McKenna WJ - Search Results

1

Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.

Tripathi S, Schultz I, Becker E, Montag J, Borchert B, Francino A, Navarro-Lopez F, Perrot A, Özcelik C, Osterziel KJ, McKenna WJ, Brenner B, Kraft T. Tripathi S, et al. Among authors: mckenna wj. Basic Res Cardiol. 2011 Nov;106(6):1041-55. doi: 10.1007/s00395-011-0205-9. Epub 2011 Jul 19. Basic Res Cardiol. 2011. PMID: 21769673 Free PMC article.

2

Mutation of the myosin converter domain alters cross-bridge elasticity.

Köhler J, Winkler G, Schulte I, Scholz T, McKenna W, Brenner B, Kraft T. Köhler J, et al. Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3557-62. doi: 10.1073/pnas.062415899. Proc Natl Acad Sci U S A. 2002. PMID: 11904418 Free PMC article.

3

Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells.

Kirschner SE, Becker E, Antognozzi M, Kubis HP, Francino A, Navarro-López F, Bit-Avragim N, Perrot A, Mirrakhimov MM, Osterziel KJ, McKenna WJ, Brenner B, Kraft T. Kirschner SE, et al. Among authors: mckenna wj. Am J Physiol Heart Circ Physiol. 2005 Mar;288(3):H1242-51. doi: 10.1152/ajpheart.00686.2004. Epub 2004 Nov 18. Am J Physiol Heart Circ Physiol. 2005. PMID: 15550524 Free article.

4

Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

Seebohm B, Matinmehr F, Köhler J, Francino A, Navarro-Lopéz F, Perrot A, Ozcelik C, McKenna WJ, Brenner B, Kraft T. Seebohm B, et al. Among authors: mckenna wj. Biophys J. 2009 Aug 5;97(3):806-24. doi: 10.1016/j.bpj.2009.05.023. Biophys J. 2009. PMID: 19651039 Free PMC article.

5

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

6

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Watkins H, et al. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

7

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.

Rosenzweig A, Watkins H, Hwang DS, Miri M, McKenna W, Traill TA, Seidman JG, Seidman CE. Rosenzweig A, et al. N Engl J Med. 1991 Dec 19;325(25):1753-60. doi: 10.1056/NEJM199112193252501. N Engl J Med. 1991. PMID: 1944483 Free article.

8

Hypertrophic cardiomyopathy: an update.

McKenna WJ. McKenna WJ. Cardiologia. 1993 Dec;38(12 Suppl 1):277-81. Cardiologia. 1993. PMID: 8020027 Review.

9

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

Anan R, Greve G, Thierfelder L, Watkins H, McKenna WJ, Solomon S, Vecchio C, Shono H, Nakao S, Tanaka H, et al. Anan R, et al. Among authors: mckenna wj. J Clin Invest. 1994 Jan;93(1):280-5. doi: 10.1172/JCI116957. J Clin Invest. 1994. PMID: 8282798 Free PMC article.

10

Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene.

Solomon SD, Wolff S, Watkins H, Ridker PM, Come P, McKenna WJ, Seidman CE, Lee RT. Solomon SD, et al. Among authors: mckenna wj. J Am Coll Cardiol. 1993 Aug;22(2):498-505. doi: 10.1016/0735-1097(93)90055-6. J Am Coll Cardiol. 1993. PMID: 8335820 Free article.

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