192 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. Overactive WASp in X-linked neutropenia leads to aberrant B-cell division and accelerated plasma cell generation
4. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.
5. Combination of tyrosine kinase inhibitors and the MCL1 inhibitor S63845 exerts synergistic antitumorigenic effects on CML cells
6. Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency
7. Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive
8. Slamf6 negatively regulates autoimmunity
9. Anti-Citrullinated Protein Antibody Reactivity towards Neutrophil-Derived Antigens : Clonal Diversity and Inter-Individual Variation
10. Characterization of Ly108-H1 Signaling Reveals Ly108-3 Expression and Additional Strain-Specific Differences in Lupus Prone Mice
11. Deletion of WASp and N-WASp in B cells cripples the germinal center response and results in production of IgM autoantibodies
12. Generation of NK cells with chimeric-switch receptors to overcome PD1-mediated inhibition in cancer immunotherapy
13. A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome
14. SAP modulates B cell functions in a genetic background-dependent manner
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. IFNγ directly counteracts imatinib-induced apoptosis of primary human CD34+ CML stem/progenitor cells potentially through the upregulation of multiple key survival factors
19. P-020: PD1-based chimeric-switch receptor expressing NK cells recover from immune checkpoint inhibition in cancer
20. Homozygous DNA Ligase IV R278H Mutation in Mice Leads to Leaky SCID and Represents a Model for Human LIG4 Syndrome
21. IFN gamma directly counteracts imatinib-induced apoptosis of primary human CD34+CML stem/progenitor cells potentially through the upregulation of multiple key survival factors
22. Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive
23. The cell surface receptor Slamf6 modulates innate immune responses during Citrobacter rodentium-induced colitis
24. SLAM family receptors and the SLAM-associated protein (SAP) modulate T cell functions
25. HtrA1 is a novel mast cell serine protease of mice and men
26. Constitutive activation of WASp leads to abnormal cytotoxic cells with increased granzyme B and degranulation response to target cells
27. Modulation of cancer pathways by inhibitors of guanylate metabolism
28. Auto-antibody production and glomerulonephritis in congenic Slamf1−/− and Slamf2−/− [B6.129] but not in Slamf1−/− and Slamf2−/− [BALB/c.129] mice
29. Polymorphism in the promoter region of the apolipoprotein A5 gene is associated with an increased susceptibility for coronary artery disease
30. ANALYSIS OF IMMUNOLOGICAL GENE EXPRESSION DATA FROM DNA MICROARRAYS
31. The development of asthma in children infected with Chlamydia pneumoniae is dependent on the modifying effect of mannose-binding lectin
32. Wiskott-Aldrich syndrome gene mutations modulate cancer susceptibility in the p53±murine model
33. Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells
34. The Wiskott-Aldrich syndrome protein regulates antigen processing and presentation by dendritic cells
35. Deletion of Wiskott-Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
36. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency
37. Deletion of Wiskott–Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
38. Congenital Defects in Neutrophil Dynamics
39. An NK cell-independent role for slamf4 in controlling humoral Autoimmunity1
40. A novel isoform of the Ly108 gene ameliorates murine lupus
41. 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
42. NKT cells support B lymphocyte functions independently of expression of the adapter SAP. (106.45)
43. 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)
44. Cutting Edge: Protein Phosphatase 2A Confers Susceptibility to Autoimmune Disease through an IL-17–Dependent Mechanism
45. Cutting Edge: An NK Cell-Independent Role for Slamf4 in Controlling Humoral Autoimmunity
46. A novel isoform of the Ly108 gene ameliorates murine lupus
47. SLAM is a microbial sensor that regulates bacterial phagosome functions in macrophages
48. Defects of B Cell Tolerance and Expansion of Immunoglobulin Secreting Cells in Rag-dependent Immunodeficiency
49. F.121. B Cell-mediated Autoimmunity in Hypomorphic rag1 and lig4 Mouse Mutants as Models for Human Leaky SCID
50. CCR5Δ32 mutation, Mycoplasma pneumoniae infection, and asthma
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