PubMed (OMIM) for id: 349382

Year	Number of Results
1988	1
1991	1
1993	2
1994	1
1995	3
1997	3
1999	1
2001	2
2024	0

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. Brown JH, et al. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8496-501. doi: 10.1073/pnas.131219198. Epub 2001 Jul 3. Proc Natl Acad Sci U S A. 2001. PMID: 11438684 Free PMC article.

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. Karibe A, et al. Circulation. 2001 Jan 2;103(1):65-71. doi: 10.1161/01.cir.103.1.65. Circulation. 2001. PMID: 11136687

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. Muthuchamy M, et al. Circ Res. 1999 Jul 9;85(1):47-56. doi: 10.1161/01.res.85.1.47. Circ Res. 1999. PMID: 10400910

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. Blanchard EM, et al. Circ Res. 1997 Dec;81(6):1005-10. doi: 10.1161/01.res.81.6.1005. Circ Res. 1997. PMID: 9400381

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. Coviello DA, et al. J Am Coll Cardiol. 1997 Mar 1;29(3):635-40. doi: 10.1016/s0735-1097(96)00538-4. J Am Coll Cardiol. 1997. PMID: 9060904 Free article.

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. Tiso N, et al. Biochem Biophys Res Commun. 1997 Jan 13;230(2):347-50. doi: 10.1006/bbrc.1996.5958. Biochem Biophys Res Commun. 1997. 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. Schleef M, et al. Genomics. 1993 Aug;17(2):519-21. doi: 10.1006/geno.1993.1361. Genomics. 1993. 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. Thierfelder L, et al. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4. doi: 10.1073/pnas.90.13.6270. Proc Natl Acad Sci U S A. 1993. PMID: 8327508 Free PMC article.

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. Thierfelder L, et al. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. 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. Watkins H, et al. N Engl J Med. 1995 Apr 20;332(16):1058-64. doi: 10.1056/NEJM199504203321603. N Engl J Med. 1995. PMID: 7898523 Free article.

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