succinyl-CoA-acetoacetate-CoA transferase

同

thiophorase, succinyl CoA:acetoacetate CoA-transferase, succinyl-CoA acetoacetate CoA transferase

WordNet

1. the 3rd letter of the Roman alphabet (同)c
2. (music) the keynote of the scale of C major
3. a general-purpose programing language closely associated with the UNIX operating system
4. any of various enzymes that move a chemical group from one compound to another compound

PrepTutorEJDIC

1. carbonの化学記号
2. cobaltの化学記号

UpToDate Contents

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• 1. ミトコンドリアミオパシー：臨床的特徴および診断 mitochondrial myopathies clinical features and diagnosis
• 2. ペルオキシソーム病 peroxisomal disorders
• 3. 幼児および小児における低血糖症の病因 etiology of hypoglycemia in infants and children
• 4. ヘキソースリン酸側路およびグルタチオン代謝関連疾患 related disorders of the hexose monophosphate shunt and glutathione metabolism
• 5. 糖尿病性ケトアシドーシスおよび高浸透圧性高血糖状態の疫学および病因 epidemiology and pathogenesis of diabetic ketoacidosis and hyperosmolar hyperglycemic state

English Journal

• Inborn errors of ketone body utilization.

• Hori T1, Yamaguchi S, Shinkaku H, Horikawa R, Shigematsu Y, Takayanagi M, Fukao T.
• Pediatrics international : official journal of the Japan Pediatric Society.Pediatr Int.2015 Feb;57(1):41-8. doi: 10.1111/ped.12585.
• Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency and mitochondrial acetoacetyl-CoA thiolase (beta-ketothiolase or T2) deficiency are classified as autosomal recessive disorders of ketone body utilization characterized by intermittent ketoacidosis. Patients with mutations retaining no residu
• PMID 25559898

• Fatty acid transport protein 1 (FATP1) localizes in mitochondria in mouse skeletal muscle and regulates lipid and ketone body disposal.

• Guitart M1, Osorio-Conles O2, Pentinat T3, Cebrià J3, García-Villoria J4, Sala D5, Sebastián D5, Zorzano A5, Ribes A4, Jiménez-Chillarón JC3, García-Martínez C6, Gómez-Foix AM2.
• PloS one.PLoS One.2014 May 23;9(5):e98109. doi: 10.1371/journal.pone.0098109. eCollection 2014.
• FATP1 mediates skeletal muscle cell fatty acid import, yet its intracellular localization and metabolic control role are not completely defined. Here, we examine FATP1 localization and metabolic effects of its overexpression in mouse skeletal muscle. The FATP1 protein was detected in mitochondrial a
• PMID 24858472

• A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.

• Shafqat N1, Kavanagh KL, Sass JO, Christensen E, Fukao T, Lee WH, Oppermann U, Yue WW.
• Journal of inherited metabolic disease.J Inherit Metab Dis.2013 Nov;36(6):983-7. doi: 10.1007/s10545-013-9589-z. Epub 2013 Feb 19.
• Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare inherited metabolic disorder of ketone metabolism, characterized by ketoacidotic episodes and often permanent ketosis. To date there are ~20 disease-associated alleles on the OXCT1 gene that encodes the mitochondrial enzyme SCOT. SC
• PMID 23420214

Related Links

• Succinyl-CoA acetoacetate transferase deficiency

According to ClinicalTrials.gov there are currently 0 additional "open" studies for "Succinyl-CoA acetoacetate transferase deficiency" (open studies are recruiting volunteers) and 0 "Succinyl-CoA acetoacetate transferase deficiency ...

• Succinyl-CoA : 3-ketoacid CoA transferase (SCOT) deficiency

Succinyl-CoA : 3-ketoacid CoA transferase (SCOT) deficiency Author: Doctor Toshiyuki FUKAO1 Creation Date: September 2001 Update: September 2004 Scientific Editor: Professor Udo WENDEL 1Department of Pediatrics, Gifu ...

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★リンクテーブル★

リンク元	「チオホラーゼ」
関連記事	「C」「transferase」「CoA」「COA」「Co」

「チオホラーゼ」

　　[★]

英

thiophorase

同

succinyl-CoA-acetoacetate-CoA transferase

[show details]

チオフォラーゼ : 1 件
チオホラーゼ : 11 件

「C」

　　[★]

• 炭素 carbon
• シトシン cytosine
• システイン cysteine
• シチジン
• セルシウス度 摂氏 degrees Celsius degree C
• 産婦人科領域で「子宮外頚 子宮外頚部 exocervix」を表現するための略語

　 　 　 　

「transferase」

　　[★]

• n.

• トランスフェラーゼ、転移酵素、付加酵素

関

lyase、synthase、transposase

　

「CoA」

　　[★]

• 大動脈縮窄症 coactation of the aorta
• 補酵素A coenzyme A

「COA」

　　[★] 補酵素A coenzyme A CoA

「Co」

　　[★] コバルト cobalt