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1. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

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

3. Prévalence des autoanticorps anti-IFNs de type I dans une cohorte prospective de patients ambulatoires dans un Service de médecine interne à Paris

4. A second update on mapping the human genetic architecture of COVID-19

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

8. 491 Recalcitrant cutaneous warts in a family with inherited ICOS deficiency

9. 489 Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions

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

13. Clonal Hematopoiesis Is Not Significantly Associated with Covid-19 Disease Severity

14. Human NLRP1 is a sensor of pathogenic coronavirus 3CL proteases in lung epithelial cells

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

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

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

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

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

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

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

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

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

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

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

27. Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines.

32. IFN-gamma and IL-12 differentially regulate CC-chemokine secretion and CCR5 expression in human T lymphocytes

34. Insufficient type I IFN immunity underlies life-threatening COVID-19 pneumonia

35. X linked susceptibility to Mycobapteria is caused by mutation in NEMO impairing CD40-dependent IL-12production

36. TLR3 deficiency in herpes simplex encephalitis: High allelic heterogeneity and recurrence risk

39. Imunodeficiência primária por défice de ZAP-70

41. DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice

43. 1401 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES VARIANTS ASSOCIATED WITH LIVER FIBROSIS PROGRESSION IN HCV-INFECTED PATIENTS

44. Interferon receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection

47. Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection.

50. Partial interferon-gamma receptor 1 deficiency in a child with tuberculoid bacillus Calmette-Guérin infection and a sibling with clinical tuberculosis.

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