Past Biodiversity: Japanese Historical Monographs Document the Epibiotic Barnacles and Cold-Stunning Event of the Hawksbill Turtle Eretmochelys imbricata von Hayashi, Ryota

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Update of recent findings in genetic hair disorders von Hayashi, Ryota, Shimomura, Yutaka

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CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells von Jacków, Joanna, Guo, Zongyou, Hansen, Corey, Abaci, Hasan E., Doucet, Yanne S., Shin, Jung U, Hayashi, Ryota, DeLorenzo, Dominick, Kabata, Yudai, Shinkuma, Satoru, Salas-Alanis, Julio C., Christiano, Angela M.

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Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia von Asano, Nobuyuki, Yasuno, Shuichiro, Hayashi, Ryota, Shimomura, Yutaka

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Distinguishing persistent effects in an undoped GaAs/AlGaAs quantum well by top-gate-dependent illumination von Fujita, Takafumi, Hayashi, Ryota, Kohda, Makoto, Ritzmann, Julian, Ludwig, Arne, Nitta, Junsaku, Wieck, Andreas D., Oiwa, Akira

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Two cases of severe congenital hypotrichosis caused by compound heterozygous mutations in the LSS gene von Murata, Mami, Hayashi, Ryota, Kawakami, Yoshio, Morizane, Shin, Shimomura, Yutaka

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Observation of Mode I Crack Growth Behavior in 4.762 mm Diameter-Silicon Nitride Ball under Compressive-Tensile Cyclic Loadings von Matsueda, Takahiro, Hayashi, Ryota, Hobo, Yasuharu, Mizobe, Koshiro, Kida, Katsuyuki

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Evidence for a dominant‐negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I von Yasuno, Shuichiro, Ansai, Osamu, Hayashi, Ryota, Nakamura, Sawako, Shimomura, Yutaka

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Potential Dependence of the Buckling Structure of the Interfacial Water Bilayer on a Graphene Electrode von Hayashi, Ryota, Hoshi, Nagahiro, Sakata, Osami, Nakamura, Masashi

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Case of transient neonatal hyperpigmentation of the proximal nail fold von Kawai, Toru, Hayashi, Ryota, Yokoyama, Rei, Abe, Riichiro

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Different degree of loss‐of‐function among four missense mutations in the EDAR gene responsible for autosomal recessive hypohidrotic ectodermal dysplasia may be associated with the... von Yagi, Sasagu, Yasuno, Shuichiro, Ansai, Osamu, Hayashi, Ryota, Shimomura, Yutaka

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CCL21‐Ser expression in melanoma cells recruits CCR7+ naïve T cells to tumor tissues and promotes tumor growth von Miyamoto, Megumi, Kawato, Yuki, Fujie, Ryonosuke, Kurowarabe, Kaoru, Fujiwara, Kakeru, Nobusawa, Reika, Hayashi, Ryota, Iida, Kei, Ohigashi, Izumi, Hayasaka, Haruko

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Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the LIPH gene at c.742C > A and c.614A > G: The first Japanese case von Yamaguchi, Natsuki, Kiniwa, Yukiko, Hayashi, Ryota, Abe, Riichiro, Katsuie, Shiho, Okuyama, Ryuhei

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A case of epidermolysis bullosa simplex‐Ogna with nail involvement von Takei, Shingo, Hayashi, Ryota, Katsumi, Tatsuya, Ansai, Osamu, Sakai, Akari, Natsuga, Ken, Abe, Riichiro

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Only plantar lesion of punctate palmoplantar keratoderma with a novel missense mutation in the AAGAB gene: Two Japanese familial case reports and review of reported mutations von Hasegawa, Akito, Hayashi, Ryota, Shimomura, Yutaka, Hirashima, Masanori, Abe, Riichiro

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Enhancement of Dark Polymerization by Oxygen Quenching during Network Formation in Ultraviolet-Light-Induced Radical Polymerization of Multifunctional Monomers and Reactive Polymer von Taki, Kentaro, Hayashi, Ryota, Taniguchi, Takatoshi, Tsuneishi, Asuka

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Expression studies of nectin-1 in human hair follicles and identification of a p63-responsive element in the NECTIN1 promoter von Hayashi, Ryota, M.D, Abe, Riichiro, M.D., Ph.D, Shimomura, Yutaka, M.D., Ph.D

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Cam-Like Mechanism in Intertarsal Joints of Ratites and its Design Framework von Ito, Kazuki, Hida, Sayaka, Kinugasa, Tetsuya, Chiba, Kentaro, Okuda, Yu, Ichikawa, Miwa, Okoshi, Tsukasa, Takasaki, Ryuji, Hayashi, Ryota, Yoshida, Koji, Osuka, Koichi

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Observation of Mode I and Mode II Fatigue Crack Growth on Silicon Nitride Balls under Cyclic Compressive Loads von Matsueda, Takahiro, Hayashi, Ryota, Kida, Katsuyuki, Matsubayashi, Soji, Matsui, Tomoya

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CADM1 is a diagnostic marker in early-stage mycosis fungoides: Multicenter study of 58 cases von Yuki, Akihiko, Shinkuma, Satoru, Hayashi, Ryota, Fujikawa, Hiroki, Kato, Taisuke, Homma, Erina, Hamade, Yohei, Onodera, Osamu, Matsuoka, Masao, Shimizu, Hiroshi, Iwata, Hiroaki, Abe, Riichiro

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