A huntingtin-associated protein enriched in brain with implications for pathology (Q24303499)

GOA release 2020-03-11

brain development

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GOA release 2020-03-11

author

Solomon Halbert Snyder

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object named as

S H Snyder

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author name string

X J Li

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S H Li

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A H Sharp

3

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F C Nucifora

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G Schilling

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A Lanahan

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P Worley

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C A Ross

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

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language of work or name

English

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publication date

23 November 1995

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published in

Nature

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volume

378

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issue

6555

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page(s)

398-402

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cites work

1 reference

7 January 2021

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

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7 January 2021

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

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

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Expression of the Huntington's disease (IT15) protein product in HD patients

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

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

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Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat.

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

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

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Inactivation of the mouse Huntington's disease gene homolog Hdh

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

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Homozygotes for Huntington's disease

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

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Molecular genetics of Huntington's disease

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Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

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Genetics and molecular biology of Huntington's disease

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When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

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Trinucleotide repeat length instability and age of onset in Huntington's disease

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The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

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

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Aging, energy, and oxidative stress in neurodegenerative diseases.

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Epithelial sodium channel related to proteins involved in neurodegeneration

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Expression and localization of amiloride-sensitive sodium channel indicate a role for non-taste cells in taste perception

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Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

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Protein interaction cloning in yeast: identification of mammalian proteins that react with the leucine zipper of Jun

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The two-hybrid system: an assay for protein-protein interactions

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10 Yeast promoters and lacZ fusions designed to study expression of cloned genes in yeast

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Eukaryotic proteins expressed in Escherichia coli: An improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase

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

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