Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 164

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.

Cell. 1994 Jun 3;77(5):701-12.

PMID:
8205619
2.

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.

Nat Genet. 1995 Dec;11(4):434-7.

PMID:
7493025
3.

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE.

Nat Genet. 1993 Apr;3(4):333-7.

PMID:
7981753
4.

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Beckmann J, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwartz K.

Nat Genet. 1995 Dec;11(4):438-40.

PMID:
7493026
5.

Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.

Watkins H, Seidman JG, Seidman CE.

Hum Mol Genet. 1995;4 Spec No:1721-7. Review.

PMID:
8541871
6.
7.

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy.

Kimura A, Harada H, Park JE, Nishi H, Satoh M, Takahashi M, Hiroi S, Sasaoka T, Ohbuchi N, Nakamura T, Koyanagi T, Hwang TH, Choo JA, Chung KS, Hasegawa A, Nagai R, Okazaki O, Nakamura H, Matsuzaki M, Sakamoto T, Toshima H, Koga Y, Imaizumi T, Sasazuki T.

Nat Genet. 1997 Aug;16(4):379-82.

PMID:
9241277
8.

Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy.

Redwood CS, Moolman-Smook JC, Watkins H.

Cardiovasc Res. 1999 Oct;44(1):20-36. Review.

PMID:
10615387
9.

Effects of two hypertrophic cardiomyopathy mutations in alpha-tropomyosin, Asp175Asn and Glu180Gly, on Ca2+ regulation of thin filament motility.

Bing W, Redwood CS, Purcell IF, Esposito G, Watkins H, Marston SB.

Biochem Biophys Res Commun. 1997 Jul 30;236(3):760-4.

PMID:
9245729
10.

Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis.

Karibe A, Tobacman LS, Strand J, Butters C, Back N, Bachinski LL, Arai AE, Ortiz A, Roberts R, Homsher E, Fananapazir L.

Circulation. 2001 Jan 2;103(1):65-71.

11.

[Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].

Ramírez CD, Padrón R.

Invest Clin. 2004 Mar;45(1):69-99. Review. Spanish.

PMID:
15058760
13.

Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy.

Erdmann J, Daehmlow S, Wischke S, Senyuva M, Werner U, Raible J, Tanis N, Dyachenko S, Hummel M, Hetzer R, Regitz-Zagrosek V.

Clin Genet. 2003 Oct;64(4):339-49.

PMID:
12974739
15.

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.

Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG, et al.

N Engl J Med. 1995 Apr 20;332(16):1058-64.

16.

Sarcomeric protein mutations in dilated cardiomyopathy.

Chang AN, Potter JD.

Heart Fail Rev. 2005 Sep;10(3):225-35. Review.

PMID:
16416045
17.

Animal models of hypertrophic cardiomyopathy.

Maass A, Leinwand LA.

Curr Opin Cardiol. 2000 May;15(3):189-96. Review.

PMID:
10952427
18.

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy.

Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, Gersh BJ.

Circulation. 2002 Dec 10;106(24):3085-90.

19.

Novel missense mutation in alpha-tropomyosin gene found in Japanese patients with hypertrophic cardiomyopathy.

Nakajima-Taniguchi C, Matsui H, Nagata S, Kishimoto T, Yamauchi-Takihara K.

J Mol Cell Cardiol. 1995 Sep;27(9):2053-8.

PMID:
8523464
20.

A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy.

Gerull B, Osterziel KJ, Witt C, Dietz R, Thierfelder L.

Hum Mutat. 1998;11(2):179-82.

PMID:
9482583

Supplemental Content

Support Center