Prevalence and spectrum of PITX2c mutations associated with congenital heart disease. - sprookjes - yvandenbroek - TriplyDB

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

http://www.wikidata.org/entity/Q37395274

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome Paired-like homeodomain 2: a novel therapeutic target for atrial fibrillation?Genetics of Primary Inherited Disorders of the Optic Nerve: Clinical Applications.An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.Analysis of PI3K pathway components in human cancers.Functional study of DAND5 variant in patients with Congenital Heart Disease and laterality defects A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.Multiple Roles of Pitx2 in Cardiac Development and Disease.Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.

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P2860

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

http://www.wikidata.org/entity/Q37395274

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on October 2013

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@en

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@nl

type

label

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@en

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@nl

prefLabel

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@en

Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

@nl

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DNA and Cell Biology

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Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

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P2093

Juan Wang

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Lei Xu

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Wen-Jun Xu

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Xin Li

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Xin-Kai Qu

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Xing-Biao Qiu

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Yi-Qing Yang

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Yuan-Feng Xin

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Zhong-Min Liu

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Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

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

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Congenital heart disease: emerging themes linking genetics and development

Genetics of congenital heart disease: the glass half empty

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

Regulation of left-right asymmetry by thresholds of Pitx2c activity

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

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10.1089/DNA.2013.2185

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