(Q41521379)

English

Kennedy disease

scientific article published on June 1997

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

1 reference

Europe PubMed Central

Kennedy disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

author name string

Fischbeck KH

1

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

publication date

1 June 1997

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

20

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

152-158

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked spinomuscular atrophy: a kindred with associated abnormal androgen receptor binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced androgen receptor gene expression with first exon CAG repeat expansion

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessive bulbospinal neuronopathy. A clinicopathological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of an expanded glutamine repeat androgen receptor in a neuronal cell culture system

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate gene for X-linked spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Embryonic mouse spinal cord motor neuron hybrid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the gene for X-linked spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessive bulbospinal neuronopathy: a report of ten cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9211187

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1005344403603

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 October 2017

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