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NKX2-5 gene
Known as:
NKX2.5, MOUSE, HOMOLOG OF
, CARDIAC-SPECIFIC HOMEOBOX 1
, CSX
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This gene plays a role in both transcriptional regulation and heart development.
National Institutes of Health
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Related topics
Related topics
9 relations
Cell Differentiation process
Homeobox Protein Nkx-2.5, human
Homo sapiens
NKX2-6 gene
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Narrower (1)
NKX2-5 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Altered transmural contractility in postmenopausal women affected by cardiac syndrome X.
C. Cadeddu
,
S. Nocco
,
M. Deidda
,
F. Pau
,
P. Colonna
,
G. Mercuro
Journal of the American Society of…
2014
Corpus ID: 41090510
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
S. M. Reamon-Buettner
,
E. Sattlegger
,
Y. Ciribilli
,
A. Inga
,
A. Wessel
,
J. Borlak
PLoS ONE
2013
Corpus ID: 10960002
Germline mutations in cardiac-specific transcription factor genes have been associated with congenital heart disease (CHD) and…
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2013
2013
Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.
S. Sabina
,
S. Pulignani
,
+6 authors
M. Andreassi
Journal of Molecular and Cellular Cardiology
2013
Corpus ID: 29382986
2013
2013
Serum uric acid and slow coronary flow in cardiac syndrome X
Z. Elbasan
,
D. Şahin
,
+6 authors
M. Çaylı
Herz
2013
Corpus ID: 31359934
ObjectiveIt has been recently shown that cardiac syndrome X (CSX) patients with slow coronary flow (SCF) have a worse long-term…
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2013
2013
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease
G. Beffagna
,
A. Cecchetto
,
+8 authors
L. Daliento
Journal of Cardiovascular Medicine
2013
Corpus ID: 13928724
Aims Heterozygous mutations in the transcription factor Nkx2.5 indicate a genetic cause for congenital heart diseases (CHDs) in…
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Review
2012
Review
2012
Frequency of Helicobacter pylori and cytotoxine associated gene A antibodies in patients with cardiac syndrome X
Yousef Rasmi
,
M. Seyyed-Mohammadzad
Journal of Cardiovascular Disease Research
2012
Corpus ID: 8159197
Background: Cardiac syndrome X (CSX) is a condition in which patients have the pain of angina despite normal coronary angiogram…
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2009
2009
GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease.
Weimin Zhang
,
Xiao-feng Li
,
+5 authors
Zhong-zhi Li
Chinese Medical Journal
2009
Corpus ID: 8923970
BACKGROUND Congenital heart disease (CHD) is the most common developmental anomaly in newborns. The germline mutations in GATA4…
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2007
2007
Gene expression of kinin receptors B1 and B2 in PBMC from patients with cardiac syndrome X
J. Dąbek
,
T. Wilczok
,
Z. Gąsior
,
S. Kucia-Kuzma
,
R. Twardowski
,
A. Kułach
Scandinavian Cardiovascular Journal
2007
Corpus ID: 9779865
Introduction. Cardiac syndrome X (CSX) is defined by typical chest pain, ST segment depression on ECG and normal coronary…
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2005
2005
Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect
山田 佳代子
,
平山 佳代子
2005
Corpus ID: 87133268
1995
1995
Assignment of cardiac homeobox gene CSX to human chromosome 5q34.
I. Shiojima
,
I. Komuro
,
+5 authors
Y. Yazaki
Genomics
1995
Corpus ID: 9711651
Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation…
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