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cTnC:cTnI:cTnT

National Institutes of Health

Papers overview

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2012
2012
Background: Cardiac troponin C mutations are rare causes of HCM. A novel mutation in TNNC1 gene was identified in a pediatric HCM… Expand
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Highly Cited
2011
Highly Cited
2011
Background: Phosphorylation of cardiac troponin I (cTnI) is critical in modulating contractility. Results: cTnI is… Expand
2009
2009
Background—Familial dilated cardiomyopathy can be caused by mutations in the proteins of the muscle thin filament. In vitro… Expand
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2008
2008
Two novel mutations (G159D and L29Q) in cardiac troponin C (CTnC) associate their phenotypic outcomes with dilated (DCM) and… Expand
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Highly Cited
2007
Highly Cited
2007
Striated muscle contraction is regulated by the binding of Ca2+ to the N-terminal regulatory lobe of the cardiac troponin C (cTnC… Expand
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Review
2005
Review
2005
Cardiac troponin I (cTnI) is a key regulatory protein in cardiac muscle contraction and relaxation, linking Ca(2+)-troponin C… Expand
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2001
2001
Ca2+-activation of cardiac muscle myofilaments is more sensitive to depression by acidic pH than is the case with skeletal… Expand
1998
1998
The goal of this study is to characterize the kinetic mechanism of Ca2+ activation and inactivation of cardiac troponin C (cTnC… Expand
Highly Cited
1995
Highly Cited
1995
The role of cardiac troponin C (cTnC) as a target protein for the calcium sensitization by levosimendan, pimobendan, MCI-154 and… Expand
Highly Cited
1989
Highly Cited
1989
The cardiac troponin T (cTNT) pre-mRNA contains a single alternative exon (exon 5) which is either included or excluded from the… Expand