Willecke K - Search Results

1

From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.

García IE, Bosen F, Mujica P, Pupo A, Flores-Muñoz C, Jara O, González C, Willecke K, Martínez AD. García IE, et al. Among authors: willecke k. J Invest Dermatol. 2016 Mar;136(3):574-583. doi: 10.1016/j.jid.2015.11.017. Epub 2016 Jan 8. J Invest Dermatol. 2016. PMID: 26777423 Free article. Review.

2

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome.

Schütz M, Auth T, Gehrt A, Bosen F, Körber I, Strenzke N, Moser T, Willecke K. Schütz M, et al. Among authors: willecke k. Hum Mol Genet. 2011 Jan 1;20(1):28-39. doi: 10.1093/hmg/ddq429. Epub 2010 Oct 6. Hum Mol Genet. 2011. PMID: 20926451

3

The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in mice.

Bosen F, Schütz M, Beinhauer A, Strenzke N, Franz T, Willecke K. Bosen F, et al. Among authors: willecke k. FEBS Lett. 2014 May 2;588(9):1795-801. doi: 10.1016/j.febslet.2014.03.040. Epub 2014 Mar 29. FEBS Lett. 2014. PMID: 24685692 Free article.

4

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

5

Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F.

Bosen F, Celli A, Crumrine D, vom Dorp K, Ebel P, Jastrow H, Dörmann P, Winterhager E, Mauro T, Willecke K. Bosen F, et al. Among authors: willecke k. FEBS Lett. 2015 Jul 8;589(15):1904-10. doi: 10.1016/j.febslet.2015.05.047. Epub 2015 Jun 9. FEBS Lett. 2015. PMID: 26070424 Free PMC article.

6

Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.

Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW. Press E, et al. Among authors: willecke k. Cell Death Dis. 2017 Jun 1;8(6):e2845. doi: 10.1038/cddis.2017.234. Cell Death Dis. 2017. PMID: 28569788 Free PMC article.

7

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: willecke k. 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

8

Abrogation of Gap Junctional Communication in ES Cells Results in a Disruption of Primitive Endoderm Formation in Embryoid Bodies.

Wörsdörfer P, Bosen F, Gebhardt M, Russ N, Zimmermann K, Komla Kessie D, Sekaran T, Egert A, Ergün S, Schorle H, Pfeifer A, Edenhofer F, Willecke K. Wörsdörfer P, et al. Among authors: willecke k. Stem Cells. 2017 Apr;35(4):859-871. doi: 10.1002/stem.2545. Epub 2016 Dec 20. Stem Cells. 2017. PMID: 27870307

9

Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.

Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW. Press E, et al. Among authors: willecke k. Cell Death Dis. 2018 May 24;9(6):630. doi: 10.1038/s41419-018-0639-1. Cell Death Dis. 2018. PMID: 29795380 Free PMC article.

10

Connexin32 can restore hearing in connexin26 deficient mice.

Degen J, Schütz M, Dicke N, Strenzke N, Jokwitz M, Moser T, Willecke K. Degen J, et al. Among authors: willecke k. Eur J Cell Biol. 2011 Oct;90(10):817-24. doi: 10.1016/j.ejcb.2011.05.001. Epub 2011 Aug 2. Eur J Cell Biol. 2011. PMID: 21813206

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