About: Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias

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About: Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1996 (uk) 1996 ഡിസംബര്‍ 1 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം (ml) im Dezember 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1996 (ast) scientific article published on 01 December 1996 (en)
publication date	wds:Q57969464-D448F76E-FE4A-41F5-A8CE-2D95BA7CBB51
publication date	1996-12-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57969464-092960DA-EF29-49FB-B180-2FE49F7DE1D8 wds:Q57969464-0944BD48-2016-4BFA-ADE5-6BEE705B82DA wds:Q57969464-3CA95C9E-DA7A-4269-BC99-9509DE88604C wds:Q57969464-53BCB088-A9ED-4FDE-9DCE-B765745EBEB9 wds:Q57969464-6717DFC3-145B-442D-B724-ED01AF21C054 wds:Q57969464-67980808-1142-4672-9972-51A266DCC8AC wds:Q57969464-7B7CA981-A5B5-4B56-ABDC-F32368A14F47 wds:Q57969464-7CC9038A-71B1-433A-A01E-80B21CB82013 wds:Q57969464-84903F77-3BEA-44DD-BDCA-5E37292835A1 wds:Q57969464-91BCD8FD-01F1-4885-9C05-C21799DCC620 wds:Q57969464-B8AE458E-B9D4-4E4F-84EB-37C4813C2A28 wds:Q57969464-CAB94CCD-B8E9-4048-B08E-517C9726B1BB wds:Q57969464-D08C2C85-5B31-4F6A-A211-0D6D69744B6F wds:Q57969464-D8816273-3C93-4993-8690-39EBB9B033E6 wds:Q57969464-E5FB976E-2198-4BAA-80E9-A29AD501A4D4
author name string	J L Mandel A Brice A Dürr T Klockgether G David I Gourfinkel-An A Benomar Y Agid G Cancel G Imbert K Bürk N Abbas D Grid O Didierjean M Abada-Bendib
rdfs:label	Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (en) Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (nl)
skos:prefLabel	Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (en) Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (nl)
name	Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (en) Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (nl)
author	wds:Q57969464-3B2B0664-5DBB-410C-B0BD-364FE68770D9 wds:Q57969464-7DCE9E09-5C80-4D8F-AF4F-ADD6B999A958 wds:Q57969464-ABC022F1-391E-4F08-8CF8-1520F462D660
author	Giovanni Stevanin Yvon Trottier Frédéric Saudou
title	wds:Q57969464-5B0D572F-D570-4EB0-9C9F-E91F32EB2174
title	Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias (en)
page(s)	wds:Q57969464-FD12359A-0488-4DCF-B8F7-C98771E15C9D
page(s)	1887-1892
instance of	wds:Q57969464-CF2FB10D-15CA-46A7-8FE9-ACA036DFCC65
instance of	scholarly article
PubMed ID	wds:Q57969464-B8F6ED8B-C7D2-4DD1-8EBF-EA8C51C6507E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8968739
PubMed ID	8968739
published in	wds:Q57969464-572CB8E8-E188-418D-8409-35ABD8F83891
published in	Human Molecular Genetics
issue	wds:Q57969464-BBCAB834-04CA-4024-B262-46181A8A4CF8
volume	wds:Q57969464-5DBEF436-AFDA-4CA2-9DE6-F252D5A0430F
issue	12
volume	5
DOI	wds:Q57969464-E4A4B11D-6FFF-4623-A4F9-18CB23B54AB2
DOI	http://dx.doi.org/10.1093/HMG/5.12.1887
DOI	10.1093/HMG/5.12.1887
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57969464
is cites work of	Transglutaminases in disease Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Parkin immunoreactivity in the brain of human and non-human primates: an immunohistochemical analysis in normal conditions and in Parkinsonian syndromes Evidence for both the nucleus and cytoplasm as subcellular sites of pathogenesis in Huntington's disease in cell culture and in transgenic mice expressing mutant huntingtin. Spinocerebellar ataxia type 4. Investigation of 34 candidate genes. Phage display screening for peptides that inhibit polyglutamine aggregation The unstable trinucleotide repeat story of major psychosis. A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involved Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's disease. Spinocerebellar ataxia 17 (SCA17) and Huntington's disease-like 4 (HDL4). Spinocerebellar ataxia with sensory neuropathy (SCA25) Recent advances in the molecular basis of inherited photoreceptor degeneration Distinct transduction profiles in the CNS via three injection routes of AAV9 and the application to generation of a neurodegenerative mouse model. Positron emission tomography and magnetic resonance imaging in spinocerebellar ataxia type 2: a study of symptomatic and asymptomatic individuals Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy Spinocerebellar ataxia with mental retardation (SCA13). Cloning of rat parkin cDNA and distribution of parkin in rat brain Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method Dominantly inherited ataxias. Part II No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24
is cites work of	wds:Q33260629-2D81258C-4300-493D-B48E-AFFE633DAE86 wds:Q34460116-F85833BB-00F5-46C5-8426-74CE2214B19C wds:Q48101492-EF035B9F-2F03-4497-9D8F-71E694A26952 wds:Q57970920-CC25B4E1-E60A-4682-B311-76C4BD7FC8A8 wds:Q28576408-FC6EF2E1-A042-43A0-A791-219625090318 wds:Q24538696-8C7DBB49-5645-451E-8A50-6520C74210A3

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