47 results on '"Duangchinda, Thaneeya"'
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2. Immunogenicity and durability against Omicron BA.1, BA.2 and BA.4/5 variants at 3–4 months after a heterologous COVID-19 booster vaccine in healthy adults with a two-doses CoronaVac vaccination
3. Persistence of immunity against Omicron BA.1 and BA.2 variants following homologous and heterologous COVID-19 booster vaccines in healthy adults after a two-dose AZD1222 vaccination
4. Immunogenicity and durability against micron BA.1, BA.2 and BA.4/5 variants at 3–4 months after a heterologous COVID-19 booster vaccine in healthy adults with a two-doses CoronaVac vaccination
5. Long-Term Dynamic Changes in Hybrid Immunity over Six Months after Inactivated and Adenoviral Vector Vaccination in Individuals with Previous SARS-CoV-2 Infection.
6. Heterologous prime-boost immunization induces protection against dengue virus infection in cynomolgus macaques
7. Dynamic Antibody Response and Hybrid Immunity Following Multiple COVID-19 Vaccine Doses and Infection: A Case Study
8. Blockade-of-Binding Activities toward Envelope-Associated, Type-Specific Epitopes as a Correlative Marker for Dengue Virus-Neutralizing Antibody
9. A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus
10. Neutralizing antibodies against omicron BA.5 among children with infection alone, vaccination alone, and hybrid immunity
11. Characterization of a potent and highly unusual minimally enhancing antibody directed against dengue virus
12. Study of dengue virus specific T lymphocytes in Thai populations
13. Comparison of the reactogenicity and immunogenicity between two‐dose mRNA COVID‐19 vaccine and inactivated COVID‐19 vaccine followed by an mRNA vaccine in children aged 5−11 years
14. Germline bias dictates cross-serotype reactivity in a common dengue-virus-specific CD8+ T cell response
15. Immunogenicity and durability against Omicron BA.1, BA.2 and BA.4/5 variants at 3 to 4 months after a heterologous COVID-19 booster vaccine in healthy adults with a two-doses CoronaVac vaccination
16. Safety and immunogenicity of intradermal administration of fractional dose CoronaVac®, ChAdOx1 nCoV-19 and BNT162b2 as primary series vaccination
17. Comparison of the reactogenicity and immunogenicity of a reduced and standard booster dose of the mRNA COVID-19 vaccine in healthy adults after two doses of inactivated vaccine
18. Effects of boosted mRNA and adenoviral‐vectored vaccines on immune responses to omicron BA.1 and BA.2 following the heterologous CoronaVac/AZD1222 vaccination
19. Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus
20. Strong Correlations between the Binding Antibodies against Wild-Type and Neutralizing Antibodies against Omicron BA.1 and BA.2 Variants of SARS-CoV-2 in Individuals Following Booster (Third-Dose) Vaccination
21. Development of a Singleplex Real-Time Reverse Transcriptase PCR Assay for Pan-Dengue Virus Detection and Quantification
22. Persistence of immunity against omicron BA.1 and BA.2 following homologous and heterologous COVID-19 booster vaccines in healthy adults after a two-doses AZD1222 vaccination
23. Omicron BA.1, BA.2 and COVID-19 Booster Vaccination
24. Neutralizing Activities Against the Omicron Variant After a Heterologous Booster in Healthy Adults Receiving Two Doses of CoronaVac Vaccination
25. COVID-19 Breakthrough Infection after Inactivated Vaccine Induced Robust Antibody Responses and Cross-Neutralization of SARS-CoV-2 Variants, but Less Immunity against Omicron
26. Immunodominant T-cell responses to dengue virus NS3 are associated with DHF
27. Cross-Reacting Antibodies Enhance Dengue Virus Infection in Humans
28. Potent programmable antiviral against dengue virus in primary human cells by Cas13b RNP with short spacer and delivery by VLP
29. Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever
30. Multi-color fluorescent reporter dengue viruses with improved stability for analysis of a multi-virus infection
31. Structural analysis of a dengue cross-reactive antibody complexed with envelope domain III reveals the molecular basis of cross-reactivity1
32. Erratum: Corrigendum: A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus
33. Enhancing cross-reactive anti-prM dominates the human antibody response in dengue infection
34. A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus
35. Invariant NKT Cell Response to Dengue Virus Infection in Human
36. Germline bias dictates cross-serotype reactivity in a common dengue-virus-specific CD8+T cell response
37. Structural Analysis of a Dengue Cross-Reactive Antibody Complexed with Envelope Domain III Reveals the Molecular Basis of Cross-Reactivity
38. The development of a novel serotyping-NS1-ELISA to identify serotypes of dengue virus
39. A Complex Interplay among Virus, Dendritic Cells, T Cells, and Cytokines in Dengue Virus Infections
40. T Cell Responses in Dengue Hemorrhagic Fever: Are Cross-Reactive T Cells Suboptimal?
41. Production of anti-dengue NS1 monoclonal antibodies by DNA immunization
42. Construction of infectious dengue 2 virus cDNA clones using high copy number plasmid
43. Corrigendum: A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus.
44. An Engineered N-Glycosylated Dengue Envelope Protein Domain III Facilitates Epitope-Directed Selection of Potently Neutralizing and Minimally Enhancing Antibodies.
45. Immunogenicity and durability against Omicron BA.1, BA.2 and BA.4/5 variants at 3-4 months after a heterologous COVID-19 booster vaccine in healthy adults with a two-doses CoronaVac vaccination.
46. Comparison of the reactogenicity and immunogenicity between two-dose mRNA COVID-19 vaccine and inactivated COVID-19 vaccine followed by an mRNA vaccine in children aged 5-11 years.
47. Safety and immunogenicity of intradermal administration of fractional dose CoronaVac ® , ChAdOx1 nCoV-19 and BNT162b2 as primary series vaccination.
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