McKenna W - Search Results

1

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Among authors: mckenna w. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

2

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. Among authors: mckenna w. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

3

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. Among authors: mckenna w. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

4

Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Watkins H, Seidman CE, MacRae C, Seidman JG, McKenna W. Watkins H, et al. Among authors: mckenna w. Br Heart J. 1992 Jan;67(1):34-8. doi: 10.1136/hrt.67.1.34. Br Heart J. 1992. PMID: 1739523 Free PMC article. Review. No abstract available.

5

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. Among authors: mckenna w. N Engl J Med. 1991 Dec 19;325(25):1753-60. doi: 10.1056/NEJM199112193252501. N Engl J Med. 1991. PMID: 1944483 Free article.

6

A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12.

Solomon SD, Geisterfer-Lowrance AA, Vosberg HP, Hiller G, Jarcho JA, Morton CC, McBride WO, Mitchell AL, Bale AE, McKenna WJ, et al. Solomon SD, et al. Among authors: mckenna wj. Am J Hum Genet. 1990 Sep;47(3):389-94. Am J Hum Genet. 1990. PMID: 1975475 Free PMC article.

7

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Among authors: mckenna w. Cell. 1990 Sep 7;62(5):999-1006. doi: 10.1016/0092-8674(90)90274-i. Cell. 1990. PMID: 1975517

8

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, Seidman JG, Seidman CE. Solomon SD, et al. Among authors: mckenna w. J Clin Invest. 1990 Sep;86(3):993-9. doi: 10.1172/JCI114802. J Clin Invest. 1990. PMID: 1975599 Free PMC article.

9

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

Jarcho JA, McKenna W, Pare JA, Solomon SD, Holcombe RF, Dickie S, Levi T, Donis-Keller H, Seidman JG, Seidman CE. Jarcho JA, et al. Among authors: mckenna w. N Engl J Med. 1989 Nov 16;321(20):1372-8. doi: 10.1056/NEJM198911163212005. N Engl J Med. 1989. PMID: 2811944

10

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Watkins H, et al. Among authors: mckenna wj. Nat Genet. 1995 Dec;11(4):434-7. doi: 10.1038/ng1295-434. Nat Genet. 1995. PMID: 7493025

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