Zobrazeno 1 - 10
of 92
pro vyhledávání: '"W. Bardenheuer"'
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 132:154-163
Autor:
W. Bardenheuer, U.R. Hengge
Publikováno v:
American Journal of Medical Genetics. :93-100
Significant progress has been made during the past decade in corrective gene therapy of the skin. This includes advances in vector technology, targeted gene expression, gene replacement, gene correction, and the availability of appropriate animal mod
Publikováno v:
Journal of stem cellsregenerative medicine. 6(2)
Publikováno v:
TumorDiagnostik & Therapie. 21:51-58
Autor:
S. Michaelis, W Bardenheuer, S. Seeber, R. Siebert, H.-J. Luboldt, A. Lux, B. Opalka, C. Willers, Jochen Schütte
Publikováno v:
British Journal of Urology. 77:524-529
Objective To determine the role of structural alterations of human chromosome region 3p12-p21 in the possible inactivation of one or more tumour-suppressor genes in the pathogenesis of renal cell carcinoma (RCC), lung cancer and other neoplasms. Mate
Publikováno v:
Annales de dermatologie et de venereologie. 132(2)
Autor:
N S, Werner, Z, Siprashvili, L Y, Fong, G, Marquitan, J K, Schröder, W, Bardenheuer, S, Seeber, K, Huebner, J, Schütte, B, Opalka
Publikováno v:
Cancer research. 60(11)
Hemizygous deletions of the fragile histidine triad (FHIT) gene at human chromosome band 3p14.2 and down-regulation of its gene product are found in the majority of renal cell carcinomas (RCCs). Functional tumor suppressive activity of Fhit in renal
Autor:
F, Bröcker, W, Bardenheuer, L, Vieten, K, Jülicher, N, Werner, G, Marquitan, D, Michael, B, Opalka, J, Schütte
Publikováno v:
Cytogenetics and cell genetics. 85(3-4)
Autor:
O. Bartsch, M. Vaiman, M.R. Matarazzo, M.P. Hande, L. Vieten, P. Marynen, T.D. Bunch, A.A. Bosma, R.A. Veitia, Marijo Kent-First, J.E. Womack, H. Aburatani, C.R. Lopes, A. Törnsten, H. Kusakabe, P.D. Pearce, N. Tanaka, A. Gelhaus, A. Wagner, H.E. McDermid, G.V.N. Velagaleti, M. Hirai, F. Apiou, P.R. Martens, C. Rogel-Gaillard, T. Ishida, N. Bourgeaux, C. Ottolenghi, L.J. Peelman, H.A. Ansari, M. Svelto, T. Antonevich, Giovanna Grimaldi, M.F. Rothschild, M. Yerle, K. Hashimoto, T. Takahashi, Y. Nakahori, R. Taneja, L. Blottière, Y. Koshizuka, M. Horie, G. Gupta, Y. Itoh, J. Schütte, W. Kreß, C.K. Tuggle, H. Hameister, K. Kikuchi, Mariano Rocchi, J.-C. Amé, P. Chardon, M. Isomura, T. Goldammer, M. Kinebuchi, I. Dunham, A. Aventin, M.D. Bishop, J. Kusuda, N. Werner, D.W. Maher, P. Laurent, P. Slijepcevic, J.M. Perez de la Lastra, T.E. Broad, Y. Hippo, D. Ferbus, D. Beare, D. Michael, G. Goubin, M.R.V. Amarante, H. Hayes, S.A. Tharapel, N. Sato, M.-T. Prospéri, B.P. Chowdhary, R.C. Michaelis, R.S. Danziger, F. Bröcker, A. Billault, A. Eggen, K. Jülicher, K. Kasai, J. Vanselow, M.-C. Bissery, M. Mattheeuws, R.D. Horstmann, M. Rosati, N.K. Rushmere, R. Hong, S. Ikegawa, B.S. Klein, B.P. Morgan, R.S. Wilroy, G. Calamita, M. Hirata, M. Bishop, A. Matsuura, M. Heß, K.E. Teague, C. Spalluto, R. Tanuma, R.M. Schmid, J. Sohal, Annamaria Franzè, A. van Zeveren, A. Zsolnai, T. Kodama, J.F. Taylor, A. Fellous, H. Levéziel, A.T. Tharapel, E.L. Jacobson, B. Dutrillaux, D.B. Zimonjic, D.S. Gallagher, P. Peeters, S.K. Davis, S.E. Long, I. Matsushita, A. Malterer, E. Seemanova, A. Mazzone, S. Liptay, B. Grandchamp, M. Schwerin, S. Nishimura, G. Rappold, M.K. Jacobson, J.D. Burzlaff, P.D. Buchanan, Y. Nakamura, B. Opalka, W. Bardenheuer, M. Vozdová, M.C. Yoshida, T. Voet, M. Van Poucke, R. Fürbass, J.T. Woitach, V. Trichet, C. Mecucci, K. Ried, K. Yamada, N.C. Popescu, A. Chase, P. Pinton, R.M. Brunner, C.L. Keck, C. Guenzi, D. Shkolny, S.S. Thorgeirsson, S. Kubíčková, J. Cools, N.C.P. Cross, J.M. Goldman, C.W. Ernst, G. Marquitan, J. Rubeš, H.-F.S. Sun, C.P. Popescu, C.H. Laundon
Publikováno v:
Cytogenetic and Genome Research. 85:327-328
Autor:
D. Michael, K Jülicher, G Marquitan, Frank Bröcker, W Bardenheuer, Bertram Opalka, Lydia Vieten, N Werner, Jochen Schütte
Publikováno v:
Cytogenetic and Genome Research. 85:267-268