Transgenic models of Huntington's disease (Q24676606)

Europe PubMed Central

title

Transgenic models of Huntington's disease (English)

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K Sathasivam

1

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C Hobbs

2

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L Mangiarini

3

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A Mahal

4

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M Turmaine

5

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P Doherty

6

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S W Davies

7

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G P Bates

Philosophical Transactions of the Royal Society B

8

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language of work or name

English

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publication date

29 June 1999

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published in

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volume

354

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issue

1386

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page(s)

963-9

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cites work

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

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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

7 April 2017

1 reference

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Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Inactivation of the mouse Huntington's disease gene homolog Hdh

7 April 2017

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Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

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

7 April 2017

1 reference

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Nonneural nuclear inclusions of androgen receptor protein in spinal and bulbar muscular atrophy

7 April 2017

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Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation

28 September 2017

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Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

28 September 2017

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Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

28 September 2017

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

28 September 2017

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Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat

28 September 2017

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Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies

28 September 2017

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When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

28 September 2017

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Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting

28 September 2017

1 reference

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Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Structural neurology: are seeds at the root of neuronal degeneration?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Widespread expression of Huntington's disease gene (IT15) protein product

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Body weight and dietary factors in Huntington's disease patients compared with matched controls

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Neuropathological classification of Huntington's disease

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Transgenic mice in the study of polyglutamine repeat expansion diseases.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Identification of an HD patient with a (CAG)180 repeat expansion and the propagation of highly expanded CAG repeats in lambda phage

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692600

Comparative sequence analysis of the human and pufferfish Huntington's disease genes

28 November 2018

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https://api.crossref.org/works/10.1098%2FRSTB.1999.0447

7 January 2021

Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology

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https://api.crossref.org/works/10.1098%2FRSTB.1999.0447

7 January 2021

Formation of polyglutamine inclusions in non-CNS tissue

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https://api.crossref.org/works/10.1098%2FRSTB.1999.0447

7 January 2021

Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.1999.0447

7 January 2021