Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population.

about

Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population.

Item

http://www.wikidata.org/entity/Q47272757

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Association of genetic polymor ...... e northern Chinese population.

@en

Association of genetic polymor ...... e northern Chinese population.

@nl

type

Item

label

Association of genetic polymor ...... e northern Chinese population.

@en

Association of genetic polymor ...... e northern Chinese population.

@nl

prefLabel

Association of genetic polymor ...... e northern Chinese population.

@en

Association of genetic polymor ...... e northern Chinese population.

@nl

P1476

Association of genetic polymor ...... e northern Chinese population.

@en

P2093

B Qiao

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

H-Y Wang

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

L-L Kuang

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

S-N Sun

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

W-Y Duan

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

P2860

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Congenital heart disease caused by mutations in the transcription factor NKX2-5

The human purH gene product, 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase. Cloning, sequencing, expression, purification, kinetic analysis, and domain mapping

Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia

Cloning of three human multifunctional de novo purine biosynthetic genes by functional complementation of yeast mutations

Assessing the association between the methylenetetrahydrofolate reductase (MTHFR) 677C>T polymorphism and blood folate concentrations: a systematic review and meta-analysis of trials and observational studies

A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development

Dietary and other lifestyle correlates of serum folate concentrations in a healthy adult population in Crete, Greece: a cross-sectional study.

Geographical distribution of MTHFR C677T, A1298C and MTRR A66G gene polymorphisms in China: findings from 15357 adults of Han nationality.

Shmt1 and de novo thymidylate biosynthesis underlie folate-responsive neural tube defects in mice.

P304

748-755

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

P31

scholarly article

P356

10.1111/CGE.12874

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

P433

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

P478

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

P50

Y-C Jiang

P577

2016-09-23T00:00:00Z

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

P698

27659940

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