393 results on '"Okamura, Ken"'
Search Results
2. Rational design of a JAK1-selective siRNA inhibitor for the modulation of autoimmunity in the skin
3. RNAi-based modulation of IFN-γ signaling in skin
4. Genetic insights into Tietz albinism‐deafness syndrome: A new dominant‐negative mutation in MITF.
5. Post‐COVID‐19 vaccination diffuse cutaneous sarcoidosis
6. Resident memory T cell contributes to the phenotype of inflammatory vitiligo
7. Why does the FDIC sue?
8. A case of acute localized exanthematous pustulosis following COVID‐19 infection
9. Pulmonary manifestation of inflammatory bowel disease: Two case reports
10. ISID0841 - A vitiligo-associated SNP (rs706779) controls IL15RA isoforms and T cell activation in epidermal keratinocytes
11. A toddler case of keratosis follicularis squamosa (Dohi) successfully treated with salicylic acid ointment
12. Activation of the NLRP1 inflammasome in human keratinocytes by the dsDNA mimetic poly(dA:dT)
13. Pulmonary and Intestinal Involvement in a Patient with Myeloperoxidase-specific Antineutrophil Cytoplasmic Antibody-positive Hermansky-Pudlak Syndrome
14. Painless thyroiditis mimicking relapse of hyperthyroidism during or after potassium iodide or thionamide therapy for Graves’ disease resulting in remission
15. Primary Cutaneous Adenoid Cystic Carcinoma Connecting to the Epidermis
16. Intralymphatic histiocytosis in a patient with lung adenocarcinoma treated with pembrolizumab: a case report
17. Successful treatment of recurrent subcutaneous abscesses using granulocyte and monocyte adsorptive apheresis.
18. Analysis of predicted factors for bronchoalveolar lavage recovery failure: An observational study
19. Characterization of melanosomes and melanin in Japanese patients with Hermansky–Pudlak syndrome types 1, 4, 6, and 9
20. The effect of a topical vitamin D3 analog on repigmentation in mice with rhododendrol-induced leukoderma
21. Author response for 'Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease'
22. Case of a neutrophilic dermatosis involving lung abscess after influenza vaccination
23. Case of Japanese Hermansky–Pudlak syndrome patient with deeply invasive squamous cell carcinoma and multiple lesions of actinic keratosis on the face and neck
24. Importance of specific reference values for evaluation of the deteriorating thyroid function in patients with end-stage renal disease on hemodialysis
25. Acute respiratory failure due to Aspergillus niger infection with acute fibrinous and organazing pneumonia: A case report
26. Novel AP3B1 mutations in a Hermansky–Pudlak syndrome type2 with neonatal interstitial lung disease
27. Contemporary geophysical surveys for marine sub-bottom sediments -Marine geophysical surveys for cable routes planning-
28. A case of Graves’ disease presenting with internal ophthalmoplegia during methylmercaptoimidazole treatment
29. Iodide-sensitive Graves’ hyperthyroidism and the strategy for resistant or escaped patients during potassium iodide treatment
30. Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 6
31. Behavior of melanocytes and keratinocytes in reticulate acropigmentation of Kitamura
32. Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene
33. Gaining Insight into Vitiligo Genetics through the Lens of a Large Epidemiologic Study
34. Novel AP3B1 mutations in a Hermansky--Pudlak syndrome type2 with neonatal pulmonary fibrosis
35. AIM2 regulates anti-tumor immunity and is a viable therapeutic target for melanoma
36. Case of Hermansky–Pudlak syndrome 1 in a Japanese infant
37. Identification of a Hashimoto Thyroiditis Susceptibility Locus Via a Genome-wide Comparison With Gravesʼ Disease
38. Remission After Potassium Iodide Therapy in Patients With Gravesʼ Hyperthyroidism Exhibiting Thionamide-Associated Side Effects
39. CHOLESTEROL CRYSTAL DEPOSITION IN BASAL CELL CARCINOMA: P-177
40. Benford’s Law and COVID-19 reporting
41. Chemoradiation using cisplatin and S-1 in locally advanced giant squamous cell carcinoma of the buttock
42. Identification of Independent Susceptible and Protective HLA Alleles in Japanese Autoimmune Thyroid Disease and Their Epistasis
43. A case of acute localized exanthematous pustulosis following COVID‐19 infection.
44. Hermansky-Pudlak Syndrome with Acute Hatred Idiopathic Pulmonary Fibrosis: All of the Patients of Oculocutaneous Albinism for Past 20 Years in Juntendo University Hospital
45. Report of two Japanese patients with piebaldism including a novel mutation in KIT
46. Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families
47. Current landscape of Oculocutaneous Albinism in Japan
48. Case of a Mongolian child with extensive Mongolian spots in mucopolysaccharidosis type VI: Identification of a novel mutation in the arylsulfatase B gene
49. Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 6.
50. Identification of two novel mutations in a Japanese patient with Hermansky–Pudlak syndrome type 5
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