Expression of discoidin domain receptor 1 and E‐cadherin in epidermis affects melanocyte behavior in rhododendrol‐induced leukoderma mouse model von Abe, Yuko, Hozumi, Yutaka, Okamura, Ken, Suzuki, Tamio

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The effect of a topical vitamin D3 analog on repigmentation in mice with rhododendrol-induced leukoderma von Abe, Yuko, Okamura, Ken, Ito, Shosuke, Hozumi, Yutaka, Suzuki, Tamio

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ADAM protease inhibitors reduce melanogenesis by regulating PMEL17 processing in human melanocytes von Kawaguchi, Masakazu, Hozumi, Yutaka, Suzuki, Tamio

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Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mouse model of rhododendrol‐induced vitiligo von Hayashi, Masahiro, Okamura, Ken, Abe, Yuko, Hozumi, Yutaka, Suzuki, Tamio

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Impact of a 4‐bp deletion variant (rs984225803) in the promoter region of SLC45A2 on color variation among a Japanese population von Okamura, Ken, Abe, Yuko, Hayashi, Masahiro, Saito, Toru, Nagatani, Kei, Tanoue, Toshihide, Wataya‐Kaneda, Mari, Hozumi, Yutaka, Suzuki, Tamio

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Report of two Japanese patients with piebaldism including a novel mutation in KIT von Nagatani, Kei, Okamura, Ken, Katagiri, Kazumoto, Ono, Ryusuke, Nishigori, Chikako, Araki, Yuta, Saito, Toru, Hozumi, Yutaka, Suzuki, Tamio

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Leukoderma induced by rhododendrol is different from leukoderma of vitiligo in pathogenesis: A novel comparative morphological study von Tsutsumi, Reiko, Sugita, Kazunari, Abe, Yuko, Hozumi, Yutaka, Suzuki, Tamio, Yamada, Nanako, Yoshida, Yuichi, Yamamoto, Osamu

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Rhododenol-induced leukoderma in a mouse model mimicking Japanese skin von Abe, Yuko, Okamura, Ken, Kawaguchi, Masakazu, Hozumi, Yutaka, Aoki, Hitomi, Kunisada, Takahiro, Ito, Shosuke, Wakamatsu, Kazumasa, Matsunaga, Kayoko, Suzuki, Tamio

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Association of melanogenesis genes with skin color variation among Japanese females von Abe, Yuko, Tamiya, Gen, Nakamura, Tomohiro, Hozumi, Yutaka, Suzuki, Tamio

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Genome‐wide association study identifies CDH13 as a susceptibility gene for rhododendrol‐induced leukoderma von Okamura, Ken, Abe, Yuko, Naka, Izumi, Ohashi, Jun, Yagami, Akiko, Matsunaga, Kayoko, Kobayashi, Yui, Fukai, Kazuyoshi, Tanemura, Atsushi, Katayama, Ichiro, Masui, Yukiko, Ito, Akiko, Yamashita, Toshiharu, Nagai, Hiroshi, Nishigori, Chikako, Oiso, Naoki, Aoyama, Yumi, Araki, Yuta, Saito, Toru, Hayashi, Masahiro, Hozumi, Yutaka, Suzuki, Tamio

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Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT5 von Okamura, Ken, Fukushima, Satoshi, Yamashita, Junji, Abe, Yuko, Hayashi, Masahiro, Hozumi, Yutaka, Ihn, Hironobu, Suzuki, Tamio

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Effects of Angiotensin II Receptor Signaling during Skin Wound Healing von Takeda, Hikaru, Katagata, Yohtaro, Hozumi, Yutaka, Kondo, Shigeo

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Microsatellite polymorphism located immediately upstream of the phosphatidylinositol glycan, class K gene ( PIGK ) affects its expression, which correlates with tyrosinase activity... von Okamura, Ken, Hayashi, Masahiro, Abe, Yuko, Araki, Yuta, Hozumi, Yutaka, Suzuki, Tamio

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Dyschromatosis symmetrica hereditaria complicated by intracranial hemangiomas and Parry-Romberg syndrome von Yanagishita, Saki, Fukai, Kazuyoshi, Tsuruta, Daisuke, Seto, Toshiyuki, Shimono, Taro, Okamura, Ken, Hozumi, Yutaka, Suzuki, Tamio

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Ultrastructural study of dyschromatosis symmetrica hereditaria with widespread pigmentary eruption von Omura, Reina, Fukai, Kazuyoshi, Sugawara, Koji, Tsuruta, Daisuke, Okamura, Ken, Hozumi, Yutaka, Suzuki, Tamio

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Knockdown of Skp2 by siRNA inhibits melanoma cell growth in vitro and in vivo von Katagiri, Yoshiyuki, Hozumi, Yutaka, Kondo, Shigeo

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Immunohistopathological analysis of frizzled-4-positive immature melanocytes from hair follicles of patients with Rhododenol-induced leukoderma von Okamura, Ken, Ohe, Rintaro, Abe, Yuko, Ueki, Masao, Hozumi, Yutaka, Tamiya, Gen, Matsunaga, Kayoko, Yamakawa, Mitsunori, Suzuki, Tamio

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Whole-exome sequencing confirmation of multiple MC1R variants associated with extensive freckles and red hair: Analysis of a Mongolian family von Araki, Yuta, Okamura, Ken, M.D., P.h.D, Munkhbat, Batmunkh, Tamiya, Gen, Erdene-Ochir, Bujin, Nemekhbaatar, Lkhasuren, Hozumi, Yutaka, Suzuki, Tamio

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Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations von Okamura, Ken, Araki, Yuta, Abe, Yuko, Shigyou, Akari, Fujiyama, Toshiharu, Baba, Atsunori, Kanekura, Takuro, Chinen, Yasutsugu, Kono, Michihiro, Niizeki, Hironori, Tsubota, Akiko, Konno, Takayuki, Hozumi, Yutaka, Suzuki, Tamio

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Dystrophic epidermolysis bullosa pruriginosa of elderly onset von HAYASHI, Masahiro, KAWAGUCHI, Masakazu, HOZUMI, Yutaka, NAKANO, Hajime, SAWAMURA, Daisuke, SUZUKI, Tamio

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