Search Results - "Morishita, Hideko"

Molecular characterization of histidinemia : identification of four missense mutations in the histidase gene by KAWAI, Yoko, MORIYAMA, Akihiko, ASAI, Kiyofumi, COLEMAN-CAMPBELL, Carrie M, SUMI, Satoshi, MORISHITA, Hideko, SUCHI, Mariko

“…Histidinemia (MIM235800) is characterized by elevated histidine in body fluids and decreased urocanic acid in blood and skin and results from histidase…”
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Inhibition in vitro linoleic acid peroxidation and haemolysis by caffeoyltryptophan by Ohnishi, Motoyo, Morishita, Hideko, Toda, Shizuo, Yase, Yoshiro, Kido, Ryo

“…Antioxidant activities of caffeoyltryptophan were investigated by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging system, the superoxide anion…”
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Enhancement by catechols of hydroxyl-radical formation in the presence of ferric ions and hydrogen peroxide by Iwahashi, H, Morishita, H, Ishii, T, Sugata, R, Kido, R

“…The effect of caffeic acid, a kind of catechol, on the Fenton reaction was examined by using the ESR spin trapping technique. Caffeic acid enhanced the…”
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Synthesis of amide compounds of ferulic acid, and their stimulatory effects on insulin secretion in vitro by Nomura, Eisaku, Kashiwada, Ayumi, Hosoda, Asao, Nakamura, Kozo, Morishita, Hideko, Tsuno, Takuo, Taniguchi, Hisaji

“…We prepared amide compounds which were derived from ferulic acid using various amines, and investigated their stimulatory effects on insulin secretion using…”
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Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome by Kobayashi, M, Morishita, H, Sugiyama, N, Yokochi, K, Nakano, M, Wada, Y, Hotta, Y, Terauchi, A, Nonaka, I

“…Muscle biopsy specimens from two patients with MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) were studied…”
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Increase of Protein Synthesis by Uridine Supplement in Lectin-Stimulated Peripheral Blood Lymphocytes and EB Virus-Transformed B Cell Line of Hereditary Orotic Aciduria Type I by YAZAKI, MAKOTO, OKAJIMA, KAZUKI, SUCHI, MARIKO, MORISHITA, HIDEKO, WADA, YOSHIRO

“…YAZAKI, M., OKAJIMA, K., SUCHI, M., MORISHITA, H. and WADA, Y. Increase of Protein Synthesis by Uridine Supplement in Lectin-Stimulated Peripheral Blood…”
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Synthesis of Novel Polyphenols Consisted of Ferulic and Gallic Acids, and Their Inhibitory Effects on Phorbol Ester-Induced Epstein–Barr Virus Activation and Superoxide Generation by Nomura, Eisaku, Hosoda, Asao, Morishita, Hideko, Murakami, Akira, Koshimizu, Koichi, Ohigashi, Hajime, Taniguchi, Hisaji

“…We prepared novel polyphenols which were esters composed of two naturally occurring products, ferulic and gallic acids, and investigated their inhibitory…”
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Molecular characterization of histidinemia: identification of four missense mutations in the histidase gene by Kawai, Yoko, Moriyama, Akihiko, Asai, Kiyofumi, Coleman-Campbell, Carrie M, Sumi, Satoshi, Morishita, Hideko, Suchi, Mariko

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Effects of valproate on mitochondrial function in epileptic patients by Kanayama, M, Sugiyama, N, Morishita, H, Ishikawa, T, Wada, Y, Akiyama, T

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Hematoma of the basal ganglia in the newborn: non-surgical treatment by Takagi, T, Matsumoto, T, Kasuga, Y, Horie, M, Morishita, H, Yasui, Y, Ishikawa, T

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Identification of glutarylcarnitine in glutaric aciduria type 1 by carboxylic acid analyzer with an ODS reverse-phase column by Kidouchi, K, Sugiyama, N, Morishita, H, Kobayashi, M, Wada, Y, Nohara, D

“…A technique for the identification of glutarylcarnitine in urine from a patient with glutaric aciduria type 1 is described. The patient's urine sample was…”
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Urinary acylcarnitines in a patient with neonatal multiple acyl-CoA dehydrogenation deficiency, quantified by a carboxylic acid analyzer with a reversed-phase column by Kidouchi, K, Niwa, T, Nohara, D, Asai, K, Sugiyama, N, Morishita, H, Kobayashi, M, Wada, Y

“…A quantitative analysis for urinary acylcarnitines in a patient with neonatal multiple acyl-CoA dehydrogenation deficiency is described. This method (liquid…”
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Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency by Kamiya, M, Eimoto, T, Kishimoto, H, Tsudzuki, T, Morishita, H, Wada, Y, Wakabayashi, T, Hashimoto, T, Goodman, S I, Frerman, F E

“…An autopsy study of glutaric aciduria type II in a 62-day-old Japanese boy is presented. The diagnosis was made by analysis of organic acids in the urine…”
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Development of histidinemic patients: follow-up study of five cases with neuropsychological symptoms by Ishikawa, M, Saito, H, Morishita, H, Ito, T, Kato, T, Wada, Y

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Effect of hypocalcemia on muscle in disorders of calcium metabolism by Ishikawa, T, Saito, M, Morishita, H, Watanabe, I

“…We reported on three hypocalcemic patients with various serum creatine kinase (CK) levels and Ca metabolic disorders. Two patients with moderate hypocalcemia…”
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