DFG-Forschergruppe
 

"Keratinocyten - Proliferation
und differenzierte Leistung in der Epidermis"

Publikationen

Der Arbeitsgruppe Willecke
seit 01.01.2000

  1. Plum, A., Hallas, G., and Willecke, K. 2002. Expression of the mouse connexin31 gene is regulated by distinct mechanisms in embryonic stem cells and keratinocytes, Genomics 79: 24-30.
  1. Theis, M., Mas, C., Döring, B., Krüger, O., Herrera, P., Meda, P., and Willecke, K. 2001. General and conditional replacement of connexin43 coding DNA by a LacZ reporter gene for cell autonomous analysis of expression, Cell Communication and Adhesion 8: 383-386.
  1. Contreras, J.E., Sánchez, H., Eugenin, E.A., Speidel, D., Theis, M., Willecke, K., Bukauskas, F.F., Bennett, M.V.L., and Sáez, J.C. 2002. Metabolic inhibition induces opening of unapposed connexin43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture. Proc. Nat. Acad. Sci., USA, 99: 495-500.
  1. Romualdi, A., Niessen, H., Dombrowski, F., Willecke, K., and Ott, T. 2002. Quantitative analysis of gap junctional intercellular communication in precision cut liver slices. Cell and Tissue Res., 307: 315-320.
  1. Willecke, K., Eiberger, J., Degen, J., Eckardt D., Romualdi, A., Güldenagel, M., Deutsch, U., and Söhl, G. 2002. Structural and functional diversity of connexin genes in the human and mouse genome. Biol. Chem. 383:725-737.
  1. Krüger, O., Beny, J.L., Charbaud, F., Traub, O., Brix, K., Kirchhoff, S., and Willecke, K. 2002. Altered dye diffusion and upregulation of connexin37 in mouse aortic endothelium deficient in connexin40, J. Vascular Res., 39:160-172.
  1. Cohen-Salmon, M., Ott, T., Michel, V., Hardelin, J.-P., Perfettini, I., Eybalin, M., Wu, T., Marcus, D. C., Wangemann, P., Willecke, K., Petit, C. 2002. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment with cell death, Current Biology, 12:1106-1111.
  1. Evert, M., Ott, T., Temme, A., Willecke, K., and Dombrowski, F. 2002. Hepatocellular preneoplastic lesions and neoplasms in connexin32 deficient mice, Carcinogenesis 23: 697-703.
  1. Thönnissen, E., Rabionet, R., Arbonès, M.L., Estivill, X., Willecke, K., and Ott, T. 2002. Human connexin26 deafness mutations affect the function of gap junction channels at different levels of protein expression. Human Genetics 111: 190-197.
  1. Teubner, B., Michel, V., Pesch, J., Lautermann, J., Cohen-Salmon, M., Söhl, G., Jahnke, K., Winterhager, E., Herberhold, C., Hardelin, J.-P., Petit, C., and Willecke, K. 2003. Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential, Human Mol. Genetics 12: 13-21
  1. Kretz, M., Euwens, C., Hombach, S., Eckardt, D., Teubner, B., Traub, O., Willecke, K., and Ott, T. 2003. Altered connexin expression and wound healing in the epidermis of connexin deficient mice, submitted for publication.
Uni-Bonn Biologie Zellbiologie BFB DFG-Forschergruppe
Verantwortlich: Impressum
Zuletzt bearbeitet: Dienstag, 9. März 2004 von K. Hedemann