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

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

4. Modulation of bone marrow and peripheral blood cytokine levels by age and clonal hematopoiesis in healthy individuals

5. Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome

6. Germline ATG2B/GSKIP-containing 14q32 duplication predisposes to early clonal hematopoiesis leading to myeloid neoplasms

7. The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

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

10. Inherited human IFN-[gamma] deficiency underlies mycobacterial disease

11. Genetic, Immunological, and Clinical Features of the First Mexican Cohort of Patients with Chronic Granulomatous Disease

16. Impaired IL-12- and IL-23-Mediated Immunity Due to IL-12Rβ1 Deficiency in Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease

17. Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency

18. A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

19. Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia

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

21. Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations

22. Persistence of Mutations in Complete Remission Including DNMT3A, TET2 and ASXL1 Mutations Is Associated with Worse Prognosis in Patients with Acute Myeloid Leukemia Treated in ALFA 0702 Study

23. Association Study of Genes Controlling IL-12-dependent IFN-γ Immunity: STAT4 Alleles Increase Risk of Pulmonary Tuberculosis in Morocco

27. Prognostic impact of early minimal residual disease combined with complete molecular evaluation in acute myeloid leukemia with mutated NPM1: a single center study

28. A partial form of inherited human USP18 deficiency underlies infection and inflammation

30. Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation

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

32. Interleukin‐18 produced by bone marrow‐derived stromal cells supports T‐cell acute leukaemia progression

33. Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds

34. Reference Values of Human Bone Marrow and Peripheral Blood Levels of 49 Cytokines According to Age and Clonal Hematopoiesis

35. Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents

37. IMMUNODEFICIENCIES: Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations

38. Germline ATG2B/GSKIP-containing 14q32 duplication predisposes to early clonal hematopoiesis leading to myeloid neoplasms

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

42. Inherited human IFN-γ deficiency underlies mycobacterial disease

46. Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus

47. Projet SYSTEM-ECO4 : Evaluation de systèmes de grandes cultures à faible usage de pesticides

49. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant

50. Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

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