Search Results - "Yarimizu, Junko"

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    Characterization of cognitive deficits in a transgenic mouse model of Alzheimer's disease and effects of donepezil and memantine by Nagakura, Akira, Shitaka, Yoshitsugu, Yarimizu, Junko, Matsuoka, Nobuya

    Published in European journal of pharmacology (05-03-2013)
    “…Alzheimer's disease is characterized by a progressive decline in cognitive function and involves β-amyloid (Aβ) in its pathogenesis. To characterize cognitive…”
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    Novel 5-HT5A receptor antagonists ameliorate scopolamine-induced working memory deficit in mice and reference memory impairment in aged rats by Yamazaki, Mayako, Okabe, Mayuko, Yamamoto, Noriyuki, Yarimizu, Junko, Harada, Katsuya

    Published in Journal of pharmacological sciences (01-03-2015)
    “…Despite the human 5-HT5A receptor being cloned in 1994, the biological function of this receptor has not been extensively characterized due to a lack of…”
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    A Comparative Study on the Hydroperoxide and Thiol Specificity of the Glutathione Peroxidase Family and Selenoprotein P by Takebe, Gen, Yarimizu, Junko, Saito, Yoshiro, Hayashi, Takaaki, Nakamura, Hajime, Yodoi, Junji, Nagasawa, Shigeharu, Takahashi, Kazuhiko

    Published in The Journal of biological chemistry (25-10-2002)
    “…Glutathione peroxidase catalyzes the reduction of hydrogen peroxide and organic hydroperoxide by glutathione and functions in the protection of cells against…”
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    Differential effects between γ-secretase inhibitors and modulators on cognitive function in amyloid precursor protein-transgenic and nontransgenic mice by Mitani, Yasuyuki, Yarimizu, Junko, Saita, Kyoko, Uchino, Hiroshi, Akashiba, Hiroki, Shitaka, Yoshitsugu, Ni, Keni, Matsuoka, Nobuya

    Published in The Journal of neuroscience (08-02-2012)
    “…γ-Secretase inhibitors (GSIs) reduce amyloid-β (Aβ) peptides but inevitably increase the β-C-terminal fragment (β-CTF) of amyloid precursor protein (APP),…”
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    5-HT5A Receptor Antagonist ASP5736 Ameliorates Several Abnormal Behaviors in an Fmr1- Targeted Transgenic Male Rat Model of Fragile X Syndrome by Yamazaki, Mayako, Arai, Takatomo, Yarimizu, Junko, Matsumoto, Mitsuyuki

    “…Abstract Background Fragile X syndrome (FXS) is a genetic condition that causes a range of developmental problems, including intellectual disability,…”
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    5-H[T.sub.5A] Receptor Antagonist ASP5736 Ameliorates Several Abnormal Behaviors in an Fmr1-Targeted Transgenic Male Rat Model of Fragile X Syndrome by Yamazaki, Mayako, Arai, Takatomo, Yarimizu, Junko, Matsumoto, Mitsuyuki

    “…Background: Fragile X syndrome (FXS) is a genetic condition that causes a range of developmental problems, including intellectual disability, aggressive…”
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    Optimization and biological evaluation of imidazopyridine derivatives as a novel scaffold for γ-secretase modulators with oral efficacy against cognitive deficits in Alzheimer’s disease model mice by Sekioka, Ryuichi, Honda, Shugo, Akashiba, Hiroki, Yarimizu, Junko, Mitani, Yasuyuki, Yamasaki, Shingo

    Published in Bioorganic & medicinal chemistry (01-06-2020)
    “…[Display omitted] Gamma-secretase modulators (GSMs) selectively lower amyloid-β42 (Aβ42) and are therefore potential disease-modifying drugs for Alzheimer’s…”
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    Efficiency of selenocysteine incorporation in human thioredoxin reductase by Yarimizu, J, Nakamura, H, Yodoi, J, Takahashi, K

    Published in Antioxidants & redox signaling (01-12-2000)
    “…Thioredoxin reductase (TR) is a flavoenzyme, containing one selenocysteine (Sec) residue at the penultimate carboxyl-terminus, that catalyzes the…”
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    Neurochemical and neuropharmacological characterization of ASP2905, a novel potent selective inhibitor of the potassium channel KCNH3 by Takahashi, Shinji, Inamura, Kohei, Yarimizu, Junko, Yamazaki, Mayako, Murai, Nobuhito, Ni, Keni

    Published in European journal of pharmacology (05-09-2017)
    “…KCNH3 (BEC1) is a member of the ether-à-go-go (KCNH) family of voltage-gated K+ channels. The aim of this study was to determine the pharmacological profiles…”
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    ASP5736, a novel 5-HT5A receptor antagonist, ameliorates positive symptoms and cognitive impairment in animal models of schizophrenia by Yamazaki, Mayako, Harada, Katsuya, Yamamoto, Noriyuki, Yarimizu, Junko, Okabe, Mayuko, Shimada, Takeshi, Ni, Keni, Matsuoka, Nobuya

    Published in European neuropsychopharmacology (01-10-2014)
    “…Abstract We recently identified ASP5736, ( N -(diaminomethylene)-1-(3,5-difluoropyridin-4-yl)-4-fluoroisoquinoline-7-carboxamide (2 E )-but-2-enedioate), a…”
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    Amelioration of cognitive deficits in plaque-bearing Alzheimer's disease model mice through selective reduction of nascent soluble A beta 42 without affecting other A beta pools by Mitani, Yasuyuki, Yarimizu, Junko, Akashiba, Hiroki, Shitaka, Yoshitsugu, Ni, Keni, Matsuoka, Nobuya

    Published in Journal of neurochemistry (01-05-2013)
    “…Given that amyloid- beta 42 (A beta 42) is believed to be a culprit in Alzheimer's disease (AD), reducing A beta 42 production should be a potential…”
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    Amelioration of cognitive deficits in plaque‐bearing Alzheimer's disease model mice through selective reduction of nascent soluble Aβ42 without affecting other Aβ pools by Mitani, Yasuyuki, Yarimizu, Junko, Akashiba, Hiroki, Shitaka, Yoshitsugu, Ni, Keni, Matsuoka, Nobuya

    Published in Journal of neurochemistry (01-05-2013)
    “…Given that amyloid‐β 42 (Aβ42) is believed to be a culprit in Alzheimer's disease (AD), reducing Aβ42 production should be a potential therapeutic approach…”
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    Amelioration of cognitive deficits in plaque-bearing Alzheimer's disease model mice through selective reduction of nascent soluble A[beta]42 without affecting other A[beta] pools by Mitani, Yasuyuki, Yarimizu, Junko, Akashiba, Hiroki, Shitaka, Yoshitsugu, Ni, Keni, Matsuoka, Nobuya

    Published in Journal of neurochemistry (01-05-2013)
    “…Given that amyloid-[beta] 42 (A[beta]42) is believed to be a culprit in Alzheimer's disease (AD), reducing A[beta]42 production should be a potential…”
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    Amelioration of cognitive deficits in plaque‐bearing A lzheimer's disease model mice through selective reduction of nascent soluble A42 without affecting other A pools by Mitani, Yasuyuki, Yarimizu, Junko, Akashiba, Hiroki, Shitaka, Yoshitsugu, Ni, Keni, Matsuoka, Nobuya

    Published in Journal of neurochemistry (01-05-2013)
    “…Abstract Given that amyloid‐β 42 (Aβ42) is believed to be a culprit in Alzheimer's disease ( AD ), reducing Aβ42 production should be a potential therapeutic…”
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    Journal Article
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