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Items: 14

1.

Deciphering the design of the tropomyosin molecule.

Brown JH, Kim KH, Jun G, Greenfield NJ, Dominguez R, Volkmann N, Hitchcock-DeGregori SE, Cohen C.

Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8496-501. Epub 2001 Jul 3.

2.

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.

3.

Mouse model of a familial hypertrophic cardiomyopathy mutation in alpha-tropomyosin manifests cardiac dysfunction.

Muthuchamy M, Pieples K, Rethinasamy P, Hoit B, Grupp IL, Boivin GP, Wolska B, Evans C, Solaro RJ, Wieczorek DF.

Circ Res. 1999 Jul 9;85(1):47-56.

4.

Targeted ablation of the murine alpha-tropomyosin gene.

Blanchard EM, Iizuka K, Christe M, Conner DA, Geisterfer-Lowrance A, Schoen FJ, Maughan DW, Seidman CE, Seidman JG.

Circ Res. 1997 Dec;81(6):1005-10.

5.

Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene.

Coviello DA, Maron BJ, Spirito P, Watkins H, Vosberg HP, Thierfelder L, Schoen FJ, Seidman JG, Seidman CE.

J Am Coll Cardiol. 1997 Mar 1;29(3):635-40.

6.

Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast.

Tiso N, Rampoldi L, Pallavicini A, Zimbello R, Pandolfo D, Valle G, Lanfranchi G, Danieli GA.

Biochem Biophys Res Commun. 1997 Jan 13;230(2):347-50.

PMID:
9016781
7.

Chromosomal localization and genomic cloning of the mouse alpha-tropomyosin gene Tpm-1.

Schleef M, Werner K, Satzger U, Kaupmann K, Jockusch H.

Genomics. 1993 Aug;17(2):519-21.

PMID:
8406508
8.

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A, et al.

Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4.

9.

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
10.

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.

11.

Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization.

Eyre H, Akkari PA, Wilton SD, Callen DC, Baker E, Laing NG.

Cytogenet Cell Genet. 1995;69(1-2):15-7.

PMID:
7835079
12.

A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.

Watkins H, Anan R, Coviello DA, Spirito P, Seidman JG, Seidman CE.

Circulation. 1995 May 1;91(9):2302-5.

13.

Human hTM alpha gene: expression in muscle and nonmuscle tissue.

MacLeod AR, Gooding C.

Mol Cell Biol. 1988 Jan;8(1):433-40.

14.

The molecular basis for tropomyosin isoform diversity.

Lees-Miller JP, Helfman DM.

Bioessays. 1991 Sep;13(9):429-37. Review.

PMID:
1796905

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