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Replacement of connexin43 by connexin26 in transgenic mice leads to dysfunctional reproductive organs and slowed ventricular conduction in the heart.
Winterhager E, Pielensticker N, Freyer J, Ghanem A, Schrickel JW, Kim JS, Behr R, Grümmer R, Maass K, Urschel S, Lewalter T, Tiemann K, Simoni M, Willecke K. Winterhager E, et al. Among authors: kim js. BMC Dev Biol. 2007 Apr 4;7:26. doi: 10.1186/1471-213X-7-26. BMC Dev Biol. 2007. PMID: 17408477 Free PMC article.
Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43.
Maass K, Ghanem A, Kim JS, Saathoff M, Urschel S, Kirfel G, Grümmer R, Kretz M, Lewalter T, Tiemann K, Winterhager E, Herzog V, Willecke K. Maass K, et al. Among authors: kim js. Mol Biol Cell. 2004 Oct;15(10):4597-608. doi: 10.1091/mbc.e04-04-0324. Epub 2004 Jul 28. Mol Biol Cell. 2004. PMID: 15282340 Free PMC article.
Cardiomyocyte-restricted deletion of connexin43 during mouse development.
Eckardt D, Kirchhoff S, Kim JS, Degen J, Theis M, Ott T, Wiesmann F, Doevendans PA, Lamers WH, de Bakker JM, van Rijen HV, Schneider MD, Willecke K. Eckardt D, et al. Among authors: kim js. J Mol Cell Cardiol. 2006 Dec;41(6):963-71. doi: 10.1016/j.yjmcc.2006.07.017. Epub 2006 Sep 11. J Mol Cell Cardiol. 2006. PMID: 16963078
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: kim js. 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.
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