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32 results on '"Jäck, Hans-Martin"'

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1. GLUT1-mediated glucose import in B cells is critical for anaplerotic balance and humoral immunity

2. SARS-CoV-2 BA.2.86 enters lung cells and evades neutralizing antibodies with high efficiency

3. Neutralisation sensitivity of SARS-CoV-2 lineages EG.5.1 and XBB.2.3

4. Neutralisation sensitivity of the SARS-CoV-2 XBB.1 lineage

6. The effect of cilgavimab and neutralisation by vaccine-induced antibodies in emerging SARS-CoV-2 BA.4 and BA.5 sublineages

7. Lung cell entry, cell–cell fusion capacity, and neutralisation sensitivity of omicron sublineage BA.2.75

8. SARS-CoV-2 Omicron sublineages show comparable cell entry but differential neutralization by therapeutic antibodies

10. BAFFR activates PI3K/AKT signaling in human naive but not in switched memory B cells through direct interactions with B cell antigen receptors

11. Comparable neutralisation evasion of SARS-CoV-2 omicron subvariants BA.1, BA.2, and BA.3

13. SARS-CoV-2 variants C.1.2 and B.1.621 (Mu) partially evade neutralization by antibodies elicited upon infection or vaccination

14. Krüppel-like factor 2 controls IgA plasma cell compartmentalization and IgA responses

15. The Omicron variant is highly resistant against antibody-mediated neutralization: Implications for control of the COVID-19 pandemic

16. Immunizations with diverse sarbecovirus receptor-binding domains elicit SARS-CoV-2 neutralizing antibodies against a conserved site of vulnerability

17. B.1.617.2 enters and fuses lung cells with increased efficiency and evades antibodies induced by infection and vaccination

18. SARS-CoV-2 variant B.1.617 is resistant to bamlanivimab and evades antibodies induced by infection and vaccination

19. SARS-CoV-2 variants B.1.351 and P.1 escape from neutralizing antibodies

20. SARS-CoV-2 mutations acquired in mink reduce antibody-mediated neutralization

21. BAFFR Activates PI3K/AKT Signaling in Human Naive But Not in Switched Memory B Cells Through Direct Interactions with B Cell Antigen Receptors

22. A web platform for the network analysis of high-throughput data in melanoma and its use to investigate mechanisms of resistance to anti-PD1 immunotherapy

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