Search Results - "Numata, Sanae"

Epiplakin Is a Paraneoplastic Pemphigus Autoantigen and Related to Bronchiolitis Obliterans in Japanese Patients by Tsuchisaka, Atsunari, Numata, Sanae, Teye, Kwesi, Natsuaki, Yohei, Kawakami, Tamihiro, Takeda, Yoshito, Wang, Wenqing, Ishikawa, Kazushi, Goto, Mizuki, Koga, Hiroshi, Sogame, Ryosuke, Ishii, Norito, Takamori, Shinzo, Hoshino, Tomoaki, Brandt, Oliver, Pas, Hendri H., Fujiwara, Sakuhei, Hashimoto, Takashi

“…All plakin family proteins are known to be autoantigens in paraneoplastic pemphigus (PNP). In this study, we first examined whether PNP sera also react with…”
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Multimerization is required for antigen binding activity of an engineered IgM/IgG chimeric antibody recognizing a skin-related antigen by Teye, Kwesi, Hashimoto, Koji, Numata, Sanae, Ohta, Kunihiro, Haftek, Marek, Hashimoto, Takashi

“…Monoclonal antibodies offer great tools for research. We encountered a potentially useful mouse IgM monoclonal antibody whose antigen is expressed in normal…”
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Shikonin Promotes Skin Cell Proliferation and Inhibits Nuclear Factor-κB Translocation via Proteasome Inhibition In Vitro by Yan, Yan, Furumura, Minao, Gouya, Takako, Iwanaga, Atsufumi, Teye, Kwesi, Numata, Sanae, Karashima, Tadashi, Li, Xiao-Guang, Hashimoto, Takashi

“…Background：Shikonin is a major active chemical component extracted from Lithospermi Radix,an effective traditional herb in various types of wound…”
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Filaggrin gene (FLG) promoter polymorphisms are associated with atopic dermatitis in the Japanese population by Teye, Kwesi, Koga, Hiroshi, Nagai, Akira, Ohata, Chika, Numata, Sanae, Hamada, Takahiro, Ishii, Norito, Nakama, Takekuni

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Establishment of IgA ELISAs of mammalian recombinant proteins of human desmocollins 1-3 by Teye, Kwesi, Numata, Sanae, Ohzono, Ayaka, Ohyama, Bungo, Tsuchisaka, Atsunari, Koga, Hiroshi, Hachiya, Takahisa, Tsuruta, Daisuke, Ishii, Norito, Hashimoto, Takashi

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Isolation of All CD44 Transcripts in Human Epidermis and Regulation of Their Expression by Various Agents by 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

“…CD44, a cell surface proteoglycan, is involved in many biological events. CD44 transcripts undergo complex alternative splicing, resulting in many functionally…”
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Functional study of TGM1 missense mutations in autosomal recessive congenital ichthyosis by Numata, Sanae, Teye, Kwesi, Karashima, Tadashi, Matsuda, Mitsuhiro, Hamada, Takahiro, 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 by Teye, Kwesi, Numata, Sanae, Krol, Rafal P, Ishii, Norito, Matsuda, Mitsuhiro, Hamada, Takahiro, 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

“…Hailey–Hailey disease (HHD) is genetic skin disorder characterized by repeated and exacerbated skin lesions in friction regions. ATP2C1 , encoding SPCA1, was…”
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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

“…Abstract Background Peeling skin syndrome (PSS) is a rare autosomal recessive form of ichthyosis showing skin exfoliation. PSS is divided into acral and…”
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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

“…Inherited keratinizing disorders are caused by mutations in the genes encoding cornified cell envelope proteins, enzymes and their inhibitors, adhesion…”
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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

“…Hailey–Hailey disease (HHD) is a dominantly inherited skin disease caused by mutations in ATP2C1 gene, which encodes secretory pathway Ca2+/Mn2+‐ATPase protein…”
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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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A three-dimensional in vitro culture model of Hailey-Hailey disease by Matsuda, Mitsuhiro, Hamada, Takahiro, Numata, Sanae, Teye, Kwesi, Ishii, Norito, Ohata, Chika, Furumura, Minao, Nakama, Takekuni, Hashimoto, Takashi

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Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients by Numata, Sanae, Harada, Eimei, Maeno, Yasuki, Ueki, Isao, Watanabe, Yoriko, Fujii, Chieko, Yanagawa, Takashi, Takenaka, Satoshi, Inoue, Toshiro, Inoue, Shinkai, Goushi, Terufumi, Yasutake, Tsutomu, Mizuta, Toshihiko, Yoshino, Makoto

“…In ten families with late-onset ornithine transcarbamylase (OTC) deficiency in male patients, three mutant alleles-R40H, R277W, and Y55D-were identified. In a…”
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Rapid quantitative analysis of human cytomegalovirus DNA by the real-time polymerase chain reaction method by Numata, Sanae, Nakamura, Yasuhiro, Imamura, Yutaka, Honda, Junichi, Momosaki, Seiya, Kojiro, Masamichi

“…Human cytomegalovirus (CMV) infection is a progressive and life-threatening complication in immunocompromised patients even now. Therefore, early and accurate…”
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Anti-Alpha-2-Macroglobulin-Like-1 Autoantibodies Are Detected Frequently and May Be Pathogenic in Paraneoplastic Pemphigus by Numata, Sanae, Teye, Kwesi, Tsuruta, Daisuke, Sogame, Ryosuke, Ishii, Norito, Koga, Hiroshi, Natsuaki, Yohei, Tsuchisaka, Atsunari, Hamada, Takahiro, Karashima, Tadashi, Nakama, Takekuni, Furumura, Minao, Ohata, Chika, Kawakami, Tamihiro, Schepens, Isabelle, Borradori, Luca, Hashimoto, Takashi

“…Paraneoplastic pemphigus (PNP) shows autoantibodies mainly to plakin and desmosomal cadherin family proteins. We have recently identified…”
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Complete Maternal Isodisomy of Chromosome 5 in a Japanese Patient with Netherton Syndrome by Numata, Sanae, Hamada, Takahiro, Teye, Kwesi, Matsuda, Mitsuhiro, Ishii, Norito, Karashima, Tadashi, Kabashima, Kenji, Furumura, Minao, Ohata, Chika, Hashimoto, Takashi

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Various peroxisome proliferator-activated receptor (PPAR)-γ agonists differently induce differentiation of cultured human keratinocytes by Yan, Yan, Furumura, Minao, Numata, Sanae, Teye, Kwesi, Karashima, Tadashi, Ohyama, Bungo, Tanida, Norifumi, Hashimoto, Takashi

“…Peroxisome proliferator‐activated receptors (PPARs) are potentially useful for the treatment of skin diseases, because they stimulate keratinocyte…”
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Functional study of TGM 1 missense mutations in autosomal recessive congenital ichthyosis by Numata, Sanae, Teye, Kwesi, Karashima, Tadashi, Matsuda, Mitsuhiro, Hamada, Takahiro, Hashimoto, Takashi

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