Search Results - "Sato, Kazuko"

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    Usefulness of second-look ultrasonography using anatomical breast structures as indicators for magnetic resonance imaging-detected breast abnormalities by Izumori, Ayumi, Kokubu, Yumi, Sato, Kazuko, Gomi, Naoya, Morizono, Hidetomo, Sakai, Takehiko, Horii, Rie, Akiyama, Futoshi, Iwase, Takuji, Ohno, Shinji

    Published in Breast cancer (Tokyo, Japan) (01-01-2020)
    “…Background Second-look ultrasonography (US) is commonly performed for breast lesions detected using magnetic resonance imaging (MRI), but the identification…”
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    Mechanism of Nucleoside Uptake in Rat Placenta and Induction of Placental CNT2 in Experimental Diabetes by Nishimura, Tomohiro, Chishu, Takuya, Tomi, Masatoshi, Nakamura, Ryo, Sato, Kazuko, Kose, Noriko, Sai, Yoshimichi, Nakashima, Emi

    “…The purpose of this study was to clarify the transport characteristics of nucleosides in rat placenta and the changes of functional expression of nucleoside…”
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    Correlation of clinical severity and ELISA indices for the NC16A domain of BP180 measured using BP180 ELISA kit in bullous pemphigoid by Tsuji-Abe, Yukiko, Akiyama, Masashi, Yamanaka, Yasuko, Kikuchi, Toshiro, Sato-Matsumura, Kazuko C., Shimizu, Hiroshi

    Published in Journal of dermatological science (01-03-2005)
    “…Titres of circulating autoantibodies detected by indirect immunofluorescence (IIF) have been used for the diagnosis and evaluation of disease activity in…”
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    Effect of a dienogest for an experimental three-dimensional endometrial culture model for endometriosis by Prechapanich, Japarath, Kajihara, Takeshi, Fujita, Keiko, Sato, Kazuko, Uchino, Satomi, Tanaka, Kayoko, Matsumoto, Sachiko, Akita, Masumi, Nagashima, Masabumi, Brosens, Jan J., Ishihara, Osamu

    Published in Medical molecular morphology (01-12-2014)
    “…The pathogenesis of endometriosis remains poorly understood at least in part because early stages of the disease process are difficult to investigate. Previous…”
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    Differential diagnosis of pelvic cystic lesions caused by hemorrhage from inflammatory abscess using CT attenuation in women with acute abdomen by Sato, Kazuko, Kajihara, Takeshi, Miki, Akinori, Hirabayashi, Eriko, Shintani, Daisuke, Niitsu, Mamoru, Ishihara, Osamu, Itakura, Atsuo

    Published in Nagoya journal of medical science (01-11-2015)
    “…To determine the efficacy of computed tomography (CT) attenuation of cystic lesions measured on an image browsing system to distinguish abscess from hematoma…”
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    Nail dystrophy and blisters as sole manifestations in myeloma-associated amyloidosis by Fujita, Yasuyuki, Tsuji-Abe, Yukiko, Sato-Matsumura, Kazuko C., Akiyama, Masashi, Shimizu, Hiroshi

    “…We report the case of a 61-year-old Japanese man with IgG λ-type multiple myeloma, who presented with nail dystrophy as the initial manifestation of systemic…”
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    The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa by Nakamura, Hiroyuki, Sawamura, Daisuke, Goto, Maki, Sato-Matsumura, Kazuko C, LaDuca, Jeffrey, Lee, Julia Yu-Yun, Masunaga, Takuji, Shimizu, Hiroshi

    Published in Journal of dermatological science (01-05-2004)
    “…Background : Glycine substitution mutations in COL7A1 not only cause dominant dystrophic epidermolysis bullosa (DDEB), but can also be silent mutations which…”
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    Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism by Goto, Maki, Sato-Matsumura, Kazuko C., Sawamura, Daisuke, Yokota, Koichi, Nakamura, Hideki, Shimizu, Hiroshi

    Published in Journal of dermatological science (01-09-2004)
    “…Oculocutaneous albinism (OCA) is a heterogeneous congenital disorder. Tyrosinase is a key enzyme in melanin biosynthesis, and tyrosinase gene mutations cause…”
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    Enhancement of Zidovudine Uptake by Dehydroepiandrosterone Sulfate in Rat Syncytiotrophoblast Cell Line TR-TBT 18d-1 by NISHIMURA, Tomohiro, SEKI, Yoshiaki, SATO, Kazuko, CHISHU, Takuya, KOSE, Noriko, TERASAKI, Tetsuya, KANG, Young-Sook, SAI, Yoshimichi, NAKASHIMA, Emi

    Published in Drug metabolism and disposition (01-10-2008)
    “…AZT (3′-azido-3′-deoxythymidine; zidovudine), which is used for the prevention of mother-to-child transmission of HIV-1, is transplacentally transferred to…”
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    The Majority of Keratinocytes Incorporate Intradermally Injected Plasmid DNA Regardless of Size but Only a Small Proportion of Cells Can Express the Gene Product by Sawamura, Daisuke, Yasukawa, Kana, Kodama, Kazuo, Yokota, Koichi, Sato-Matsumura, Kazuko C., Shimizu, Hiroshi, Toshihiro, Tanaka

    Published in Journal of investigative dermatology (01-06-2002)
    “…The expression of intradermally injected DNA by keratinocytes is found mainly in the upper and middle layers of the epidermis. To investigate the mechanism of…”
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    Microbiome biomarkers associated with the gut contraction response elicited by the Japanese traditional medicine daikenchuto by Wada, Yu, Nishiyama, Mitsue, Uehara, Hideaki, Sato, Kazuko, Hamamoto, Yoshihiko, Ogihara, Hiroyuki, Nishi, Akinori, Asakawa, Takeshi, Yamamoto, Masahiro

    Published in Gene (05-06-2022)
    “…•Statistical pattern recognition can find markers of multi-target drugs such as Kampo.•The balance of gut microbiota may be related to clinical effect of…”
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    Distribution of IL-18 and IL-18 receptor in human skin : various forms of IL-18 are produced in keratinocytes by KOIZUMI, Hiroko, SATO-MATSUMURA, Kazuko C, NAKAMURA, Hideki, SHIDA, Kyoko, KIKKAWA, Satomi, MATSUMOTO, Misako, TOYOSHIMA, Kumao, SEYA, Tsukasa

    Published in Archives of Dermatological Research (01-07-2001)
    “…Human interleukin-18 (IL-18) enhances IL-12-mediated IFN-gamma production by lymphocytes and Fas/perforin-mediated cytolysis by NK cells. IL-18 is synthesized…”
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    COL7A1 mutation G2037E causes epidermal retention of type VII collagen by Sawamura, Daisuke, Sato-Matsumura, Kazuko, Shibata, Satoko, Tashiro, Akari, Furue, Masutaka, Goto, Maki, Sakai, Kaori, Akiyama, Masashi, Nakamura, Hideki, Shimizu, Hiroshi

    Published in Journal of human genetics (01-05-2006)
    “…COL7A1 glycine substitution (GS) mutations result in dominant and recessive dystrophic epidermolysis bullosa (DDEB and RDEB). Here, we report a DDEB family in…”
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