(Q58125486)

1

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Akiyo Hineno

2

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Kunihiro Yoshida

3

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Yoshiki Sekijima

4

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Naoko Hanaoka-Tachibana

5

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Yo-Ichi Takei

6

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Shinji Ohara

7

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Shu-Ichi Ikeda

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

8

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publication date

September 2012

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published in

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volume

13

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issue

5

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page(s)

479-486

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cites work

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

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SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in management

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Electrodiagnostic criteria for diagnosis of ALS.

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An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4.

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Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase.

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Early-onset ALS with long-term survival associated with spastin gene mutation

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Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions

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The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.

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The G93C Mutation in Superoxide Dismutase 1

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Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles

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Metal-free superoxide dismutase forms soluble oligomers under physiological conditions: a possible general mechanism for familial ALS

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Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis

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Disulfide bond mediates aggregation, toxicity, and ubiquitylation of familial amyotrophic lateral sclerosis-linked mutant SOD1.

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Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature

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Increased affinity for copper mediated by cysteine 111 in forms of mutant superoxide dismutase 1 linked to amyotrophic lateral sclerosis

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