(Q36589172)

15 August 2017

1 reference

title

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA. (English)

1 reference

15 August 2017

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Kinya Ishikawa

1

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15 August 2017

Hidehiro Mizusawa

series ordinal

2

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15 August 2017

publication date

1 August 2006

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15 August 2017

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15 August 2017

volume

26

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15 August 2017

issue

4

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15 August 2017

page(s)

352-360

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Protein aggregation and neurodegenerative disease

15 August 2017

cites work

1 reference

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An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

21 January 2018

1 reference

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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

21 January 2018

1 reference

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Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00719.X

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia

21 January 2018

1 reference

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A candidate gene for human neurodegenerative disorders: a rat PKC gamma mutation causes a Parkinsonian syndrome.

21 January 2018

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PKC gamma mutant mice exhibit mild deficits in spatial and contextual learning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00719.X

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2006.00719.X

New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.

21 January 2018

1 reference

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Altered trafficking of membrane proteins in purkinje cells of SCA1 transgenic mice

21 January 2018

1 reference

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Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.

21 January 2018

1 reference

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A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]

21 January 2018

1 reference

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Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype

21 January 2018

1 reference

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Ataxia and paroxysmal dyskinesia in mice lacking axonally transported FGF14.

21 January 2018

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The hereditary spinocerebellar ataxias in Japan

21 January 2018

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Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

21 January 2018

1 reference

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Cloning and identification of the human LPAAT-zeta gene, a novel member of the lysophosphatidic acid acyltransferase family

21 January 2018

1 reference

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An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor dom

21 January 2018

1 reference

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A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.

21 January 2018

1 reference

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The clinical and genetic spectrum of spinocerebellar ataxia 14

21 January 2018

1 reference

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10.1111/J.1440-1789.2006.00719.X

21 January 2018

Identifiers

DOI

1 reference

release_z5xqgprfufhhbomgtfixn5m6km

15 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/z5xqgprfufhhbomgtfixn5m6km

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference