Potter JD - Search Results

1

Functional consequences of the human cardiac troponin I hypertrophic cardiomyopathy mutation R145G in transgenic mice.

Wen Y, Pinto JR, Gomes AV, Xu Y, Wang Y, Wang Y, Potter JD, Kerrick WG. Wen Y, et al. Among authors: potter jd. J Biol Chem. 2008 Jul 18;283(29):20484-94. doi: 10.1074/jbc.M801661200. Epub 2008 Apr 22. J Biol Chem. 2008. PMID: 18430738 Free PMC article.

2

Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy.

Lang R, Gomes AV, Zhao J, Housmans PR, Miller T, Potter JD. Lang R, et al. Among authors: potter jd. J Biol Chem. 2002 Apr 5;277(14):11670-8. doi: 10.1074/jbc.M108912200. Epub 2002 Jan 18. J Biol Chem. 2002. PMID: 11801593 Free article.

3

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. Gomes AV, et al. Among authors: potter jd. J Biol Chem. 2002 Sep 20;277(38):35341-9. doi: 10.1074/jbc.M204118200. Epub 2002 Jul 1. J Biol Chem. 2002. PMID: 12093807 Free article.

4

Different functional properties of troponin T mutants that cause dilated cardiomyopathy.

Venkatraman G, Harada K, Gomes AV, Kerrick WG, Potter JD. Venkatraman G, et al. Among authors: potter jd. J Biol Chem. 2003 Oct 24;278(43):41670-6. doi: 10.1074/jbc.M302148200. Epub 2003 Aug 14. J Biol Chem. 2003. PMID: 12923187 Free article.

5

Molecular and cellular aspects of troponin cardiomyopathies.

Gomes AV, Potter JD. Gomes AV, et al. Among authors: potter jd. Ann N Y Acad Sci. 2004 May;1015:214-24. doi: 10.1196/annals.1302.018. Ann N Y Acad Sci. 2004. PMID: 15201162 Review.

6

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. Gomes AV, et al. Among authors: potter jd. J Biol Chem. 2004 Nov 26;279(48):49579-87. doi: 10.1074/jbc.M407340200. Epub 2004 Sep 9. J Biol Chem. 2004. PMID: 15358779 Free article.

7

Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene.

Gomes AV, Potter JD. Gomes AV, et al. Among authors: potter jd. Mol Cell Biochem. 2004 Aug;263(1-2):99-114. doi: 10.1023/B:MCBI.0000041852.42291.aa. Mol Cell Biochem. 2004. PMID: 15524171 Review.

8

Role of troponin T in disease.

Gomes AV, Barnes JA, Harada K, Potter JD. Gomes AV, et al. Among authors: potter jd. Mol Cell Biochem. 2004 Aug;263(1-2):115-29. doi: 10.1023/B:MCBI.0000041853.20588.a0. Mol Cell Biochem. 2004. PMID: 15524172 Review.

9

Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform.

Venkatraman G, Gomes AV, Kerrick WG, Potter JD. Venkatraman G, et al. Among authors: potter jd. J Biol Chem. 2005 May 6;280(18):17584-92. doi: 10.1074/jbc.M409337200. Epub 2004 Dec 28. J Biol Chem. 2005. PMID: 15623536 Free article.

10

Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development.

Gomes AV, Liang J, Potter JD. Gomes AV, et al. Among authors: potter jd. J Biol Chem. 2005 Sep 2;280(35):30909-15. doi: 10.1074/jbc.M500287200. Epub 2005 Jun 15. J Biol Chem. 2005. PMID: 15961398 Free article.

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