McNally EM - Search Results

1

Population-based variation in cardiomyopathy genes.

Golbus JR, Puckelwartz MJ, Fahrenbach JP, Dellefave-Castillo LM, Wolfgeher D, McNally EM. Golbus JR, et al. Among authors: mcnally em. Circ Cardiovasc Genet. 2012 Aug 1;5(4):391-9. doi: 10.1161/CIRCGENETICS.112.962928. Epub 2012 Jul 4. Circ Cardiovasc Genet. 2012. PMID: 22763267 Free PMC article.

2

Lamin A/C truncation in dilated cardiomyopathy with conduction disease.

MacLeod HM, Culley MR, Huber JM, McNally EM. MacLeod HM, et al. Among authors: mcnally em. BMC Med Genet. 2003 Jul 10;4:4. doi: 10.1186/1471-2350-4-4. BMC Med Genet. 2003. PMID: 12854972 Free PMC article.

3

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.

4

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.

5

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.

6

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis.

Attali R, Warwar N, Israel A, Gurt I, McNally E, Puckelwartz M, Glick B, Nevo Y, Ben-Neriah Z, Melki J. Attali R, et al. Hum Mol Genet. 2009 Sep 15;18(18):3462-9. doi: 10.1093/hmg/ddp290. Epub 2009 Jun 19. Hum Mol Genet. 2009. PMID: 19542096

7

Nesprin-1 mutations in human and murine cardiomyopathy.

Puckelwartz MJ, Kessler EJ, Kim G, Dewitt MM, Zhang Y, Earley JU, Depreux FF, Holaska J, Mewborn SK, Pytel P, McNally EM. Puckelwartz MJ, et al. Among authors: mcnally em. J Mol Cell Cardiol. 2010 Apr;48(4):600-8. doi: 10.1016/j.yjmcc.2009.11.006. Epub 2009 Nov 24. J Mol Cell Cardiol. 2010. PMID: 19944109 Free PMC article.

8

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.

9

The genetics of dilated cardiomyopathy.

Dellefave L, McNally EM. Dellefave L, et al. Among authors: mcnally em. Curr Opin Cardiol. 2010 May;25(3):198-204. doi: 10.1097/HCO.0b013e328337ba52. Curr Opin Cardiol. 2010. PMID: 20186049 Free PMC article. Review.

10

Cardiomyocyte sulfonylurea receptor 2-KATP channel mediates cardioprotection and ST segment elevation.

Stoller DA, Fahrenbach JP, Chalupsky K, Tan BH, Aggarwal N, Metcalfe J, Hadhazy M, Shi NQ, Makielski JC, McNally EM. Stoller DA, et al. Among authors: mcnally em. Am J Physiol Heart Circ Physiol. 2010 Oct;299(4):H1100-8. doi: 10.1152/ajpheart.00084.2010. Epub 2010 Jul 23. Am J Physiol Heart Circ Physiol. 2010. PMID: 20656890 Free PMC article.

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