Similar articles for PMID: 11113119

Year	Number of Results
1988	1
1994	1
1996	1
1998	4
1999	8
2000	9
2001	6
2002	1
2003	4
2004	3
2005	6
2006	5
2007	4
2008	9
2009	6
2010	5
2011	4
2012	7
2013	8
2014	9
2015	7
2016	5
2017	8
2018	5
2019	5
2020	3
2021	3
2023	2
2024	0

1

Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathy.

Knollmann BC, Blatt SA, Horton K, de Freitas F, Miller T, Bell M, Housmans PR, Weissman NJ, Morad M, Potter JD. Knollmann BC, et al. J Biol Chem. 2001 Mar 30;276(13):10039-48. doi: 10.1074/jbc.M006745200. Epub 2000 Dec 11. J Biol Chem. 2001. PMID: 11113119 Free article.

2

Differential effect of troponin T mutations on the inotropic responsiveness of mouse hearts--role of myofilament Ca2+ sensitivity increase.

Sirenko SG, Potter JD, Knollmann BC. Sirenko SG, et al. J Physiol. 2006 Aug 15;575(Pt 1):201-13. doi: 10.1113/jphysiol.2006.107557. Epub 2006 Jun 15. J Physiol. 2006. PMID: 16777946 Free PMC article.

3

Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling.

Knollmann BC, Kirchhof P, Sirenko SG, Degen H, Greene AE, Schober T, Mackow JC, Fabritz L, Potter JD, Morad M. Knollmann BC, et al. Circ Res. 2003 Mar 7;92(4):428-36. doi: 10.1161/01.RES.0000059562.91384.1A. Epub 2003 Feb 6. Circ Res. 2003. PMID: 12600890

4

Hypertrophic cardiomyopathy-linked mutation in troponin T causes myofibrillar disarray and pro-arrhythmic action potential changes in human iPSC cardiomyocytes.

Wang L, Kim K, Parikh S, Cadar AG, Bersell KR, He H, Pinto JR, Kryshtal DO, Knollmann BC. Wang L, et al. J Mol Cell Cardiol. 2018 Jan;114:320-327. doi: 10.1016/j.yjmcc.2017.12.002. Epub 2017 Dec 5. J Mol Cell Cardiol. 2018. PMID: 29217433 Free PMC article.

5

Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponin T (I79N) mutation.

Miller T, Szczesna D, Housmans PR, Zhao J, de Freitas F, Gomes AV, Culbreath L, McCue J, Wang Y, Xu Y, Kerrick WG, Potter JD. Miller T, et al. J Biol Chem. 2001 Feb 9;276(6):3743-55. doi: 10.1074/jbc.M006746200. Epub 2000 Nov 1. J Biol Chem. 2001. PMID: 11060294 Free article.

6

Pathogenic troponin T mutants with opposing effects on myofilament Ca²⁺ sensitivity attenuate cardiomyopathy phenotypes in mice.

Dieseldorff Jones KM, Koh Y, Weller RS, Turna RS, Ahmad F, Huke S, Knollmann BC, Pinto JR, Hwang HS. Dieseldorff Jones KM, et al. Arch Biochem Biophys. 2019 Jan;661:125-131. doi: 10.1016/j.abb.2018.11.006. Epub 2018 Nov 13. Arch Biochem Biophys. 2019. PMID: 30445044 Free PMC article.

7

Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models.

Ferrantini C, Coppini R, Pioner JM, Gentile F, Tosi B, Mazzoni L, Scellini B, Piroddi N, Laurino A, Santini L, Spinelli V, Sacconi L, De Tombe P, Moore R, Tardiff J, Mugelli A, Olivotto I, Cerbai E, Tesi C, Poggesi C. Ferrantini C, et al. J Am Heart Assoc. 2017 Jul 22;6(7):e005407. doi: 10.1161/JAHA.116.005407. J Am Heart Assoc. 2017. PMID: 28735292 Free PMC article.

8

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy.

Szczesna D, Zhang R, Zhao J, Jones M, Guzman G, Potter JD. Szczesna D, et al. J Biol Chem. 2000 Jan 7;275(1):624-30. doi: 10.1074/jbc.275.1.624. J Biol Chem. 2000. PMID: 10617660 Free article.

9

F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers.

Hernandez OM, Szczesna-Cordary D, Knollmann BC, Miller T, Bell M, Zhao J, Sirenko SG, Diaz Z, Guzman G, Xu Y, Wang Y, Kerrick WG, Potter JD. Hernandez OM, et al. J Biol Chem. 2005 Nov 4;280(44):37183-94. doi: 10.1074/jbc.M508114200. Epub 2005 Aug 22. J Biol Chem. 2005. PMID: 16115869 Free article.

10

Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations.

Gilda JE, Lai X, Witzmann FA, Gomes AV. Gilda JE, et al. Mol Cell Proteomics. 2016 Jun;15(6):1962-81. doi: 10.1074/mcp.M115.057380. Epub 2016 Mar 28. Mol Cell Proteomics. 2016. PMID: 27022107 Free PMC article.

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