Willecke K - Search Results

1

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: willecke k. 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.

2

The connexin31 F137L mutant mouse as a model for the human skin disease erythrokeratodermia variabilis (EKV).

Schnichels M, Wörsdörfer P, Dobrowolski R, Markopoulos C, Kretz M, Schwarz G, Winterhager E, Willecke K. Schnichels M, et al. Among authors: willecke k. Hum Mol Genet. 2007 May 15;16(10):1216-24. doi: 10.1093/hmg/ddm068. Epub 2007 Apr 19. Hum Mol Genet. 2007. PMID: 17446259

3

Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels.

Dobrowolski R, Sommershof A, Willecke K. Dobrowolski R, et al. Among authors: willecke k. J Membr Biol. 2007 Oct;219(1-3):9-17. doi: 10.1007/s00232-007-9055-7. Epub 2007 Aug 9. J Membr Biol. 2007. PMID: 17687502

4

Connexin-caused genetic diseases and corresponding mouse models.

Dobrowolski R, Willecke K. Dobrowolski R, et al. Among authors: willecke k. Antioxid Redox Signal. 2009 Feb;11(2):283-95. doi: 10.1089/ars.2008.2128. Antioxid Redox Signal. 2009. PMID: 18831677 Review.

5

Human Connexin43E42K mutation from a sudden infant death victim leads to impaired ventricular activation and neonatal death in mice.

Lübkemeier I, Bosen F, Kim JS, Sasse P, Malan D, Fleischmann BK, Willecke K. Lübkemeier I, et al. Among authors: willecke k. Circ Cardiovasc Genet. 2015 Feb;8(1):21-9. doi: 10.1161/CIRCGENETICS.114.000793. Epub 2014 Dec 10. Circ Cardiovasc Genet. 2015. PMID: 25504652

6

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: willecke k. 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.

7

Functional properties of mouse connexin30.2 expressed in the conduction system of the heart.

Kreuzberg MM, Söhl G, Kim JS, Verselis VK, Willecke K, Bukauskas FF. Kreuzberg MM, et al. Among authors: willecke k. Circ Res. 2005 Jun 10;96(11):1169-77. doi: 10.1161/01.RES.0000169271.33675.05. Epub 2005 May 5. Circ Res. 2005. PMID: 15879306 Free PMC article.

8

Connexin30.2 containing gap junction channels decelerate impulse propagation through the atrioventricular node.

Kreuzberg MM, Schrickel JW, Ghanem A, Kim JS, Degen J, Janssen-Bienhold U, Lewalter T, Tiemann K, Willecke K. Kreuzberg MM, et al. Among authors: willecke k. Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5959-64. doi: 10.1073/pnas.0508512103. Epub 2006 Mar 29. Proc Natl Acad Sci U S A. 2006. PMID: 16571663 Free PMC article.

9

Cardiac morphogenetic defects and conduction abnormalities in mice homozygously deficient for connexin40 and heterozygously deficient for connexin45.

Krüger O, Maxeiner S, Kim JS, van Rijen HV, de Bakker JM, Eckardt D, Tiemann K, Lewalter T, Ghanem A, Lüderitz B, Willecke K. Krüger O, et al. Among authors: willecke k. J Mol Cell Cardiol. 2006 Nov;41(5):787-97. doi: 10.1016/j.yjmcc.2006.07.005. Epub 2006 Aug 17. J Mol Cell Cardiol. 2006. PMID: 16919680

10

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: willecke k. 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

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