Showing results (21-30 of 78) with videos related to
Sort By:
Pageof 8
Journal of Neuropathology and Experimental Neurology|June 16, 2009
Intracerebral interleukin 12 induces glioma rejection in the brain predominantly by CD8+ T cells and independently of interferon-gammaMarcus Vetter, Markus J Hofer, Evelyn Roth, et al.Journal of Neuropathology and Experimental Neurology|June 15, 2006
Metalloproteinase disintegrins ADAM8 and ADAM19 are highly regulated in human primary brain tumors and their expression levels and activities are associated with invasivenessDirk Wildeboer, Silvia Naus, Qing-Xiang Amy Sang, et al.Journal of Virology|October 18, 2005
CD8 T cells require gamma interferon to clear borna disease virus from the brain and prevent immune system-mediated neuronal damageJürgen Hausmann, Axel Pagenstecher, Karen Baur, et al.Stroke|January 2, 2009
Involvement of PTEN promoter methylation in cerebral cavernous malformationsYuan Zhu, Andreas Wloch, Qun Wu, et al.Journal of Virology|January 15, 2004
Borna disease virus multiplication in mouse organotypic slice cultures is site-specifically inhibited by gamma interferon but not by interleukin-12Gregor Friedl, Markus Hofer, Bernd Auber, et al.Journal of Virology|January 11, 2008
Antiviral CD8 T cells recognize borna disease virus antigen transgenically expressed in either neurons or astrocytesKaren Baur, Mathias Rauer, Kirsten Richter, et al.Epilepsia|September 11, 2007
Intraoperative ultrasound to define focal cortical dysplasia in epilepsy surgeryDorothea Miller, Susanne Knake, Sebastian Bauer, et al.European Journal of Immunology|September 5, 2002
Gelatinase B deficiency protects against endotoxin shockBénédicte Dubois, Sofie Starckx, Axel Pagenstecher, et al.Biochemical and Biophysical Research Communications|June 25, 2021
DYRK3 contributes to differentiation and hypoxic control in neuroblastomaEkaterina Ivanova, Shrey Dharamvir Sharma, Anna Brichkina, et al.Molecular and Cellular Biology|March 14, 2007
Nuclear factor I X deficiency causes brain malformation and severe skeletal defectsKatrin Driller, Axel Pagenstecher, Markus Uhl, et al.Pageof 8