BS
Benjamin A. H. Smith
Also known as: Benjie Smith
Stanford University, Pomona College
Research areas: Medicine · Oncology · Glycosylation and Glycoproteins Research · Cancer Immunotherapy and Biomarkers · Carbohydrate Chemistry and Synthesis
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Publications (17)
- Beta-2 adrenergic receptor agonism alters astrocyte phagocytic activity and has potential applications to psychiatric disease Save
- MYC-driven synthesis of Siglec ligands is a glycoimmune checkpoint Save
- Lineage plasticity dictates responsiveness to anti-GD2 therapy in neuroblastoma. Save
- Lineage plasticity dictates responsiveness to anti-GD2 therapy in neuroblastoma. Save
- Beta-2 adrenergic receptor agonism alters astrocyte phagocytic activity and has potential applications to psychiatric disease Save
- Transition to a mesenchymal state in neuroblastoma confers resistance to anti-GD2 antibody via reduced expression of ST8SIA1. Save
- Anti-GD2 synergizes with CD47 blockade to mediate tumor eradication Save
- Small RNAs are modified with N-glycans and displayed on the surface of living cells Save
- Author Correction: The clinical impact of glycobiology: targeting selectins, Siglecs and mammalian glycans Save
- The clinical impact of glycobiology: targeting selectins, Siglecs and mammalian glycans Save
- Genome-wide CRISPR screens reveal a specific ligand for the glycan-binding immune checkpoint receptor Siglec-7 Save
- GD2 is a macrophage checkpoint molecule and combined GD2/CD47 blockade results in synergistic effects and tumor clearance in xenograft models of neuroblastoma and osteosarcoma Save
- CRISPR-Cas9 screens identify regulators of antibody–drug conjugate toxicity Save
- CD22 blockade restores homeostatic microglial phagocytosis in ageing brains Save
- MicroRNA-155 deficient dendritic cells cause less severe GvHD through reduced migration and defective inflammasome activation. Save
- Therapeutic activity of multiple common γ-chain cytokine inhibition in acute and chronic GVHD. Save
- Impact of mammalian target of rapamycin inhibition on lymphoid homing and tolerogenic function of nanoparticle-labeled dendritic cells following allogeneic hematopoietic cell transplantation. Save