(Q29615357)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

title

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice (English)

2 references

PubMed

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

1 reference

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20 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

L Mangiarini

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

K Sathasivam

1 reference

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20 October 2019

M Seller

1 reference

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20 October 2019

B Cozens

1 reference

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20 October 2019

A Harper

1 reference

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20 October 2019

C Hetherington

1 reference

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20 October 2019

M Lawton

1 reference

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20 October 2019

H Lehrach

1 reference

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20 October 2019

S W Davies

1 reference

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

20 October 2019

language of work or name

1 reference

30 April 2017

publication date

1 November 1996

2 references

PubMed

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

493-506

2 references

PubMed

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

30 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

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

20 October 2019

cites work

1 reference

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7 January 2021

Morphometric demonstration of atrophic changes in the cerebral cortex, white matter, and neostriatum in Huntington's disease

1 reference

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7 January 2021

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

1 reference

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7 January 2021

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

A huntingtin-associated protein enriched in brain with implications for pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Clinical and neuropathologic assessment of severity in Huntington's disease

1 reference

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7 January 2021

Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleus

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

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

1 reference

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7 January 2021

Neuropathological classification of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Vesico-urethral function in Huntington's chorea

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981369-0

7 January 2021

10.1016/S0092-8674(00)81369-0

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=8898202

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8898202%20AND%20SRC:MED&resulttype=core&format=json