長尾アイソザイム
WordNet
- Kamarupan languages spoken in northeastern India and western Burma
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. ホスホグリセリン酸キナーゼ欠損症およびホスホグリセリン酸ムターゼ欠損症phosphoglycerate kinase deficiency and phosphoglycerate mutase deficiency [show details]
…Human PGAM is a dimer consisting of different amounts of muscle (MM) isozyme, brain (BB) isozyme, and the intermediate hybrid (MB) isozyme. Inheritance is autosomal recessive. Various distinct point mutations…
- 2. アスピリン:リウマチ性疾患における作用機序、主な毒性、および使用aspirin mechanism of action major toxicities and use in rheumatic diseases [show details]
…site of aspirin and nonsalicylate NSAID binding . Mammalian cells contain two related but unique isozymes of COX: PG endoperoxide H2 synthase-1 and -2 (COX-1 and COX-2, respectively). Both catalyze the …
- 3. グリコーゲン代謝のその他の障害:GLUT2欠損症およびアルドラーゼA欠損症other disorders of glycogen metabolism glut2 deficiency and aldolase a deficiency [show details]
…#611881) is a rare GSD associated with hereditary hemolytic anemia. In the glycolytic pathway, three isozymes of aldolase (A, B, and C) are responsible for the conversion of fructose-1,6-biphosphate into g …
- 4. 家族性アルドステロン症familial hyperaldosteronism [show details]
…the zona fasciculata. Two isozymes of 11-beta-hydroxylase encoded by two genes on chromosome 8 are responsible for the biosynthesis of aldosterone and cortisol : The isozyme in the zona glomerulosa (CYP11B2 …
- 5. 筋ホスホリラーゼ欠損症(糖原病V型、マッカードル病)myophosphorylase deficiency glycogen storage disease v mcardle disease [show details]
…been shortened to approximately 4 glucosyl units. Glycogen phosphorylase exists in three distinct isozymes (muscle [PYGM], liver [PYGL], and brain [PYGB]), but diseases are only described for muscle and …
English Journal
- Safety and effectiveness of enzyme replacement therapy with agalsidase alfa in patients with Fabry disease: Post-marketing surveillance in Japan.
- Sasa H, Nagao M, Kino K.
- Molecular genetics and metabolism. 2019 04;126(4)448-459.
- Fabry disease is a rare X-linked inherited multisystem disorder resulting from deficiency of the lysosomal enzyme alpha-galactosidase A. Currently, specific therapies, including enzyme replacement therapies, are available for Fabry disease, but clinical trials provide limited information on long-ter
- PMID 30803893
- Regional Spread of CTX-M-2-Producing Proteus mirabilis with the Identical Genetic Structure in Japan.
- Kato K, Matsumura Y, Yamamoto M, Nagao M, Takakura S, Ichiyama S.
- Microbial drug resistance (Larchmont, N.Y.). 2017 Jul;23(5)590-595.
- In this study, we analyzed the molecular epidemiology of extended-spectrum β-lactamase (ESBL)-producing Proteus mirabilis isolates collected from the central region of Japan. Between 2005 and 2012, 820 clinical P. mirabilis isolates were obtained from ten acute care hospitals in Japan. We character
- PMID 27834610
- Evaluating the Risk of a Fifth Metatarsal Stress Fracture by Measuring the Serum 25-Hydroxyvitamin D Levels.
- Shimasaki Y, Nagao M, Miyamori T, Aoba Y, Fukushi N, Saita Y, Ikeda H, Kim SG, Nozawa M, Kaneko K, Yoshimura M.
- Foot & ankle international. 2016 Mar;37(3)307-11.
- The fifth metatarsal bone is a common site of stress fractures in soccer athletes. Although several endocrine risk factors for stress fractures have been proposed, the endocrine risks for fifth metatarsal (5-MT) stress fractures have not been evaluated. To evaluate the endocrine risks of fifth metat
- PMID 26596794
Japanese Journal
- プレチラクロームや活性酸素により誘導されるGSTアイソザイムの比較
- <Abstract of Published Report>Effects of cAMP-phosphodiesterase Isozyme Inhibitor on Cytokine Production by Lipopolysaccharide-stimulated Human Peripheral Blood Mononuclear Cells.
- Yomoaki YOSHIMURA,Chikako KURITA,Tomomi NAGAO,Eiseki USAMI,Toshiya NAKAO,Shino WATANABE,Joji KOBAYASHI,Futoshi YAMAZAKI,Hiroyuki TANAKA,Hiroichi NAGAI
- 岐阜藥科大學紀要 = The annual proceedings of Gifu College of Pharmacy (47), 74, 1998-06-30
- NAID 120005563044
- <Abstract of Published Report>Effects of cAMP-phosphodiesterase Isozyme Inhibitor on Cytokine Production by Lipopolysaccharide-stimulated Human Peripheral Blood Mononuclear Cells.
- YOSHIMURA Yomoaki,KURITA Chikako,NAGAO Tomomi,USAMI Eiseki,NAKAO Toshiya,WATANABE Shino,KOBAYASHI Joji,YAMAZAKI Futoshi,TANAKA Hiroyuki,NAGAI Hiroichi
- 岐阜藥科大學紀要 47, 74, 1998-06-30
- NAID 110000054090
Related Links
- No.1 医学電子出版物配信サイトへ!医書.jpは医学専門書籍・雑誌の幅広い医学情報を共通プラットフォームより配信します ALP分離の試行錯誤 血清アルカリホスファターゼ(ALP)のアイソザイムを検査室に導入しようとして,私たちは第一歩から難関にぶつかった.原著どおりの条件で実施して ...
- A full-length placental alkaline phosphatase (PLAP) cDNA was used to identify and clone the PLAP-like Nagao isozyme gene from human genomic libraries. The entire nucleotide sequence of the gene reveals the existence of 11 ...
- [CANCER RESEARCH 33, 1657-1661, July 1973] Phenotypes of the Regan Isoenzyme and Identity between the Placental D-Variant and the Nagao Isoenzyme1 Norma R. Inglis, Sandra Kirley, L. L. Stolbach, and William H. Fishman ...
★リンクテーブル★
[★]
- 英
- Nagao isozyme
- 関
- 耐熱性アルカリホスファターゼ
[★]
アイソザイム、イソ酵素
- 関
- isoenzyme、isozymic