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Pathogenetic role of the deafness-related M34T mutation of Cx26.
Bicego M, Beltramello M, Melchionda S, Carella M, Piazza V, Zelante L, Bukauskas FF, Arslan E, Cama E, Pantano S, Bruzzone R, D'Andrea P, Mammano F. Bicego M, et al. Among authors: bukauskas ff. Hum Mol Genet. 2006 Sep 1;15(17):2569-87. doi: 10.1093/hmg/ddl184. Epub 2006 Jul 18. Hum Mol Genet. 2006. PMID: 16849369 Free PMC article.
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
Dobrowolski R, Sasse P, Schrickel JW, Watkins M, Kim JS, Rackauskas M, Troatz C, Ghanem A, Tiemann K, Degen J, Bukauskas FF, Civitelli R, Lewalter T, Fleischmann BK, Willecke K. Dobrowolski R, et al. Among authors: bukauskas ff. Hum Mol Genet. 2008 Feb 15;17(4):539-54. doi: 10.1093/hmg/ddm329. Epub 2007 Nov 13. Hum Mol Genet. 2008. PMID: 18003637 Free PMC article.
The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice.
Lübkemeier I, Andrié R, Lickfett L, Bosen F, Stöckigt F, Dobrowolski R, Draffehn AM, Fregeac J, Schultze JL, Bukauskas FF, Schrickel JW, Willecke K. Lübkemeier I, et al. Among authors: bukauskas ff. J Mol Cell Cardiol. 2013 Dec;65:19-32. doi: 10.1016/j.yjmcc.2013.09.008. Epub 2013 Sep 21. J Mol Cell Cardiol. 2013. PMID: 24060583
120 results