Year |
Citation |
Score |
2023 |
Hwang HS, Kahmini AR, Prascak J, Cejas-Carbonell A, Valera IC, Champion S, Corrigan M, Mumbi F, Parvatiyar MS. Sarcospan Deficiency Increases Oxidative Stress and Arrhythmias in Hearts after Acute Ischemia-Reperfusion Injury. International Journal of Molecular Sciences. 24. PMID 37511627 DOI: 10.3390/ijms241411868 |
0.393 |
|
2021 |
Marques MA, Landim-Vieira M, Moraes AH, Sun B, Johnston JR, Dieseldorff Jones KM, Cino EA, Parvatiyar MS, Valera IC, Silva JL, Galkin VE, Chase PB, Kekenes-Huskey PM, de Oliveira GAP, Pinto JR. Anomalous structural dynamics of minimally frustrated residues in cardiac troponin C triggers hypertrophic cardiomyopathy. Chemical Science. 12: 7308-7323. PMID 34163821 DOI: 10.1039/d1sc01886h |
0.437 |
|
2020 |
Valera IC, Wacker AL, Hwang HS, Holmes C, Laitano O, Landstrom AP, Parvatiyar MS. Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies. Advances in Medical Sciences. 66: 52-71. PMID 33387942 DOI: 10.1016/j.advms.2020.12.004 |
0.337 |
|
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 |
0.337 |
|
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 |
0.351 |
|
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 |
0.447 |
|
2020 |
Coscarella IL, Landim Vieira M, Valera IC, Wacker AL, Chase PB, Pinto JR, Parvatiyar MS. Connecting Cardiac Sarcolemma Protein Content with Sarcomeric Function Biophysical Journal. 118: 595a. DOI: 10.1016/J.Bpj.2019.11.3219 |
0.413 |
|
2020 |
Dieseldorff Jones KM, Vied C, Valera IC, Chase PB, Parvatiyar MS, Pinto JR. Sex Differences in Regulating the Cardiac Transcriptome within a Murine Model for Hypertrophic Cardiomyopathy Biophysical Journal. 118: 594a-595a. DOI: 10.1016/J.Bpj.2019.11.3217 |
0.382 |
|
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 |
0.759 |
|
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 |
0.345 |
|
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 |
0.817 |
|
2015 |
Parvatiyar MS, Marshall JL, Nguyen RT, Jordan MC, Richardson VA, Roos KP, Crosbie-Watson RH. Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy. Journal of the American Heart Association. 4. PMID 26702077 DOI: 10.1161/Jaha.115.002481 |
0.708 |
|
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 |
0.442 |
|
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 |
0.635 |
|
2014 |
Martins AS, Parvatiyar MS, Turna R, Badger CD, Griffin B, Zorio D, Vukmirovic M, Sanchez-Gonzalez MA, Dweck D, Ruiz EL, Liang J, Wang Y, Overton J, Pinto JR. In Vivo Analysis of Troponin C Knock-In (A8V) Mice: Evidence that TNNC1 is a Hypertrophic Cardiomyopathy Susceptibility Gene Biophysical Journal. 106: 723a. DOI: 10.1016/J.Bpj.2013.11.3995 |
0.814 |
|
2012 |
Monte E, Chen H, Kolmakova M, Parvatiyar M, Vondriska TM, Franklin S. Quantitative analysis of chromatin proteomes in disease. Journal of Visualized Experiments : Jove. PMID 23299252 DOI: 10.3791/4294 |
0.363 |
|
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 |
0.695 |
|
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 |
0.733 |
|
2012 |
Parvatiyar MS, Liang J, Jones MA, Potter JD, Pinto JR. Pseudo-Phosphorylation of Cardiac Troponin I Containing the RCM Troponin T Deletion Glutamic Acid 96 is not an Accurate Indicator of the Phosphorylation Effects by PKA in Skinned Fibers Biophysical Journal. 102: 157a. DOI: 10.1016/J.Bpj.2011.11.856 |
0.69 |
|
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 |
0.702 |
|
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 |
0.763 |
|
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 |
0.792 |
|
2011 |
Pinto JR, Yang SW, Hitz M, Parvatiyar MS, Jones MA, Liang J, Kokta V, 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 Biophysical Journal. 100: 114a-115a. DOI: 10.1016/J.Bpj.2010.12.834 |
0.759 |
|
2011 |
Parvatiyar MS, Landstrom AP, Pinto JR, Liang J, Ackerman MJ, Potter JD. A Novel Mutation in TNNC1-ENCODED Cardiac Troponin C Predisposes to Hypertrophic Cardiomyopathy and Recurrent Episodes of Aborted Sudden Cardiac Death Biophysical Journal. 100: 114a. DOI: 10.1016/J.Bpj.2010.12.832 |
0.745 |
|
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 |
0.799 |
|
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 |
0.748 |
|
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 |
0.707 |
|
2010 |
Dweck D, Pinto JR, Reynaldo DP, Parvatiyar M, Jones MA, Liang J, Sorenson MM, Potter JD. Strong Crossbridges are Required to Recapitulate the Ca2+ Affinity Changes Produced by HCM-cTnC Mutants in Skinned Fibers Biophysical Journal. 98: 149a. DOI: 10.1016/J.Bpj.2009.12.802 |
0.793 |
|
2010 |
Jones MA, Pinto JR, Xu Q, Gomes AV, Parvatiyar M, Liang J, Potter JD. Biophysical and Biochemical Studies of Human Slow Skeletal Troponin T Isoforms in Slow Skeletal Muscle Biophysical Journal. 98: 352a. DOI: 10.1016/J.Bpj.2009.12.1904 |
0.655 |
|
2010 |
Parvatiyar MS, Yang SW, Pinto JR, Jones MA, Liang J, Andelfinger GU, Potter JD. Functional Consequences of a Novel Cardiac Troponin T Mutation Linked to Infantile Restrictive Cardiomyopathy Biophysical Journal. 98: 352a. DOI: 10.1016/J.Bpj.2009.12.1903 |
0.716 |
|
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 |
0.578 |
|
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 |
0.719 |
|
2009 |
Parvatiyar MS, Pinto JR, Liang J, Jones MA, Potter JD. Troponin T Deletion 96 Related to Restrictive Cardiomyopathy Ablates the Effects of Cardiac Troponin I PKA Pseudo-Phosphorylation on Ca2+ Sensitivity of Force Development Biophysical Journal. 96: 67a. DOI: 10.1016/J.Bpj.2008.12.246 |
0.723 |
|
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 |
0.686 |
|
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 |
0.654 |
|
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 |
0.736 |
|
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 |
0.522 |
|
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