(Q28245736)

1

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Yuichi Hashimoto

2

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Takako Niikura

3

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Sadakazu Aiso

4

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Ikuo Nishimoto

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

30 April 2004

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published in

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volume

279

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issue

18

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page(s)

19247-56

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cites work

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Aβ

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

A novel centrosomal ring-finger protein, dorfin, mediates ubiquitin ligase activity

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

Neurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313236200

Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313236200

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

21 January 2018

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Mutated human SOD1 causes dysfunction of oxidative phosphorylation in mitochondria of transgenic mice.

21 January 2018

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Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

21 January 2018

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Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis show enhanced formation of aggregates in vitro

21 January 2018

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 January 2018

1 reference

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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313236200

ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene

21 January 2018

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Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons

21 January 2018

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Neurotoxic mechanisms triggered by Alzheimer's disease-linked mutant M146L presenilin 1: involvement of NO synthase via a novel pertussis toxin target

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Neurotoxic mechanisms by Alzheimer's disease-linked N141I mutant presenilin 2.

21 January 2018

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Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity

21 January 2018

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Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

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Molecular genetics of Alzheimer's disease.

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

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Involvement of c-Jun N-terminal kinase in amyloid precursor protein-mediated neuronal cell death.

21 January 2018

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Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis

21 January 2018

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The pleckstrin homology domain mediates transformation by oncogenic dbl through specific intracellular targeting

21 January 2018

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Modulation of oncogenic DBL activity by phosphoinositol phosphate binding to pleckstrin homology domain.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M313236200

Regulation of proto-Dbl by intracellular membrane targeting and protein stability

21 January 2018

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AnALS2gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

21 January 2018

1 reference

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