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2. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

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

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

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

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

7. 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

43. Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds

45. Genetic inhibition of CARD9 accelerates the development of atherosclerosis in mice through CD36 dependent-defective autophagy

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

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

50. Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

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