TPI deficiency

同

triose phosphate isomerase

WordNet

1. the 20th letter of the Roman alphabet (同)t

PrepTutorEJDIC

1. 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
2. tritiumの化学記号

UpToDate Contents

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• 1. 急性虚血性脳卒中における経静脈的線維素溶解（血栓溶解）治療：治療的使用 intravenous fibrinolytic thrombolytic therapy in acute ischemic stroke therapeutic use
• 2. ST上昇型心筋梗塞に対する線溶療法：治療開始 fibrinolytic therapy in acute st elevation myocardial infarction initiation of therapy
• 3. IgG サブクラス欠乏症 igg subclass deficiency
• 4. 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
• 5. アデノシンデアミナーゼ欠損症：治療 adenosine deaminase deficiency treatment

English Journal

• Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency.

• Roland BP1, Amrich CG2, Kammerer CJ1, Stuchul KA1, Larsen SB1, Rode S3, Aslam AA2, Heroux A4, Wetzel R3, VanDemark AP5, Palladino MJ6.
• Biochimica et biophysica acta.Biochim Biophys Acta.2015 Jan;1852(1):61-9. doi: 10.1016/j.bbadis.2014.10.010. Epub 2014 Oct 16.
• Triosephosphate isomerase (TPI) is a glycolytic enzyme which homodimerizes for full catalytic activity. Mutations of the TPI gene elicit a disease known as TPI Deficiency, a glycolytic enzymopathy noted for its unique severity of neurological symptoms. Evidence suggests that TPI Deficiency pathogene
• PMID 25463631

• Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiency.

• Aissa K1, Kamoun F, Sfaihi L, Ghedira ES, Aloulou H, Kamoun T, Pissard S, Hachicha M.
• Fetal and pediatric pathology.Fetal Pediatr Pathol.2014 Aug;33(4):234-8. doi: 10.3109/15513815.2014.915365. Epub 2014 May 19.
• We have reported the first Tunisian case of triosephosphate isomerase (TPI) deficiency in a 2-year-old girl. She was the first child of a nonconsanguineous couple. The disease included a neonatal onset of chronic hemolytic anemia, recurrent low-respiratory infections then progressive neurological in
• PMID 24840153

• The mechanism by which TATA-box polymorphisms associated with human hereditary diseases influence interactions with the TATA-binding protein.

• Drachkova I1, Savinkova L, Arshinova T, Ponomarenko M, Peltek S, Kolchanov N.
• Human mutation.Hum Mutat.2014 May;35(5):601-8. doi: 10.1002/humu.22535. Epub 2014 Mar 31.
• SNPs in ТАТА boxes are the cause of monogenic diseases, contribute to a large number of complex diseases, and have implications for human sensitivity to external and internal environmental signals. The aim of this work was to explore the kinetic characteristics of the formation of human ТВР c
• PMID 24616209

Related Links

• Triose Phosphate Isomerase (TPI) Deficiency Prognosis

Triose Phosphate Isomerase (TPI) Deficiency Prognosis Triose Phosphate Isomerase (TPI) deficiency is a rare inherited disorder in glycolysis, one of the principal pathways by which cells generate energy. Affected children who inherit ...

• Triose phosphate isomerase deficiency | Definition and ...

Triose phosphate isomerase (TPI) deficiency is a rare non-sex-linked (autosomal) disorder that is a result of an insufficient amount of the enzyme triose phosphate isomerase. This disorder is inherited as a dominant trait and it is ...

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★リンクテーブル★

関連記事	「deficiency」「T」「TPI」「TP」

「deficiency」

　　[★]

• n.

• 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
• 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの

関

absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve

　

「T」

　　[★]

• T波 T wave
• チミン thymine
• ツイスト数
• スレオニントレオニン threonine

　 　

「TPI」

　　[★]

同

トリオースリン酸イソメラーゼ

同

トリオースリン酸イソメラーゼ

「TP」

　　[★]

• 総蛋白 total protein
• 足趾圧力 足指圧力 toe pressure