Search Results - "Nakashima, Masato"
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TAK-071, a muscarinic M1 receptor positive allosteric modulator, attenuates scopolamine-induced quantitative electroencephalogram power spectral changes in cynomolgus monkeys
Published in PloS one (01-03-2019)“…Activation of the muscarinic M1 receptor is a promising approach to improve cognitive deficits associated with cholinergic dysfunction in Alzheimer's disease,…”
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Selective regulation of the chitin‐induced defense response by the Arabidopsis receptor‐like cytoplasmic kinase PBL27
Published in The Plant journal : for cell and molecular biology (01-07-2014)“…Recognition of microbe‐associated molecular patterns (MAMPs) initiates pattern‐triggered immunity in host plants. Pattern recognition receptors (PRRs) and…”
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Practicality of multilayer round window reinforcement in the surgical management of superior semicircular canal dehiscence syndrome: a case report of long-term follow-up
Published in Frontiers in neurology (19-06-2024)“…Several surgical techniques have been documented for approaching and repairing superior semicircular canal dehiscence syndrome (SCDS). These techniques…”
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Autophosphorylation of Specific Threonine and Tyrosine Residues in Arabidopsis CERK1 is Essential for the Activation of Chitin-Induced Immune Signaling
Published in Plant and cell physiology (01-11-2016)“…Pattern recognition receptors on the plant cell surface mediate the recognition of microbe/damage-associated molecular patterns (MAMPs/DAMPs) and activate…”
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Electrical impedance myography detects dystrophin-related muscle changes in mdx mice
Published in Skeletal muscle (18-11-2023)“…The lack of functional dystrophin protein in Duchenne muscular dystrophy (DMD) causes chronic skeletal muscle inflammation and degeneration. Therefore, the…”
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Discovery of a Novel Series of Pyrazolo[1,5-a]pyrimidine-Based Phosphodiesterase 2A Inhibitors Structurally Different from N-((1S)-1-(3-Fluoro-4-(trifluoromethoxy)phenyl)-2-methoxyethyl)-7-methoxy-2-oxo-2,3-dihydropyrido[2,3-b]pyrazine-4(1H)-carboxamide (TAK-915), for the Treatment of Cognitive Disorders
Published in Chemical & pharmaceutical bulletin (2017)“…It has been hypothesized that selective inhibition of phosphodiesterase (PDE) 2A could potentially be a novel approach to treat cognitive impairment in…”
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Participation of prostaglandin E receptor EP4 subtype in duodenal bicarbonate secretion in rats
Published in American journal of physiology: Gastrointestinal and liver physiology (01-07-2004)“…We examined, by using a specific PGE receptor subtype EP4 agonist and antagonist, the involvement of EP4 receptors in duodenal HCO(3)(-) secretion induced by…”
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Facilitation by endogenous prostaglandins of capsaicin-induced gastric protection in rodents through EP2 and IP receptors
Published in The Journal of pharmacology and experimental therapeutics (01-03-2003)“…We investigated the role that prostaglandins (PGs) and EP receptors play in facilitating the gastroprotective action of capsaicin against HCl/ethanol in rats…”
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Tonsillar cyst of the false vocal cord
Published in Auris, nasus, larynx (01-03-2007)“…To report, for the first time, tonsillar cyst of the false vocal cord. Case report. Case presentation and literature review. A 74-year-old woman with a mass in…”
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TAK-915, a phosphodiesterase 2A inhibitor, ameliorates the cognitive impairment associated with aging in rodent models
Published in Behavioural brain research (30-12-2019)“…•TAK-915 facilitated the spatial learning in aged rats in the Morris water maze task.•TAK-915 attenuated scopolamine-induced memory deficits in rats.•TAK-915…”
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A case of nasal natural killer/T lymphoma revealed by repeated deep neck abscess
Published in American journal of otolaryngology (01-07-2009)“…Abstract A diagnosis of natural killer (NK)/T-cell lymphoma was clarified after repeated deep neck abscess in a 63-year-old man. The absolute number of…”
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Discovery of a Potent and Orally Bioavailable Melatonin Receptor Agonist
Published in Journal of medicinal chemistry (25-03-2021)“…To develop potent and orally bioavailable melatonin receptor (MT1 and MT2) agonists, a novel series of 5–6–5 tricyclic derivatives was designed, synthesized,…”
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TAK-071, a muscarinic M.sub.1 receptor positive allosteric modulator, attenuates scopolamine-induced quantitative electroencephalogram power spectral changes in cynomolgus monkeys
Published in PloS one (11-03-2019)“…Activation of the muscarinic M.sub.1 receptor is a promising approach to improve cognitive deficits associated with cholinergic dysfunction in Alzheimer's…”
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IgG4-related Mikulicz's disease: a report of 3 cases
Published in Nippon Jibi Inkoka Gakkai Kaiho (2010)“…We report three cases of hyper-IgG4 disease with synchronous or asynchronous lymphocytic infiltration onset, IgG4 positive plasma cell infiltration, and fibril…”
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Urine titin as a novel biomarker for Duchenne muscular dystrophy
Published in Neuromuscular disorders : NMD (01-04-2023)“…•Mdx mice lacking dystrophin have elevated urine titin levels.•Treatment with an exon skipping method rescued dystrophin expression and decreased urine titin…”
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Orexin 2 receptor-selective agonist danavorexton (TAK-925) promotes wakefulness in non-human primates and healthy individuals
Published in Journal of sleep research (01-10-2023)“…The orexin 2 receptor-selective agonist danavorexton (TAK-925) has been shown to produce wake-promoting effects in wild-type mice, narcolepsy-model mice, and…”
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Regulatory mechanism of the gastric hyperemic response following barrier disruption: roles of cyclooxygenase-1, the prostaglandin E2/EP1 receptor and sensory neurons
Published in Current pharmaceutical design (2015)“…We herein reviewed the mechanism underlying the gastric hyperemic response following barrier disruption, with a focus on cyclooxygenase (COX) isozymes,…”
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Synthesis of a Novel Series of Tricyclic Dihydrofuran Derivatives: Discovery of 8,9-Dihydrofuro[3,2-c]pyrazolo[1,5-a]pyridines as Melatonin Receptor (MT1/MT2) Ligands
Published in Journal of medicinal chemistry (23-06-2011)“…Novel tricyclic dihydrofuran derivatives were designed, synthesized, and evaluated as melatonin receptor (MT1/MT2) ligands based on the previously reported…”
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Discovery of potent, selective, orally active benzoxazepine-based Orexin-2 receptor antagonists
Published in Bioorganic & medicinal chemistry letters (01-11-2011)“…During our efforts to identify a series of potent, selective, orally active human Orexin-2 Receptor (OX2R) antagonists, we elucidated structure-activity…”
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