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1. Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

2. Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

4. Glycosylation-Dependent IFN-γR Partitioning in Lipid and Actin Nanodomains Is Critical for JAK Activation

5. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases

7. Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

9. Mycobacterial Disease and Impaired IFN-γ Immunity in Humans with Inherited ISG15 Deficiency

10. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

11. Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency

12. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

13. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

14. Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing

15. In vitro differentiation of human macrophages with enhanced antimycobacterial activity

16. Inhibitors selective for mycobacterial versus human proteasomes

17. A partial form of recessive STAT1 deficiency in humans

18. IFN-γ mediates the rejection of haematopoietic stem cells in IFN-γR1-deficient hosts

19. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

23. Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

26. Systemic Modelling in Bioethics

29. [The ownership of genetic data: from data to information]

31. Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France

32. La propriété des données génétiques: De la donnée à l’information

33. French‐style genetics v. 2.0: The “e‐CohortE” project

36. IRF4 haploinsufficiency in a family with Whipple’s disease

37. Author response: IRF4 haploinsufficiency in a family with Whipple’s disease

38. AIDS vaccine developments

39. IRF4 haploinsufficiency in a family with Whipple’s disease

43. Molecular Tumor Boards: Ethical Issues in the New Era of Data Medicine.

44. X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

47. Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

48. Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

49. Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

50. A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

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