HTRA2 variations in Taiwanese Parkinson's disease.

about

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease.Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease.

P2860

Q34792986-F84C64DD-9FE6-476E-8690-755DDE4C8DDB Q37627534-52CD56BA-123E-405D-A74E-CEE13CED1993

P2860

HTRA2 variations in Taiwanese Parkinson's disease.

Item

http://www.wikidata.org/entity/Q54441120

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh-hant

name

HTRA2 variations in Taiwanese Parkinson's disease.

@en

HTRA2 variations in Taiwanese Parkinson's disease.

@nl

type

Item

label

HTRA2 variations in Taiwanese Parkinson's disease.

@en

HTRA2 variations in Taiwanese Parkinson's disease.

@nl

prefLabel

HTRA2 variations in Taiwanese Parkinson's disease.

@en

HTRA2 variations in Taiwanese Parkinson's disease.

@nl

P1476

HTRA2 variations in Taiwanese Parkinson's disease.

@en

P2093

Chi-Mei Lee

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

Chih-Hsin Lin

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

Chin-Hsia Hsieh

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

Chiung-Mei Chen

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

Chun-Hsien Wu

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

Guey-Jen Lee-Chen

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

I-Cheng Chen

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

Li-Ching Lee

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

Yi-Chun Chen

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

Yih-Ru Wu

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

P2860

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

Neuroprotective role of the Reaper-related serine protease HtrA2/Omi revealed by targeted deletion in mice

Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls.

Hyperexcitable substantia nigra dopamine neurons in PINK1- and HtrA2/Omi-deficient mice.

Role of mendelian genes in "sporadic" Parkinson's disease.

Diagnostic criteria for Parkinson disease.

Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.

Expanding insights of mitochondrial dysfunction in Parkinson's disease.

P2888

s00702-013-1131-9

P304

491-498

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

P31

scholarly article

P356

10.1007/S00702-013-1131-9

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

P433

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

P478

121

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

P577

2013-12-12T00:00:00Z

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

P698

24337630

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

HTRA2 variations in Taiwanese Parkinson's disease.

about

P2860

P2860

HTRA2 variations in Taiwanese Parkinson's disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698