183 results on '"Keszei, Marton"'
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2. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients
3. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.
4. Combination of tyrosine kinase inhibitors and the MCL1 inhibitor S63845 exerts synergistic antitumorigenic effects on CML cells
5. Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency
6. Slamf6 negatively regulates autoimmunity
7. Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive
8. Characterization of Ly108-H1 Signaling Reveals Ly108-3 Expression and Additional Strain-Specific Differences in Lupus Prone Mice
9. Anti-Citrullinated Protein Antibody Reactivity towards Neutrophil-Derived Antigens : Clonal Diversity and Inter-Individual Variation
10. Generation of NK cells with chimeric-switch receptors to overcome PD1-mediated inhibition in cancer immunotherapy
11. A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome
12. IFNγ directly counteracts imatinib-induced apoptosis of primary human CD34+ CML stem/progenitor cells potentially through the upregulation of multiple key survival factors
13. P-020: PD1-based chimeric-switch receptor expressing NK cells recover from immune checkpoint inhibition in cancer
14. IFN gamma directly counteracts imatinib-induced apoptosis of primary human CD34+CML stem/progenitor cells potentially through the upregulation of multiple key survival factors
15. SAP expression in invariant NKT cells is required for cognate help to support B-cell responses
16. Wiskott-Aldrich syndrome protein (WASP) and N-WASP are critical for peripheral B-cell development and function
17. B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice
18. Overactive WASp in X-linked neutropenia leads to aberrant B-cell division and accelerated plasma cell generation
19. Homozygous DNA Ligase IV R278H Mutation in Mice Leads to Leaky SCID and Represents a Model for Human LIG4 Syndrome
20. Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive
21. The cell surface receptor Slamf6 modulates innate immune responses during Citrobacter rodentium-induced colitis
22. SLAM family receptors and the SLAM-associated protein (SAP) modulate T cell functions
23. Constitutive activation of WASp leads to abnormal cytotoxic cells with increased granzyme B and degranulation response to target cells
24. HtrA1 is a novel mast cell serine protease of mice and men
25. Auto-antibody production and glomerulonephritis in congenic Slamf1−/− and Slamf2−/− [B6.129] but not in Slamf1−/− and Slamf2−/− [BALB/c.129] mice
26. ANALYSIS OF IMMUNOLOGICAL GENE EXPRESSION DATA FROM DNA MICROARRAYS
27. Wiskott-Aldrich syndrome gene mutations modulate cancer susceptibility in the p53±murine model
28. The Wiskott-Aldrich syndrome protein regulates antigen processing and presentation by dendritic cells
29. Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells
30. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency
31. Deletion of Wiskott-Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
32. Congenital Defects in Neutrophil Dynamics
33. Deletion of Wiskott–Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
34. An NK cell-independent role for slamf4 in controlling humoral Autoimmunity1
35. Deletion of WASp and N-WASp in B cells cripples the germinal center response and results in production of IgM autoantibodies
36. A novel isoform of the Ly108 gene ameliorates murine lupus
37. SAP modulates B cell functions in a genetic background-dependent manner
38. Expansion of an osteopontin‐expressing T follicular helper cell subset correlates with autoimmunity in B6.Sle1b mice and is suppressed by the H1‐isoform of the Slamf6 receptor
39. NKT cells support B lymphocyte functions independently of expression of the adapter SAP. (106.45)
40. The H1-isoform of the cell surface receptor Slamf6 suppresses expansion of PD-1+ OPN+ CD4+ T Follicular Helper cells in the lupus-prone B6.Sle1b mice. (123.5)
41. Cutting Edge: Protein Phosphatase 2A Confers Susceptibility to Autoimmune Disease through an IL-17–Dependent Mechanism
42. Cutting Edge: An NK Cell-Independent Role for Slamf4 in Controlling Humoral Autoimmunity
43. A novel isoform of the Ly108 gene ameliorates murine lupus
44. SLAM is a microbial sensor that regulates bacterial phagosome functions in macrophages
45. Defects of B Cell Tolerance and Expansion of Immunoglobulin Secreting Cells in Rag-dependent Immunodeficiency
46. F.121. B Cell-mediated Autoimmunity in Hypomorphic rag1 and lig4 Mouse Mutants as Models for Human Leaky SCID
47. CCR5Δ32 mutation, Mycoplasma pneumoniae infection, and asthma
48. Progesterone-Induced Blocking Factor Activates STAT6 via Binding to a Novel IL-4 Receptor
49. Wiskott-Aldrich syndrome gene mutations modulate cancer susceptibility in the p53± murine model.
50. Β cell-intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice.
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