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Thomas Brocker | doi.page

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Thomas Brocker

LMU Klinikum(DE)Urologische Klinik München(DE)Ludwig-Maximilians-Universität München(DE)

Publications by Year

Research Areas

Immunotherapy and Immune Responses, T-cell and B-cell Immunology, Immune Cell Function and Interaction, CAR-T cell therapy research, RNA Interference and Gene Delivery

Most-Cited Works

→ Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways(2013)1,413 cited
→ Constitutive ablation of dendritic cells breaks self-tolerance of CD4 T cells and results in spontaneous fatal autoimmunity(2009)560 cited
→ Targeted Expression of Major Histocompatibility Complex (MHC) Class II Molecules Demonstrates that Dendritic Cells Can Induce Negative but Not Positive Selection of Thymocytes In Vivo(1997)441 cited
→ The T cell receptor/CD3 complex is composed of at least two autonomous transduction modules(1992)430 cited
→ Survival of Mature CD4 T Lymphocytes Is Dependent on Major Histocompatibility Complex Class II–expressing Dendritic Cells(1997)394 cited
→ Signals through T cell receptor-zeta chain alone are insufficient to prime resting T lymphocytes.(1995)285 cited

→ Compromised Ox40 Function in Cd28-Deficient Mice Is Linked with Failure to Develop Cxc Chemokine Receptor 5–Positive Cd4 Cells and Germinal Centers(1999)276 cited

→ Soluble CD40 ligand can replace the normal T cell-derived CD40 ligand signal to B cells in T cell-dependent activation.(1993)252 cited

→ Innate control of actin nucleation determines two distinct migration behaviours in dendritic cells(2015)215 cited

→ CD4 T cell traffic control:in vivo evidence that ligation of OX40 on CD4 T cells by OX40-ligand expressed on dendritic cells leads to the accumulation of CD4 T cells in B follicles(1999)185 cited