Michelle Parvatiyar

Transgenic mice expressing Na+-K+-ATPase in smooth muscle decreases blood pressure.

A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin.

Troponin and cardiomyopathy.

Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C.

A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy.

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.

Predicting cardiomyopathic phenotypes by altering Ca2+ affinity of cardiac troponin C.

Cardiac troponin mutations and restrictive cardiomyopathy.

Strong cross-bridges potentiate the Ca(2+) affinity changes produced by hypertrophic cardiomyopathy cardiac troponin C mutants in myofilaments: a fast kinetic approach.

Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach.

Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy.

A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation.

Structural considerations for chromatin state models with transcription as a functional readout.

The functional properties of human slow skeletal troponin T isoforms in cardiac muscle regulation.