Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (4) Bähring, Sylvia Dr. (1) Birchmeier, Walter Prof. Dr. (1) Gotthardt, Michael Prof. Dr. (1) Hübner, Norbert Prof. Dr. (13) Hummel, Oliver (1) Klaassen, Sabine Prof. Dr. med. (1) Klaus-Bergmann, Alexandra Dr. (1) Lee, Young-Ae Prof. Dr. (4) Lewin, Gary Prof. Dr. (1) Luft, Friedrich Prof. Dr. (1) Maatz, Henrike Dr. (1) Marenholz, Ingo Dr. (1) Müller, Marion (1) Perrot, Andreas (1) Radke, Michael Dr. (1) Saar, Kathrin Dr. (5) Schiattarella, Gabriele G. 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Lee N. Hübner D. Ganten September 12, 1995 / Proc Natl Acad Sci U S A Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10 R. Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten February 01, 2012 / FASEB J Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells J. Grosse M. Wehland J. Pietsch X. Ma C. Ulbrich H. Schulz K. Saar N. Huebner J. Hauslage R. Hemmersbach M. Braun J. van Loon N. Vagt M. Infanger C. Eilles M. Egli P. Richter T. Baltz R. Einspanier S. Sharbati D. Grimm December 15, 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 September 01, 2012 / Stem Cells Dev Gene expression signatures defining fundamental biological processes in pluripotent, early, and late differentiated embryonic stem cells J.A. Gaspar M.X. Doss J. Winkler V. Wagh J. Hescheler R. Kolde J. Vilo H. Schulz A. Sachinidis February 10, 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 Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
September 12, 1995 / Proc Natl Acad Sci U S A Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10 R. Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner
January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner
January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner
November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner
January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten
February 01, 2012 / FASEB J Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells J. Grosse M. Wehland J. Pietsch X. Ma C. Ulbrich H. Schulz K. Saar N. Huebner J. Hauslage R. Hemmersbach M. Braun J. van Loon N. Vagt M. Infanger C. Eilles M. Egli P. Richter T. Baltz R. Einspanier S. Sharbati D. Grimm
December 15, 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
September 01, 2012 / Stem Cells Dev Gene expression signatures defining fundamental biological processes in pluripotent, early, and late differentiated embryonic stem cells J.A. Gaspar M.X. Doss J. Winkler V. Wagh J. Hescheler R. Kolde J. Vilo H. Schulz A. Sachinidis
February 10, 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