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The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction.
Chiang DY, Verkerk AO, Victorio R, Shneyer BI, van der Vaart B, Jouni M, Narendran N, Kc A, Sampognaro JR, Vetrano-Olsen F, Oh JS, Buys E, de Jonge B, Shah DA, Kiviniemi T, Burridge PW, Bezzina CR, Akhmanova A, MacRae CA. Chiang DY, et al. Among authors: bezzina cr. Circ Res. 2024 Jan 5;134(1):46-59. doi: 10.1161/CIRCRESAHA.123.323231. Epub 2023 Dec 14. Circ Res. 2024. PMID: 38095085 Free article.
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, van Langen IM, Tan-Sindhunata G, Bink-Boelkens MT, van Der Hout AH, Mannens MM, Wilde AA. Bezzina C, et al. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249
Genetic control of sodium channel function.
Tan HL, Bezzina CR, Smits JP, Verkerk AO, Wilde AA. Tan HL, et al. Among authors: bezzina cr. Cardiovasc Res. 2003 Mar 15;57(4):961-73. doi: 10.1016/s0008-6363(02)00714-9. Cardiovasc Res. 2003. PMID: 12650874 Review.
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.
Bezzina CR, Verkerk AO, Busjahn A, Jeron A, Erdmann J, Koopmann TT, Bhuiyan ZA, Wilders R, Mannens MM, Tan HL, Luft FC, Schunkert H, Wilde AA. Bezzina CR, et al. Cardiovasc Res. 2003 Jul 1;59(1):27-36. doi: 10.1016/s0008-6363(03)00342-0. Cardiovasc Res. 2003. PMID: 12829173
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.
Coronel R, Casini S, Koopmann TT, Wilms-Schopman FJ, Verkerk AO, de Groot JR, Bhuiyan Z, Bezzina CR, Veldkamp MW, Linnenbank AC, van der Wal AC, Tan HL, Brugada P, Wilde AA, de Bakker JM. Coronel R, et al. Among authors: bezzina cr. Circulation. 2005 Nov 1;112(18):2769-77. doi: 10.1161/CIRCULATIONAHA.105.532614. Circulation. 2005. PMID: 16267250
Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD.
Remme CA, Verkerk AO, Nuyens D, van Ginneken AC, van Brunschot S, Belterman CN, Wilders R, van Roon MA, Tan HL, Wilde AA, Carmeliet P, de Bakker JM, Veldkamp MW, Bezzina CR. Remme CA, et al. Among authors: bezzina cr. Circulation. 2006 Dec 12;114(24):2584-94. doi: 10.1161/CIRCULATIONAHA.106.653949. Epub 2006 Dec 4. Circulation. 2006. PMID: 17145985
225 results