Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. - Wikidata - awgldk - TriplyDB

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

http://www.wikidata.org/entity/Q30445013

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Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington’s Disease Genomewide association study for onset age in Parkinson disease.Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics.Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.Genetic background modulates behavioral impairments in R6/2 mice and suggests a role for dominant genetic modifiers in Huntington’s disease pathogenesis.Genetic analysis of the GRIK2 modifier effect in Huntington's disease.Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease.Normal-repeat-length polyglutamine peptides accelerate aggregation nucleation and cytotoxicity of expanded polyglutamine proteins Chromosome substitution strain assessment of a Huntington's disease modifier locus RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression.Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds.Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.Modifier genes as therapeutics: the nuclear hormone receptor Rev Erb alpha (Nr1d1) rescues Nr2e3 associated retinal disease A brief history of triplet repeat diseases.Molecular mechanisms and potential therapeutical targets in Huntington's disease.The clinical and genetic features of Huntington disease.Genetic modifiers of neurological disease The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology Genetic modifiers of Huntington's disease.Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction.Modulation at age of onset in tunisian huntington disease patients: implication of new modifier genes Response to Falush: a role for cis-element polymorphisms in HD.A retrospective study of the impact of lifestyle on age at onset of Huntington disease.The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot study.Molecular characterization of genes modifying the age at onset in Huntington's Disease in Uruguayan patients.

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P2860

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

http://www.wikidata.org/entity/Q30445013

description

2004 nî lūn-bûn

@nan

2004 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի մարտին հրատարակված գիտական հոդված

@hy

2004年の論文

@ja

2004年論文

@yue

2004年論文

@zh-hant

2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

@zh-tw

2004年论文

@wuu

name

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@ast

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@en

type

label

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@ast

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@en

prefLabel

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@ast

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

@en

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Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16

@en

P2093

Adam Rosenblatt

http://www.w3.org/2001/XMLSchema#string

Alexandra Durr

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Andrea Zanko

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Beth Knowlton

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Catherine Dode

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David Mayo Cabrero

http://www.w3.org/2001/XMLSchema#string

Elisabeth W Almqvist

http://www.w3.org/2001/XMLSchema#string

Elizabeth McCusker

http://www.w3.org/2001/XMLSchema#string

Estrella Gómez-Tortosa

http://www.w3.org/2001/XMLSchema#string

Jayalakshmi Mysore

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A nonsense mutation in MSX1 causes Witkop syndrome

The role of MSX1 in human tooth agenesis

Huntington disease: genetics and epidemiology

Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease

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

The Huntington's disease candidate region exhibits many different haplotypes

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

Structure and sequence of the human homeobox gene HOX7.

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

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s10048-004-0175-2

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109-114

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2

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5

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James F. Gusella

Andrea Novelletto

L. Adrienne Cupples

Richard H Myers

Jane S. Paulsen

Ryan R Brinkman

Marcy E. MacDonald

Michael R. Hayden

Christopher A Ross

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2004-03-17T00:00:00Z

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8672779

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15029481

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Huntington disease

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1866166

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