activated endocytosis. |
Journal |
|
Reference |
|
Authors |
Hadano S, Kunita R, Otomo A, Suzuki-Utsunomiya K, Ikeda JE |
Title |
Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degeneration. |
Journal |
|
Reference |
|
Authors |
Ruffoli R, Bartalucci A, Frati A, Fornai F |
Title |
Ultrastructural studies of ALS mitochondria connect altered function and permeability with defects of mitophagy and mitochondriogenesis. |
Journal |
|
Reference |
|
Authors |
Menzies FM, Fleming A, Rubinsztein DC |
Title |
Compromised autophagy and neurodegenerative diseases. |
Journal |
|
Reference |
|
Authors |
Casterton RL, Hunt RJ, Fanto M |
Title |
Pathomechanism Heterogeneity in the Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Disease Spectrum: Providing Focus Through the Lens of Autophagy. |
Journal |
|
Reference |
|
Authors |
Lin G, Mao D, Bellen HJ |
Title |
Amyotrophic Lateral Sclerosis Pathogenesis Converges on Defects in Protein Homeostasis Associated with TDP-43 Mislocalization and Proteasome-Mediated Degradation Overload. |
Journal |
|
Reference |
|
Authors |
Hetz C, Mollereau B |
Title |
Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases. |
Journal |
|
Reference |
|
Authors |
Xiang C, Wang Y, Zhang H, Han F |
Title |
The role of endoplasmic reticulum stress in neurodegenerative disease. |
Journal |
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Reference |
|
Authors |
Hughes D, Mallucci GR |
Title |
The unfolded protein response in neurodegenerative disorders - therapeutic modulation of the PERK pathway. |
Journal |
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Reference |
|
Authors |
Doyle KM, Kennedy D, Gorman AM, Gupta S, Healy SJ, Samali A |
Title |
Unfolded proteins and endoplasmic reticulum stress in neurodegenerative disorders. |
Journal |
|
Reference |
|
Authors |
Turner BJ, Atkin JD |
Title |
ER stress and UPR in familial amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Nishitoh H, Kadowaki H, Nagai A, Maruyama T, Yokota T, Fukutomi H, Noguchi T, Matsuzawa A, Takeda K, Ichijo H |
Title |
ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1. |
Journal |
|
Reference |
|
Authors |
Walker AK, Atkin JD |
Title |
Stress signaling from the endoplasmic reticulum: A central player in the pathogenesis of amyotrophic lateral sclerosis. |
Journal |
|
Reference |
|
Authors |
Renaud L, Picher-Martel V, Codron P, Julien JP |
Title |
Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia. |
Journal |
|
Reference |
|
Authors |
Nguyen HP, Van Broeckhoven C, van der Zee J |
Title |
ALS Genes in the Genomic Era and their Implications for FTD. |
Journal |
|
Reference |
|
Authors |
Atkin G, Paulson H |
Title |
Ubiquitin pathways in neurodegenerative disease. |
Journal |
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Reference |
|
Authors |
Kim JM, Billington E, Reyes A, Notarianni T, Sage J, Agbas E, Taylor M, Monast I, Stanford JA, Agbas A |
Title |
Impaired Cu-Zn Superoxide Dismutase (SOD1) and Calcineurin (Cn) Interaction in ALS: A Presumed Consequence for TDP-43 and Zinc Aggregation in Tg SOD1(G93A) Rodent Spinal Cord Tissue. |
Journal |
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Reference |
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Authors |
Benarroch EE |
Title |
Sigma-1 receptor and amyotrophic lateral sclerosis. |
Journal |
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Reference |
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Authors |
Millecamps S, Julien JP |
Title |
Axonal transport deficits and neurodegenerative diseases. |
Journal |
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Related pathway |
hsa04141 | Protein processing in endoplasmic reticulum |
hsa04810 | Regulation of actin cytoskeleton |
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KO pathway |
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