261 results on '"Deswarte, Caroline"'
Search Results
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
9. High prevalence of clonal hematopoiesis in the blood and bone marrow of healthy volunteers
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
12. IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis
13. LINE-1-Mediated AluYa5 Insertion Underlying Complete Autosomal Recessive IFN-γR1 Deficiency
14. Molecular, Immunological, and Clinical Features of 16 Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease
15. A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate
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
24. Leukocyte Adhesion Deficiency Type 1 (LAD1) with Expressed but Nonfunctional CD11/CD18
25. Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience
26. Disseminated Mycobacterium avium Complex Infection in a Child with Partial Dominant Interferon Gamma Receptor 1 Deficiency in India
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
29. MAIZEWALL. Database and Developmental Gene Expression Profiling of Cell Wall Biosynthesis and Assembly in Maize
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
36. Diagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiency
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
40. Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency
41. The c.273+11dup genetic change in the WAS gene is a functionally neutral polymorphism
42. Inherited human IFN-γ deficiency underlies mycobacterial disease
43. A novel variant in the neutrophil cytosolic factor 2 (NCF2) gene results in severe disseminated BCG infectious disease: A clinical report and literature review
44. Acute Lymphoblastic Leukemia and Cutaneous Mastocytosis in Two Children
45. Disseminated abscesses due to Mycoplasma faucium in a patient with activated PI3Kδ syndrome type 2
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
48. Skewed X-inactivation in a Female Carrier with X-linked Chronic Granulomatous Disease
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
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.