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NKX2-5 gene

Known as: NKX2.5, MOUSE, HOMOLOG OF, CARDIAC-SPECIFIC HOMEOBOX 1, CSX 
This gene plays a role in both transcriptional regulation and heart development.
National Institutes of Health

Papers overview

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2013
2013
Germline mutations in cardiac-specific transcription factor genes have been associated with congenital heart disease (CHD) and… 
2013
2013
ObjectiveIt has been recently shown that cardiac syndrome X (CSX) patients with slow coronary flow (SCF) have a worse long-term… 
2013
2013
Aims Heterozygous mutations in the transcription factor Nkx2.5 indicate a genetic cause for congenital heart diseases (CHDs) in… 
Review
2012
Review
2012
Background: Cardiac syndrome X (CSX) is a condition in which patients have the pain of angina despite normal coronary angiogram… 
2009
2009
BACKGROUND Congenital heart disease (CHD) is the most common developmental anomaly in newborns. The germline mutations in GATA4… 
2007
2007
Introduction. Cardiac syndrome X (CSX) is defined by typical chest pain, ST segment depression on ECG and normal coronary… 
1995
1995
Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation…