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Journal of Molecular Neuroscience : MN|December 3, 2013
A novel missense mutation in AFG3L2 associated with late onset and slow progression of spinocerebellar ataxia type 28Anna Mareike Löbbe, Jun-Suk Kang, Rüdiger Hilker, et al.
Cellular Immunology|March 9, 2010
Tumor necrosis factor alpha gene variants do not display allelic imbalance in circulating myeloid cellsSandra Wienzek, Karin Kissel, Kirstin Breithaupt, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|May 25, 2022
Emergency Use of Convalescent Plasma: Perception of the Regulatory Framework from a Clinical PerspectivePatrick Möhnle, Andreas Humpe, Markus Boeck, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 9, 2005
Low TLR4 expression by liver dendritic cells correlates with reduced capacity to activate allogeneic T cells in response to endotoxinAn De Creus, Masanori Abe, Audrey H Lau, et al.
Oncotarget|November 29, 2017
The tumor suppressor RASSF1A induces the YAP1 target gene <i>ANKRD1</i> that is epigenetically inactivated in human cancers and inhibits tumor growthAdriana P Jiménez, Annalena Traum, Thomas Boettger, et al.
Plos One|April 13, 2011
The cyclophilin-binding agent Sanglifehrin A is a dendritic cell chemokine and migration inhibitorSabrina N Immecke, Nelli Baal, Jochen Wilhelm, et al.
Cellular Immunology|September 6, 2011
The TLR7/8 ligand resiquimod targets monocyte-derived dendritic cell differentiation via TLR8 and augments functional dendritic cell generationHolger Hackstein, Angela Knoche, Angelika Nockher, et al.
European Urology|October 12, 2004
Alpha-1-antitrypsin levels and genetic variation of the alpha-1-antitrypsin gene in Peyronie's diseaseEkkehard W Hauck, Arne Hauptmann, Simone M Haag, et al.
Cancer Immunology, Immunotherapy : CII|November 2, 2024
Interdependence of coagulation with immunotherapy and BRAF/MEK inhibitor therapy: results from a prospective studyMalte Beckmann, Julian Schlüter, Michael Erdmann, et al.
Thrombosis Journal|February 12, 2024
SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiencyMaximilian Ruf, Sarah Cunningham, Alexandra Wandersee, et al.
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