RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.

about

Developmental YAPdeltaC determines adult pathology in a model of spinocerebellar ataxia type 1.The central role of DNA damage and repair in CAG repeat diseases.

P2860

Q47131805-B9C10D1D-BD99-4502-97E1-8985FB6A314B Q50118950-BC21F2C5-EC9D-4D2F-9D60-DEEF1DB528D3

P2860

RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.

Item

http://www.wikidata.org/entity/Q40341497

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

RpA1 ameliorates symptoms of m ...... nd enhances DNA damage repair.

@en

type

Item

label

RpA1 ameliorates symptoms of m ...... nd enhances DNA damage repair.

@en

prefLabel

RpA1 ameliorates symptoms of m ...... nd enhances DNA damage repair.

@en

P1476

RpA1 ameliorates symptoms of m ...... nd enhances DNA damage repair.

@en

P2093

Hidenori Homma

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

Hitoshi Okazawa

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

Juliana Bosso Taniguchi

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

Kanoh Kondo

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

Kazuhiko Tagawa

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

Kei Watase

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

Kyota Fujita

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

Shin-Ichi Muramatsu

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

Takeaki Sudo

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

Takuya Tamura

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

P2860

Suppression of the novel ER protein Maxer by mutant ataxin-1 in Bergman glia contributes to non-cell-autonomous toxicity

RPA-coated single-stranded DNA as a platform for post-translational modifications in the DNA damage response

PQBP-1/Npw38, a nuclear protein binding to the polyglutamine tract, interacts with U5-15kD/dim1p via the carboxyl-terminal domain

Evidence that dim1 associates with proteins involved in pre-mRNA splicing, and delineation of residues essential for dim1 interactions with hnRNP F and Npw38/PQBP-1

PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival

A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome

Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death

Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1

Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse model.

Increased RPA1 gene dosage affects genomic stability potentially contributing to 17p13.3 duplication syndrome

P304

4432-4447

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

P31

scholarly article

P356

10.1093/HMG/DDW272

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

P433

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

P478

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

P577

2016-10-01T00:00:00Z

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

P698

28173122

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

P921

DNA damage

RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.

about

P2860

P2860

RpA1 ameliorates symptoms of mutant ataxin-1 knock-in mice and enhances DNA damage repair.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921