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

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About: Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	articolo scientifico (it) vedecký článok (publikovaný 1995/05/01) (sk) vědecký článek publikovaný v roce 1995 (cs) مقالة علمية (نشرت في مايو 1995) (ar) artículu científicu espublizáu en 1995 (ast) 1995 թվականի մայիսին հրատարակված գիտական հոդված (hy) 1995 թուականի Մայիսին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в травні 1995 (uk) article scientifique publié en 1995 (fr) scientific journal article (en) im Mai 1995 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 1995/05/01) (nl)
publication date	wds:Q28509836-71103861-ED94-47D0-A007-BA578FF9C576
publication date	1995-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28509836-BEC164B9-9379-420A-916A-757E2556DFC7
language of work or name	English
exact match	wds:Q28509836-344FA1E7-A867-48F3-B9DD-97AA82C9A1DD
exact match	https://scigraph.springernature.com/pub.10.1038/ng0595-104
cites work	wds:Q28509836-015A32BB-03F8-458D-BED0-EB9A0ACE2BD5 wds:Q28509836-0614771B-585A-46AE-A12B-E9F05735B9DF wds:Q28509836-13B0D428-4D28-496C-8AEC-0898A64CAC5B wds:Q28509836-2C2020EF-E9FE-4DEB-8A3D-80B5701DA058 wds:Q28509836-369E98AD-1814-452B-AA56-61AD1132EDED wds:Q28509836-4874A1F6-C512-43D9-9C26-25289CF061F6 wds:Q28509836-48AB3102-DB2B-434C-BBD2-BD6BC37665BB wds:Q28509836-4F64237A-AD2E-40FC-9F63-1E42E4923488 wds:Q28509836-51FFE4D8-720B-472D-8BB0-BFD420171AC7 wds:Q28509836-53411943-1A1F-4AC3-84CA-BED4A6928979 wds:Q28509836-58E9BF88-C92A-40D0-8F5C-41915018BC44 wds:Q28509836-590C06D0-9D26-4A4B-A79C-4FD6937524CD wds:Q28509836-5B4EEBDA-5A93-4976-9705-8A0F30463F4E wds:Q28509836-5BE60A10-2B72-415A-8D55-4E6DAE65CF45 wds:Q28509836-5EBA54A6-4B44-4BC8-AAE9-947E5264E7F2 wds:Q28509836-637DFC63-F800-4233-A2B8-042757D60D48 wds:Q28509836-696D9CED-05AF-4CF9-9E85-4D795964C602 wds:Q28509836-69A9A3FF-3386-4038-81A3-7DAE9E380B30 wds:Q28509836-6AEA8B6D-50C3-4001-AEDA-B89BD680A86A wds:Q28509836-7152363C-885E-48F5-888E-87A67D52D944 wds:Q28509836-72F93C64-37FF-4B2A-BBA2-26B227685B7D wds:Q28509836-8DCD01E9-C129-42F3-8CAA-97BBAAA93A54 wds:Q28509836-98782FED-4BBD-4D50-9CAF-FA7EECB9F63A wds:Q28509836-9A999A52-3EC3-4026-81C7-C93DC7E256E5 wds:Q28509836-9DB0EC07-8CFB-4233-9823-B34CB32B8982 wds:Q28509836-A66C5A22-0EB6-47A0-81F1-C79C6C6B12F9 wds:Q28509836-A9511C28-1404-4C3D-B86E-9683DD488859 wds:Q28509836-C0BFCF07-D79F-4401-96E7-D047AFBC4318 wds:Q28509836-C765C4FD-322E-4CF2-85C6-9E77BA28F724 wds:Q28509836-CEC86CA3-4AB6-4CFB-8528-21D8038DF403 wds:Q28509836-D3B15887-588C-43D9-A794-5E574721C456 wds:Q28509836-D3E898C0-595D-404C-A744-7F4597B77345 wds:Q28509836-D477727B-31D2-4CBF-8DFF-66B6EBF85BDC wds:Q28509836-DA1600D2-B6D1-4D68-811F-767A43CAA64D wds:Q28509836-E550837B-4307-40FE-A82C-386EAF1B3138 wds:Q28509836-F163A90D-8258-47EB-A27F-8D838E043AC7
cites work	CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 Huntington's disease and repeating trinucleotides Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism Characterization and localization of the Huntington disease gene product Transcriptional activation modulated by homopolymeric glutamine and proline stretches Huntington's disease gene (IT15) is widely expressed in human and rat tissues Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues Neuropathological classification of Huntington's disease Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Huntington's disease. Pathogenesis and management Selective sparing of a class of striatal neurons in Huntington's disease The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats The epidemiology of Huntington's disease Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA) Differences in tyrosine hydroxylase-like immunoreactivity characterize the mesostriatal innervation of striosomes and extrastriosomal matrix at maturity Mouse Huntington's disease gene homolog (Hdh). Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected] The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27. Genetics and molecular biology of Huntington's disease High efficiency gene transfer into mammalian cells Melanized dopaminergic neurons are differentially susceptible to degeneration in Parkinson's disease Trinucleotide repeat length instability and age of onset in Huntington's disease Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie? Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease Identification and characterization of the gene causing type 1 spinocerebellar ataxia. Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset
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OpenCitations bibliographic resource ID	wds:Q28509836-3B4F6261-DD86-471F-B576-FB03B5980AC4
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/2331150

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