Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.
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The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptorsThe ER stress factor XBP1s prevents amyloid-beta neurotoxicityXBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagyThe Unfolded Protein Response and the Role of Protein Disulfide Isomerase in NeurodegenerationMolecular motor proteins and amyotrophic lateral sclerosisProtein disulfide isomerases in neurodegeneration: from disease mechanisms to biomedical applicationsRedox regulation in amyotrophic lateral sclerosisALS-associated TDP-43 induces endoplasmic reticulum stress, which drives cytoplasmic TDP-43 accumulation and stress granule formationAn inducer of VGF protects cells against ER stress-induced cell death and prolongs survival in the mutant SOD1 animal models of familial ALSFunctional contribution of the transcription factor ATF4 to the pathogenesis of amyotrophic lateral sclerosisFunctional Role of the Disulfide Isomerase ERp57 in Axonal RegenerationThe Cu, Zn Superoxide Dismutase: Not Only a Dismutase EnzymeReview: Modulating the unfolded protein response to prevent neurodegeneration and enhance memoryProtein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosisSOD1 aggregation in astrocytes following ischemia/reperfusion injury: a role of NO-mediated S-nitrosylation of protein disulfide isomerase (PDI)The critical role of membralin in postnatal motor neuron survival and diseaseAmyotrophic lateral sclerosis multiprotein biomarkers in peripheral blood mononuclear cellsModulation of proteostasis by transcription factor NRF2 and impact in neurodegenerative diseasesPalmitoylation of superoxide dismutase 1 (SOD1) is increased for familial amyotrophic lateral sclerosis-linked SOD1 mutantsA random set scoring model for prioritization of disease candidate genes using protein complexes and data-mining of GeneRIF, OMIM and PubMed records.Probing mechanisms of axonopathy. Part I: Protein targets of 1,2-diacetylbenzene, the neurotoxic metabolite of aromatic solvent 1,2-diethylbenzeneAltered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosisProtein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities?Variation in the Subcellular Localization and Protein Folding Activity among Arabidopsis thaliana Homologs of Protein Disulfide Isomerase.Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia ContinuumEndoplasmic reticulum stress and inflammation in the central nervous systemInhibitors of protein disulfide isomerase suppress apoptosis induced by misfolded proteins.Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.Bacitracin is not a specific inhibitor of protein disulfide isomerase.Bim links ER stress and apoptosis in cells expressing mutant SOD1 associated with amyotrophic lateral sclerosis.Guanabenz, which enhances the unfolded protein response, ameliorates mutant SOD1-induced amyotrophic lateral sclerosis.The unfolded protein response in familial amyotrophic lateral sclerosis.Activation of interferon signaling pathways in spinal cord astrocytes from an ALS mouse model.Domain a' of protein disulfide isomerase plays key role in inhibiting alpha-synuclein fibril formation.The endoplasmic reticulum-resident chaperone heat shock protein 47 protects the Golgi apparatus from the effects of O-glycosylation inhibition.Mechanisms of neuroprotection by protein disulphide isomerase in amyotrophic lateral sclerosis.Mutant TDP-43 deregulates AMPK activation by PP2A in ALS models.Altered oxido-reductive state in the diabetic heart: loss of cardioprotection due to protein disulfide isomeraseActivation of the endoplasmic reticulum stress response in skeletal muscle of G93A*SOD1 amyotrophic lateral sclerosis mice.Novel roles for protein disulphide isomerase in disease states: a double edged sword?
P2860
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P2860
Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Induction of the unfolded prot ...... e with superoxide dismutase 1.
@en
type
label
Induction of the unfolded prot ...... e with superoxide dismutase 1.
@en
prefLabel
Induction of the unfolded prot ...... e with superoxide dismutase 1.
@en
P2093
P2860
P356
P1476
Induction of the unfolded prot ...... e with superoxide dismutase 1.
@en
P2093
Alan Rembach
Bradley J Turner
Doris Tomas
Janelle Nunan
Judith A Lysaght
Julie D Atkin
Malcolm K Horne
Manal A Farg
Philip M Beart
Phillip Nagley
P2860
P304
30152-30165
P356
10.1074/JBC.M603393200
P407
P577
2006-07-17T00:00:00Z