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(32) Perrot, Andreas (10) Pezzutto, Antonio Prof. Dr. (8) Pilz, Bernhard Dr. (1) Pischon, Tobias Prof. Dr. (29) Pombo, Ana Prof. Dr. (14) Popova, Elena Dr. (2) Potente, Michael Prof. Dr. (4) Poulet, James Prof. Dr. (3) Preibisch, Stephan Dr. (9) Prigione, Alessandro Prof. Dr. (9) Qadri, Fatimunnisa Dr. (6) Quedenau, Claudia (1) Räbel, Katrin (1) Rademann, Joerg Prof. Dr. (3) Radke, Michael Dr. (2) Rahn, Hans-Peter Dr. (2) Rajewsky, Klaus Prof. Dr. (7) Rajewsky, Nikolaus Prof. Dr. (10) Rathjen, Fritz Prof. Dr. (5) Rehm, Armin Dr. (3) Rocks, Oliver Dr. (3) Rosenthal, Walter Prof. Dr. (4) Roske, Yvette Dr. (5) Rother, Franziska Dr. (1) Rousselle, Anthony (1) Rybak-Wolf, Agnieszka Dr. (3) Saar, Kathrin Dr. (9) Sander, Maike Prof. Dr. (7) Sanders, Ashley Dr. (1) Sawamiphak, Suphansa Dr. (2) Schäfer, Gesa Dr. (1) Scheidereit, Claus Prof. Dr. (2) Schiattarella, Gabriele G. Dr. (10) Schlag, Peter M. Prof. Dr. (35) Schmidt, Sabine (1) Schmidt-Krüger, Vanessa Dr. (6) Schmidt-Ullrich, Ruth Dr. (3) Schmitt, Clemens Prof. Dr. (6) Schnögl, Sigrid (2) Schreiber, Adrian PD Dr. med. 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Dezember 2012 / OncoImmunology HER2/neu DNA vaccination by intradermal gene delivery in a mouse tumor model: gene gun is superior to jet injector in inducing CTL responses and protective immunity T. Nguyen-Hoai D. Kobelt O. Hohn M.D. Vu P.M. Schlag B. Doerken S. Norley M. Lipp W. Walther A. Pezzutto J. Westermann 15. Dezember 2012 / Hum Mol Genet Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 M. Steffens C. Leu A.K. Ruppert F. Zara P. Striano A. Robbiano G. Capovilla P. Tinuper A. Gambardella A. Bianchi A. La Neve G. Crichiutti C.G.F. de Kovel D. Kasteleijn-Nolst Trenite G.J. de Haan D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche B.J. Steinhoff A.A. Kleefuss-Lie W.S. Kunz R. Surges C.E. Elger H. Muhle S. von Spiczak P. Ostertag I. Helbig U. Stephani R.S. Moller H. Hjalgrim L.M. Dibbens S. Bellows K. Oliver S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren M. Guipponi A. Malafosse P. Thomas R. Nabbout S. Baulac E. Leguern R. Guerrero J.M. Serratosa P.S. Reif F. Rosenow M. Mörzinger M. Feucht F. Zimprich C. Kapser C.J. Schankin A. Suls K. Smets P. De Jonghe A. Jordanova H. Caglayan Z. Yapici D.A. Yalcin B. Baykan N. Bebek U. Ozbek C. Gieger H.E. Wichmann T. Balschun D. Ellinghaus A. Franke C. Meesters T Becker T.F. Wienker A. Hempelmann H. Schulz F. Rueschendorf M. Leber S.M. Pauck H. Trucks M.R. Toliat P. Nuernberg G. Avanzini B.P. Koeleman T. Sander 10. Februar 2012 / Am J Hum Genet Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss M. Baumann C. Giunta B. Krabichler F. Rueschendorf N. Zoppi M. Colombi R.E. Bittner S. Quijano-Roy F. Muntoni S. Cirak G. Schreiber Y. Zou Y. Hu N.B. Romero R.Y. Carlier A. Amberger A. Deutschmann V. Straub M. Rohrbach B. Steinmann K. Rostasy D. Karall C.G. Boennemann J. Zschocke C. Fauth Januar 2010 / J Mol Med MACC1 - more than metastasis? Facts and predictions about a novel gene U. Stein M. Dahlmann W. Walther 01. Dezember 2010 / Biophys J Routes of epithelial water flow: aquaporins versus cotransporters R. Mollajew F. Zocher A. Horner B. Wiesner E. Klussmann P. Pohl 15. Mai 2010 / Biochem J Selective SUMO modification of cAMP-specific phosphodiesterase-4D5 (PDE4D5) regulates the functional consequences of phosphorylation by PKA and ERK X. Li S. Vadrevu A. Dunlop J. Day N. Advant J. Troeger E. Klussmann E. Jaffrey R.T. Hay D.R. Adams M.D. Houslay G.S. Baillie Dezember 2012 / Nephrol Dial Transplant Vasopressin increases S261 phosphorylation in AQP2-P262L, a mutant in recessive nephrogenic diabetes insipidus C. Trimpert D.T.M. van den Berg R.A. Fenton E. Klussmann P.M.T. Deen 01. Dezember 2012 / J Cell Sci A key phosphorylation site in AC8 mediates regulation of Ca2+-dependent cAMP dynamics by an AC8-AKAP79-PKA signalling complex D. Willoughby M.L. Halls K.L. Everett P. Skroblin E. Klussmann D.M.F. Cooper August 2012 / Hum Gene Ther Methods Intratumoral dispersion, retention, systemic biodistribution, and clearance of a small-size tumor necrosis factor-α-expressing MIDGE vector after nonviral in vivo jet-injection gene transfer N. Galling D. Kobelt J. Aumann M. Schmidt B. Wittig P.M. Schlag W. Walther 08. Juni 2012 / Invest Ophthalmol Vis Sci Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy M.N. Preising N. Hausotter-Will M.C. Solbach C. Friedburg F. Rueschendorf B. Lorenz Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 Nächste Seite Next › Letzte Seite Last »
01. Dezember 2012 / OncoImmunology HER2/neu DNA vaccination by intradermal gene delivery in a mouse tumor model: gene gun is superior to jet injector in inducing CTL responses and protective immunity T. Nguyen-Hoai D. Kobelt O. Hohn M.D. Vu P.M. Schlag B. Doerken S. Norley M. Lipp W. Walther A. Pezzutto J. Westermann
15. Dezember 2012 / Hum Mol Genet Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 M. Steffens C. Leu A.K. Ruppert F. Zara P. Striano A. Robbiano G. Capovilla P. Tinuper A. Gambardella A. Bianchi A. La Neve G. Crichiutti C.G.F. de Kovel D. Kasteleijn-Nolst Trenite G.J. de Haan D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche B.J. Steinhoff A.A. Kleefuss-Lie W.S. Kunz R. Surges C.E. Elger H. Muhle S. von Spiczak P. Ostertag I. Helbig U. Stephani R.S. Moller H. Hjalgrim L.M. Dibbens S. Bellows K. Oliver S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren M. Guipponi A. Malafosse P. Thomas R. Nabbout S. Baulac E. Leguern R. Guerrero J.M. Serratosa P.S. Reif F. Rosenow M. Mörzinger M. Feucht F. Zimprich C. Kapser C.J. Schankin A. Suls K. Smets P. De Jonghe A. Jordanova H. Caglayan Z. Yapici D.A. Yalcin B. Baykan N. Bebek U. Ozbek C. Gieger H.E. Wichmann T. Balschun D. Ellinghaus A. Franke C. Meesters T Becker T.F. Wienker A. Hempelmann H. Schulz F. Rueschendorf M. Leber S.M. Pauck H. Trucks M.R. Toliat P. Nuernberg G. Avanzini B.P. Koeleman T. Sander
10. Februar 2012 / Am J Hum Genet Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss M. Baumann C. Giunta B. Krabichler F. Rueschendorf N. Zoppi M. Colombi R.E. Bittner S. Quijano-Roy F. Muntoni S. Cirak G. Schreiber Y. Zou Y. Hu N.B. Romero R.Y. Carlier A. Amberger A. Deutschmann V. Straub M. Rohrbach B. Steinmann K. Rostasy D. Karall C.G. Boennemann J. Zschocke C. Fauth
Januar 2010 / J Mol Med MACC1 - more than metastasis? Facts and predictions about a novel gene U. Stein M. Dahlmann W. Walther
01. Dezember 2010 / Biophys J Routes of epithelial water flow: aquaporins versus cotransporters R. Mollajew F. Zocher A. Horner B. Wiesner E. Klussmann P. Pohl
15. Mai 2010 / Biochem J Selective SUMO modification of cAMP-specific phosphodiesterase-4D5 (PDE4D5) regulates the functional consequences of phosphorylation by PKA and ERK X. Li S. Vadrevu A. Dunlop J. Day N. Advant J. Troeger E. Klussmann E. Jaffrey R.T. Hay D.R. Adams M.D. Houslay G.S. Baillie
Dezember 2012 / Nephrol Dial Transplant Vasopressin increases S261 phosphorylation in AQP2-P262L, a mutant in recessive nephrogenic diabetes insipidus C. Trimpert D.T.M. van den Berg R.A. Fenton E. Klussmann P.M.T. Deen
01. Dezember 2012 / J Cell Sci A key phosphorylation site in AC8 mediates regulation of Ca2+-dependent cAMP dynamics by an AC8-AKAP79-PKA signalling complex D. Willoughby M.L. Halls K.L. Everett P. Skroblin E. Klussmann D.M.F. Cooper
August 2012 / Hum Gene Ther Methods Intratumoral dispersion, retention, systemic biodistribution, and clearance of a small-size tumor necrosis factor-α-expressing MIDGE vector after nonviral in vivo jet-injection gene transfer N. Galling D. Kobelt J. Aumann M. Schmidt B. Wittig P.M. Schlag W. Walther
08. Juni 2012 / Invest Ophthalmol Vis Sci Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy M.N. Preising N. Hausotter-Will M.C. Solbach C. Friedburg F. Rueschendorf B. Lorenz