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TNNT2 wt Allele

Known as: cTnT, CMPD2, TnTC 
Human TNNT2 wild-type allele is located in the vicinity of 1q32 and is approximately 19 kb in length. This allele, which encodes troponin T, cardiac… Expand
National Institutes of Health

Papers overview

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2014
2014
Lung bioengineering based on decellularized organ scaffolds is a potential alternative for transplantation. Freezing/thawing, a… Expand
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Highly Cited
2009
Highly Cited
2009
AIMS Both serum cardiac troponin T (cTnT) and renal function are prognostic predictors in patients with chronic heart failure… Expand
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2009
2009
Naturally occurring mutations in cardiac troponin T (cTnT) result in a clinical subset of familial hypertrophic cardiomyopathy… Expand
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Highly Cited
2009
Highly Cited
2009
OBJECTIVES The purpose of this study was to determine whether different profiles of cardiac troponin T (cTnT) values assessed… Expand
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Highly Cited
2009
Highly Cited
2009
BackgroundStem cell therapy has emerged as a potential therapeutic option for tissue engineering and regenerative medicine, but… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Myonecrosis after percutaneous coronary intervention (PCI) has been correlated with a worse prognosis, but controversy… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND The progression of chronic heart failure (CHF) is related to ongoing myocyte loss, which can be detected by cardiac… Expand
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Right ventricular failure is a leading cause of death in patients with chronic pulmonary hypertension (PH). We checked… Expand
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Highly Cited
1997
Highly Cited
1997
OBJECTIVES The present study investigated whether myocyte injury can be assessed sensitively by measurement of serum levels of… Expand
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Highly Cited
1996
Highly Cited
1996
BACKGROUND Familial hypertrophic cardiomyopathy is a phenotypically and genetically heterogeneous disease. In some families, the… Expand
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