Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy (Q44173664)

30 November 2017

title

Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy (English)

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30 November 2017

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2

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30 November 2017

10

Gen Sobue

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30 November 2017

Masahisa Katsuno

1

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30 November 2017

Akito Kume

3

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30 November 2017

Mei Li

4

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30 November 2017

Yuji Nakagomi

5

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30 November 2017

Hisayoshi Niwa

6

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30 November 2017

Chen Sang

7

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30 November 2017

Yasushi Kobayashi

8

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30 November 2017

Manabu Doyu

9

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30 November 2017

language of work or name

English

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publication date

1 August 2002

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30 November 2017

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30 November 2017

volume

35

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30 November 2017

issue

5

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30 November 2017

page(s)

843-854

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Expression of expanded repeat androgen receptor produces neurologic disease in transgenic mice

30 November 2017

cites work

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Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

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Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability

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7 January 2021

Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy

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7 January 2021

Transcriptional activation by the androgen receptor in X-linked spinal and bulbar muscular atrophy

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7 January 2021

CAG-repeat expansion in androgen receptor in Kennedy's disease is not a loss of function mutation

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7 January 2021

Efficient selection for high-expression transfectants with a novel eukaryotic vector

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Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor--gene expression level.

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7 January 2021

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7 January 2021

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

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7 January 2021

Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70.

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7 January 2021

Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract

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7 January 2021

Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

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7 January 2021

Glutamine repeats and neurodegeneration

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7 January 2021

10.1016/S0896-6273(02)00834-6

Identifiers

DOI

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30 November 2017

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