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1. Comparative analysis of spike-specific IgG Fc glycoprofiles elicited by adenoviral, mRNA, and protein-based SARS-CoV-2 vaccines

3. The BNT162b2 mRNA SARS-CoV-2 vaccine induces transient afucosylated IgG1 in naive but not in antigen-experienced vaccinees

7. IgG1 glycosylation highlights premature aging in Down syndrome.

8. Biological and structural characterization of murine TRALI antibody reveals increased Fc-mediated complement activation

9. Afucosylated Plasmodium falciparum-specific IgG is induced by infection but not by subunit vaccination

10. Comparative analysis of spike-specific IgG Fc glycoprofiles elicited by adenoviral, mRNA, and protein-based SARS-CoV-2 vaccines

11. Phagocytosis of platelets opsonized with differently glycosylated anti-HLA hIgG1 by monocyte-derived macrophages.

12. Factors affecting IgG4-mediated complement activation

13. Phagocytosis of platelets opsonized with differently glycosylated anti-HLA hIgG1 by monocyte-derived macrophages

14. Factors affecting IgG4-mediated complement activation

16. Factors affecting IgG4-mediated complement activation

17. mRNA vaccines against SARS-CoV-2 induce comparably low long-term IgG Fc galactosylation and sialylation levels but increasing long-term IgG4 responses compared to an adenovirus-based vaccine

18. The BNT162b2 mRNA SARS-CoV-2 vaccine induces transient afucosylated IgG1 in naive but not in antigen-experienced vaccinees

19. Phagocytosis of platelets opsonized with differently glycosylated anti-HLA hIgG1 by monocyte-derived macrophages

20. Immunoassay for quantification of antigen-specific IgG fucosylation

21. Immunoassay for quantification of antigen-specific IgG fucosylation

22. Immunoglobulin G1 Fc glycosylation as an early hallmark of severe COVID-19

23. Fc galactosylation of anti-platelet human IgG1 alloantibodies enhances complement activation on platelets

24. The BNT162b2 mRNA SARS-CoV-2 Vaccine Induces Transient Afucosylated IgG1 in Naive But Not in Antigen-Experienced Vaccinees

25. mRNA vaccines against SARSCoV-2 induce comparably low long-term IgG Fc galactosylation and sialylation levels but increasing long-term IgG4 responses compared to an adenovirus-based vaccine.

26. Aberrant glycosylation of anti-SARS-CoV-2 spike IgG is a prothrombotic stimulus for platelets

27. Association of Antibody-Dependent Neutrophil Phagocytosis With Distinct Antibody Glycosylation Profiles Following Typhoid Vaccination

29. The IgG glycome of SARS-CoV-2 infected individuals reflects disease course and severity.

30. High titers and low fucosylation of early human anti–SARS-CoV-2 IgG promote inflammation by alveolar macrophages

31. Afucosylated IgG characterizes enveloped viral responses and correlates with COVID-19 severity

32. Large-Scale Analysis of Apolipoprotein CIII Glycosylation by Ultrahigh Resolution Mass Spectrometry

34. Afucosylated Plasmodium falciparum-specific IgG is induced by infection but not by subunit vaccination

36. Capillary Electrophoresis-Mass Spectrometry at Trial by Metabo-Ring: Effective Electrophoretic Mobility for Reproducible and Robust Compound Annotation

37. Serum N‐Glycome analysis reveals pancreatic cancer disease signatures

38. A Matrix-Assisted Laser Desorption/Ionization—Mass Spectrometry Assay for the Relative Quantitation of Antennary Fucosylated N-Glycans in Human Plasma

40. Highly sensitive CE-ESI-MS analysis of N-glycans from complex biological samples

43. Quantification of serum apolipoproteins A-I and B-100 in clinical samples using an automated SISCAPA–MALDI-TOF-MS workflow

45. Ag85B–ESAT-6 adjuvanted with IC31® promotes strong and long-lived Mycobacterium tuberculosis specific T cell responses in volunteers with previous BCG vaccination or tuberculosis infection

46. Ag85B–ESAT-6 adjuvanted with IC31® promotes strong and long-lived Mycobacterium tuberculosis specific T cell responses in naïve human volunteers

47. Analysis of Mycobacterium tuberculosis-Specific CD8 T-Cells in Patients with Active Tuberculosis and in Individuals with Latent Infection

48. Detection and Functional Analysis of CD8+ T Cells Specific for PRAME: a Target for T-Cell Therapy

50. Activation of Dendritic Cells That Cross-Present Tumor-Derived Antigen Licenses CD8+ CTL to Cause Tumor Eradication

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