Lepka, K., K. Volbracht, E. Bill, R. Schneider, N. Rios, T. Hildebrandt, J. Ingwersen, T. Prozorovski, C. H. Lillig, J. van Horssen, L. Steinman, H.-P. Hartung, R. Radi, A. Holmgren, O. Aktas and C. Berndt: Iron-sulfur glutaredoxin 2 protects oligodendrocytes against damage induced by nitric oxide release from activated microglia. In: GLIA 65, 9, 1521-1534 (2017).
doi: 10.1002/glia.23178
Lill, C. M., M. Schilling, S. Ansaloni, J. Schröder, M. Jaedicke, F. Luessi, B.-M. Schjeide, A. Mashychev, C. Graetz, D. A. Akkad, L.-A. Gerdes, A. Kroner, P. Blaschke, S. Hoffjan, A. Winkelmann, T. Dörner, P. Rieckmann, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, H.-P. Hartung, O. Aktas, P. Lohse, M. Buttmann, T. Kümpfel, C. Kubisch, U. K. Zettl, J. T. Epplen, F. Zipp and L. Bertram: Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis. In: Neurogenetics 15, 2, 129-134 (2014).
doi: 10.1007/s10048-014-0396-y
Lill, C. M., B.-M. Schjejde, C. Graetz, M. Ban, A. Alcina, M. A. Ortiz, J. Pérez, V. Damotte, D. Booth, A. Lopez de Lapuente, L. Broer, M. Schilling, D. A. Akkad, O. Aktas, I. Alloza, A. Antigüedad, R. Arroyo, P. Blaschke, M. Buttmann, A. Chan, A. Compston, I. Cournu-Rebeix, T. Dörner, J. T. Epplen, Ó. Fernández, L.-A. Gerdes, L. Guillot-Noël, H.-P. Hartung, S. Hoffjan, G. Izquierdo, A. Kemppinen, A. Kroner, C. Kubisch, T. Kümpfel, S.-C. Li, U. Lindenberger, P. Lohse, C. Lubetzki, F. Luessi, S. Malhotra, J. Mescheriakova, X. Montalban, C. Papeix, L. F. Paredes, P. Rieckmann, E. Steinhagen-Thiessen, A. Winkelmann, U. K. Zettl, R. Hintzen, K. Vandenbroeck, G. Stewart, B. Fontaine, M. Comabella, E. Urcelay, F. Matesanz, S. Sawcer, L. Bertram, F. Zipp and International Multiple Sclerosis Genetics Consortium: MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. In: Brain 136, 6, 1778-1782 (2013).
doi: 10.1093/brain/awt101
Lill, C. M., B.-M. Schjeide, C. Graetz, T. Liu, V. Damotte, D. A. Akkad, P. Blaschke, L.-A. Gerdes, A. Kroner, F. Luessi, I. Cournu-Rebeix, S. Hoffjan, A. Winkelmann, E. Touze, F. Pico, P. Corcia, D. Otaegui, A. Antigüedad, A. Alcina, M. Comabella, X. Montalban, J. Olascoaga, F. Matesanz, T. Dörner, S.-C. Li, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, P. Rieckmann, H.-P. Hartung, O. Aktas, P. Lohse, M. Buttmann, T. Kümpfel, C. Kubisch, U. K. Zettl, J. T. Epplen, B. Fontaine, F. Zipp, K. Vandenbroeck and L. Bertram: Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. In: Journal of Medical Genetics 50, 3, 140-143 (2013).
doi: 10.1136/jmedgenet-2012-101411
Lill, C. M., B.-M. Schjejde, D. A. Akkad, P. Blaschke, A. Winkelmann, L.-A. Gerdes, S. Hoffjan, F. Luessi, T. Dörner, S.-C. Li, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, H.-P. Hartung, O. Aktas, P. Lohse, T. Kümpfel, C. Kubisch, J. T. Epplen, U. K. Zettl, L. Bertram and F. Zipp: Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample. In: Neurogenetics 13, 1, 83-86 (2012).
doi: 10.1007/s10048-011-0305-6
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.