Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Markus Schülke"'
Autor:
Selene Lickfett, Carmen Menacho, Annika Zink, Markus Schülke, Andrea Rossi, Sidney Cambridge, Alessandro Prigione
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S184- (2023)
Externí odkaz:
https://doaj.org/article/9ac0c858904f40479d2ff9be7313a30c
Autor:
Carmen Menacho, Satoshi Okawa, Laura Petersilie, Annette Seibt, Markus Schülke, Felix Distelmaier, Christine R. Rose, Antonio Del Sol, Alessandro Prigione
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S188- (2023)
Externí odkaz:
https://doaj.org/article/c5f67a05b81945489eb9f13d3e3acc3b
Autor:
Andreas Marg, Helena Escobar, Nikos Karaiskos, Stefanie A. Grunwald, Eric Metzler, Janine Kieshauer, Sascha Sauer, Diana Pasemann, Edoardo Malfatti, Dominique Mompoint, Susanna Quijano-Roy, Anastasiya Boltengagen, Joanna Schneider, Markus Schülke, Séverine Kunz, Robert Carlier, Carmen Birchmeier, Helge Amthor, Andreas Spuler, Christine Kocks, Nikolaus Rajewsky, Simone Spuler
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Skeletal muscle stem cells express the transcription factor Pax7. Here, the authors isolate, from human muscle, cells that are positive for the endothelial marker CLEC14A and show that despite not expressing pax7, these cells regenerate muscle and co
Externí odkaz:
https://doaj.org/article/ce96cb57dae14384b0b97d2a3e6fda84
Autor:
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tzung-Chien Hsieh, Hartmut Engels, Sophia Peters, Alexej Knaus, Shahida Moosa, Luisa Averdunk, Felix Boschann, Henrike Sczakiel, Sarina Schwartzmann, Martin Atta Mensah, Jean Tori Pantel, Manuel Holtgrewe, Annemarie Bösch, Claudia Weiß, Natalie Weinhold, Aude-Annick Suter, Corinna Stoltenburg, Julia Neugebauer, Tillmann Kallinich, Angela M. Kaindl, Susanne Holzhauer, Christoph Bührer, Philip Bufler, Uwe Kornak, Claus-Eric Ott, Markus Schülke, Hoa Huu Phuc Nguyen, Sabine Hoffjan, Corinna Grasemann, Tobias Rothoeft, Folke Brinkmann, Nora Matar, Sugirthan Sivalingam, Claudia Perne, Elisabeth Mangold, Martina Kreiss, Kirsten Cremer, Regina C. Betz, Tim Bender, Martin Mücke, Lorenz Grigull, Thomas Klockgether, Spier Isabel, Heimbach André, Bender Tim, Fabian Brand, Christiane Stieber, Alexandra Marzena Morawiec, Pantelis Karakostas, Valentin S. Schäfer, Sarah Bernsen, Patrick Weydt, Sergio Castro-Gomez, Ahmad Aziz, Marcus Grobe-Einsler, Okka Kimmich, Xenia Kobeleva, Demet Önder, Hellen Lesmann, Sheetal Kumar, Pawel Tacik, Min Ae Lee-Kirsch, Reinhard Berner, Catharina Schuetz, Julia Körholz, Tanita Kretschmer, Nataliya Di Donato, Evelin Schröck, André Heinen, Ulrike Reuner, Amalia-Mihaela Hanßke, Frank J. Kaiser, Eva Manka, Martin Munteanu, Alma Kuechler, Kiewert Cordula, Raphael Hirtz, Elena Schlapakow, Christian Schlein, Jasmin Lisfeld, Christian Kubisch, Theresia Herget, Maja Hempel, Christina Weiler-Normann, Kurt Ullrich, Christoph Schramm, Cornelia Rudolph, Franziska Rillig, Maximilian Groffmann, Ania Muntau, Alexandra Tibelius, Eva M. C. Schwaibold, Christian P. Schaaf, Michal Zawada, Lilian Kaufmann, Katrin Hinderhofer, Pamela M. Okun, Urania Kotzaeridou, Georg F. Hoffmann, Daniela Choukair, Markus Bettendorf, Malte Spielmann, Annekatrin Ripke, Martje Pauly, Alexander Münchau, Katja Lohmann, Irina Hüning, Britta Hanker, Tobias Bäumer, Rebecca Herzog, Yorck Hellenbroich, Dominik S. Westphal, Tim Strom, Reka Kovacs, Korbinian M. Riedhammer, Katharina Mayerhanser, Elisabeth Graf, Melanie Brugger, Julia Hoefele, Konrad Oexle, Nazanin Mirza-Schreiber, Riccardo Berutti, Ulrich Schatz, Martin Krenn, Christine Makowski, Heike Weigand, Sebastian Schröder, Meino Rohlfs, Vill Katharina, Fabian Hauck, Ingo Borggraefe, Wolfgang Müller-Felber, Ingo Kurth, Miriam Elbracht, Cordula Knopp, Matthias Begemann, Florian Kraft, Johannes R. Lemke, Julia Hentschel, Konrad Platzer, Vincent Strehlow, Rami Abou Jamra, Martin Kehrer, German Demidov, Stefanie Beck-Wödl, Holm Graessner, Marc Sturm, Lena Zeltner, Ludger J. Schöls, Janine Magg, Andrea Bevot, Christiane Kehrer, Nadja Kaiser, Denise Horn, Annette Grüters-Kieslich, Christoph Klein, Stefan Mundlos, Markus Nöthen, Olaf Riess, Thomas Meitinger, Heiko Krude, Peter M. Krawitz, Tobias Haack, Nadja Ehmke, Matias Wagner
Most individuals with rare diseases initially consult their primary care physician. For a subset of rare diseases, efficient diagnostic pathways are available. However, ultra-rare diseases often require both expert clinical knowledge and comprehensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51d2fffa10e3858a273179e9636175f6
https://doi.org/10.1101/2023.04.19.23288824
https://doi.org/10.1101/2023.04.19.23288824
Autor:
Samuele Garda, Freyda Lenihan-Geels, Sebastian Proft, Stefanie Hochmuth, Markus Schülke, Dominik Seelow, Ulf Leser
Publikováno v:
Database : the journal of biological databases and curation. 2022
High-throughput technologies led to the generation of a wealth of data on regulatory DNA elements in the human genome. However, results from disease-driven studies are primarily shared in textual form as scientific articles. Information extraction (I
Autor:
Michelangelo Mancuso, Robert McFarland, Thomas Klopstock, Michio Hirano, Rafael Artuch, Enrico Bertini, Laurence Bindoff, Valerio Carelli, Grainne Gorman, Rita Horvath, Petra Kaufmann, Yasutoshi Koga, Saskia Koene, Costanza Lamperti, Julio Montoya, Francisco Javier Pérez-Mínguez Caneda, Vincent Procaccio, Holger Prokisch, Shamima Rahman, Piero Santantonio, Markus Schülke, Serenella Servidei, Dikoma C. Shungu, Gabriele Siciliano, Jan Smeitink, Tanja Taivassalo, John L.P. Thompson, Doug Turnbull, Elja Van der Veer, Philip E. Yeske, Massimo Zeviani
Publikováno v:
Neuromuscular Disorders. 27:1126-1137
Publikováno v:
Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics.
Publikováno v:
Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics.
Autor:
Petkova, Mina
Publikováno v:
Cellular Biology. Université Pierre et Marie Curie-Paris VI; Freie Universität (Berlin). Fachbereich Biologie, 2016. English. ⟨NNT : 2016PA066090⟩
Dystrophin is a rod-shaped cytoplasmic protein that physically links the cytoskeleton to the ECM through the dystrophin-associated protein complex (DAPC), thereby providing sarcolemmal stability. Mutations in the dystrophin encoding DMD gene cause th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::eb5513ec073f7abc86101c9e3b59a268
https://tel.archives-ouvertes.fr/tel-01458772
https://tel.archives-ouvertes.fr/tel-01458772
Autor:
Stantzou, Amalia
Publikováno v:
Molecular biology. Université Pierre et Marie Curie-Paris VI; Freie Universität (Berlin). Fachbereich Biologie, 2015. English. ⟨NNT : 2015PA066337⟩
Growth factors from several families of signaling molecules regulate muscle development and regeneration, and thereby determine correct muscle function. However, the regulatory mechanisms that coordinate the timing of muscle precursor generation, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e8936529315111bc4143733e14e1c689
https://doi.org/10.17169/refubium-8142
https://doi.org/10.17169/refubium-8142