22 results on '"Nakamura, Motonobu"'
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2. Effect of cis-urocanic acid on atopic dermatitis in NC/Nga mice
3. Resolvin E1 inhibits dendritic cell migration in the skin and attenuates contact hypersensitivity responses
4. Expression of activation induced deaminase (AID) and BRAF V600E mutation in malignant melanoma
5. Induction of S100 calcium-binding protein A2 expression in keratinocytes by telaprevir and trichloroethylene
6. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: Ten novel mutations of the ADAR1 gene
7. Increased frequencies of Th17 cells in drug eruptions
8. A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis
9. D1-like dopamine receptors antagonist inhibits cutaneous immune reactions mediated by Th2 and mast cells
10. Identification of a mutation in GJB6 gene, encoding a gap junction protein Cx30, in a family with Clouston syndrome
11. Galectin-7, induced by cis-urocanic acid and ultraviolet B irradiation, down-modulates cytokine production by T lymphocytes
12. CCR5 expression on melanoma cells affects the disease progression
13. Role of prostaglandin E2-EP2/EP4 signaling in the development of photosensitivity in pellagra
14. GJB6, of which mutations underlie Clouston syndrome, is a potential direct target gene of p63
15. Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
16. A group of atopic dermatitis without IgE elevation or barrier impairment shows a high Th1 frequency: Possible immunological state of the intrinsic type
17. Heparin serves as a natural stimulant of the inflammasome and exacerbates the symptoms of tumor necrosis factor receptor-associated periodic syndrome (TRAPS)
18. Modulation of semaphorin 3A expression by calcium concentration and histamine in human keratinocytes and fibroblasts
19. Epithelial–mesenchymal transition in the skin
20. A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
21. High expression of activation induced deaminase in recurrent or metastatic squamous cell carcinoma.
22. Expression of activation induced deaminase (AID) and BRAFV600E mutation in malignant melanoma.
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