Search

Your search keyword '"Casanova Jean-Laurent"' showing total 825 results

Search Constraints

Start Over You searched for: Author "Casanova Jean-Laurent" Remove constraint Author: "Casanova Jean-Laurent" Publication Year Range Last 3 years Remove constraint Publication Year Range: Last 3 years
825 results on '"Casanova Jean-Laurent"'

Search Results

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

2. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.

4. Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.

5. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

6. TMEFF1 is a neuron-specific restriction factor for herpes simplex virus

7. Human TMEFF1 is a restriction factor for herpes simplex virus in the brain

8. Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.

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

10. Correction to: Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency

11. A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries

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

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

16. Role of IL-27 in Epstein–Barr virus infection revealed by IL-27RA deficiency

18. Inherited CARD9 Deficiency Due to a Founder Effect in East Asia

20. Toll-Like Receptor 3 Mediates Aortic Stenosis Through a Conserved Mechanism of Calcification.

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

22. Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

23. Unlocking life-threatening COVID-19 through two types of inborn errors of type I IFNs

24. Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

26. Contributors

27. Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling

28. Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seq.

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

31. Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population

33. New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome

35. IgG4-related disease and B-cell malignancy due to an IKZF1 gain-of-function variant

36. Pandemic-associated pernio harbors footprints of an abortive SARS-CoV-2 infection

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

43. Neutralizing IFN-[gamma] autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals

44. Dissecting human population variation in single-cell responses to SARS-CoV-2

45. Autoantibodies Neutralizing Type I IFNs in the Bronchoalveolar Lavage of at Least 10% of Patients During Life-Threatening COVID-19 Pneumonia

48. FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

Catalog

Books, media, physical & digital resources