Wolf CM - Search Results

1

Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.

Wolf CM, Moskowitz IP, Arno S, Branco DM, Semsarian C, Bernstein SA, Peterson M, Maida M, Morley GE, Fishman G, Berul CI, Seidman CE, Seidman JG. Wolf CM, et al. Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):18123-8. doi: 10.1073/pnas.0509145102. Epub 2005 Dec 6. Proc Natl Acad Sci U S A. 2005. PMID: 16332958 Free PMC article.

2

Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy.

Ahmad F, Arad M, Musi N, He H, Wolf C, Branco D, Perez-Atayde AR, Stapleton D, Bali D, Xing Y, Tian R, Goodyear LJ, Berul CI, Ingwall JS, Seidman CE, Seidman JG. Ahmad F, et al. Circulation. 2005 Nov 15;112(20):3140-8. doi: 10.1161/CIRCULATIONAHA.105.550806. Epub 2005 Nov 7. Circulation. 2005. PMID: 16275868

3

Inherited conduction system abnormalities--one group of diseases, many genes.

Wolf CM, Berul CI. Wolf CM, et al. J Cardiovasc Electrophysiol. 2006 Apr;17(4):446-55. doi: 10.1111/j.1540-8167.2006.00427.x. J Cardiovasc Electrophysiol. 2006. PMID: 16643374 Review.

4

A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development.

Moskowitz IP, Kim JB, Moore ML, Wolf CM, Peterson MA, Shendure J, Nobrega MA, Yokota Y, Berul C, Izumo S, Seidman JG, Seidman CE. Moskowitz IP, et al. Among authors: wolf cm. Cell. 2007 Jun 29;129(7):1365-76. doi: 10.1016/j.cell.2007.04.036. Cell. 2007. PMID: 17604724 Free article.

5

Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia.

Song L, Alcalai R, Arad M, Wolf CM, Toka O, Conner DA, Berul CI, Eldar M, Seidman CE, Seidman JG. Song L, et al. Among authors: wolf cm. J Clin Invest. 2007 Jul;117(7):1814-23. doi: 10.1172/JCI31080. J Clin Invest. 2007. PMID: 17607358 Free PMC article.

6

Cardiac electrophysiological characteristics of the mdx ( 5cv ) mouse model of Duchenne muscular dystrophy.

Branco DM, Wolf CM, Sherwood M, Hammer PE, Kang PB, Berul CI. Branco DM, et al. Among authors: wolf cm. J Interv Card Electrophysiol. 2007 Nov;20(1-2):1-7. doi: 10.1007/s10840-007-9168-z. Epub 2007 Oct 17. J Interv Card Electrophysiol. 2007. PMID: 17940855

7

Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations.

Wolf CM, Arad M, Ahmad F, Sanbe A, Bernstein SA, Toka O, Konno T, Morley G, Robbins J, Seidman JG, Seidman CE, Berul CI. Wolf CM, et al. Circulation. 2008 Jan 15;117(2):144-54. doi: 10.1161/CIRCULATIONAHA.107.726752. Epub 2007 Dec 24. Circulation. 2008. PMID: 18158359 Free PMC article.

8

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.

Wolf CM, Wang L, Alcalai R, Pizard A, Burgon PG, Ahmad F, Sherwood M, Branco DM, Wakimoto H, Fishman GI, See V, Stewart CL, Conner DA, Berul CI, Seidman CE, Seidman JG. Wolf CM, et al. J Mol Cell Cardiol. 2008 Feb;44(2):293-303. doi: 10.1016/j.yjmcc.2007.11.008. Epub 2007 Dec 3. J Mol Cell Cardiol. 2008. PMID: 18182166 Free PMC article.

9

Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features.

Dansithong W, Wolf CM, Sarkar P, Paul S, Chiang A, Holt I, Morris GE, Branco D, Sherwood MC, Comai L, Berul CI, Reddy S. Dansithong W, et al. Among authors: wolf cm. PLoS One. 2008;3(12):e3968. doi: 10.1371/journal.pone.0003968. Epub 2008 Dec 18. PLoS One. 2008. PMID: 19092997 Free PMC article.

10

Molecular mechanisms of inherited arrhythmias.

Wolf CM, Berul CI. Wolf CM, et al. Curr Genomics. 2008 May;9(3):160-8. doi: 10.2174/138920208784340768. Curr Genomics. 2008. PMID: 19440513 Free PMC article.

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