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Anomalous structural dynamics of minimally frustrated residues in cardiac troponin C triggers hypertrophic cardiomyopathy.
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. Marques MA, et al. Among authors: parvatiyar ms. Chem Sci. 2021 Apr 29;12(21):7308-7323. doi: 10.1039/d1sc01886h. Chem Sci. 2021. PMID: 34163821 Free PMC article.
Cardiac troponin mutations and restrictive cardiomyopathy.
Parvatiyar MS, Pinto JR, Dweck D, Potter JD. Parvatiyar MS, et al. J Biomed Biotechnol. 2010;2010:350706. doi: 10.1155/2010/350706. Epub 2010 Jun 8. J Biomed Biotechnol. 2010. PMID: 20617149 Free PMC article. Review.
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.
Pinto JR, Yang SW, Hitz MP, Parvatiyar MS, Jones MA, Liang J, Kokta V, Talajic M, Tremblay N, Jaeggi M, Andelfinger G, Potter JD. Pinto JR, et al. Among authors: parvatiyar ms. J Biol Chem. 2011 Jun 10;286(23):20901-12. doi: 10.1074/jbc.M111.234336. Epub 2011 Apr 18. J Biol Chem. 2011. PMID: 21502316 Free PMC article.
36 results