McNally EM - Search Results

1

Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.

Dellefave LM, Pytel P, Mewborn S, Mora B, Guris DL, Fedson S, Waggoner D, Moskowitz I, McNally EM. Dellefave LM, et al. Among authors: mcnally em. Circ Cardiovasc Genet. 2009 Oct;2(5):442-9. doi: 10.1161/CIRCGENETICS.109.861955. Epub 2009 Jul 24. Circ Cardiovasc Genet. 2009. PMID: 20031619 Clinical Trial.

2

Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle.

Allikian MJ, Hack AA, Mewborn S, Mayer U, McNally EM. Allikian MJ, et al. Among authors: mcnally em. J Cell Sci. 2004 Aug 1;117(Pt 17):3821-30. doi: 10.1242/jcs.01234. Epub 2004 Jul 13. J Cell Sci. 2004. PMID: 15252120

3

A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex.

MacLeod H, Pytel P, Wollmann R, Chelmicka-Schorr E, Silver K, Anderson RB, Waggoner D, McNally EM. MacLeod H, et al. Among authors: mcnally em. Neuromuscul Disord. 2007 Apr;17(4):285-9. doi: 10.1016/j.nmd.2007.01.005. Epub 2007 Mar 1. Neuromuscul Disord. 2007. PMID: 17336067

4

Muscle diseases: the muscular dystrophies.

McNally EM, Pytel P. McNally EM, et al. Annu Rev Pathol. 2007;2:87-109. doi: 10.1146/annurev.pathol.2.010506.091936. Annu Rev Pathol. 2007. PMID: 18039094 Review.

5

The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusion.

Doherty KR, Demonbreun AR, Wallace GQ, Cave A, Posey AD, Heretis K, Pytel P, McNally EM. Doherty KR, et al. Among authors: mcnally em. J Biol Chem. 2008 Jul 18;283(29):20252-60. doi: 10.1074/jbc.M802306200. Epub 2008 May 23. J Biol Chem. 2008. PMID: 18502764 Free PMC article.

6

Sarcomere mutations in cardiomyopathy, noncompaction, and the developing heart.

Dellefave L, McNally EM. Dellefave L, et al. Among authors: mcnally em. Circulation. 2008 Jun 3;117(22):2847-9. doi: 10.1161/CIRCULATIONAHA.108.781518. Circulation. 2008. PMID: 18519860 Review. No abstract available.

7

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.

Puckelwartz MJ, Kessler E, Zhang Y, Hodzic D, Randles KN, Morris G, Earley JU, Hadhazy M, Holaska JM, Mewborn SK, Pytel P, McNally EM. Puckelwartz MJ, et al. Among authors: mcnally em. Hum Mol Genet. 2009 Feb 15;18(4):607-20. doi: 10.1093/hmg/ddn386. Epub 2008 Nov 13. Hum Mol Genet. 2009. PMID: 19008300 Free PMC article.

8

Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy.

Pytel P, Husain A, Moskowitz I, Raman J, MacLeod H, Anderson AS, Burke M, McNally EM. Pytel P, et al. Among authors: mcnally em. Cardiovasc Pathol. 2010 Mar-Apr;19(2):e33-6. doi: 10.1016/j.carpath.2008.09.004. Epub 2008 Nov 21. Cardiovasc Pathol. 2010. PMID: 19026577 Free PMC article.

9

Sarcomere mutations in cardiogenesis and ventricular noncompaction.

McNally E, Dellefave L. McNally E, et al. Trends Cardiovasc Med. 2009 Jan;19(1):17-21. doi: 10.1016/j.tcm.2009.03.003. Trends Cardiovasc Med. 2009. PMID: 19467449 Review.

10

Impaired exercise tolerance and skeletal muscle myopathy in sulfonylurea receptor-2 mutant mice.

Stoller D, Pytel P, Katz S, Earley JU, Collins K, Metcalfe J, Lang RM, McNally EM. Stoller D, et al. Among authors: mcnally em. Am J Physiol Regul Integr Comp Physiol. 2009 Oct;297(4):R1144-53. doi: 10.1152/ajpregu.00081.2009. Epub 2009 Aug 12. Am J Physiol Regul Integr Comp Physiol. 2009. PMID: 19675276 Free PMC article.

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