Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ramona Zeh"'
Autor:
Lore Becker, Eva Kling, Evelyn Schiller, Ramona Zeh, Anja Schrewe, Sabine M Hölter, Ilona Mossbrugger, Julia Calzada-Wack, Valentina Strecker, Ilka Wittig, Iulia Dumitru, Tina Wenz, Andreas Bender, Michaela Aichler, Dirk Janik, Frauke Neff, Axel Walch, Leticia Quintanilla-Fend, Thomas Floss, Raffi Bekeredjian, Valérie Gailus-Durner, Helmut Fuchs, Wolfgang Wurst, Thomas Meitinger, Holger Prokisch, Martin Hrabě de Angelis, Thomas Klopstock
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e114918 (2014)
Recently, mutations in the mitochondrial translation optimization factor 1 gene (MTO1) were identified as causative in children with hypertrophic cardiomyopathy, lactic acidosis and respiratory chain defect. Here, we describe an MTO1-deficient mouse
Externí odkaz:
https://doaj.org/article/5fb946e312a94325a7492aee89c6f092
Autor:
Jivko Stoyanov, Ramona Zeh, Marija Glisic, Simona Capossela, Alessandro Bertolo, Ezra Valido, Gerold Stucki, Jürgen Pannek, Inge Eriks-Hoogland, Xavier Jordan, Margret Hund-Georgiadis
Objectives To describe the concept, establishment and the operationalization of the biobank of the Swiss Spinal Cord Injury Cohort Study (SwiSCI), the available biosamples, and demographic and clinical characteristics of study participants. Setting:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ad9ba6eeab8c0ef80aee6ac4b64f251
https://doi.org/10.21203/rs.3.rs-1850636/v1
https://doi.org/10.21203/rs.3.rs-1850636/v1
Autor:
Markus Nussbaumer, Rainer Landgraf, Rupert Palme, Marina Zimbelmann, Ramona Zeh, Hendrik Stein, Mirjam Bunck, Lisa Glasl, Michael Wolferstätter, Chadi Touma, Florian Holsboer
Publikováno v:
Psychoneuroendocrinology. 33:839-862
Affective disorders such as major depression are among the most prevalent and costly diseases of the central nervous system, but the underlying mechanisms are still poorly understood. In recent years, it has become evident that alterations of the str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::916d43fe8f60407022e4d6965f23585d
https://doi.org/10.1016/j.psyneuen.2008.03.013
https://doi.org/10.1016/j.psyneuen.2008.03.013
Autor:
Ilona Mossbrugger, Frauke Neff, Ilka Wittig, Evelyn Schiller, Wolfgang Wurst, Valentina Strecker, Andreas Bender, Anja Schrewe, Thomas Floss, Sabine M. Hölter, Valerie Gailus-Durner, Helmut Fuchs, Julia Calzada-Wack, Thomas Meitinger, Thomas Klopstock, Raffi Bekeredjian, Martin Hrabě de Angelis, Michaela Aichler, Tina Wenz, Holger Prokisch, Ramona Zeh, Lore Becker, Dirk Janik, Iulia Dumitru, Leticia Quintanilla-Fend, Eva Kling, Axel Walch
Publikováno v:
PLOS ONE
PLoS ONE, Vol 9, Iss 12, p e114918 (2014)
PLOS ONE 9(12), e114918 (2014). doi:10.1371/journal.pone.0114918
PLoS ONE
PLoS ONE 9:e114918 (2014)
PLoS ONE, Vol 9, Iss 12, p e114918 (2014)
PLOS ONE 9(12), e114918 (2014). doi:10.1371/journal.pone.0114918
PLoS ONE
PLoS ONE 9:e114918 (2014)
Recently, mutations in the mitochondrial translation optimization factor 1 gene (MTO1) were identified as causative in children with hypertrophic cardiomyopathy, lactic acidosis and respiratory chain defect. Here, we describe an MTO1-deficient mouse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b033069bfd68b8c8ab8906cb3f52db82
https://hdl.handle.net/11858/00-001M-0000-0026-BE61-511858/00-001M-0000-0026-BE5F-D
https://hdl.handle.net/11858/00-001M-0000-0026-BE61-511858/00-001M-0000-0026-BE5F-D
Autor:
Oliver Eickelberg, Hugo A. Katus, Oliver Puk, Minxuan Sun, Gabriele Möller, Dirk H. Busch, Eva Janas, Jack Favor, Melanie Kahle, Ralph Steinkamp, Wilfried Szymczak, Markus Ollert, Markus F. Scheerer, Susanne Neschen, Andreas Zimmer, Holger Maier, Thure Adler, Valerie Gailus-Durner, Jan Rozman, Ali Önder Yildirim, Claudia Stöger, Tonia Ludwig, Julia Calzada-Wack, Christoph Lengger, Martin Klingenspor, Anja Schrewe, Ingrid L. Vargas Panesso, Sabine M. Hölter, Evelyn Schiller, Monja Willershäuser, Luciana Caminha Afonso, Barbara Fridrich, Beatrix Naton, Michael Räß, Alexander Götz, Christian M. Cohrs, Eckhard Wolf, Jerzy Adamski, Martin Hrabě de Angelis, Anja Hurt, Ildiko Racz, Birgit Rathkolb, Alexander Bohla, Ramona Zeh, Thomas Klopstock, Tanja Klein-Rodewald, Lore Becker, Kateryna Micklich, Frauke Neff, Alexandra Vernaleken, Tobias Stöger, Annemarie Wolff-Muscate, Juan Antonio Aguilar-Pimentel, Dirk Janik, Wolfgang Hans, Cornelia Prehn, Raffi Bekeredjian, Wolfgang Wurst, Susan Marschall, Christoph Höschen, Helmut Fuchs, Heinz Höfler, Lisa Glasl, Lillian Garrett, Anna Dewert, Martin Kistler, Irina Treise, Jochen Graw, Holger Schulz, Johannes Beckers, Marion Horsch
Publikováno v:
Mamm. Genome 23, 611-622 (2012)
Mammalian genome 23(9-10), 611-622 (2012). doi:10.1007/s00335-012-9415-1
Mammalian Genome
Mammalian genome 23(9-10), 611-622 (2012). doi:10.1007/s00335-012-9415-1
Mammalian Genome
Under the label of the German Mouse Clinic (GMC), a concept has been developed and implemented that allows the better understanding of human diseases on the pathophysiological and molecular level. This includes better understanding of the crosstalk b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4c9113cf82c123a12ff3d46acda9d4
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=10697
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=10697
Autor:
Eckhard Wolf, Claudia Stöger, Jerzy Adamski, Melanie Kahle, Hugo A. Katus, Holger Maier, Andreas Zimmer, Alexander Bohla, Valerie Gailus-Durner, Wolfgang Hans, Tonia Ludwig, Kateryna Micklich, Markus Ollert, Beatrix Naton, Michael Räß, Julia Calzada-Wack, Alexander Götz, Martin Kistler, Christian M. Cohrs, Christoph Lengger, Martin Klingenspor, Luciana Caminha Afonso, Irina Treise, Juan Antonio Aguilar-Pimentel, Birgit Rathkolb, Michael Hagn, Wolfgang Wurst, Tanja Klein-Rodewald, Lillian Garrett, Ildiko Racz, Markus F. Scheerer, Oliver Puk, Raffi Bekeredjian, Frauke Neff, Susanne Neschen, Felix Schöfer, Jochen Graw, Gabriele Möller, Ali Önder Yildirim, Susan Marschall, Monja Willershäuser, Ramona Zeh, Anja Schrewe, Lore Becker, Martin Hrabě de Angelis, Sabine M. Hölter, Jan Rozman, Annemarie Wolff-Muscate, Holger Schulz, Johannes Beckers, Marion Horsch, Tobias Stöger, Andras Franko, Evelyn Schiller, Thure Adler, Lisa Glasl, Jack Favor, Ralph Steinkamp, Sibylle Wagner, Thomas Klopstock, Cornelia Prehn, Helmut Fuchs, Dirk H. Busch
Publikováno v:
Genetics Meets Metabolomics ISBN: 9781461416883
The mouse is widely considered as a toolbox for modeling human diseases: mice are easy to handle and breed, there exist inbred strains, and the mouse genome sequence is available. Mutant mouse lines can be generated by different technologies, and sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2731ab37a11246f3266e4d4c2acbcc4
https://doi.org/10.1007/978-1-4614-1689-0_7
https://doi.org/10.1007/978-1-4614-1689-0_7
Autor:
Thure Adler, Claudia Stöger, Luciana Caminha Afonso, Raffi Bekeredjian, Irene Esposito, Felix Schöfer, Helmut Fuchs, Susanne Neschen, Gabriele Möller, Johannes Beckers, Holger Maier, Frauke Neff, Marion Horsch, Beatrix Naton, Patricia da Silva-Buttkus, Monja Willershäuser, Jerzy Adamski, Jan Rozman, Markus F. Scheerer, Irina Treise, Hugo A. Katus, Birgit Rathkolb, Cornelia Prehn, Frank Thiele, Juan Antonio Aguilar-Pimentel, Markus Ollert, Heinz Höfler, Martin Hrabě de Angelis, Kateryna Micklich, Valerie Gailus-Durner, Eckhard Wolf, Tonia Ludwig, Monica Tost, Christoph Lengger, Martin Klingenspor, Wolfgang Hans, Julia Calzada-Wack, Melanie Kahle, Dirk H. Busch, Anja Schrewe, Thomas Klopstock, Ramona Zeh, Lore Becker, Ralph Steinkamp, Christian M. Cohrs, Evelyn Schiller
Publikováno v:
Mouse as a Model Organism ISBN: 9789400707498
Next challenges in functional annotation of mammalian genomes are yet of a much larger scope than previous genomics initiatives. Mouse mutant resources must be phenotyped systematically (one after the other) and systemically (assessing all organ syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba6b552be204d6d98810f2afa9904de
https://doi.org/10.1007/978-94-007-0750-4_2
https://doi.org/10.1007/978-94-007-0750-4_2
Autor:
Leticia Quintanilla-Martinez, Magdalena Kallnik, Werner Müller, Irene Esposito, Juan Antonio Aguilar Pimentel, Bastian Pasche, B. Ferwagner, Nicolas Fasnacht, Heidrun Behrendt, R. Schreiner, Gerhard Heldmaier, Jochen Graw, Claudia Dalke, Wolfgang Hans, Ralph Steinkamp, Jan Rozman, Stefan Schreiber, Susanne Neschen, Christoph Lengger, Martin Klingenspor, Eva Kling, Nicole Ehrhardt, Frank Thiele, Holger Maier, Philip Rosenstiel, Klaus Schughart, Wolfgang Wurst, Markus Brielmeier, Ilona Mossbrugger, Hannelore Daniel, Christian Sina, M. H. de Angelis, Birgit Rathkolb, Helmut Fuchs, Eckhard Wolf, Ursula Frischmann, Beatrix Naton, Thure Adler, Anja Schrewe, T. Klopstock, Monja Willershäuser, C. Morth, Sabine M. Hölter, Julia Calzada-Wack, Heinz Höfler, U. Noth, Boris Ivandic, Jerzy Adamski, Martin Mempel, Andreas Zimmer, Hugo A. Katus, K. Schäble, Johannes Beckers, Marion Horsch, Gabriele Hölzlwimmer, Oliver Puk, Anahita Javaheri, Jack Favor, V. Gailus-Durner, Markus Ollert, Ramona Zeh, Lore Becker, Ines Bolle, Ildiko Racz, Julie A. Schmidt, Gerhard K. H. Przemeck, Holger Schulz, Cornelia Prehn, Andreas Lengeling, Dirk H. Busch
Publikováno v:
Curr. Pharm. Biotechnol. 10, 236-243 (2009)
The German Mouse Clinic (GMC) is a large scale phenotyping center where mouse mutant lines are analyzed in a standardized and comprehensive way. The result is an almost complete picture of the phenotype of a mouse mutant line--a systemic view. At the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::132f54a4c7c1934a5531713db1953f2b
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=1112
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=1112
Publikováno v:
Frontiers in Neuroendocrinology. 27:56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88ab9081cd19a902cbe512964ce53628
https://doi.org/10.1016/j.yfrne.2006.03.114
https://doi.org/10.1016/j.yfrne.2006.03.114