Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

about

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

Item

http://www.wikidata.org/entity/Q36303336

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@ast

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@en

type

Item

label

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@ast

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@en

prefLabel

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@ast

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@en

P1476

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

@en

P2093

Jian Guo

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

Nan Ding

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

Ren Yu Guo

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

Song Bai

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

Xiao Feng Li

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

Zhong Zhi Li

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

P2860

Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart

Neighbourhood Deprivation, Individual-Level and Familial-Level Socio-demographic Factors and Risk of Congenital Heart Disease: A Nationwide Study from Sweden

Direct biomechanical induction of endogenous calcineurin inhibitor Down Syndrome Critical Region-1 in cardiac myocytes

The incidence of congenital heart disease

Dscr1, a novel endogenous inhibitor of calcineurin signaling, is expressed in the primitive ventricle of the heart and during neurogenesis.

Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory.

Prevalence of birth defects and risk-factor analysis from a population-based survey in Inner Mongolia, China.

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.

The maternal-age-associated risk of congenital heart disease is modifiable.

P304

3536-3539

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

P31

scholarly article

P356

10.12659/MSM.894830

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

P478

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

P577

2015-11-16T00:00:00Z

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

P698

26569438

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

P921

birth defect

P932

4654592

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