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5. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

7. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

8. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

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

10. Erratum: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome (J. Exp. Med. (2020) 217:6 Doi:10.1084/jem.20191804)

11. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

12. Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

13. cpbAg1encodes an active carboxypeptidase B expressed in the midgut ofAnopheles gambiae.

15. Serial Analysis of Gene Expression in Plasmodium berghei salivary gland sporozoites

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

17. Human genetic and immunological determinants of critical COVID-19 pneumonia

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

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

20. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

21. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.

22. A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

23. T cell defects in patients with ARPC1B germline mutations account for their combined immunodeficiency

24. Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.

25. Phenotypes of 126 Moroccan HIES patients according to NIH Score.

26. IL-7-dependent and -independent lineages of IL-7R-dependent human T cells.

27. Comprehensive Catalog of Variants Potentially Associated with Hidradenitis Suppurativa, Including Newly Identified Variants from a Cohort of 100 Patients.

28. Inherited human RelB deficiency impairs innate and adaptive immunity to infection.

29. Tuberculosis in otherwise healthy adults with inherited TNF deficiency.

31. A microglia clonal inflammatory disorder in Alzheimer's Disease.

32. Mechanism of neurodegeneration mediated by clonal inflammatory microglia.

33. Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

34. ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis.

35. Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency.

36. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children.

37. Genetics and clinical phenotypes in common variable immunodeficiency.

38. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

39. Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites.

40. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

41. Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity.

43. Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling.

44. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia.

45. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

46. Is Your Kid Actin Out? A Series of Six Patients With Inherited Actin-Related Protein 2/3 Complex Subunit 1B Deficiency and Review of the Literature.

47. Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria.

48. Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.

49. Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination.

50. Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

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