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Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy.

Parvatiyar MS, Marshall JL, Nguyen RT, Jordan MC, Richardson VA, Roos KP, Crosbie-Watson RH.

J Am Heart Assoc. 2015 Dec 23;4(12). pii: e002481. doi: 10.1161/JAHA.115.002481.


X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy.

Nakamura A.

Pharmaceuticals (Basel). 2015 Jun 9;8(2):303-20. doi: 10.3390/ph8020303. Review.


Mechanotransduction in cardiac hypertrophy and failure.

Lyon RC, Zanella F, Omens JH, Sheikh F.

Circ Res. 2015 Apr 10;116(8):1462-76. doi: 10.1161/CIRCRESAHA.116.304937. Review.



Mestroni L, Brun F, Spezzacatene A, Sinagra G, Taylor MR.

Prog Pediatr Cardiol. 2014 Dec;37(1-2):13-18.


Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27.

Tsuda T, Fitzgerald K, Scavena M, Gidding S, Cox MO, Marks H, Flanigan KM, Moore SA.

J Hum Genet. 2015 Mar;60(3):151-5. doi: 10.1038/jhg.2014.112. Epub 2014 Dec 24.


Early right ventricular fibrosis and reduction in biventricular cardiac reserve in the dystrophin-deficient mdx heart.

Meyers TA, Townsend D.

Am J Physiol Heart Circ Physiol. 2015 Feb 15;308(4):H303-15. doi: 10.1152/ajpheart.00485.2014. Epub 2014 Dec 5.


Inherited cardiomyopathies.

Towbin JA.

Circ J. 2014;78(10):2347-56. Epub 2014 Sep 2. Review.


Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex.

Townsend D.

Anat Rec (Hoboken). 2014 Sep;297(9):1694-705. doi: 10.1002/ar.22974. Review.


Proteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathy.

Holland A, Ohlendieck K.

Biomed Res Int. 2014;2014:246195. doi: 10.1155/2014/246195. Epub 2014 Mar 20. Review.


Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.

Feldman AM, Begay RL, Knezevic T, Myers VD, Slavov DB, Zhu W, Gowan K, Graw SL, Jones KL, Tilley DG, Coleman RC, Walinsky P, Cheung JY, Mestroni L, Khalili K, Taylor MR.

J Cell Physiol. 2014 Nov;229(11):1697-702. doi: 10.1002/jcp.24615.


Mendelian forms of structural cardiovascular disease.

MacRae CA.

Curr Cardiol Rep. 2013 Oct;15(10):399. doi: 10.1007/s11886-013-0399-6. Review.


The costamere bridges sarcomeres to the sarcolemma in striated muscle.

Peter AK, Cheng H, Ross RS, Knowlton KU, Chen J.

Prog Pediatr Cardiol. 2011 May;31(2):83-88.


Inherited cardiomyopathies caused by troponin mutations.

Lu QW, Wu XY, Morimoto S.

J Geriatr Cardiol. 2013 Mar;10(1):91-101. doi: 10.3969/j.issn.1671-5411.2013.01.014.


Proteasome inhibitor (MG132) rescues Nav1.5 protein content and the cardiac sodium current in dystrophin-deficient mdx (5cv) mice.

Rougier JS, Gavillet B, Abriel H.

Front Physiol. 2013 Mar 26;4:51. doi: 10.3389/fphys.2013.00051. eCollection 2013.


Exclusive skeletal muscle correction does not modulate dystrophic heart disease in the aged mdx model of Duchenne cardiomyopathy.

Wasala NB, Bostick B, Yue Y, Duan D.

Hum Mol Genet. 2013 Jul 1;22(13):2634-41. doi: 10.1093/hmg/ddt112. Epub 2013 Mar 3.


Injection of vessel-derived stem cells prevents dilated cardiomyopathy and promotes angiogenesis and endogenous cardiac stem cell proliferation in mdx/utrn-/- but not aged mdx mouse models for duchenne muscular dystrophy.

Chun JL, O'Brien R, Song MH, Wondrasch BF, Berry SE.

Stem Cells Transl Med. 2013 Jan;2(1):68-80. doi: 10.5966/sctm.2012-0107. Epub 2012 Dec 27. Erratum in: Stem Cells Transl Med. 2013 Feb;2(2):following 158.


Clinical utility gene card for: dilated cardiomyopathy (CMD).

Posafalvi A, Herkert JC, Sinke RJ, van den Berg MP, Mogensen J, Jongbloed JD, van Tintelen JP.

Eur J Hum Genet. 2013 Oct;21(10). doi: 10.1038/ejhg.2012.276. Epub 2012 Dec 19. No abstract available.


Cardiomyopathy classification: ongoing debate in the genomics era.

McCartan C, Mason R, Jayasinghe SR, Griffiths LR.

Biochem Res Int. 2012;2012:796926. doi: 10.1155/2012/796926. Epub 2012 Aug 8.


Cardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathy.

Dees E, Miller PM, Moynihan KL, Pooley RD, Hunt RP, Galindo CL, Rottman JN, Bader DM.

Dis Model Mech. 2012 Jul;5(4):468-80. doi: 10.1242/dmm.008680. Epub 2012 Mar 22.

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