Výsledky vyhledávání - Claudius Werner
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Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia Autor Johanna Raidt, Julia Wallmeier, Rim Hjeij, Jörg Große Onnebrink, Petra Pennekamp, Niki T. Loges, Heike Olbrich, Karsten Häffner, Gerard W. Dougherty, Heymut Omran, Claudius Werner
Vydáno 2014Artigo -
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Mutations in <i>CCDC11</i> , which Encodes a Coiled-Coil Containing Ciliary Protein, Causes <i>Situs Inversus</i> Due to Dysmotility of Monocilia in the Left-Right Organizer Autor Vijayashankaranarayanan Narasimhan, Rim Hjeij, Shubha Vij, Niki T. Loges, Julia Wallmeier, Cordula Koerner‐Rettberg, Claudius Werner, Surin Kumar Thamilselvam, Adrian Boey, Semil P. Choksi, Petra Pennekamp, Sudipto Roy, Heymut Omran
Vydáno 2014Artigo -
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Study protocol, rationale and recruitment in a European multi-centre randomized controlled trial to determine the efficacy and safety of azithromycin maintenance therapy for 6 mont... Autor Helene Kobbernagel, Frederik Buchvald, Eric G. Haarman, Carmen Casaulta, Samuel A. Collins, Claire Hogg, Claudia E. Kuehni, Jane S. Lucas, Heymut Omran, Alexandra L. Quittner, Claudius Werner, Kim G. Nielsen
Vydáno 2016Artigo -
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Systematic Analysis of<i>CCNO</i>Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis Autor Israel Amirav, Julia Wallmeier, Niki T. Loges, Tabea Menchen, Petra Pennekamp, Huda Mussaffi, Revital Abitbul, Avraham Avital, Lea Bentur, Gerard W. Dougherty, Nael Elias, Moran Lavie, Heike Olbrich, Claudius Werner, Chris Kintner, Heymut Omran
Vydáno 2016Artigo -
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The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans Autor Maureen Wirschell, Heike Olbrich, Claudius Werner, Douglas Tritschler, Raqual Bower, Winfield S. Sale, Niki T. Loges, Petra Pennekamp, Staffan I. Lindberg, Unne Stenram, Birgitta Carlén, Elisabeth Horak, Gabriele Köhler, Peter Nürnberg, Gudrun Nürnberg, Mary E. Porter, Heymut Omran
Vydáno 2013Artigo -
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Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex Autor Heike Olbrich, Carolin Cremers, Niki T. Loges, Claudius Werner, Kim G. Nielsen, June K. Marthin, Maria C. Philipsen, Julia Wallmeier, Petra Pennekamp, Tabea Menchen, Christine Edelbusch, Gerard W. Dougherty, Oliver Schwartz, Hölger Thiele, Janine Altmüller, Frank Rommelmann, Heymut Omran
Vydáno 2015Artigo -
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Efficacy and safety of azithromycin maintenance therapy in primary ciliary dyskinesia (BESTCILIA): a multicentre, double-blind, randomised, placebo-controlled phase 3 trial Autor Helene Kobbernagel, Frederik Buchvald, Eric G. Haarman, Carmen Casaulta, Samuel A. Collins, Claire Hogg, Claudia E. Kuehni, Jane S. Lucas, Claus Moser, Alexandra L. Quittner, Johanna Raidt, Susanne Rosthøj, Anne L. Sørensen, Kim Thomsen, Claudius Werner, Heymut Omran, Kim G. Nielsen
Vydáno 2020Artigo -
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Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling Pathways Autor Monika Abedin Sigg, Tabea Menchen, Chanjae Lee, Jeffery R. Johnson, Melissa K. Jungnickel, Semil P. Choksi, Galo García, Henriette Busengdal, Gerard W. Dougherty, Petra Pennekamp, Claudius Werner, Fabian Rentzsch, Harvey M. Florman, Nevan J. Krogan, John B. Wallingford, Heymut Omran, Jeremy F. Reiter
Vydáno 2017Artigo -
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Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects Autor Tamara Paff, Niki T. Loges, Isabella Aprea, Kaman Wu, Zeineb Bakey, Eric G. Haarman, Johannes M.A. Daniels, Erik A. Sistermans, Natalija Bogunovic, Gerard W. Dougherty, Inga M. Höben, Jörg Große-Onnebrink, Anja Matter, Heike Olbrich, Claudius Werner, Gerard Pals, Miriam Schmidts, Heymut Omran, Dimitra Micha
Vydáno 2016Artigo -
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An international registry for primary ciliary dyskinesia Autor Claudius Werner, Martin Lablans, Maximilian Ataian, Johanna Raidt, Julia Wallmeier, Jörg Große-Onnebrink, Claudia E. Kuehni, Eric G. Haarman, Margaret W. Leigh, Alexandra L. Quittner, Jane S. Lucas, Claire Hogg, Michał Witt, Kostas Ν. Priftis, Panayiotis K. Yiallouros, Kim G. Nielsen, Francesca Santamaria, Frank Ückert, Heymut Omran
Vydáno 2015Artigo -
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Genotype alone does not predict the clinical course of<i>SFTPC</i>deficiency in paediatric patients Autor Carolin Kröner, Simone Reu, Veronika Teusch, Andrea Schams, Ann-Christin Grimmelt, Michael Barker, Joerg Brand, Monika Gappa, Richard J. Kitz, Boris W. Kramer, Lars Lange, Susanne Lau, Claus Pfannenstiel, Marijke Proesmans, Jürgen Seidenberg, Tuğba Şişmanlar Eyüboğlu, Ayşe Tana Aslan, Claudius Werner, Stefan Zielen, Ralf Zarbock, Frank Brasch, Peter Lohse, Matthias Griese
Vydáno 2015Artigo -
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Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry Autor Heike Olbrich, Miriam Schmidts, Claudius Werner, Alexandros Onoufriadis, Niki T. Loges, Johanna Raidt, Nóra Fanni Bánki, Amelia Shoemark, Thomas Burgoyne, Saeed Al Turki, Matthew E. Hurles, Gabriele Köhler, Josef Schroeder, Gudrun Nürnberg, Peter Nürnberg, Eddie M.K. Chung, Richard Reinhardt, June K. Marthin, Kim G. Nielsen, Hannah M. Mitchison, Heymut Omran
Vydáno 2012Artigo -
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TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization Autor Julia Wallmeier, Hidetaka Shiratori, Gerard W. Dougherty, Christine Edelbusch, Rim Hjeij, Niki T. Loges, Tabea Menchen, Heike Olbrich, Petra Pennekamp, Johanna Raidt, Claudius Werner, Katsura Minegishi, Kyosuke Shinohara, Yasuko Asai, Katsuyoshi Takaoka, Chanjae Lee, Matthias Griese, Yasin Memari, Richard Durbin, Anja Kolb‐Kokocinski, Sascha Sauer, John B. Wallingford, Hiroshi Hamada, Heymut Omran
Vydáno 2016Artigo -
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Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects Autor Adrien Frommer, Rim Hjeij, Niki T. Loges, Christine Edelbusch, Charlotte Jahnke, Johanna Raidt, Claudius Werner, Julia Wallmeier, Jörg Große-Onnebrink, Heike Olbrich, Sandra Cindrić, Martine Jaspers, Mieke Boon, Yasin Memari, Richard Durbin, Anja Kolb‐Kokocinski, Sascha Sauer, June K. Marthin, Kim G. Nielsen, Israel Amirav, Nael Elias, Eitan Kerem, David Shoseyov, Karsten Häeffner, Heymut Omran
Vydáno 2015Artigo -
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Mutations of<i>DNAH11</i>in patients with primary ciliary dyskinesia with normal ciliary ultrastructure Autor Michael R. Knowles, Margaret W. Leigh, Johnny L. Carson, Stephanie D. Davis, Sharon Dell, Thomas W. Ferkol, Kenneth N. Olivier, Scott D. Sagel, Margaret Rosenfeld, Kimberlie A. Burns, Susan L. Minnix, Michael C. Armstrong, Adriana Lori, Milan J. Hazucha, Niki T. Loges, Heike Olbrich, Anita Becker-Heck, Miriam Schmidts, Claudius Werner, Heymut Omran, Maimoona A. Zariwala
Vydáno 2011Artigo -
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MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia Autor Mieke Boon, Julia Wallmeier, Lina Ma, Niki T. Loges, Martine Jaspers, Heike Olbrich, Gerard W. Dougherty, Johanna Raidt, Claudius Werner, Israel Amirav, Avigdor Hevroni, Revital Abitbul, Avraham Avital, Ruth Soferman, Marja W. Wessels, Christopher O’Callaghan, Eddie M.K. Chung, Andrew Rutman, Robert A. Hirst, Eduardo Moya, Hannah M. Mitchison, Sabine Van daele, K. De Boeck, Mark Jorissen, Chris Kintner, Harry Cuppens, Heymut Omran
Vydáno 2014Artigo -
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The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results Autor Myrofora Goutaki, Elisabeth Maurer, Florian S. Halbeisen, Israel Amirav, Angelo Barbato, Laura Behan, Mieke Boon, Carmen Casaulta, Annick Clément, Suzanne Crowley, Eric G. Haarman, Claire Hogg, Bülent Karadağ, Cordula Koerner‐Rettberg, Margaret W. Leigh, Michael R. Loebinger, Henryk Mazurek, Lucy Morgan, Kim G. Nielsen, Heymut Omran, Nicolaus Schwerk, Sergio Scigliano, Claudius Werner, Panayiotis K. Yiallouros, Zorica Živković, Jane S. Lucas, Claudia E. Kuehni
Vydáno 2016Artigo
Vyhledávací nástroje:
Související témata
Biology
Medicine
Internal medicine
Genetics
Lung
Bronchiectasis
Primary ciliary dyskinesia
Cilium
Gene
Cell biology
Motile cilium
Flagellum
Microtubule
Dynein
Pediatrics
Axoneme
Pathology
Disease
Anatomy
Mutation
Phenotype
Intensive care medicine
Intraflagellar transport
Mutant
Dyskinesia
Parkinson's disease
Pregnancy
Zebrafish
Ciliogenesis
Clinical trial