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The Journal of Dermatology|October 23, 2025
Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical ManifestationsKen Okamura, Tamio SuzukiJournal of Dermatological Science|January 31, 2025
Genetics and epigenetics in vitiligoKen Okamura, Tamio SuzukiPigment Cell & Melanoma Research|September 24, 2020
Current landscape of Oculocutaneous Albinism in JapanKen Okamura, Tamio SuzukiThe Journal of Dermatology|August 10, 2020
Expression of discoidin domain receptor 1 and E-cadherin in epidermis affects melanocyte behavior in rhododendrol-induced leukoderma mouse modelYuko Abe, Yutaka Hozumi, Ken Okamura, et al.Journal of Dermatological Science|December 7, 2016
Microsatellite polymorphism located immediately upstream of the phosphatidylinositol glycan, class K gene (PIGK) affects its expression, which correlates with tyrosinase activity in human melanocytesKen Okamura, Masahiro Hayashi, Yuko Abe, et al.Pigment Cell & Melanoma Research|July 19, 2018
A 4-bp deletion promoter variant (rs984225803) is associated with mild OCA4 among Japanese patientsKen Okamura, Masahiro Hayashi, Osamu Nakajima, et al.Pigment Cell & Melanoma Research|September 27, 2020
Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese familiesYuta Araki, Ken Okamura, Toru Saito, et al.Pigment Cell & Melanoma Research|February 24, 2025
Synonymous but Significant: New Findings of Pathological Variants in Hermansky-Pudlak SyndromeJunnosuke Kawaguchi, Ken Okamura, Toru Saito, et al.Pigment Cell & Melanoma Research|March 5, 2024
Genetic insights into Tietz albinism-deafness syndrome: A new dominant-negative mutation in MITFKohei Yamamoto, Ken Okamura, Kazumasa Wakamatsu, et al.Pigment Cell & Melanoma Research|December 6, 2021
Impact of a SLC24A5 variant on the retinal pigment epithelium of a Japanese patient with oculocutaneous albinism type 6Toru Saito, Ken Okamura, Rika Kosaki, et al.Pageof 16