34 results on '"Sijts, Alice J.A.M."'
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2. Generation and characterization of novel co-stimulatory anti-mouse TNFR2 antibodies
3. A novel efficient bispecific antibody format, combining a conventional antigen-binding fragment with a single domain antibody, avoids potential heavy-light chain mis-pairing
4. Intranasal delivery of Salmonella OMVs decorated with Chlamydia trachomatis antigens induces specific local and systemic immune responses
5. Immunogenicity Testing of Lipidoids In Vitro and In Silico: Modulating Lipidoid-Mediated TLR4 Activation by Nanoparticle Design
6. Hollow microneedle-mediated intradermal delivery of model vaccine antigen-loaded PLGA nanoparticles elicits protective T cell-mediated immunity to an intracellular bacterium
7. Multi-level Strategy for Identifying Proteasome-Catalyzed Spliced Epitopes Targeted by CD8+ T Cells during Bacterial Infection
8. Strategies to enhance immunogenicity of cDNA vaccine encoded antigens by modulation of antigen processing
9. Supplementary Figure SF4 from Mouse IgG2a Isotype Therapeutic Antibodies Elicit Superior Tumor Growth Control Compared with mIgG1 or mIgE
10. Supplementary Table ST2 from Mouse IgG2a Isotype Therapeutic Antibodies Elicit Superior Tumor Growth Control Compared with mIgG1 or mIgE
11. Data from Mouse IgG2a Isotype Therapeutic Antibodies Elicit Superior Tumor Growth Control Compared with mIgG1 or mIgE
12. Basophil-Derived Amphiregulin Is Essential for UVB Irradiation–Induced Immune Suppression
13. Mouse IgG2a Isotype Therapeutic Antibodies Elicit Superior Tumor Growth Control Compared with mIgG1 or mIgE
14. Canonical Wnt Signaling Negatively Modulates Regulatory T Cell Function
15. Stabilization of the Transcription Factor Foxp3 by the Deubiquitinase USP7 Increases Treg-Cell-Suppressive Capacity
16. Amphiregulin Enhances Regulatory T Cell-Suppressive Function via the Epidermal Growth Factor Receptor
17. Induction of humoral and cellular immune responses by antigen-expressing immunostimulatory liposomes
18. Pre-existing virus-specific CD8+ T-cells provide protection against pneumovirus-induced disease in mice
19. Human milk extracellular vesicles target nodes in interconnected signalling pathways that enhance oral epithelial barrier function and dampen immune responses
20. Human milk extracellular vesicles target nodes in interconnected signalling pathways that enhance oral epithelial barrier function and dampen immune responses
21. PI31 is a modulator of proteasome formation and antigen processing
22. Human milk extracellular vesicles target nodes in interconnected signalling pathways that enhance oral epithelial barrier function and dampen immune responses
23. Hsp70 and NF-kB Mediated Control of Innate Inflammatory Responses in a Canine Macrophage Cell Line
24. Efficient Generation of a Hepatitis B Virus Cytotoxic T Lymphocyte Epitope Requires the Structural Features of Immunoproteasomes
25. Hsp70 and NF-kB Mediated Control of Innate Inflammatory Responses in a Canine Macrophage Cell Line
26. MHC class I antigen processing of Listeria monocytogenes proteins: implications for dominant and subdominant CTL responses
27. Enhanced Intracellular Dissociation of Major Histocompatibility Complex Class I-associated Peptides: A Mechanism for Optimizing the Spectrum of Cell Surface-Presented Cytotoxic T Lymphocyte Epitopes
28. Immunogenicity Testing of Lipidoids In Vitro and In Silico: Modulating Lipidoid-Mediated TLR4 Activation by Nanoparticle Design
29. The proteasome inhibitor PI31 competes with PA28 for binding to 20S proteasomes
30. Dissecting antigen processing and presentation routes in dermal vaccination strategies
31. An unexpected major role for proteasome-catalyzed peptide splicing in generation of T cell epitopes: Is there relevance for vaccine development?
32. An unexpected major role for proteasome-catalyzed peptide splicing in generation of T cell epitopes: Is there relevance for vaccine development?
33. Multi-level Strategy for Identifying Proteasome-Catalyzed Spliced Epitopes Targeted by CD8+T Cells during Bacterial Infection
34. The Listeria monocytogenes-secreted p60 Protein Is an N-end Rule Substrate in the Cytosol of Infected Cells
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