Distinct Characteristics in Japanese Dermatitis Herpetiformis : A Review of All 91 Japanese Patients over the Last 35 Years by Ohata, Chika, Ishii, Norito, Hamada, Takahiro, Shimomura, Yutaka, Niizeki, Hironori, Dainichi, Teruki, Furumura, Minao, Tsuruta, Daisuke, Hashimoto, Takashi

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Factors Affecting Postoperative Spinal Epidural Hematoma and the Optimal Order of Vertebral Body Decompression in Multivertebral Microendoscopic Laminectomy by Soejima, Yu, Arizono, Takeshi, Bekki, Hirofumi, Inokuchi, Akihiko, Izumi, Teiyu, Imamura, Ryuta, Hamada, Takahiro, Nakamura, Kimitaka, Sakai, Mamiko, Yoshimoto, Masakazu, Yamamoto, Masatoshi

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Autoantibodies to extracellular matrix protein 1 in lichen sclerosus by Oyama, Noritaka, Chan, Ien, Neill, Sallie M, Hamada, Takahiro, South, Andrew P, Wessagowit, Vesarat, Wojnarowska, Fenella, D'Cruz, David, Hughes, Graham J, Black, Martin M, McGrath, John A

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A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases by 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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An attempt to develop mouse model for anti-laminin γ1 pemphigoid by Koga, Hiroshi, Ishii, Norito, Dainichi, Teruki, Tsuruta, Daisuke, Hamada, Takahiro, Ohata, Chika, Karashima, Tadashi, Furumura, Minao, Hashimoto, Takashi

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A Novel Microduplication Spanning Exons 8–16 of ATP2C1 That Was Undetectable by Standard Sanger Sequencing in a Japanese Patient With Hailey–Hailey Disease by Teye, Kwesi, Koga, Hiroshi, Hamada, Takahiro, Matsuda, Mitsuhiro, Ichiki, Mikio, Numata, Sanae, Ishii, Norito, Nakama, Takekuni

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Plant-specific microtubule-associated protein SPIRAL2 is required for anisotropic growth in Arabidopsis. [Erratum: 2005 Mar., v. 137, no. 3, p. 1169.] by Shoji, T, Narita, N.N, Hayashi, K, Asada, J, Hamada, T, Sonobe, S, Nakajima, K, Hashimoto, T

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Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A by Nagy, Nikoletta, Wedgeworth, Emma, Hamada, Takahiro, White, Jonathan M, Hashimoto, Takashi, McGrath, John A

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

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How do keratinizing disorders and blistering disorders overlap? by Hamada, Takahiro, Tsuruta, Daisuke, Fukuda, Shunpei, Ishii, Norito, Teye, Kwesi, Numata, Sanae, Dainichi, Teruki, Karashima, Tadashi, Ohata, Chika, Furumura, Minao, Hashimoto, Takashi

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Mutation-dependent effects on mRNA and protein expressions in cultured keratinocytes of Hailey-Hailey disease by Matsuda, Mitsuhiro, Hamada, Takahiro, Numata, Sanae, Teye, Kwesi, Okazawa, Hiromi, Imafuku, Shinichi, Ohata, Chika, Furumura, Minao, Hashimoto, Takashi

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A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene by Yasuda, Hazuki, Kanazawa, Nobuo, Matsuda, Mitsuhiro, Hamada, Takahiro, Furumura, Minao, Hashimoto, Takashi, Nakama, Takekuni, Furukawa, Fukumi

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Epidermal polymeric immunoglobulin receptors: leads from intraepidermal neutrophilic IgA dermatosis-type IgA pemphigus by Tsuchisaka, Atsunari, Ishii, Norito, Hamada, Takahiro, Teye, Kwesi, Sogame, Ryosuke, Koga, Hiroshi, Tsuruta, Daisuke, Ohata, Chika, Furumura, Minao, Hashimoto, Takashi

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Interaction of plectin and intermediate filaments by Karashima, Tadashi, Tsuruta, Daisuke, Hamada, Takahiro, Ishii, Norito, Ono, Fumitake, Hashikawa, Keiko, Ohyama, Bungo, Natsuaki, Yohei, Fukuda, Shunpei, Koga, Hiroshi, Sogame, Ryosuke, Nakama, Takekuni, Dainichi, Teruki, Hashimoto, Takashi

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Microtubule-Associated Kinase-like Protein RUNKEL Needed for Cell Plate Expansion in Arabidopsis Cytokinesis by Krupnova, Tamara, Sasabe, Michiko, Ghebreghiorghis, Luam, Gruber, Christian W., Hamada, Takahiro, Dehmel, Verena, Strompen, Georg, Stierhof, York-Dieter, Lukowitz, Wolfgang, Kemmerling, Birgit, Machida, Yasunori, Hashimoto, Takashi, Mayer, Ulrike, Jürgens, Gerd

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Late-onset Darier's disease due to a novel missense mutation in the ATP2A2 gene: A different missense mutation affecting the same codon has been previously reported in acrokeratosi... by Ueo, Daisuke, Hamada, Takahiro, Hashimoto, Takashi, Hatano, Yutaka, Okamoto, Osamu, Fujiwara, Sakuhei

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RNA Processing Bodies, Peroxisomes, Golgi Bodies, Mitochondria, and Endoplasmic Reticulum Tubule Junctions Frequently Pause at Cortical Microtubules by Hamada, Takahiro, Tominaga, Motoki, Fukaya, Takashi, Nakamura, Masayoshi, Nakano, Akihiko, Watanabe, Yuichiro, Hashimoto, Takashi, Baskin, Tobias I.

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Morphological changes of the hair roots in alopecia areata: A scanning electron microscopic study by Karashima, Tadashi, Tsuruta, Daisuke, Hamada, Takahiro, Ishii, Norito, Ono, Fumitake, Ueda, Akihiro, Abe, Toshifumi, Nakama, Takekuni, Dainichi, Teruki, Hashimoto, Takashi

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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia by 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 by 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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