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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Springe zu: 2023 | 2020 | 2018 | 2016 | 2014
Anzahl der Publikationen: 8

2023

Djannatian, Minou; Radha, Swathi; Weikert, Ulrich; Safaiyan, Shima; Wrede, Christoph; Deichsel, Cassandra; Kislinger, Georg; Rhomberg, Agata; Ruhwedel, Torben; Campbell, Douglas S.; van Ham, Tjakko; Schmid, Bettina; Hegermann, Jan; Moebius, Wiebke; Schifferer, Martina und Simons, Mikael (2023): Myelination generates aberrant ultrastructure that is resolved by microglia. In: Journal of Cell Biology, Bd. 222, Nr. 3, e202204010 [PDF, 6MB]

2020

Rachev, Ev; Schuster-Gossler, Karin; Fuhl, Franziska; Ott, Tim; Tveriakhina, Lena; Beckers, Anja; Hegermann, Jan; Boldt, Karsten; Mai, Michaela; Kremmer, Elisabeth; Ueffing, Marius; Blum, Martin und Gossler, Achim (2020): CFAP43 modulates ciliary beating in mouse and Xenopus. In: Developmental Biology, Bd. 459, Nr. 2: S. 109-125

Beckers, Anja; Adis, Christian; Schuster-Gossler, Karin; Tveriakhina, Lena; Ott, Tim; Fuhl, Franziska; Hegermann, Jan; Boldt, Karsten; Serth, Katrin; Rachev, Ev; Alten, Leonie; Kremmer, Elisabeth; Ueffing, Marius; Blum, Martin und Gossler, Achim (2020): The FOXJ1 target Cfap206 is required for sperm motility, mucociliary clearance of the airways and brain development. In: Development, Bd. 147, Nr. 21, dev188052

2018

Schindlbeck, Ulrike; Wittnnann, Thomas; Hoeppner, Stefanie; Kinting, Susanna; Liebisch, Gerhard; Hegermann, Jan und Griese, Matthias (2018): ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes. In: Human Mutation, Bd. 39, Nr. 6: S. 841-850

2016

Wittmann, Thomas; Frixel, Sabrina; Höppner, Stefanie; Schindlbeck, Ulrike; Schams, Andrea; Kappler, Matthias; Hegermann, Jan; Wrede, Christoph; Liebisch, Gerhard; Vierzig, Anne; Zacharasiewicz, Angela; Kopp, Matthias Volkmar; Poets, Christian F.; Baden, Winfried; Hartl, Dominik; Kaam, Anton H. van; Lohse, Peter; Aslanidis, Charalampos; Zarbock, Ralf und Griese, Matthias (2016): Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3. In: Molecular Medicine, Bd. 22 [PDF, 1MB]

Wittmann, Thomas; Schindlbeck, Ulrike; Höppner, Stefanie; Kinting, Susanna; Frixel, Sabrina; Kröner, Carolin; Liebisch, Gerhard; Hegermann, Jan; Aslanidis, Charalampos; Brasch, Frank; Reu, Simone; Lasch, Peter; Zarbock, Ralf und Griese, Matthias (2016): Tools to explore ABCA3 mutations causing interstitial lung disease. In: Pediatric Pulmonology, Bd. 51, Nr. 12: S. 1284-1294

Schlosser, Anders; Pilecki, Bartosz; Hemstra, Line E.; Kejling, Karin; Kristmannsdottir, Gudlaug B.; Wulf-Johansson, Helle; Moeller, Jesper B.; Füchtbauer, Ernst-Martin; Nielsen, Ole; Kirketerp-Møller, Katrine; Dubey, Lalit K.; Hansen, Pernille B. L.; Stubbe, Jane; Wrede, Christoph; Hegermann, Jan; Ochs, Matthias; Rathkolb, Birgit; Schrewe, Anja; Bekeredjian, Raffi; Wolf, Eckhard; Gailus-Durner, Valérie; Fuchs, Helmut; Hrabě de Angelis, Martin; Lindholt, Jes S.; Holmskov, Uffe und Sorensen, Grith L. (2016): MFAP4 Promotes Vascular Smooth Muscle Migration, Proliferation and Accelerates Neointima Formation. In: Arteriosclerosis thrombosis and Vascular Biology, Bd. 36, Nr. 1: S. 122-133

2014

Campo, Ilaria; Zorzetto, Michele; Mariani, Francesca; Kadija, Zamir; Morbini, Patrizia; Dore, Roberto; Kaltenborn, Eva; Frixel, Sabrina; Zarbock, Ralf; Liebisch, Gerhard; Hegermann, Jan; Wrede, Christoph; Griese, Matthias und Luisetti, Maurizio (2014): A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant. In: Respiratory Research 15:43 [PDF, 2MB]

Diese Liste wurde am Sat Nov 23 23:37:05 2024 CET erstellt.