A modifier of Huntington's disease onset at the MLH1 locus.

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R-loops: targets for nuclease cleavage and repeat instability.HttQ111/+ Huntington's Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic Dysfunction.Population-specific genetic modification of Huntington's disease in Venezuela.

P2860

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P2860

A modifier of Huntington's disease onset at the MLH1 locus.

Item

http://www.wikidata.org/entity/Q49962235

description

2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

A modifier of Huntington's disease onset at the MLH1 locus.

@en

A modifier of Huntington's disease onset at the MLH1 locus.

@nl

type

Item

label

A modifier of Huntington's disease onset at the MLH1 locus.

@en

A modifier of Huntington's disease onset at the MLH1 locus.

@nl

prefLabel

A modifier of Huntington's disease onset at the MLH1 locus.

@en

A modifier of Huntington's disease onset at the MLH1 locus.

@nl

P1476

A modifier of Huntington's disease onset at the MLH1 locus.

@en

P2093

Jong-Min Lee

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

Kawther Abu Elneel

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

Lesley Jones

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

Michael J Chao

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

Peter Holmans

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

Richard H Myers

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

Seung Kwak

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

Vanessa C Wheeler

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

P2860

Identification of the Wnt signaling activator leucine-rich repeat in Flightless interaction protein 2 by a genome-wide functional analysis

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

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

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

Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

A review of the clinical relevance of mismatch-repair deficiency in ovarian cancer

METAL: fast and efficient meta-analysis of genomewide association scans

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

P304

3859-3867

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P31

scholarly article

P356

10.1093/HMG/DDX286

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P433

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P478

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2017-10-01T00:00:00Z

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28934397

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P921

Huntington disease

P932

6455020

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A modifier of Huntington's disease onset at the MLH1 locus.

about

P2860

P2860

A modifier of Huntington's disease onset at the MLH1 locus.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932