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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

Related topics

Related topics

9 relations
Cell Differentiation processHomeobox Protein Nkx-2.5, humanHomo sapiensNKX2-6 gene

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NKX2-5 wt Allele

Papers overview

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2014
2014
Altered transmural contractility in postmenopausal women affected by cardiac syndrome X.
2013
2013
Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease
Germline mutations in cardiac-specific transcription factor genes have been associated with congenital heart disease (CHD) and… 
2013
2013
Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.
2013
2013
Serum uric acid and slow coronary flow in cardiac syndrome X
ObjectiveIt has been recently shown that cardiac syndrome X (CSX) patients with slow coronary flow (SCF) have a worse long-term… 
2013
2013
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease
Aims Heterozygous mutations in the transcription factor Nkx2.5 indicate a genetic cause for congenital heart diseases (CHDs) in… 
Review
2012
Review
2012
Frequency of Helicobacter pylori and cytotoxine associated gene A antibodies in patients with cardiac syndrome X
Background: Cardiac syndrome X (CSX) is a condition in which patients have the pain of angina despite normal coronary angiogram… 
2009
2009
GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease.
BACKGROUND Congenital heart disease (CHD) is the most common developmental anomaly in newborns. The germline mutations in GATA4… 
2007
2007
Gene expression of kinin receptors B1 and B2 in PBMC from patients with cardiac syndrome X
Introduction. Cardiac syndrome X (CSX) is defined by typical chest pain, ST segment depression on ECG and normal coronary… 
2005
2005
Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect
1995
1995
Assignment of cardiac homeobox gene CSX to human chromosome 5q34.
Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation… 
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