698 results on '"Latour, Sylvain"'
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2. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
3. Inactivation of cytidine triphosphate synthase 1 prevents fatal auto-immunity in mice
4. Role of IL-27 in Epstein–Barr virus infection revealed by IL-27RA deficiency
5. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
6. Loss-of-phosphorylation of IKZF1 results in gain-of-function associated with immune dysregulation
7. Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature
8. A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature
9. NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells
10. Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
11. Inborn errors of immunity underlying defective T-cell memory
12. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
13. Characteristics of circulating KSHV-infected viroblasts during active KSHV+ multicentric Castleman disease
14. An update on molecular features and therapeutic perspectives of pediatric classical Hodgkin Lymphoma. What the clinician needs to know?
15. Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence
16. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India
17. Late-Onset Progressive Multifocal Leukoencephalopathy (PML) and Lymphoma in a 65-Year-Old Patient with XIAP Deficiency
18. Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies
19. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency
20. Combined Flow‐Fluorescence in situ hybridization to HHV‐8 and EBV reveals the viral heterogeneity of primary effusion lymphoma.
21. Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts
22. A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature
23. Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced dysfunction
24. Late-Onset EBV Susceptibility and Refractory Pure Red Cell Aplasia Revealing DADA2
25. MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation
26. Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
27. Hematopoietic stem cell transplantation for cytidine triphosphate synthase 1 (CTPS1) deficiency
28. Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study
29. Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency
30. Comprehensive molecular diagnosis of Epstein–Barr virus-associated lymphoproliferative diseases using next-generation sequencing
31. Loss of RASGRP1 in humans impairs T‐cell expansion leading to Epstein‐Barr virus susceptibility
32. CTP Synthase 1 Is a Novel Therapeutic Target in Lymphoma
33. SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling
34. Somatic reversion of pathogenic DOCK8 variants alters lymphocyte differentiation and function to effectively cure DOCK8 deficiency
35. Differential roles of CTP synthetases CTPS1 and CTPS2 in cell proliferation.
36. Impaired thymic AIRE expression underlies autoantibodies against type I IFNs in humans with inborn errors of the alternative NF-kB pathway
37. Characteristics of circulating KSHV-infected viroblasts during active KSHV+ multicentric Castleman disease
38. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
39. Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations
40. Characteristics of Circulating KSHV-Infected Cells during Active KSHV+ Multicentric Castleman Disease
41. Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
42. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
43. Characterization of Crohn disease in X-linked inhibitor of apoptosis–deficient male patients and female symptomatic carriers
44. Human T-bet governs the generation of a distinct subset of CD11c high CD21 low B cells
45. Epstein-Barr Virus Genome Deletions in Epstein-Barr Virus-Positive T/NK Cell Lymphoproliferative Diseases
46. Inherited TNFSF9 deficiency causes broad Epstein–Barr virus infection with EBV+ smooth muscle tumors
47. Human iNKT and MAIT cells exhibit a PLZF-dependent proapoptotic propensity that is counterbalanced by XIAP
48. Lymphoproliferative Syndrome, X-linked
49. X-linked Inhibitor of Apoptosis Protein Deficiency: More than an X-linked Lymphoproliferative Syndrome
50. Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation
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