Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Blachut, Susanne (1) Hübner, Norbert Prof. Dr. (6) Hummel, Oliver (1) Jentsch, Thomas Prof. Dr. (1) Kirchner, Marieluise Dr. (1) Lee, Young-Ae Prof. Dr. (19) Lisewski, Ulrike Dr. (1) Lopez Carballo, Jacobo (1) Luft, Friedrich Prof. Dr. (1) Marenholz, Ingo Dr. (11) Mertins, Philipp Dr. (1) Patone, Giannino Dr. (2) Radke, Michael Dr. (3) Sander, Maike Prof. Dr. (13) (-) Gotthardt, Michael Prof. Dr. (13) (-) Saar, Kathrin Dr. (2) AG Müller/Dechend (ECRC) (5) Animal Phenotyping (3) Genetik und Genomik von Herz- Kreislauferkrankungen (29) Hochschulambulanz für Pädiatrische Allergologie und Neurodermitis (7) Hypertonie-vermittelter Endorganschaden (5) Hypertonie bedingte Endorganschäden (5) Kardiale MRT (1) Molekularbiologie von Hormonen im Herz-Kreislaufssystem (1) (-) Molekulare Genetik allergischer Erkrankungen (7) (-) Pancreatic Organoid Research and Disease Modeling (1) Proteomforschung und molekulare Mechanismen bei neurodegenerativen Erkrankungen (1) Proteomics (1) (-) Translationale Kardiologie und Funktionelle Genomforschung (13) 1994 (1) 1996 (1) 1997 (1) 1998 (1) 1999 (1) 2000 (6) (-) 2001 (2) 2002 (3) 2003 (3) 2004 (2) 2005 (3) 2006 (3) 2007 (6) 2008 (5) (-) 2009 (8) 2010 (3) 2011 (4) 2012 (1) (-) 2013 (4) 2014 (6) 2015 (6) 2016 (2) 2017 (4) 2018 (7) 2019 (8) (-) 2020 (7) 2021 (7) 2022 (5) 2023 (8) 2024 (3) 21 Ergebnisse: Active Filter: Gotthardt, Michael Prof. Dr.Saar, Kathrin Dr.Molekulare Genetik allergischer Erkrankungen Pancreatic Organoid Research and Disease ModelingTranslationale Kardiologie und Funktionelle Genomforschung2001200920132020 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 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 01. Februar 2013 / Hypertension Loss of epidermal growth factor receptor in vascular smooth muscle cells and cardiomyocytes causes arterial hypotension and cardiac hypertrophy B. Schreier S. Rabe B. Schneider M. Bretschneider S. Rupp S. Ruhs J. Neumann U. Rueckschloss M. Sibilia M. Gotthardt C. Grossmann M. Gekle 01. Juli 2013 / Arch Biochem Biophys Calcium sensitivity and myofilament lattice structure in titin N2B KO mice E.J. Lee J. Nedrud P. Schemmel M. Gotthardt T.C. Irving H.L. Granzier 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 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 19. Juni 2020 / Nat Commun Deconstructing sarcomeric structure-function relations in titin-BioID knock-in mice F. Rudolph C. Fink J. Hüttemeister M. Kirchner M.H. Radke J. Lopez Carballo E. Wagner T. Kohl S.E. Lehnart P. Mertins M. Gotthardt 30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman 03. August 2020 / eLife A human ESC-based screen identifies a role for the translated lncRNA LINC00261 in pancreatic endocrine differentiation B. Gaertner S. van Heesch V. Schneider-Lunitz J.F. Schulz F. Witte S. Blachut S. Nguyen R. Wong I. Matta N. Hübner M. Sander 08. September 2020 / Cell Rep iPSC modeling of RBM20-deficient DCM identifies upregulation of RBM20 as a therapeutic strategy F. Briganti H. Sun W. Wei J. Wu C. Zhu M. Liss I. Karakikes S. Rego A. Cipriano M. Snyder B. Meder Z. Xu G. Millat M. Gotthardt M. Mercola L.M. Steinmetz Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
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
01. Februar 2013 / Hypertension Loss of epidermal growth factor receptor in vascular smooth muscle cells and cardiomyocytes causes arterial hypotension and cardiac hypertrophy B. Schreier S. Rabe B. Schneider M. Bretschneider S. Rupp S. Ruhs J. Neumann U. Rueckschloss M. Sibilia M. Gotthardt C. Grossmann M. Gekle
01. Juli 2013 / Arch Biochem Biophys Calcium sensitivity and myofilament lattice structure in titin N2B KO mice E.J. Lee J. Nedrud P. Schemmel M. Gotthardt T.C. Irving H.L. Granzier
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
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
19. Juni 2020 / Nat Commun Deconstructing sarcomeric structure-function relations in titin-BioID knock-in mice F. Rudolph C. Fink J. Hüttemeister M. Kirchner M.H. Radke J. Lopez Carballo E. Wagner T. Kohl S.E. Lehnart P. Mertins M. Gotthardt
30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman
03. August 2020 / eLife A human ESC-based screen identifies a role for the translated lncRNA LINC00261 in pancreatic endocrine differentiation B. Gaertner S. van Heesch V. Schneider-Lunitz J.F. Schulz F. Witte S. Blachut S. Nguyen R. Wong I. Matta N. Hübner M. Sander
08. September 2020 / Cell Rep iPSC modeling of RBM20-deficient DCM identifies upregulation of RBM20 as a therapeutic strategy F. Briganti H. Sun W. Wei J. Wu C. Zhu M. Liss I. Karakikes S. Rego A. Cipriano M. Snyder B. Meder Z. Xu G. Millat M. Gotthardt M. Mercola L.M. Steinmetz