Zobrazeno 1 - 10 of 152 pro vyhledávání: '"Hiroshi TERASHIMA"'
1
Akademický článek
Treatment of tubular damage in high-fat-diet-fed obese mice using sodium-glucose co-transporter inhibitors.
Autor: Sei Saitoh, Takashi Takaki, Kazuki Nakajima, Bao Wo, Hiroshi Terashima, Satoshi Shimo, Huy Bang Nguyen, Truc Quynh Thai, Kanako Kumamoto, Kazuo Kunisawa, Shizuko Nagao, Akihiro Tojo, Nobuhiko Ohno, Kazuo Takahashi
Publikováno v: PLoS ONE, Vol 18, Iss 2, p e0281770 (2023)
A long-term high-fat diet (HFD) causes obesity and changes in renal lipid metabolism and lysosomal dysfunction in mice, causing renal damage. Sodium-glucose co-transporter inhibitors, including phlorizin, exert nephroprotective effects in patients wi
Externí odkaz: https://doaj.org/article/480b788ebb394b8aa85d01e5bfcc0fff
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2
Akademický článek
Mechanism of transient photothermal inactivation of bacteria using a wavelength-tunable nanosecond pulsed laser
Autor: Ichiro Tatsuno, Yuna Niimi, Makoto Tomita, Hiroshi Terashima, Tadao Hasegawa, Takahiro Matsumoto
Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract There is a great demand for novel disinfection technologies to inactivate various pathogenic viruses and bacteria. In this situation, ultraviolet (UVC) disinfection technologies seem to be promising because biocontaminated air and surfaces a
Externí odkaz: https://doaj.org/article/1b4e974ac2c848509e89eeb660ac8a47
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3
Akademický článek
A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10
Autor: Noriomi Suzuki, Hideki Mutai, Fuyuki Miya, Tatsuhiko Tsunoda, Hiroshi Terashima, Noriko Morimoto, Tatsuo Matsunaga
Publikováno v: BMC Pediatrics, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Waardenburg syndrome type 1 (WS1) can be distinguished from Waardenburg syndrome type 2 (WS2) by the presence of dystopia canthorum. About 96% of WS1 are due to PAX3 mutations, and SOX10 mutations have been reported in 15% of WS2.
Externí odkaz: https://doaj.org/article/57b47a4867204a07b1c77ee825d08698
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4
Akademický článek
Aerodynamic instability of flare-type membrane inflatable vehicle in suborbital reentry demonstration
Autor: Tatsushi OHASHI, Yusuke TAKAHASHI, Hiroshi TERASHIMA, Nobuyuki OSHIMA
Publikováno v: Journal of Fluid Science and Technology, Vol 13, Iss 3, Pp JFST0020-JFST0020 (2018)
An inflatable membrane reentry vehicle has been developed as one of the innovative reentry technologies. A suborbital reentry demonstration using a sounding rocket was carried out in 2012. Contrary to the result of a preliminary study, the vehicle al
Externí odkaz: https://doaj.org/article/c4f1c86751224d2ea486d39518f6d681
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5
Unsteady Aerodynamics Around a Pitching Airfoil with Shock and Shock-Induced Boundary-Layer Separation
Autor: Noah D. Oyeniran, Toma Miyake, Hiroshi Terashima, Ryoto Seki, Keiichi Ishiko, Taku Nonomura
Publikováno v: AIAA Journal. 60:6557-6565
This study numerically investigated the characteristics of unsteady aerodynamic forces around a pitching airfoil in the transonic flow regime. The unsteady Reynolds-averaged compressible Navier–Stokes (URANS) equations were solved using a Spalart
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c64d2141a35de3b145138d16498cb4d5
https://doi.org/10.2514/1.j062054
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6
A nationwide survey of monocarboxylate transporter 8 deficiency in Japan: Its incidence, clinical course, MRI and laboratory findings
Autor: Masaya, Kubota, Akiko, Yakuwa, Hiroshi, Terashima, Hideki, Hoshino
Publikováno v: Brain and Development. 44:699-705
Monocarboxylate transporter 8 (MCT8) deficiency is an X-linked recessive developmental disorder characterized by initially marked truncal hypotonia, later athetotic posturing, and severe intellectual disability caused by mutations in SLC16A2, which i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166de9e4a4426aa289c5adcdae3f55fe
https://doi.org/10.1016/j.braindev.2022.07.007
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8
Differentiating early clinical features of Panayiotopoulos syndrome from acute encephalopathy
Autor: Saori Kawakami, Masaya Kubota, Hiroshi Terashima, Chie Nagata, Akira Ishiguro
Publikováno v: Brain and Development. 44:386-390
Panayiotopoulos syndrome (PS) is a common benign epilepsy in childhood, characterized by predominantly autonomic symptoms such as emesis, pallor, and seizures, which are often prolonged. In an emergency room (ER), particularly when unconsciousness is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e0a053d9452d35af53bd9c3e09b182
https://doi.org/10.1016/j.braindev.2022.01.006
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