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The European Respiratory Journal|February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.The American Journal of Gastroenterology|December 29, 2007
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German populationJürgen Glas, Astrid Konrad, Silke Schmechel, et al.Thorax|August 13, 2016
Lung disease caused by <i>ABCA3</i> mutationsCarolin Kröner, Thomas Wittmann, Simone Reu, et al.Neurogenetics|November 19, 2011
Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sampleChristina M Lill, Brit-Maren M Schjeide, Denis A Akkad, et al.Human Mutation|July 27, 2012
Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1βHella Luksch, Michael J Romanowski, Osvaldo Chara, et al.Neurogenetics|March 19, 2014
Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosisChristina M Lill, Marcel Schilling, Sara Ansaloni, et al.The Journal of Allergy and Clinical Immunology|May 31, 2015
Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseasesDirk Holzinger, Selina Kathleen Fassl, Wilco de Jager, et al.Journal of Medical Genetics|September 14, 2012
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjectsChristina M Lill, Tian Liu, Brit-Maren M Schjeide, et al.G3 (Bethesda, Md.)|May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis PatientsA Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.Pageof 13