McKenna W - Search Results

1

Disparate effects of different mutations in plakoglobin on cell mechanical behavior.

Huang H, Asimaki A, Lo D, McKenna W, Saffitz J. Huang H, et al. Among authors: mckenna w. Cell Motil Cytoskeleton. 2008 Dec;65(12):964-78. doi: 10.1002/cm.20319. Cell Motil Cytoskeleton. 2008. PMID: 18937352 Free PMC article.

2

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy.

Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ. Asimaki A, et al. Am J Hum Genet. 2007 Nov;81(5):964-73. doi: 10.1086/521633. Epub 2007 Sep 28. Am J Hum Genet. 2007. PMID: 17924338 Free PMC article.

3

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.

Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, Zambartas C, Stefanadis C, McKenna WJ, Protonotarios N. Antoniades L, et al. Eur Heart J. 2006 Sep;27(18):2208-16. doi: 10.1093/eurheartj/ehl184. Epub 2006 Aug 7. Eur Heart J. 2006. PMID: 16893920

4

A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy.

Asimaki A, Tandri H, Huang H, Halushka MK, Gautam S, Basso C, Thiene G, Tsatsopoulou A, Protonotarios N, McKenna WJ, Calkins H, Saffitz JE. Asimaki A, et al. N Engl J Med. 2009 Mar 12;360(11):1075-84. doi: 10.1056/NEJMoa0808138. N Engl J Med. 2009. PMID: 19279339 Free article.

5

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

Gehmlich K, Asimaki A, Cahill TJ, Ehler E, Syrris P, Zachara E, Re F, Avella A, Monserrat L, Saffitz JE, McKenna WJ. Gehmlich K, et al. Heart Rhythm. 2010 Oct;7(10):1446-53. doi: 10.1016/j.hrthm.2010.08.007. Epub 2010 Aug 11. Heart Rhythm. 2010. PMID: 20708101 Free PMC article.

6

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations.

Gehmlich K, Syrris P, Peskett E, Evans A, Ehler E, Asimaki A, Anastasakis A, Tsatsopoulou A, Vouliotis AI, Stefanadis C, Saffitz JE, Protonotarios N, McKenna WJ. Gehmlich K, et al. Cardiovasc Res. 2011 Apr 1;90(1):77-87. doi: 10.1093/cvr/cvq353. Epub 2010 Nov 9. Cardiovasc Res. 2011. PMID: 21062920 Free PMC article.

7

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions.

Gehmlich K, Lambiase PD, Asimaki A, Ciaccio EJ, Ehler E, Syrris P, Saffitz JE, McKenna WJ. Gehmlich K, et al. Heart Rhythm. 2011 May;8(5):711-8. doi: 10.1016/j.hrthm.2011.01.010. Epub 2011 Jan 7. Heart Rhythm. 2011. PMID: 21220045 Free PMC article.

8

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele.

Gehmlich K, Syrris P, Reimann M, Asimaki A, Ehler E, Evans A, Quarta G, Pantazis A, Saffitz JE, McKenna WJ. Gehmlich K, et al. Cardiovasc Pathol. 2012 Jul-Aug;21(4):275-82. doi: 10.1016/j.carpath.2011.09.005. Epub 2011 Oct 27. Cardiovasc Pathol. 2012. PMID: 22036071

9

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

Gomes J, Finlay M, Ahmed AK, Ciaccio EJ, Asimaki A, Saffitz JE, Quarta G, Nobles M, Syrris P, Chaubey S, McKenna WJ, Tinker A, Lambiase PD. Gomes J, et al. Eur Heart J. 2012 Aug;33(15):1942-53. doi: 10.1093/eurheartj/ehr472. Epub 2012 Jan 11. Eur Heart J. 2012. PMID: 22240500 Free PMC article.

10

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2.

Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, McKenna WJ. Syrris P, et al. Am J Hum Genet. 2006 Nov;79(5):978-84. doi: 10.1086/509122. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033975 Free PMC article.

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