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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
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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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2005
2005
Protein kinase C (PKC)-induced phosphorylation of cardiac troponin I (cTnI) depresses the acto-myosin interaction and may be… 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
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1998
1998
The goal of this study is to characterize the kinetic mechanism of Ca2+ activation and inactivation of cardiac troponin C (cTnC… Expand
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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
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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
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