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Genome-wide association study identifies CDH13 as a susceptibility gene for rhododendrol-induced leukoderma.
Okamura K, Abe Y, Naka I, Ohashi J, Yagami A, Matsunaga K, Kobayashi Y, Fukai K, Tanemura A, Katayama I, Masui Y, Ito A, Yamashita T, Nagai H, Nishigori C, Oiso N, Aoyama Y, Araki Y, Saito T, Hayashi M, Hozumi Y, Suzuki T. Okamura K, et al. Pigment Cell Melanoma Res. 2020 Nov;33(6):826-833. doi: 10.1111/pcmr.12904. Epub 2020 Jun 29. Pigment Cell Melanoma Res. 2020. PMID: 32558222
Oculocutaneous albinism (OCA) in Japanese patients: five novel mutations.
Okamura K, Yoshizawa J, Abe Y, Hanaoka K, Higashi N, Togawa Y, Nakagawa S, Kambe N, Funasaka Y, Ohko K, Hozumi Y, Suzuki T. Okamura K, et al. J Dermatol Sci. 2014 May;74(2):173-4. doi: 10.1016/j.jdermsci.2013.12.011. Epub 2014 Jan 10. J Dermatol Sci. 2014. PMID: 24461674 No abstract available.
Case of Hermansky-Pudlak syndrome 1 in a Japanese infant.
Tanaka M, Yang L, Wataya-Kaneda M, Suzuki T, Okamura K, Hozumi Y, Yang F, Katayama I. Tanaka M, et al. Among authors: okamura k. J Dermatol. 2015 Sep;42(9):906-7. doi: 10.1111/1346-8138.12937. Epub 2015 May 19. J Dermatol. 2015. PMID: 25988314 No abstract available.
Rhododenol-induced leukoderma in a mouse model mimicking Japanese skin.
Abe Y, Okamura K, Kawaguchi M, Hozumi Y, Aoki H, Kunisada T, Ito S, Wakamatsu K, Matsunaga K, Suzuki T. Abe Y, et al. Among authors: okamura k. J Dermatol Sci. 2016 Jan;81(1):35-43. doi: 10.1016/j.jdermsci.2015.10.011. Epub 2015 Oct 27. J Dermatol Sci. 2016. PMID: 26547111
Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.
Okamura K, Araki Y, Abe Y, Shigyou A, Fujiyama T, Baba A, Kanekura T, Chinen Y, Kono M, Niizeki H, Tsubota A, Konno T, Hozumi Y, Suzuki T. Okamura K, et al. J Dermatol Sci. 2016 Feb;81(2):140-2. doi: 10.1016/j.jdermsci.2015.10.014. Epub 2015 Oct 31. J Dermatol Sci. 2016. PMID: 26573111 No abstract available.
1,723 results