NK2 Homeobox 5 抗体
(NK2 Homeobox 5 (NKX2-5))
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].
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Latest Publications for our NK2 Homeobox 5 抗体
: "iPSC-derived human cardiac progenitor cells improve ventricular remodelling via angiogenesis and interstitial networking of infarcted myocardium." in: Journal of cellular and molecular medicine, Vol. 20, Issue 2, pp. 323-32, (2016) (PubMed).
: "Evaluation of sarcomeric organization in human pluripotent stem cell-derived cardiomyocytes." in: Methods in molecular biology (Clifton, N.J.), Vol. 1299, pp. 161-6, (2015) (PubMed).
: "Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5." in: PLoS ONE, Vol. 6, Issue 9, pp. e24812, (2011) (PubMed).
: "Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects." in: Circulation research, Vol. 103, Issue 6, pp. 580-90, (2008) (PubMed).
: "RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression." in: Nature genetics, Vol. 40, Issue 1, pp. 61-8, (2007) (PubMed).
: "GATA factors lie upstream of Nkx 2.5 in the transcriptional regulatory cascade that effects cardiogenesis." in: Stem cells and development, Vol. 14, Issue 4, pp. 425-39, (2005) (PubMed).
: "Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease." in: Circulation journal : official journal of the Japanese Circulation Society, Vol. 66, Issue 6, pp. 561-3, (2002) (PubMed).
: "Evaluation of sarcomeric organization in human pluripotent stem cell-derived cardiomyocytes." in: Methods in molecular biology (Clifton, N.J.), Vol. 1299, pp. 161-6, (2015) (PubMed).
: "Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5." in: PLoS ONE, Vol. 6, Issue 9, pp. e24812, (2011) (PubMed).
: "Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects." in: Circulation research, Vol. 103, Issue 6, pp. 580-90, (2008) (PubMed).
: "RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression." in: Nature genetics, Vol. 40, Issue 1, pp. 61-8, (2007) (PubMed).
: "GATA factors lie upstream of Nkx 2.5 in the transcriptional regulatory cascade that effects cardiogenesis." in: Stem cells and development, Vol. 14, Issue 4, pp. 425-39, (2005) (PubMed).
: "Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease." in: Circulation journal : official journal of the Japanese Circulation Society, Vol. 66, Issue 6, pp. 561-3, (2002) (PubMed).
Aliases for NK2 Homeobox 5 抗体
NK2 homeobox 5 (NKX2-5) 抗体NK2 homeobox 5 (Nkx2-5) 抗体
NK2 homeobox 5 (nkx2.5) 抗体
NK2 homeobox 5 S homeolog (nkx2-5.S) 抗体
NK2 homeobox 5 (nkx2-5) 抗体
AR2 抗体
CHNG5 抗体
CNKX-2.5 抗体
CSX 抗体
Csx 抗体
csx 抗体
CSX1 抗体
csx1 抗体
HLHS2 抗体
nk2.5 抗体
Nkx-2.5 抗体
nkx-2.5 抗体
NKX-2.5 抗体
nkx2-5 抗体
NKX2-5 抗体
Nkx2-5 抗体
nkx2-5b 抗体
NKX2.5 抗体
Nkx2.5 抗体
nkx2.5 抗体
NKX2E 抗体
nkx2e 抗体
NKX4-1 抗体
tinman 抗体
VSD3 抗体
XNkx-2.5 抗体
XNkx2-5 抗体
zgc:111912 抗体
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