Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease (Q38443001)

3 September 2017

title

Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease (English)

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3 September 2017

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Sm Reamon-Buettner

1

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3 September 2017

J Borlak

series ordinal

2

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3 September 2017

publication date

1 May 2005

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3 September 2017

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3 September 2017

volume

1

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3 September 2017

issue

3

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3 September 2017

page(s)

355-361

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The incidence of congenital heart disease

3 September 2017

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Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies

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

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A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

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Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

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Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations

21 January 2018

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Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

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Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

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Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation

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TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts

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A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

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Tbx5specifies the left/right ventricles and ventricular septum position during cardiogenesis

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The zinc finger-containing transcription factors GATA-4, -5, and -6. Ubiquitously expressed regulators of tissue-specific gene expression.

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GATA transcription factors in the developing and adult heart

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Somatic gene mutation and human disease other than cancer

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The endothelin axis: emerging role in cancer

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Oxidative DNA damage: mechanisms, mutation, and disease

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Oxidative DNA damage and disease: induction, repair and significance

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A genetic blueprint for cardiac development

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Homeodomain factor Nkx2-5 in heart development and disease

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Identifiers

DOI

10.1517/14796678.1.3.355

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3 September 2017

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