Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 275

1.

Sarcomere protein gene mutations and inherited heart disease: a beta-cardiac myosin heavy chain mutation causing endocardial fibroelastosis and heart failure.

Kamisago M, Schmitt JP, McNamara D, Seidman C, Seidman JG.

Novartis Found Symp. 2006;274:176-89; discussion 189-95, 272-6. Review.

PMID:
17019812
2.

A novel beta-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model.

Kaneda T, Naruse C, Kawashima A, Fujino N, Oshima T, Namura M, Nunoda S, Mori S, Konno T, Ino H, Yamagishi M, Asano M.

Clin Sci (Lond). 2008 Mar;114(6):431-40.

PMID:
17956225
3.

Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy.

Tsoutsman T, Kelly M, Ng DC, Tan JE, Tu E, Lam L, Bogoyevitch MA, Seidman CE, Seidman JG, Semsarian C.

Circulation. 2008 Apr 8;117(14):1820-31. doi: 10.1161/CIRCULATIONAHA.107.755777. Epub 2008 Mar 24.

4.

Mutations in sarcomere protein genes in left ventricular noncompaction.

Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L.

Circulation. 2008 Jun 3;117(22):2893-901. doi: 10.1161/CIRCULATIONAHA.107.746164. Epub 2008 May 27.

5.

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.

Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, Bristow MR, Mestroni L.

Circulation. 2005 Jul 5;112(1):54-9.

6.

Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.

Mohapatra B, Jimenez S, Lin JH, Bowles KR, Coveler KJ, Marx JG, Chrisco MA, Murphy RT, Lurie PR, Schwartz RJ, Elliott PM, Vatta M, McKenna W, Towbin JA, Bowles NE.

Mol Genet Metab. 2003 Sep-Oct;80(1-2):207-15.

PMID:
14567970
7.

Comparison of two murine models of familial hypertrophic cardiomyopathy.

McConnell BK, Fatkin D, Semsarian C, Jones KA, Georgakopoulos D, Maguire CT, Healey MJ, Mudd JO, Moskowitz IP, Conner DA, Giewat M, Wakimoto H, Berul CI, Schoen FJ, Kass DA, Seidman CE, Seidman JG.

Circ Res. 2001 Mar 2;88(4):383-9.

8.

Sarcomere mutations in cardiogenesis and ventricular noncompaction.

McNally E, Dellefave L.

Trends Cardiovasc Med. 2009 Jan;19(1):17-21. doi: 10.1016/j.tcm.2009.03.003. Review.

PMID:
19467449
9.

Novel locus for an inherited cardiomyopathy maps to chromosome 7.

Song L, DePalma SR, Kharlap M, Zenovich AG, Cirino A, Mitchell R, McDonough B, Maron BJ, Seidman CE, Seidman JG, Ho CY.

Circulation. 2006 May 9;113(18):2186-92. Epub 2006 May 1.

10.

[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
11.

Mutation of Arg723Gly in beta-myosin heavy chain gene in five Chinese families with hypertrophic cardiomyopathy.

Yang JH, Zheng DD, Dong NZ, Yang XJ, Song JP, Jiang TB, Cheng XJ, Li HX, Zhou BY, Zhao CM, Jiang WP.

Chin Med J (Engl). 2006 Nov 5;119(21):1785-9.

PMID:
17097032
12.

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.

Rai TS, Ahmad S, Bahl A, Ahuja M, Ahluwalia TS, Singh B, Talwar KK, Khullar M.

Mol Cell Biochem. 2009 Jan;321(1-2):189-96. doi: 10.1007/s11010-008-9932-0. Epub 2008 Oct 25.

PMID:
18953637
13.

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

Daehmlow S, Erdmann J, Knueppel T, Gille C, Froemmel C, Hummel M, Hetzer R, Regitz-Zagrosek V.

Biochem Biophys Res Commun. 2002 Oct 18;298(1):116-20.

PMID:
12379228
14.

Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.

Kärkkäinen S, Heliö T, Jääskeläinen P, Miettinen R, Tuomainen P, Ylitalo K, Kaartinen M, Reissell E, Toivonen L, Nieminen MS, Kuusisto J, Laakso M, Peuhkurinen K.

Eur J Heart Fail. 2004 Dec;6(7):861-8.

15.

Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.

Rajan S, Ahmed RP, Jagatheesan G, Petrashevskaya N, Boivin GP, Urboniene D, Arteaga GM, Wolska BM, Solaro RJ, Liggett SB, Wieczorek DF.

Circ Res. 2007 Jul 20;101(2):205-14. Epub 2007 Jun 7. Erratum in: Circ Res. 2007 Sep 14;101(6):e80.

16.

The molecular and cellular biology of heart failure.

Mayer NJ, Rubin SA.

Curr Opin Cardiol. 1995 May;10(3):238-45. Review.

PMID:
7612972
17.

Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.

Ware SM, Quinn ME, Ballard ET, Miller E, Uzark K, Spicer RL.

Clin Genet. 2008 Feb;73(2):165-70. Epub 2007 Dec 12.

PMID:
18076673
18.

The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model.

Semsarian C, Ahmad I, Giewat M, Georgakopoulos D, Schmitt JP, McConnell BK, Reiken S, Mende U, Marks AR, Kass DA, Seidman CE, Seidman JG.

J Clin Invest. 2002 Apr;109(8):1013-20.

19.

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.

Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS.

Eur J Hum Genet. 2005 Feb;13(2):161-5. Erratum in: Eur J Hum Genet. 2005 May;13(5):694.

20.

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.

Andersen PS, Havndrup O, Hougs L, Sørensen KM, Jensen M, Larsen LA, Hedley P, Thomsen AR, Moolman-Smook J, Christiansen M, Bundgaard H.

Hum Mutat. 2009 Mar;30(3):363-70. doi: 10.1002/humu.20862.

PMID:
19035361

Supplemental Content

Support Center