162 results on '"Lenoir, Christelle"'
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2. NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells
3. Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
4. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
5. Defects in mucosal immunity and nasopharyngeal dysbiosis in HSC-transplanted SCID patients with IL2RG/JAK3 deficiency
6. Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence
7. Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome
8. Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency
9. Loss of RASGRP1 in humans impairs T‐cell expansion leading to Epstein‐Barr virus susceptibility
10. SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling
11. Characterization of Crohn disease in X-linked inhibitor of apoptosis–deficient male patients and female symptomatic carriers
12. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited
13. Human iNKT and MAIT cells exhibit a PLZF-dependent proapoptotic propensity that is counterbalanced by XIAP
14. Epstein-Barr Virus Genome Deletions in Epstein-Barr Virus-Positive T/NK Cell Lymphoproliferative Diseases
15. Inherited TNFSF9 deficiency causes broad Epstein–Barr virus infection with EBV+ smooth muscle tumors
16. Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG
17. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
18. Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation
19. CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
20. DEF6 deficiency, a mendelian susceptibility to EBV infection, lymphoma, and autoimmunity
21. MD-2 controls bacterial lipopolysaccharide hyporesponsiveness in human intestinal epithelial cells
22. Antibody-coated microbiota in nasopharynx of healthy individuals and IVIg-treated patients with hypogammaglobulinemia
23. Refractory monogenic Crohn’s disease due to X-linked inhibitor of apoptosis deficiency
24. A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency
25. Intestinal dysbiosis in inflammatory bowel disease associated with primary immunodeficiency
26. Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study
27. Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutation
28. Antibody-coated microbiota in nasopharynx of healthy individuals and hypogammaglobulinemia patients
29. Diagnostic yield of next-generation sequencing in very early-onset inflammatory bowel diseases: A multicentre study
30. 1-Benzyl-2-acetamido-2-deoxy-α-D-galactopyranoside Blocks the Apical Biosynthetic Pathway in Polarized HT-29 Cells
31. Intestinal dysbiosis in Inflammatory Bowel Disease associated with primary 1 immunodeficiency. 2
32. Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells
33. TCR density in early iNKT cell precursors regulates agonist selection and subset differentiation in mice
34. The Cytoplasmic/Transmembrane Domain of Dipeptidyl Peptidase IV, A Type II Glycoprotein, Contains an Apical Targeting Signal That Does Not Specifically Interact with Lipid Rafts
35. Apical Secretion and Sialylation of Soluble Dipeptidyl Peptidase IV Are Two Related Events
36. Loss of RASGRP 1 in humans impairs T‐cell expansion leading to Epstein‐Barr virus susceptibility
37. Inherited CD70 deficiency in humans reveals a critical role for the CD70–CD27 pathway in immunity to Epstein-Barr virus infection
38. SLAM‐associated protein favors the development of iNKT2 over iNKT17 cells
39. A hematopoietic cell–driven mechanism involving SLAMF6 receptor, SAP adaptors and SHP-1 phosphatase regulates NK cell education
40. Refractory monogenic Crohn’s disease due to X-linked inhibitor of apoptosis deficiency
41. Erratum: CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
42. Hsp70 Negatively Controls Rotavirus Protein Bioavailability in Caco-2 Cells Infected by the Rotavirus RF Strain
43. Dipeptidyl Aminopeptidase IV (DPP IV/CD26)
44. Characterization of a Di-leucine–based Signal in the Cytoplasmic Tail of the Nucleotide-pyrophosphatase NPP1 That Mediates Basolateral Targeting but not Endocytosis
45. Inherited CD70 deficiency in humans reveals a critical role for the CD70–CD27 pathway in immunity to Epstein-Barr virus infection
46. Signaux moléculaires de tri des protéines dans les cellules épithéliales : implication du domaine transmembranaire et des processus de maturation post-traductionnels
47. Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study.
48. Antibodies against restricted sequences in human c-ErbA hinge domain recognize differentially natural mammalian α- or β-type triiodothyronine receptors and interfere differently with hormone binding
49. Nuclear factors specifically favor thyroid hormone binding to c‐ErbAα1 protein (thyroid hormone receptor α) over‐expressed in E. coli
50. Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAPin association with a rare polymorphism in CD40LG
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