Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Alenina, Natalia Dr. (172) Bader, Michael Prof. Dr. (681) Bähring, Sylvia Dr. (4) Bartels-Klein, Eireen (1) Bartolomaeus, Hendrik (1) Bartolomaeus, Theda (4) Birchmeier-Kohler, Carmen Prof. Dr. (2) Borodina, Tatiana Dr. (2) Castilho de Barros, Carlos Prof. Dr. (6) Chen, Chia-Yu (1) Chen, Wei Prof. Dr. (2) Dechend, Ralf Priv. Doz. (24) Diecke, Sebastian Dr. (1) Escobar Fernandez, Helena Dr. (1) Fielitz, Jens Dr. (4) Forslund, Sofia Dr. (4) Fritsche, Raphaela Dr. (1) Geisberger, Sabrina Yasmin Dr. (1) Gösele, Claudia Dr. (1) Haase, Nadine Dr. (10) Heinemann, Udo Prof. Dr. (2) Herse, Florian PD Dr. (8) Heuser, Arnd Dr. (12) Hinze, Christian Dr. med. Dipl.-Math. (1) Hodge, Russell (4) Hollfinger, Irene (1) Hübner, Norbert Prof. Dr. (8) Hummel, Oliver (1) Infante Duarte, Carmen (1) Ivics, Zoltan Dr. (1) Izsvak, Zsuzsanna Dr. (1) Janke, Jürgen Dr. (1) Jarosch, Ernst Dr. (1) Jentsch, Thomas Prof. Dr. (1) Kamer, Ilona (2) Kempa, Stefan Dr. (1) Kettenmann, Helmut Prof. Dr. (3) Kettritz, Ralph Prof. Dr. (1) Kirwan, Jennifer Dr. (1) Klaassen, Sabine Prof. Dr. med. 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(2) Willnow, Thomas Prof. Dr. (3) Wolf, Susanne Dr. (1) Zühlke, Kerstin Dr. (2) (-) Marg, Andreas Dr. (1) 2015 (1) 2018 (1) Advanced Light Microscopy (2) AG Müller/Dechend (ECRC) (2) AG Schreiber [ECRC] (1) Anchored Signalling (1) Animal Phenotyping (1) Bioinformatics and Omics Data Science (2) Cancer Genetics and Cellular Stress Responses (1) Computational Regulatory Genomics (1) Developmental Biology / Signal Transduction (6) Developmental Neurobiology (2) Electron Microscopy (1) Endocrinology, Diabetes and Nutritional Medicine (1) Epigenetic Modifications in Neuroblastoma (1) Genetics and Genomics of Cardiovascular Diseases (85) Genetics of Congenital Heart Disease (1) Genome Diversification & Integrity (5) Genome Engineering & Disease Models (1) Genomics (3) Hypertension-caused End-Organ Damage (2) Hypertension-Mediated End-Organ Damage (2) In Situ Structural Biology (1) Integrative Vascular Biology (1) Mathematical Cell Physiology (3) Mathematical Modelling of Cellular Processes (1) Mobile DNA (3) (-) Molecular Biology of Peptide Hormones (2) Molecular Cardiovascular Research (2) Molecular Genetics of Chronic Inflammation and Allergic Disease (23) Molecular Physiology of Somatic Sensation (2) Myology (17) Nephrology and Inflammatory Vascular Diseases (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (2) Organoids (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (23) Pluripotent Stem Cells (2) Proteome Dynamics (11) Proteomics (34) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Quantitative Developmental Biology (3) RNA Biology and Posttranscriptional Regulation (3) Stem Cell Modeling of Development and Disease (1) Structural Biology of Membrane-Associated Processes (7) Synaptic Transmission and Plasticity (1) Systems Biology of Gene Regulatory Elements (5) Transgenics (1) Translational Bioinformatics (4) Translational Cardiology and Functional Genomics (6) Tumor heterogeneity and treatment resistance in pediatric cancer (1) 2 Results: Active Filter: Marg, Andreas Dr.Molecular Biology of Peptide Hormones Sort: Result score Newest to oldest Oldest to newest December 07, 2018 / Mol Ther Nucleic Acids Exon skipping in a Dysf-missense mutant mouse model J. Malcher L. Heidt A. Goyenvalle H. Escobar A. Marg C. Beley R. Benchaouir M. Bader S. Spuler L. García V. Schöwel June 01, 2015 / Nat Genet PDE3A mutations cause autosomal dominant hypertension with brachydactyly P.G. Maass A. Aydin F.C. Luft C. Schächterle A. Weise S. Stricker C. Lindschau M. Vaegler F. Qadri H.R. Toka H. Schulz P.M. Krawitz D. Parkhomchuk J. Hecht I. Hollfinger Y. Wefeld-Neuenfeld E. Bartels-Klein A. Mühl M. Kann H. Schuster D. Chitayat M.G. Bialer T.F. Wienker J. Ott K. Rittscher T. Liehr J. Jordan G. Plessis J. Tank K. Mai R. Naraghi R. Hodge M. Hopp L.O. Hattenbach A. Busjahn A. Rauch F. Vandeput M. Gong F. Rüschendorf N. Hübner H. Haller S. Mundlos N. Bilginturan M.A. Movsesian E. Klussmann O. Toka S. Bähring
December 07, 2018 / Mol Ther Nucleic Acids Exon skipping in a Dysf-missense mutant mouse model J. Malcher L. Heidt A. Goyenvalle H. Escobar A. Marg C. Beley R. Benchaouir M. Bader S. Spuler L. García V. Schöwel
June 01, 2015 / Nat Genet PDE3A mutations cause autosomal dominant hypertension with brachydactyly P.G. Maass A. Aydin F.C. Luft C. Schächterle A. Weise S. Stricker C. Lindschau M. Vaegler F. Qadri H.R. Toka H. Schulz P.M. Krawitz D. Parkhomchuk J. Hecht I. Hollfinger Y. Wefeld-Neuenfeld E. Bartels-Klein A. Mühl M. Kann H. Schuster D. Chitayat M.G. Bialer T.F. Wienker J. Ott K. Rittscher T. Liehr J. Jordan G. Plessis J. Tank K. Mai R. Naraghi R. Hodge M. Hopp L.O. Hattenbach A. Busjahn A. Rauch F. Vandeput M. Gong F. Rüschendorf N. Hübner H. Haller S. Mundlos N. Bilginturan M.A. Movsesian E. Klussmann O. Toka S. Bähring