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Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.
Lakdawala NK, Dellefave L, Redwood CS, Sparks E, Cirino AL, Depalma S, Colan SD, Funke B, Zimmerman RS, Robinson P, Watkins H, Seidman CE, Seidman JG, McNally EM, Ho CY. Lakdawala NK, et al. Among authors: robinson p. J Am Coll Cardiol. 2010 Jan 26;55(4):320-9. doi: 10.1016/j.jacc.2009.11.017. J Am Coll Cardiol. 2010. PMID: 20117437 Free PMC article.
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
Robinson P, Mirza M, Knott A, Abdulrazzak H, Willott R, Marston S, Watkins H, Redwood C. Robinson P, et al. J Biol Chem. 2002 Oct 25;277(43):40710-6. doi: 10.1074/jbc.M203446200. Epub 2002 Aug 18. J Biol Chem. 2002. PMID: 12186860 Free article.
The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.
Mirza M, Robinson P, Kremneva E, Copeland O, Nikolaeva O, Watkins H, Levitsky D, Redwood C, El-Mezgueldi M, Marston S. Mirza M, et al. Among authors: robinson p. J Biol Chem. 2007 May 4;282(18):13487-97. doi: 10.1074/jbc.M701071200. Epub 2007 Mar 13. J Biol Chem. 2007. PMID: 17360712 Free article.
4,464 results