Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31. - Wikidata - awgldk - TriplyDB

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

http://www.wikidata.org/entity/Q34805963

about

Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1 Neuromyelitis Optica Spectrum Disorder Coinciding with Spinocerebellar Ataxia Type 31 Hsp20 Protects against Oxygen-Glucose Deprivation/Reperfusion-Induced Golgi Fragmentation and Apoptosis through Fas/FasL Pathway Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region.Case Study: Somatic Sprouts and Halo-Like Amorphous Materials of the Purkinje Cells in Huntington's Disease.Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.Cerebellar neurodegeneration in a new rat model of episodic hepatic encephalopathy.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

http://www.wikidata.org/entity/Q34805963

description

2013 nî lūn-bûn

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2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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type

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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prefLabel

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

@ast

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31.

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Emi Suzuki-Kouyama

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Kenichi Tabata

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Kiyomitsu Oyanagi

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Kunihiro Yoshida

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Masayuki Shintaku

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Mika Asakawa

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Shu-Ichi Ikeda

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P2860

Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis

Fragmentation of the Golgi apparatus in neurodegenerative diseases and cell death.

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

Golgi apparatus and neurodegenerative diseases.

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians.

The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of Neuropathology.

Identification of a synaptic vesicle-specific 38,000-dalton protein by monoclonal antibodies.

Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia: an autopsy case report with some new observations on cerebellar pathology.

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261-267

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10.1111/NEUP.12090

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3

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34

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2013-12-17T00:00:00Z

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