Michelle S. Parvatiyar, Ph.D. - Publications

2009 University of Miami, Coral Gables, FL 
Pharmacology, Physiology Biology, Molecular Biology

23 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Reinoso TR, Landim-Vieira M, Shi Y, Johnston JR, Chase PB, Parvatiyar MS, Landstrom AP, Pinto JR, Tadros HJ. A comprehensive guide to genetic variants and post-translational modifications of cardiac troponin C. Journal of Muscle Research and Cell Motility. PMID 33179204 DOI: 10.1007/s10974-020-09592-5  0.56
2020 Tadros HJ, Life CS, Garcia G, Pirozzi E, Jones EG, Datta S, Parvatiyar MS, Chase PB, Allen HD, Kim JJ, Pinto JR, Landstrom AP. Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hotspots that are associated with worse clinical outcomes. Journal of Molecular and Cellular Cardiology. PMID 32278834 DOI: 10.1016/j.yjmcc.2020.04.005  0.56
2020 Dieseldorff Jones KM, Vied C, Valera IC, Chase PB, Parvatiyar MS, Pinto JR. Sexual dimorphism in cardiac transcriptome associated with a troponin C murine model of hypertrophic cardiomyopathy. Physiological Reports. 8: e14396. PMID 32189431 DOI: 10.14814/phy2.14396  0.56
2019 Parvatiyar MS, Brownstein AJ, Kanashiro-Takeuchi RM, Collado JR, Dieseldorff Jones KM, Gopal J, Hammond KG, Marshall JL, Ferrel A, Beedle AM, Chamberlain JS, Pinto JR, Crosbie RH. Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy. Jci Insight. 5. PMID 31039133 DOI: 10.1172/jci.insight.123855  0.56
2018 de A Marques M, Parvatiyar MS, Yang W, de Oliveira GP, Pinto JR. The missing links within troponin. Archives of Biochemistry and Biophysics. PMID 30584890 DOI: 10.1016/j.abb.2018.12.026  0.56
2017 Veltri T, Landim-Vieira M, Parvatiyar MS, Gonzalez-Martinez D, Dieseldorff Jones KM, Michell CA, Dweck D, Landstrom AP, Chase PB, Pinto JR. Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation. Frontiers in Physiology. 8: 221. PMID 28473771 DOI: 10.3389/fphys.2017.00221  0.56
2015 Martins AS, Parvatiyar MS, Feng HZ, Bos JM, Gonzalez-Martinez D, Vukmirovic M, Turna RS, Sanchez-Gonzalez MA, Badger CD, Zorio DA, Singh RK, Wang Y, Jin JP, Ackerman MJ, Pinto JR. In vivo Analysis of Troponin C Knock-in (A8V) Mice: Evidence that TNNC1 Is a Hypertrophic Cardiomyopathy Susceptibility Gene. Circulation. Cardiovascular Genetics. PMID 26304555 DOI: 10.1161/CIRCGENETICS.114.000957  0.56
2015 Parvatiyar MS, Pinto JR. Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca2+ sensitivity. Biochimica Et Biophysica Acta. 1850: 365-72. PMID 25450489 DOI: 10.1016/j.bbagen.2014.09.029  0.56
2012 Pinto JR, Gomes AV, Jones MA, Liang J, Nguyen S, Miller T, Parvatiyar MS, Potter JD. The functional properties of human slow skeletal troponin T isoforms in cardiac muscle regulation. The Journal of Biological Chemistry. 287: 37362-70. PMID 22977240 DOI: 10.1074/jbc.M112.364927  0.56
2012 Chen H, Monte E, Parvatiyar MS, Rosa-Garrido M, Franklin S, Vondriska TM. Structural considerations for chromatin state models with transcription as a functional readout. Febs Letters. 586: 3548-54. PMID 22940112 DOI: 10.1016/j.febslet.2012.08.018  0.56
2012 Parvatiyar MS, Landstrom AP, Figueiredo-Freitas C, Potter JD, Ackerman MJ, Pinto JR. A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation. The Journal of Biological Chemistry. 287: 31845-55. PMID 22815480 DOI: 10.1074/jbc.M112.377713  0.56
2011 Pinto JR, Siegfried JD, Parvatiyar MS, Li D, Norton N, Jones MA, Liang J, Potter JD, Hershberger RE. Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy. The Journal of Biological Chemistry. 286: 34404-12. PMID 21832052 DOI: 10.1074/jbc.M111.267211  0.56
2011 Pinto JR, Yang SW, Hitz MP, Parvatiyar MS, Jones MA, Liang J, Kokta V, Talajic M, Tremblay N, Jaeggi M, Andelfinger G, Potter JD. 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. The Journal of Biological Chemistry. 286: 20901-12. PMID 21502316 DOI: 10.1074/jbc.M111.234336  0.56
2011 Pinto JR, Reynaldo DP, Parvatiyar MS, Dweck D, Liang J, Jones MA, Sorenson MM, Potter JD. Strong cross-bridges potentiate the Ca(2+) affinity changes produced by hypertrophic cardiomyopathy cardiac troponin C mutants in myofilaments: a fast kinetic approach. The Journal of Biological Chemistry. 286: 1005-13. PMID 21056975 DOI: 10.1074/jbc.M110.168583  0.56
2010 Parvatiyar MS, Pinto JR, Dweck D, Potter JD. Cardiac troponin mutations and restrictive cardiomyopathy. Journal of Biomedicine & Biotechnology. 2010: 350706. PMID 20617149 DOI: 10.1155/2010/350706  0.56
2010 Parvatiyar MS, Pinto JR, Liang J, Potter JD. Predicting cardiomyopathic phenotypes by altering Ca2+ affinity of cardiac troponin C. The Journal of Biological Chemistry. 285: 27785-97. PMID 20566645 DOI: 10.1074/jbc.M110.112326  0.56
2010 Willott RH, Gomes AV, Chang AN, Parvatiyar MS, Pinto JR, Potter JD. Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? Journal of Molecular and Cellular Cardiology. 48: 882-92. PMID 19914256 DOI: 10.1016/j.yjmcc.2009.10.031  0.56
2009 Hershberger RE, Pinto JR, Parks SB, Kushner JD, Li D, Ludwigsen S, Cowan J, Morales A, Parvatiyar MS, Potter JD. Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy. Circulation. Cardiovascular Genetics. 2: 306-13. PMID 20031601 DOI: 10.1161/CIRCGENETICS.108.846733  0.56
2009 Pinto JR, Parvatiyar MS, Jones MA, Liang J, Ackerman MJ, Potter JD. A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy. The Journal of Biological Chemistry. 284: 19090-100. PMID 19439414 DOI: 10.1074/jbc.M109.007021  0.56
2008 Landstrom AP, Parvatiyar MS, Pinto JR, Marquardt ML, Bos JM, Tester DJ, Ommen SR, Potter JD, Ackerman MJ. Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C. Journal of Molecular and Cellular Cardiology. 45: 281-8. PMID 18572189 DOI: 10.1016/j.yjmcc.2008.05.003  0.56
2008 Chang AN, Parvatiyar MS, Potter JD. Troponin and cardiomyopathy. Biochemical and Biophysical Research Communications. 369: 74-81. PMID 18157941 DOI: 10.1016/j.bbrc.2007.12.081  0.56
2008 Pinto JR, Parvatiyar MS, Jones MA, Liang J, Potter JD. A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin. The Journal of Biological Chemistry. 283: 2156-66. PMID 18032382 DOI: 10.1074/jbc.M707066200  0.56
2007 Pritchard TJ, Parvatiyar M, Bullard DP, Lynch RM, Lorenz JN, Paul RJ. Transgenic mice expressing Na+-K+-ATPase in smooth muscle decreases blood pressure. American Journal of Physiology. Heart and Circulatory Physiology. 293: H1172-82. PMID 17468335 DOI: 10.1152/ajpheart.00279.2007  0.56
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