These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
175 related articles for article (PubMed ID: 15623536)
1. Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform. Venkatraman G; Gomes AV; Kerrick WG; Potter JD J Biol Chem; 2005 May; 280(18):17584-92. PubMed ID: 15623536 [TBL] [Abstract][Full Text] [Related]
2. The miscommunicative cardiac cell: when good proteins go bad. Gomes AV; Venkatraman G; Potter JD Ann N Y Acad Sci; 2005 Jun; 1047():30-7. PubMed ID: 16093482 [TBL] [Abstract][Full Text] [Related]
3. Different functional properties of troponin T mutants that cause dilated cardiomyopathy. Venkatraman G; Harada K; Gomes AV; Kerrick WG; Potter JD J Biol Chem; 2003 Oct; 278(43):41670-6. PubMed ID: 12923187 [TBL] [Abstract][Full Text] [Related]
4. Cardiac troponin T isoforms affect the Ca(2+) sensitivity of force development in the presence of slow skeletal troponin I: insights into the role of troponin T isoforms in the fetal heart. Gomes AV; Venkatraman G; Davis JP; Tikunova SB; Engel P; Solaro RJ; Potter JD J Biol Chem; 2004 Nov; 279(48):49579-87. PubMed ID: 15358779 [TBL] [Abstract][Full Text] [Related]
5. A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin. Pinto JR; Parvatiyar MS; Jones MA; Liang J; Potter JD J Biol Chem; 2008 Jan; 283(4):2156-66. PubMed ID: 18032382 [TBL] [Abstract][Full Text] [Related]
6. Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization. Lu QW; Morimoto S; Harada K; Du CK; Takahashi-Yanaga F; Miwa Y; Sasaguri T; Ohtsuki I J Mol Cell Cardiol; 2003 Dec; 35(12):1421-7. PubMed ID: 14654368 [TBL] [Abstract][Full Text] [Related]
7. Cardiac troponin T isoforms affect the Ca2+ sensitivity and inhibition of force development. Insights into the role of troponin T isoforms in the heart. Gomes AV; Guzman G; Zhao J; Potter JD J Biol Chem; 2002 Sep; 277(38):35341-9. PubMed ID: 12093807 [TBL] [Abstract][Full Text] [Related]
8. Molecular mechanisms and structural features of cardiomyopathy-causing troponin T mutants in the tropomyosin overlap region. Gangadharan B; Sunitha MS; Mukherjee S; Chowdhury RR; Haque F; Sekar N; Sowdhamini R; Spudich JA; Mercer JA Proc Natl Acad Sci U S A; 2017 Oct; 114(42):11115-11120. PubMed ID: 28973951 [TBL] [Abstract][Full Text] [Related]
9. Dilated cardiomyopathy mutation (R174W) in troponin T attenuates the length-mediated increase in cross-bridge recruitment and myofilament Ca Reda SM; Chandra M Am J Physiol Heart Circ Physiol; 2019 Sep; 317(3):H648-H657. PubMed ID: 31373515 [TBL] [Abstract][Full Text] [Related]
10. Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity. Memo M; Leung MC; Ward DG; dos Remedios C; Morimoto S; Zhang L; Ravenscroft G; McNamara E; Nowak KJ; Marston SB; Messer AE Cardiovasc Res; 2013 Jul; 99(1):65-73. PubMed ID: 23539503 [TBL] [Abstract][Full Text] [Related]
11. The functional effect of dilated cardiomyopathy mutation (R144W) in mouse cardiac troponin T is differently affected by α- and β-myosin heavy chain isoforms. Gollapudi SK; Tardiff JC; Chandra M Am J Physiol Heart Circ Physiol; 2015 Apr; 308(8):H884-93. PubMed ID: 25681424 [TBL] [Abstract][Full Text] [Related]
12. An R111C polymorphism in wild turkey cardiac troponin I accompanying the dilated cardiomyopathy-related abnormal splicing variant of cardiac troponin T with potentially compensatory effects. Biesiadecki BJ; Schneider KL; Yu ZB; Chong SM; Jin JP J Biol Chem; 2004 Apr; 279(14):13825-32. PubMed ID: 14736877 [TBL] [Abstract][Full Text] [Related]
13. Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype. Mirza M; Marston S; Willott R; Ashley C; Mogensen J; McKenna W; Robinson P; Redwood C; Watkins H J Biol Chem; 2005 Aug; 280(31):28498-506. PubMed ID: 15923195 [TBL] [Abstract][Full Text] [Related]
14. Differential expression of TnI and TnT isoforms in rabbit heart during the perinatal period and during cardiovascular stress. Gao L; Kennedy JM; Solaro RJ J Mol Cell Cardiol; 1995 Jan; 27(1):541-50. PubMed ID: 7760375 [TBL] [Abstract][Full Text] [Related]
15. Gene transfer of troponin I isoforms, mutants, and chimeras. Westfall MV; Metzger JM Adv Exp Med Biol; 2003; 538():169-74; discussion 174. PubMed ID: 15098664 [TBL] [Abstract][Full Text] [Related]
16. Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca2+ sensitivity. Parvatiyar MS; Pinto JR Biochim Biophys Acta; 2015 Feb; 1850(2):365-72. PubMed ID: 25450489 [TBL] [Abstract][Full Text] [Related]
17. Interplay Between the Effects of Dilated Cardiomyopathy Mutation (R206L) and the Protein Kinase C Phosphomimic (T204E) of Rat Cardiac Troponin T Are Differently Modulated by α- and β-Myosin Heavy Chain Isoforms. Michael JJ; Chandra M J Am Heart Assoc; 2016 Mar; 5(3):e002777. PubMed ID: 27001966 [TBL] [Abstract][Full Text] [Related]
18. Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. Morimoto S; Lu QW; Harada K; Takahashi-Yanaga F; Minakami R; Ohta M; Sasaguri T; Ohtsuki I Proc Natl Acad Sci U S A; 2002 Jan; 99(2):913-8. PubMed ID: 11773635 [TBL] [Abstract][Full Text] [Related]
19. Recombinant troponin I substitution and calcium responsiveness in skinned cardiac muscle. Strauss JD; Van Eyk JE; Barth Z; Kluwe L; Wiesner RJ; Maéda K; Rüegg JC Pflugers Arch; 1996 Apr; 431(6):853-62. PubMed ID: 8927501 [TBL] [Abstract][Full Text] [Related]
20. Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin. Sommese RF; Nag S; Sutton S; Miller SM; Spudich JA; Ruppel KM PLoS One; 2013; 8(12):e83403. PubMed ID: 24367593 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]