Search

Your search keyword '"Hoffmann, Markus"' showing total 90 results

Search Constraints

Start Over You searched for: Author "Hoffmann, Markus" Remove constraint Author: "Hoffmann, Markus" Publisher elsevier bv Remove constraint Publisher: elsevier bv
90 results on '"Hoffmann, Markus"'

Search Results

1. Cytoskeletal β-tubulin and cysteine cathepsin L deregulation by SARS-CoV-2 spike protein interaction with the neuronal model cell line SH-SY5Y

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

4. Humoral and cellular immune responses following BNT162b2 XBB.1.5 vaccination

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

6. Safety and immunogenicity against ancestral, Delta and Omicron virus variants following a booster dose of an inactivated whole-virus COVID-19 vaccine (VLA2001): Interim analysis of an open-label extension of the randomized, controlled, phase 3 COV-COMPARE trial

9. The impact of palliative radiotherapy on health-related quality of life in patients with head and neck cancer – results of a multicenter prospective cohort study

10. Prognostic implications of p16 and HPV discordance in oropharyngeal cancer (HNCIG-EPIC-OPC): a multicentre, multinational, individual patient data analysis

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

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

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

17. The loss of pancreatic islet NADPH oxidase (NOX)2 improves islet transplantation

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

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

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

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

29. Heterologous ChAdOx1 nCoV-19 and BNT162b2 prime-boost vaccination elicits potent neutralizing antibody responses and T cell reactivity against prevalent SARS-CoV-2 variants

31. Improved cellular and humoral immunity upon a second BNT162b2 and mRNA-1273 boost in prime-boost vaccination no/low responders with end-stage renal disease

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

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

35. The complement system drives local inflammatory tissue priming by metabolic reprogramming of synovial fibroblasts

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

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

38. Camostat mesylate inhibits SARS-CoV-2 activation by TMPRSS2-related proteases and its metabolite GBPA exerts antiviral activity

43. No association between HPV-status in tonsillar tissue and sexual behavior of the patients in a northern German population - Critical view of the link between HPV natural history and HPV-driven carcinogenesis

44. Pharmacological Inhibition of Acid Sphingomyelinase Prevents Uptake of SARS-CoV-2 by Epithelial Cells

45. Sphingosine prevents binding of SARS–CoV-2 spike to its cellular receptor ACE2

46. Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases

47. Structural Basis for Potent Neutralization of Betacoronaviruses by Single-Domain Camelid Antibodies

49. Structural Basis for Potent Neutralization of Betacoronaviruses by Single-Domain Camelid Antibodies

50. SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

Catalog

Books, media, physical & digital resources