Misfolded SOD1 is not a primary component of sporadic ALS.
about
Parsing Disease-relevant Protein Modifications from Epiphenomena: Perspective on the Structural Basis of SOD1-Mediated ALS.Amyotrophic lateral sclerosis-like superoxide dismutase 1 proteinopathy is associated with neuronal loss in Parkinson's disease brain.A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model.The Enigmatic Role of C9ORF72 in AutophagySpinal cord homogenates from SOD1 familial amyotrophic lateral sclerosis induce SOD1 aggregation in living cells.Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111.Accumulation of dysfunctional SOD1 protein in Parkinson's disease is not associated with mutations in the SOD1 gene.MIF inhibits the formation and toxicity of misfolded SOD1 amyloid aggregates: implications for familial ALS.Misfolded SOD1 pathology in sporadic Amyotrophic Lateral SclerosisLarge SOD1 aggregates, unlike trimeric SOD1, do not impact cell viability in a model of amyotrophic lateral sclerosis
P2860
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P2860
Misfolded SOD1 is not a primary component of sporadic ALS.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
@zh-cn
2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
Misfolded SOD1 is not a primary component of sporadic ALS.
@en
Misfolded SOD1 is not a primary component of sporadic ALS.
@nl
type
label
Misfolded SOD1 is not a primary component of sporadic ALS.
@en
Misfolded SOD1 is not a primary component of sporadic ALS.
@nl
prefLabel
Misfolded SOD1 is not a primary component of sporadic ALS.
@en
Misfolded SOD1 is not a primary component of sporadic ALS.
@nl
P2093
P2860
P1476
Misfolded SOD1 is not a primary component of sporadic ALS.
@en
P2093
Derek Schulte
Donald P Pizzo
Jennifer Stauffer
John Ravits
Melissa McAlonis-Downes
Philippe A Parone
Sandra K Lee
Sandrine Da Cruz
Shahram Saberi
P2860
P2888
P304
P356
10.1007/S00401-017-1688-8
P577
2017-02-28T00:00:00Z
P6179
1084021471