Publications
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“Effects of sex and age on chicken TBC1D1 gene mRNA expression”, vol. 14, pp. 7704-7714, 2015.
, “Lack of mutations of G4.5 in three families from China with noncompaction of the ventricular myocardium”, vol. 12, pp. 53-58, 2013.
, Bleyl SB, Mumford BR, Thompson V, Carey JC, et al. (1997). Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome. Am. J. Hum. Genet. 61: 868-872.
http://dx.doi.org/10.1086/514879
PMid:9382097 PMCid:1715997
Chen R, Tsuji T, Ichida F, Bowles KR, et al. (2002). Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction. Mol. Genet. Metab. 77: 319-325.
http://dx.doi.org/10.1016/S1096-7192(02)00195-6
Chin TK, Perloff JK, Williams RG, Jue K, et al. (1990). Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 82: 507-513.
http://dx.doi.org/10.1161/01.CIR.82.2.507
PMid:2372897
Ichida F, Tsubata S, Bowles KR, Haneda N, et al. (2001). Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome. Circulation 103: 1256-1263.
http://dx.doi.org/10.1161/01.CIR.103.9.1256
PMid:11238270
Jenni R, Oechslin E, Schneider J, Attenhofer JC, et al. (2001). Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy. Heart 86: 666-671.
http://dx.doi.org/10.1136/heart.86.6.666
PMid:11711464 PMCid:1730012
Kasifoglu T, Cavusoglu Y, Korkmaz C and Birdane A (2007). Noncompaction of the ventricular myocardium in a patient with Behcet's disease showing multiple thrombus formations in the right atrium, inferior vena cava and right iliac vein: A case report. Int. J. Angiol. 16: 69-72.
http://dx.doi.org/10.1055/s-0031-1278252
PMid:22477276 PMCid:2733008
Kenton AB, Sanchez X, Coveler KJ, Makar KA, et al. (2004). Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12. Mol. Genet. Metab. 82: 162-166.
http://dx.doi.org/10.1016/j.ymgme.2004.02.009
PMid:15172004
Klaassen S, Probst S, Oechslin E, Gerull B, et al. (2008). Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation 117: 2893-2901.
http://dx.doi.org/10.1161/CIRCULATIONAHA.107.746164
PMid:18506004
Maron BJ, Towbin JA, Thiene G, Antzelevitch C, et al. (2006). Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 113: 1807-1816.
http://dx.doi.org/10.1161/CIRCULATIONAHA.106.174287
PMid:16567565
Richardson P, McKenna W, Bristow M, Maisch B, et al. (1996). Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 93: 841-842.
http://dx.doi.org/10.1161/01.CIR.93.5.841
PMid:8598070
Sasse-Klaassen S, Gerull B, Oechslin E, Jenni R, et al. (2003). Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients. Am. J. Med. Genet. A 119A: 162-167.
http://dx.doi.org/10.1002/ajmg.a.20075
PMid:12749056
Weiford BC, Subbarao VD and Mulhern KM (2004). Noncompaction of the ventricular myocardium. Circulation 109: 2965-2971.
http://dx.doi.org/10.1161/01.CIR.0000132478.60674.D0
PMid:15210614
Zambrano E, Marshalko SJ, Jaffe CC and Hui P (2002). Isolated noncompaction of the ventricular myocardium: clinical and molecular aspects of a rare cardiomyopathy. Lab Invest 82: 117-122.
http://dx.doi.org/10.1038/labinvest.3780404
PMid:11850525