Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (1) Akalin, Altuna Dr. (1) Bader, Michael Prof. Dr. (2) Beule, Dieter Dr. (1) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Conrad, Thomas Dr. (1) Eisenberger, Alina (1) Fritsche, Raphaela Dr. (1) Gerhardt, Holger Prof. Dr. (1) Gerlach, Kerstin (1) Gösele, Claudia Dr. (1) Gotthardt, Michael Prof. Dr. (6) Greiner, Johannes (1) Hammes-Lewin, Annette Dr. (16) Haucke, Volker Professor (2) Heuser, Arnd Dr. (1) Höpken, Uta Elisabeth PD Dr. (1) Hübner, Norbert Prof. Dr. (5) Juul-Madsen, Kristian Dr. rer. nat. (3) Kalnytska, Oleksandra (2) Kempa, Stefan Dr. (2) Kirchner, Marieluise Dr. (2) Kirwan, Jennifer Dr. (2) Kitt Dr. (1) Ku, Min-Chi Dr. (1) Kühn, Ralf Dr. (1) Kunz, Severine Dr. (1) Lewin, Gary Prof. Dr. (2) Liang, Ning Dr. (1) Lisek, Kamil Dr. (1) Luft, Friedrich Prof. Dr. (4) Lund Ovesen, Peter Dr. (2) Margineanu, Anca Dr. (1) Mastrobuoni, Guido Dr. (1) Mertins, Philipp Dr. (2) Morano, Ingo Prof. Dr. (1) Niendorf, Thoralf Prof. Dr. (1) Popp, Oliver Dr. (3) Poulet, James Prof. Dr. (1) Rajewsky, Nikolaus Prof. Dr. (1) Rehm, Armin Dr. (2) Rudolph, Ina-Maria Dr. (3) Ruiz Orera, Jorge Dr. (1) Schlag, Peter M. Prof. Dr. (1) Schmidt-Krüger, Vanessa Dr. (24) Selbach, Matthias Prof. Dr. (1) Shih, Alexis Zi Le Dr. (1) Siffrin, Volker (1) Spagnoli, Francesca Dr. (1) Sporbert, Anje Dr. (2) Sunaga-Franze, Daniele Yumi Dr. (1) Todiras, Mihail (1) Uckert, Wolfgang Prof. Dr. (1) Uyar, Bora Dr. (1) Wellner, Maren Dr. (3) Willimsky, Gerald Dr. (1) Willnow, David (1) Willnow, Thomas Prof. Dr. (171) Wolf, Jana Prof. Dr. (1) Wolf, Susanne Dr. (1) Ziehm, Matthias Dr. (1) Zywitza, Vera Dr. (1) (-) Diecke, Sebastian Dr. (3) (-) Zauber, Henrik Dr. (1) 2005 (1) 2006 (2) 2007 (1) 2008 (1) 2009 (1) 2010 (1) 2011 (1) 2012 (3) 2014 (1) 2015 (1) 2018 (2) 2019 (2) 2020 (4) 2021 (1) 2024 (1) AG Müller/Dechend (ECRC) (1) Anchored Signalling (2) Animal Phenotyping (1) Biobank (1) Bioinformatics and Omics Data Science (2) Cellular Neurosciences (1) Clinical Research Unit (1) Computational Regulatory Genomics (4) Developmental Biology / Signal Transduction (3) Electron Microscopy (1) Epigenetic Modifications in Neuroblastoma (1) Genetics and Genomics of Cardiovascular Diseases (4) Genome Diversification & Integrity (1) Genome Engineering & Disease Models (5) Genomics (4) Host-microbiome factors in cardiovascular disease (1) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Immune Mechanisms and Human Antibodies (22) Immune Regulation and Cancer (3) Integrative Vascular Biology (5) Intracellular Proteolysis (1) Mathematical Modelling of Cellular Processes (14) Mobile DNA (1) Molecular Biology of Peptide Hormones (4) (-) Molecular Cardiovascular Research (23) Molecular Epidemiology (1) Myology (3) Neuroimmunology Laboratory (1) Organoids (1) Out-patient Clinic for Neuroimmunology (3) Pluripotent Stem Cells (68) Proteome Dynamics (17) Proteomics (4) Proteomics and Metabolomics (2) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (7) Quantitative Stem Cell Biology (2) RNA Biology and Posttranscriptional Regulation (4) Stem Cell Modeling of Development and Disease (1) Structural Biology of Membrane-Associated Processes (1) Synaptic Transmission and Plasticity (2) Systems Biology of Gene Regulatory Elements (3) Transgenics (5) Translational Bioinformatics (1) Translational Cardiology and Functional Genomics (1) Translational Oncology of Solid Tumors (1) 23 Results: Active Filter: Diecke, Sebastian Dr.Zauber, Henrik Dr.Molecular Cardiovascular Research Sort: Result score Newest to oldest Oldest to newest July 01, 2007 / Hum Mol Genet L1 retrotransposition can occur early in human embryonic development J.A. van den Hurk I.C. Meij M.C. Seleme H. Kano K. Nikopoulos L.H. Hoefsloot E.A. Sistermans I.J. de Wijs A. Mukhopadhyay A.S. Plomp P.T. de Jong H.H. Kazazian F.P. Cremers April 01, 2006 / Hum Mol Genet Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail D. Mueller P.J. Kausalya I.C. Meij W. Hunziker April 01, 2005 / Organogenesis The European Renal Genome Project: An integrated approach towards understanding the genetics of kidney development and disease T.E. Willnow C. Antignac A.W. Braendli E.I. Christensen R.D. Cox D. Davidson J.A. Davies O. Devuyst G. Eichele N.D. Hastie P.J. Verroust A. Schedl I.C. Meij August 01, 2006 / J Clin Endocrinol Metab Unusual clinical presentation and possible rescue of a novel Claudin-16 mutation D. Mueller P.J. Kausalya D. Bockenhauer J. Tumfart I.C. Meij M.J. Dillon W. van't Hoff W. Hunziker May 01, 2010 / Am J Physiol Renal Physiol Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting C. Will T. Breiderhoff J. Thumfart M. Stuiver K. Kopplin K. Sommer D. Guenzel U. Querfeld I.C. Meij Q. Shan M. Bleich T.E. Willnow D. Mueller July 01, 2009 / Nephrol Dial Transplant EUNEFRON, the European Network for the Study of Orphan Nephropathies O. Devuyst I. Meij X. Jeunemaitre P. Ronco C. Antignac E.I. Christensen N.V. Knoers E.N. Levtchenko P.M. Deen D. Mueller C.A. Wagner L. Rampoldi W.G. van't Hoff October 09, 2008 / Am J Physiol Renal Physiol Magnesium stimulates renal phosphate reabsorption J. Thumfart S. Jung S. Amasheh S. Kraemer H. Peters K. Sommer J. Biber H. Murer I.C. Meij U. Querfeld C.A. Wagner D. Mueller March 11, 2011 / Am J Hum Genet CNNM2, encoding a basolateral protein required for renal Mg(2+) handling, is mutated in dominant hypomagnesemia M. Stuiver S. Lainez C. Will S. Terryn D. Guenzel H. Debaix K. Sommer K. Kopplin J. Thumfart N.B. Kampik U. Querfeld T.E. Willnow V. Nemec C.A. Wagner J.G. Hoenderop O. Devuyst N.V. Knoers R.J. Bindels I.C. Meij D. Mueller August 01, 2014 / Acta Neuropathol Disturbed function of the blood-cerebrospinal fluid barrier aggravates neuro-inflammation G. Kooij K. Kopplin R. Blasig M. Stuiver N. Koning G. Goverse S.M.A. van der Pol B. van het Hof M. Gollasch J.A.R. Drexhage A. Reijerkerk I.C. Meij R. Mebius T.E. Willnow D. Müller I.E. Blasig H.E. de Vries September 20, 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach Pagination Current page 1 Page 2 Page 3 Next page Next › Last page Last »
July 01, 2007 / Hum Mol Genet L1 retrotransposition can occur early in human embryonic development J.A. van den Hurk I.C. Meij M.C. Seleme H. Kano K. Nikopoulos L.H. Hoefsloot E.A. Sistermans I.J. de Wijs A. Mukhopadhyay A.S. Plomp P.T. de Jong H.H. Kazazian F.P. Cremers
April 01, 2006 / Hum Mol Genet Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail D. Mueller P.J. Kausalya I.C. Meij W. Hunziker
April 01, 2005 / Organogenesis The European Renal Genome Project: An integrated approach towards understanding the genetics of kidney development and disease T.E. Willnow C. Antignac A.W. Braendli E.I. Christensen R.D. Cox D. Davidson J.A. Davies O. Devuyst G. Eichele N.D. Hastie P.J. Verroust A. Schedl I.C. Meij
August 01, 2006 / J Clin Endocrinol Metab Unusual clinical presentation and possible rescue of a novel Claudin-16 mutation D. Mueller P.J. Kausalya D. Bockenhauer J. Tumfart I.C. Meij M.J. Dillon W. van't Hoff W. Hunziker
May 01, 2010 / Am J Physiol Renal Physiol Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting C. Will T. Breiderhoff J. Thumfart M. Stuiver K. Kopplin K. Sommer D. Guenzel U. Querfeld I.C. Meij Q. Shan M. Bleich T.E. Willnow D. Mueller
July 01, 2009 / Nephrol Dial Transplant EUNEFRON, the European Network for the Study of Orphan Nephropathies O. Devuyst I. Meij X. Jeunemaitre P. Ronco C. Antignac E.I. Christensen N.V. Knoers E.N. Levtchenko P.M. Deen D. Mueller C.A. Wagner L. Rampoldi W.G. van't Hoff
October 09, 2008 / Am J Physiol Renal Physiol Magnesium stimulates renal phosphate reabsorption J. Thumfart S. Jung S. Amasheh S. Kraemer H. Peters K. Sommer J. Biber H. Murer I.C. Meij U. Querfeld C.A. Wagner D. Mueller
March 11, 2011 / Am J Hum Genet CNNM2, encoding a basolateral protein required for renal Mg(2+) handling, is mutated in dominant hypomagnesemia M. Stuiver S. Lainez C. Will S. Terryn D. Guenzel H. Debaix K. Sommer K. Kopplin J. Thumfart N.B. Kampik U. Querfeld T.E. Willnow V. Nemec C.A. Wagner J.G. Hoenderop O. Devuyst N.V. Knoers R.J. Bindels I.C. Meij D. Mueller
August 01, 2014 / Acta Neuropathol Disturbed function of the blood-cerebrospinal fluid barrier aggravates neuro-inflammation G. Kooij K. Kopplin R. Blasig M. Stuiver N. Koning G. Goverse S.M.A. van der Pol B. van het Hof M. Gollasch J.A.R. Drexhage A. Reijerkerk I.C. Meij R. Mebius T.E. Willnow D. Müller I.E. Blasig H.E. de Vries
September 20, 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach