PD Dr. Julian Strobel

Medizinische Fakultät

Functional Heterogeneity of Umbilical Cord Blood Monocyte-Derived Dendritic Cells (2024) Schweiger P, Hamann L, Strobel J, Weisbach V, Wandersee A, Christ J, Kehl S, et al. Journal article Adoptive transfer of donor B lymphocytes: a phase 1/2a study for patients after allogeneic stem cell transplantation. (2024) Winkler J, Tittlbach H, Schneider A, Vasova I, Strobel J, Herold S, Maas S, et al. Journal article HLA-C*04:09N is expressed at the cell surface and triggers peptide-specific T-cell activation. (2024) Welters C, Welters ML, Stadler S, Bullinger L, Strobel J, Hackstein H, Dhamodaran A, et al. Journal article SERPINC1 c.1247dupC: a novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency (2024) Ruf M, Cunningham S, Wandersee A, Brox R, Achenbach S, Strobel J, Hackstein H, Schneider S Journal article, Original article The Protein S Erlangen Mutation PROS1c.1904T>C (F635S) Suppresses Secretion. (2024) Reißig J, Cunningham S, Wandersee A, Brox R, Achenbach S, Strobel J, Hackstein H, Schneider S Journal article, Original article Virus-reactive T cells expanded in aplastic anemia eliminate hematopoietic progenitor cells by molecular mimicry (2024) Ben Hamza A, Welters C, Stadler S, Brüggemann M, Dietze K, Brauns O, Brümmendorf TH, et al. Journal article Prevention of CMV/EBV reactivation by double-specific T cells in patients after allogeneic stem cell transplantation: results from the randomized phase I/IIa MULTIVIR-01 study (2023) Gerbitz A, Gary R, Aigner M, Moosmann A, Kremer A, Schmid C, Hirschbuehl K, et al. Journal article An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis. (2023) Kramer RA, Zimmermann R, Strobel J, Achenbach S, Stroebel A, Hackstein H, Messerer DAC, Schneider S Journal article Immune Phenotypes and Target Antigens of Clonally Expanded Bone Marrow T Cells in Treatment-Naïve Multiple Myeloma (2022) Welters C, Lammoglia Cobo MF, Stein CA, Hsu MT, Ben Hamza A, Penter L, Chen X, et al. Journal article Protein S Erlangen: a novel PROS1 gene mutation associated with quantitative protein S deficiency (2022) Schneider S, Reissig J, Weisbach VG, Achenbach S, Hackstein H, Strobel J Journal article