Isolation of All CD44 Transcripts in Human Epidermis and Regulation of Their Expression by Various Agents von Teye, Kwesi, Numata, Sanae, Ishii, Norito, Krol, Rafal P, Tsuchisaka, Atsunari, Hamada, Takahiro, Koga, Hiroshi, Karashima, Tadashi, Ohata, Chika, Tsuruta, Daisuke, Saya, Hideyuki, Haftek, Marek, Hashimoto, Takashi

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Immunological and Statistical Studies of Anti-BP180 Antibodies in Paraneoplastic Pemphigus von Tsuchisaka, Atsunari, Kawano, Hideo, Yasukochi, Atsushi, Teye, Kwesi, Ishii, Norito, Koga, Hiroshi, Sogame, Ryosuke, Ohzono, Ayaka, Krol, Rafal P., Kawakami, Tamihiro, Furumura, Minao, Ohata, Chika, Li, Xiaoguang, Hashimoto, Takashi

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Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea von Teye, Kwesi, Numata, Sanae, Krol, Rafal P, Ishii, Norito, Matsuda, Mitsuhiro, Hamada, Takahiro, Hashimoto, Takashi

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Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips von Deguchi, Sayaka, Kosugi, Kaori, Hashimoto, Rina, Sakamoto, Ayaka, Yamamoto, Masaki, Krol, Rafal P, Gee, Peter, Negoro, Ryosuke, Noda, Takeshi, Yamamoto, Takuya, Torisawa, Yu-Suke, Nagao, Miki, Takayama, Kazuo

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SARS-CoV-2-induced disruption of a vascular bed in a microphysiological system caused by type-I interferon from bronchial organoids von Fujimoto, Kazuya, Kameda, Yoshikazu, Nagano, Yuta, Deguchi, Sayaka, Yamamoto, Takuya, Krol, Rafal P, Gee, Peter, Matsumura, Yasufumi, Okamoto, Toru, Nagao, Miki, Takayama, Kazuo, Yokokawa, Ryuji

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Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease von Teye, Kwesi, Hamada, Takahiro, Krol, Rafal P, Numata, Sanae, Ishii, Norito, Matsuda, Mitsuhiro, Ohata, Chika, Furumura, Minao, Hashimoto, Takashi

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Ten cases of severe oral lichen planus showing granular C3 deposition in oral mucosal basement membrane zone von Hashimoto, Takashi, Fukuda, Aoi, Himejima, Akio, Morita, Shosuke, Tsuruta, Daisuke, Koga, Hiroshi, Krol, Rafal P., Ishii, Norito

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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners von Li, Xiaoguang, Qian, Hua, Ono, Fumitake, Tsuchisaka, Atsunari, Krol, Rafal P., Ohara, Koji, Hayakawa, Taihei, Matsueda, Satoko, Sasada, Tetsuro, Ohata, Chika, Furumura, Minao, Hamada, Takahiro, Hashimoto, Takashi

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Identification of CD44 transcripts that segregate with proliferation, redox and differentiation activities in human epidermal keratinocytes von Teye, Kwesi, Numata, Sanae, Ishii, Norito, Krol, Rafal P, Hamada, Takahiro, Koga, Hiroshi, Tsuruta, Daisuke, Saya, Hideyuki, Haftek, Marek, Hashimoto, Takashi

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Molecular diagnosis of Nagashima-type palmoplantar keratoderma von Krol, Rafal P, Numata, Sanae, Teye, Kwesi, Hamada, Takahiro, Matsuda, Mitsuhiro, Ishii, Norito, Ohyama, Bungo, Ohata, Chika, Furumura, Minao, Hashimoto, Takashi

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Isolation of all CD44 transcripts in human epidermis and regulation of their expression by various agents von Teye, Kwesi, Numata, Sanae, Krol, Rafal P, Hamada, Takahiro, Tsuchisaka, Atsunari, Karashima, Tadashi, Ohata, Chika, Furumura, Minao, Haftek, Marek, Ishii, Norito, Hashimoto, Takashi

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A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome von Numata, Sanae, Teye, Kwesi, Krol, Rafal P., Okamatsu, Yuki, Hashikawa, Keiko, Matsuda, Mitsuhiro, Fortugno, Paola, Di Zenzo, Giovanni, Castiglia, Daniele, Zambruno, Giovanna, Hamada, Takahiro, Hashimoto, Takashi

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A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases von Teye, Kwesi, Suga, Yasushi, Numata, Sanae, Soejima, Mikiko, Ishii, Norito, Krol, Rafal P, Ohata, Chika, Matsuda, Mitsuhiro, Honma, Masaru, Ishida-Yamamoto, Akemi, Hamada, Takahiro, Koda, Yoshiro, Hashimoto, Takashi

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Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A.D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases von Nishikawa, Ryuhei, Takahashi, Hitoshi, Matsuda, Mitsuhiro, Imaoka, Kaoru, Ogawa, Masahiro, Teye, Kwesi, Tsuchisaka, Atsunari, Koga, Hiroshi, Komorowski, Lars, Probst, Christian, Hachiya, Takahisa, Fritzler, Marvin J., Ishii, Norito, Ohata, Chika, Furumura, Minao, Krol, Rafal P., Muro, Yoshinao, Morita, Eishin, Hashimoto, Takashi

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Towards understanding mechanisms of autoimmune bullous skin diseases von Krol, Rafal P, Yasukochi, Atsushi, Hashimoto, Takashi

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Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (201... von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A.D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome von KAITO, Hiroshi, NOZU, Kandai, MATSUO, Masafumi, FU, Xue J, KAMIOKA, Ichiro, FUJITA, Teruo, KANDA, Kyoko, KROL, Rafal P, SUMINAGA, Ryo, ISHIDA, Akihito, IIJIMA, Kazumoto

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A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK 5 causes splicing disorder and mild phenotype in Netherton syndrome von Numata, Sanae, Teye, Kwesi, Krol, Rafal P., Okamatsu, Yuki, Hashikawa, Keiko, Matsuda, Mitsuhiro, Fortugno, Paola, Di Zenzo, Giovanni, Castiglia, Daniele, Zambruno, Giovanna, Hamada, Takahiro, Hashimoto, Takashi

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