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Number of items: 3.

Journal Article

Gaertner, Vincent D., Michel, Sven, Curtin, John A., Pulkkinen, Ville, Acevedo, Nathalie, Soderhall, Cilla, von Berg, Andrea, Bufe, Albrecht, Laub, Otto, Rietschel, Ernst, Heinzmann, Andrea, Simma, Burkhard, Vogelberg, Christian, Pershagen, Goeran, Melen, Erik, Simpson, Angela ORCID: 0000-0003-2733-6666, Custovic, Adnan ORCID: 0000-0001-5218-7071, Kere, Juha ORCID: 0000-0003-1974-0271 and Kabesch, Michael (2019). Nocturnal asthma is affected by genetic interactions between RORA and NPSR1. Pediatr. Pulmonol., 54 (6). S. 847 - 858. HOBOKEN: WILEY. ISSN 1099-0496

Schieck, Maximilian ORCID: 0000-0001-5878-0546, Schouten, Jan P., Michel, Sven, Suttner, Kathrin, Toncheva, Antoaneta A., Gaertner, Vincent D., Illig, Thomas, Lipinski, Simone ORCID: 0000-0002-9322-7372, Franke, Andre ORCID: 0000-0003-1530-5811, Klintschar, Michael, Kalayci, Omer, Sahiner, Umit M., Birben, Esra, Melen, Erik, Pershagen, Goeran, Freidin, Maxim B., Ogorodova, Ludmila M., Granell, Raquel ORCID: 0000-0002-4890-4012, Henderson, John, Brunekreef, Bert, Smit, Henriette A., Vogelberg, Christian, von Berg, Andrea, Bufe, Albrecht, Heinzmann, Andrea, Laub, Otto, Rietschel, Ernst, Simma, Burkhard, Genuneit, Jon, Jonigk, Danny, Postma, Dirkje S., Koppelman, Gerard H., Vonk, Judith M., Timens, Wim ORCID: 0000-0002-4146-6363, Boezen, H. Marike and Kabesch, Michael (2016). Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages. J. Allergy Clin. Immunol., 138 (2). S. 421 - 432. NEW YORK: MOSBY-ELSEVIER. ISSN 1097-6825

Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Noethe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas ORCID: 0000-0002-6699-0014, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhan B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmueller, Janine, Krenz, Henrike, Woeste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J. and Omran, Heymut (2019). De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. Am. J. Hum. Genet., 105 (5). S. 1030 - 1040. CAMBRIDGE: CELL PRESS. ISSN 1537-6605

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