Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Akalin, Altuna Dr. (14) Alenina, Natalia Dr. (25) Alp, Keziban Merve (1) Altmueller, Janine Dr.med. (24) Annibale, Paolo Dr. (7) Bader, Michael Prof. Dr. (101) Bähring, Sylvia Dr. (4) Bartolomaeus, Hendrik (4) Bartolomaeus, Theda (3) Bayram, Safak (1) Begay-Müller, Valerie Dr. (2) Bernert, Carola (1) Berruezo Llacuna, Maria (1) Beule, Dieter Dr. (16) Birchmeier, Walter Prof. Dr. (23) Birchmeier-Kohler, Carmen Prof. Dr. (31) Birol, Melissa Dr. (1) Blachut, Susanne (1) Blankenstein, Thomas Prof. Dr. (13) Blüthgen, Nils (2) Bock-Bierbaum, Tobias Dr. (2) Braeuning, Caroline (1) Bunina, Daria Dr. (2) Bunse, Mario Dr. (1) Burkert, Christian Martin (1) Castilho de Barros, Carlos Prof. Dr. (2) Chakrabarti, Sampurna Dr. (1) Chekulaeva, Marina Dr. (3) Chen, Wei Prof. Dr. (21) Chu, Van Trung Dr. (3) Cöl Arslan, Seda Dr. (3) Collins, Russell Thomas Dr. (1) Conrad, Thomas Dr. (2) Coscia, Fabian Dr. (3) Dahlmann, Mathias Dr. (4) Dang Ngoc, Tu Dr. (1) Daniel, Peter Prof. Dr. (16) Daumke, Oliver Prof. Dr. (14) Dechend, Ralf Priv. Doz. 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(10) Schulz-Menger, Jeanette Prof. Dr. (42) Schütz, Anja Dr. (7) Schwarz, Roland Dr. (10) Selbach, Matthias Prof. Dr. (19) Semtner, Marcus Dr. (3) Serresi, Michela Dr. (1) Siffrin, Volker (7) Sigal, Michael Dr. (3) Simon, Katja Prof. Dr. (6) Simon, Mareike Dr. (1) Singh, Manvendra Dr. (3) Smith, Janice (4) Sommer, Thomas Prof. Dr. (10) Spagnoli, Francesca Dr. (5) Spanjaard, Bastiaan Dr. (1) Spatt, Lisa (1) Specker, Edgar Dr. (1) Sperling, Silke Prof. Dr. (5) Sporbert, Anje Dr. (3) Spuler, Simone Prof. (17) Starke, Ludger Benedikt (2) Stein, Ulrike Prof. Dr. (29) Sugimoto, Yoichiro Dr. (3) Sunaga-Franze, Daniele Yumi Dr. (3) Taube, Martin (1) Telugu, Narasimha Swamy Dr. (5) Todiras, Mihail (11) Toscano, Elisa (1) Treier, Mathias Prof. Dr. (3) Trombke, Janine (1) Tsybulskyi, Volodymyr (1) Tursun, Baris Dr. (7) Uckert, Wolfgang Prof. Dr. (9) Udhayachandran, Annapoorani Dr. (1) Uyar, Bora Dr. (1) Vidal, Marie Dr. (1) Volkwein, Corinna (1) von Kries, Jens Peter Dr. (4) Waiczies, Helmar Dr. (8) Waiczies, Sonia PD Dr. (11) Wallukat, Gerd Dr. (18) Walther, Wolfgang Prof. Dr. (17) Wanker, Erich Prof. Dr. (31) Welke, Robert-William (1) Wellner, Maren Dr. (2) Wenzel, Katrin Dr. (3) Wilck, Nicola Dr. med. 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Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali 23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit 09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck 13. Februar 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke 05. November 2020 / JCI Insight Transient enlargement of brain ventricles during relapsing-remitting multiple sclerosis and experimental autoimmune encephalomyelitis J.M. Millward P.R. Delgado A. Smorodchenko L. Boehmert J. Periquito H.M. Reimann C. Prinz A. Els M. Scheel J. Bellmann-Strobl H. Waiczies J. Wuerfel C. Infante-Duarte C. Chien J. Kuchling A. Pohlmann F. Zipp F. Paul T. Niendorf S. Waiczies 02. November 2020 / Sci Rep Assessment of nanoindentation in stiffness measurement of soft biomaterials: kidney, liver, spleen and uterus G. Wu M. Gotthardt M. Gollasch 11. November 2020 / Genes Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families J. Doll B. Vona L. Schnapp F. Rüschendorf I. Khan S. Khan N. Muhammad S. Alam Khan H. Nawaz A. Khan N. Ahmad S.M. Kolb L. Kühlewein J.D.J. Labonne L.C. Layman M.A.H. Hofrichter T. Röder M. Dittrich T. Müller T.D. Graves I.K. Kong I. Nanda H.G. Kim T. Haaf 19. Mai 2020 / Cells Concerted EP2 and EP4 receptor signaling stimulates autocrine prostaglandin E(2) activation in human podocytes E. Mangelsen M. Rothe A. Schulz A. Kourpa D. Panáková R. Kreutz J. Bolbrinker 29. Mai 2020 / Front Physiol Deleting titin's C-terminal PEVK exons increases passive stiffness, alters splicing, and induces cross-sectional and longitudinal hypertrophy in skeletal muscle R.J. van der Pijl B. Hudson T. Granzier-Nakajima F. Li A.M. Knottnerus J. Smith C.S. Chung M. Gotthardt H.L. Granzier C.A.C. Ottenheijm Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit
09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck
13. Februar 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke
05. November 2020 / JCI Insight Transient enlargement of brain ventricles during relapsing-remitting multiple sclerosis and experimental autoimmune encephalomyelitis J.M. Millward P.R. Delgado A. Smorodchenko L. Boehmert J. Periquito H.M. Reimann C. Prinz A. Els M. Scheel J. Bellmann-Strobl H. Waiczies J. Wuerfel C. Infante-Duarte C. Chien J. Kuchling A. Pohlmann F. Zipp F. Paul T. Niendorf S. Waiczies
02. November 2020 / Sci Rep Assessment of nanoindentation in stiffness measurement of soft biomaterials: kidney, liver, spleen and uterus G. Wu M. Gotthardt M. Gollasch
11. November 2020 / Genes Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families J. Doll B. Vona L. Schnapp F. Rüschendorf I. Khan S. Khan N. Muhammad S. Alam Khan H. Nawaz A. Khan N. Ahmad S.M. Kolb L. Kühlewein J.D.J. Labonne L.C. Layman M.A.H. Hofrichter T. Röder M. Dittrich T. Müller T.D. Graves I.K. Kong I. Nanda H.G. Kim T. Haaf
19. Mai 2020 / Cells Concerted EP2 and EP4 receptor signaling stimulates autocrine prostaglandin E(2) activation in human podocytes E. Mangelsen M. Rothe A. Schulz A. Kourpa D. Panáková R. Kreutz J. Bolbrinker
29. Mai 2020 / Front Physiol Deleting titin's C-terminal PEVK exons increases passive stiffness, alters splicing, and induces cross-sectional and longitudinal hypertrophy in skeletal muscle R.J. van der Pijl B. Hudson T. Granzier-Nakajima F. Li A.M. Knottnerus J. Smith C.S. Chung M. Gotthardt H.L. Granzier C.A.C. Ottenheijm