175 results on '"Yasuda, Koubun"'
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2. IL-33-induced keratoconjunctivitis is mediated by group 2 innate lymphoid cells in mice
3. Monitoring Cellular Movement with Photoconvertible Fluorescent Protein and Single-Cell RNA Sequencing Reveals Cutaneous Group 2 Innate Lymphoid Cell Subtypes, Circulating ILC2 and Skin-Resident ILC2
4. RAGE in circulating immune cells is fundamental for hippocampal inflammation and cognitive decline in a mouse model of latent chronic inflammation
5. Dupilumab Effects on Innate Lymphoid Cell and Helper T Cell Populations in Patients with Atopic Dermatitis
6. Periostin forms a functional complex with IgA in human serum
7. IL-33–Induced Atopic Dermatitis–Like Inflammation in Mice Is Mediated by Group 2 Innate Lymphoid Cells in Concert with Basophils
8. Human cystatin SN is an endogenous protease inhibitor that prevents allergic rhinitis
9. Allergen endotoxins induce T-cell–dependent and non–IgE-mediated nasal hypersensitivity in mice
10. Anti-interleukin-6 receptor antibody treatment ameliorates postoperative adhesion formation
11. IL-33-induced keratoconjunctivitis is mediated by group 2 innate lymphoid cells in mice
12. Host responses to intestinal nematodes
13. Skin-specific expression of IL-33 activates group 2 innate lymphoid cells and elicits atopic dermatitis-like inflammation in mice
14. Epithelial-derived nuclear IL-33 aggravates inflammation in the pathogenesis of reflux esophagitis
15. Contribution of IL-33–activated type II innate lymphoid cells to pulmonary eosinophilia in intestinal nematode-infected mice
16. Contribution of IL-18 to Atopic-Dermatitis-Like Skin Inflammation Induced by Staphylococcus aureus Product in Mice
17. Murine allergic rhinitis and nasal Th2 activation are mediated via TSLP- and IL-33-signaling pathways
18. Thymic stromal lymphopoietin contributes to protection of mice from Strongyloides venezuelensis infection by CD4+ T cell-dependent and -independent pathways
19. Lung fibroblasts produce IL-33 in response to stimulation with retinoblastoma-binding protein 9 via production of prostaglandin E2
20. Regnase-1 degradation is crucial for IL-33– and IL-25–mediated ILC2 activation
21. Contribution of IL-18 to eosinophilic airway inflammation induced by immunization and challenge with Staphylococcus aureus proteins
22. Contribution of IL-33 to induction and augmentation of experimental allergic conjunctivitis
23. Role of eosinophils in protective immunity against secondary nematode infections
24. Administration of IL-33 induces airway hyperresponsiveness and goblet cell hyperplasia in the lungs in the absence of adaptive immune system
25. Type 1 cytokine/chemokine production by mouse NK cells following activation of their TLR/MyD88-mediated pathways
26. ASC is essential for LPS-induced activation of procaspase-1 independently of TLR-associated signal adaptor molecules
27. Persistent secretion of IL-18 in the skin contributes to IgE response in mice
28. Interleukin-1/-33 Signaling Pathways as Therapeutic Targets for Endometriosis
29. Interleukin-18 in Health and Disease
30. Nematode-Infected Mice Acquire Resistance to Subsequent Infection With Unrelated Nematode by Inducing Highly Responsive Group 2 Innate Lymphoid Cells in the Lung
31. B cells with aberrant activation of Notch1 signaling promote Treg and Th2 cell–dominant T-cell responses via IL-33
32. Lung fibroblasts produce IL-33 in response to stimulation with retinoblastoma-binding protein 9 via production of prostaglandin E2.
33. Lung fibroblasts produce IL-33 in response to stimulation with retinoblastoma-binding protein 9 via production of prostaglandin E2.
34. Expression of IL-33 in ocular surface epithelium induces atopic keratoconjunctivitis with activation of group 2 innate lymphoid cells in mice
35. Ablation of IL-33 gene exacerbate myocardial remodeling in mice with heart failure induced by mechanical stress
36. Activation of group 2 innate lymphoid cells exacerbates and confers corticosteroid resistance to mouse nasal type 2 inflammation
37. Murine allergic rhinitis and nasal T h2 activation are mediated via TSLP- and IL-33-signaling pathways
38. Epithelial-derived nuclear IL-33 aggravates inflammation in the pathogenesis of reflux esophagitis
39. Immediate-type contact hypersensitivity is reduced in interleukin-33 knockout mice
40. Tu1883 Esophageal Epithelial-Derived IL-33 Acts As an Exaggerator of Inflammation in the Pathogenesis of GERD
41. Importance of Both Innate Immunity and Acquired Immunity for Rapid Expulsion of S. venezuelensis
42. IgG and IgE Collaboratively Accelerate Expulsion of Strongyloides venezuelensis in a Primary Infection
43. Contribution of IL-33 to contact urticaria model
44. 40 Contribution of IL-33 and Nuocyte to Experimental Allergic Dermatitis
45. The Jmjd3-Irf4 axis regulates M2 macrophage polarization and host responses against helminth infection
46. Erratum to “Neutrophil-dominant psoriasis-like skin inflammation induced by epidermal-specific expression of Raf in mice” [J. Dermatol. Sci. 58 (2010) 28–35]
47. Neutrophil-dominant psoriasis-like skin inflammation induced by epidermal-specific expression of Raf in mice
48. IL-27 suppresses Th2 cell development and Th2 cytokines production from polarized Th2 cells: a novel therapeutic way for Th2-mediated allergic inflammation.
49. Contribution of TIR domain-containing adapter inducing IFN-β-mediated IL-18 release to LPS-induced liver injury in mice
50. Basophils contribute to TH2-IgE responses in vivo via IL-4 production and presentation of peptide–MHC class II complexes to CD4+ T cells
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