Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy (Q33894661)

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English	Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy	scientific article

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14 March 2020

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy (English)

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14 March 2020

motor neuron disease

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muscular atrophy

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Don W. Cleveland

12

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14 March 2020

Albert R. La Spada

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Albert R La Spada

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14 March 2020

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Constanza J Cortes

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14 March 2020

Shuo-Chien Ling

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14 March 2020

Ling T Guo

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14 March 2020

Gene Hung

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14 March 2020

Taiji Tsunemi

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14 March 2020

Linda Ly

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14 March 2020

Seiya Tokunaga

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14 March 2020

Edith Lopez

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14 March 2020

Bryce L Sopher

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14 March 2020

C Frank Bennett

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14 March 2020

G Diane Shelton

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1 April 2014

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14 March 2020

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14 March 2020

82

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14 March 2020

2

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14 March 2020

295-307

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14 March 2020

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11 June 2022

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Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy

1 reference

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5 July 2018

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5 July 2018

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Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model

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5 July 2018

Increased IGF-1 in muscle modulates the phenotype of severe SMA mice

1 reference

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1 reference

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5 July 2018

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1 reference

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Overexpression of wild-type androgen receptor in muscle recapitulates polyglutamine disease.

1 reference

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Androgen-dependent pathology demonstrates myopathic contribution to the Kennedy disease phenotype in a mouse knock-in model

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based on heuristic

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Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1016/J.NEURON.2014.03.001

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14 March 2020

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14 March 2020

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14 March 2020

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