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Items: 1 to 20 of 160

1.

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.

2.

Alpha-tropomyosin mutations in inherited cardiomyopathies.

Redwood C, Robinson P.

J Muscle Res Cell Motil. 2013 Aug;34(3-4):285-94. doi: 10.1007/s10974-013-9358-5. Epub 2013 Sep 5. Review.

PMID:
24005378
3.

Functional consequences of sarcomeric protein abnormalities in failing myocardium.

LeWinter MM.

Heart Fail Rev. 2005 Sep;10(3):249-57. Review.

PMID:
16416047
4.

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

Willott RH, Gomes AV, Chang AN, Parvatiyar MS, Pinto JR, Potter JD.

J Mol Cell Cardiol. 2010 May;48(5):882-92. doi: 10.1016/j.yjmcc.2009.10.031. Epub 2009 Nov 12. Review.

PMID:
19914256
5.

[Calcium regulation by troponin and its genetic disorder in striated muscle contraction].

Ohtsuki I.

Nihon Yakurigaku Zasshi. 2002 Nov;120(1):20P-23P. Review. Japanese.

PMID:
12491770
6.

Sarcomeric protein mutations in dilated cardiomyopathy.

Chang AN, Potter JD.

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

PMID:
16416045
7.
8.

Sarcoplasmic reticulum Ca-ATPase-phospholamban interactions and dilated cardiomyopathy.

Haghighi K, Gregory KN, Kranias EG.

Biochem Biophys Res Commun. 2004 Oct 1;322(4):1214-22. Review.

PMID:
15336969
9.

Role of troponin T in disease.

Gomes AV, Barnes JA, Harada K, Potter JD.

Mol Cell Biochem. 2004 Aug;263(1-2):115-29. Review.

PMID:
15524172
10.

[Genetics of dilated cardiomyopathy].

Osterziel KJ, Scheffold T, Perrot A, Dietz R; Netzwerk Myokardiale Erkrankungen.

Z Kardiol. 2001 Jul;90(7):461-9. Review. German.

PMID:
11515275
12.

The role of tropomyosin in the regulation of myocardial contraction and relaxation.

Wolska BM, Wieczorek DM.

Pflugers Arch. 2003 Apr;446(1):1-8. Epub 2003 Feb 18. Review.

PMID:
12690456
13.

A study of tropomyosin's role in cardiac function and disease using thin-filament reconstituted myocardium.

Bai F, Wang L, Kawai M.

J Muscle Res Cell Motil. 2013 Aug;34(3-4):295-310. doi: 10.1007/s10974-013-9343-z. Epub 2013 May 23. Review.

14.
15.

[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
16.

Biochemical characterisation of Troponin C mutations causing hypertrophic and dilated cardiomyopathies.

Kalyva A, Parthenakis FI, Marketou ME, Kontaraki JE, Vardas PE.

J Muscle Res Cell Motil. 2014 Apr;35(2):161-78. doi: 10.1007/s10974-014-9382-0. Epub 2014 Apr 18. Review.

PMID:
24744096
17.

Cardiac and skeletal myopathies: can genotype explain phenotype?

Marston SB, Hodgkinson JL.

J Muscle Res Cell Motil. 2001;22(1):1-4. Review.

PMID:
11563546
18.

[Mutations in genes for sarcomeric proteins].

Kimura A.

Nihon Rinsho. 2000 Jan;58(1):117-22. Review. Japanese.

PMID:
10885298
19.
20.

Models of dilated cardiomyopathy in the mouse and the hamster.

Ikeda Y, Ross J Jr.

Curr Opin Cardiol. 2000 May;15(3):197-201. Review.

PMID:
10952428

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