チトクロム酸化酵素欠損症、チトクロム酸化酵素欠乏症、チトクロム酸化酵素欠乏
WordNet
- (biochemistry) a class of hemoprotein whose principal biological function is electron transfer (especially in cellular respiration)
- any of the enzymes that catalyze biological oxidation
PrepTutorEJDIC
- 〈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
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- 1. 新生児における筋緊張低下を引き起こす末梢神経および筋肉の障害に関する概要 overview of peripheral nerve and muscle disorders causing hypotonia in the newborn
- 2. 先天性代謝異常：分類 inborn errors of metabolism classification
- 3. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
- 4. 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
- 5. ミトコンドリア細胞症における腎病変 renal involvement in the mitochondrial cytopathies
English Journal
- Investigating the role of the physiological isoform switch of cytochrome c oxidase subunits in reversible mitochondrial disease.
- Boczonadi V1, Giunta M1, Lane M1, Tulinius M2, Schara U3, Horvath R4.
- The international journal of biochemistry & cell biology.Int J Biochem Cell Biol.2015 Jun;63:32-40. doi: 10.1016/j.biocel.2015.01.025. Epub 2015 Feb 7.
- Reversible infantile respiratory chain deficiency is characterised by spontaneous recovery of mitochondrial myopathy in infants. We studied whether a physiological isoform switch of nuclear cytochrome c oxidase subunits contributes to the age-dependent manifestation and spontaneous recovery in rever
- PMID 25666558
- Cytochrome c oxidase deficit is associated with the seizure onset zone in young patients with focal cortical dysplasia Type II.
- Miles L1, Greiner HM, Mangano FT, Horn PS, Leach JL, Miles MV.
- Metabolic brain disease.Metab Brain Dis.2015 May 10. [Epub ahead of print]
- It has been postulated that mitochondrial dysfunction may be an important factor in epileptogenesis of intractable epilepsy. The current study tests the hypothesis that mitochondrial Complex IV (CIV) or cytochrome c oxidase dysfunction is associated with the seizure onset zone (SOZ) in patients with
- PMID 25957585
- Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome c Oxidase Assembly Links Two Mitochondrial Cardiomyopathies.
- Pacheu-Grau D1, Bareth B1, Dudek J1, Juris L1, Vögtle FN2, Wissel M1, Leary SC3, Dennerlein S1, Rehling P4, Deckers M1.
- Cell metabolism.Cell Metab.2015 May 6. pii: S1550-4131(15)00167-9. doi: 10.1016/j.cmet.2015.04.012. [Epub ahead of print]
- Three mitochondria-encoded subunits form the catalytic core of cytochrome c oxidase, the terminal enzyme of the respiratory chain. COX1 and COX2 contain heme and copper redox centers, which are integrated during assembly of the enzyme. Defects in this process lead to an enzyme deficiency and manifes
- PMID 25959673
Japanese Journal
- High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency
- Vondrackova Alzbeta,Vesela Katerina,Hansikova Hana [他],DOCEKALOVA Dagmar Zajicova,ROZSYPALOVA Eva,ZEMAN Jiri,TESAROVA Marketa
- Journal of human genetics 57(7), 442-448, 2012-07-01
- NAID 10030965683
- Mechanism of increased respiration in an H⁺ -ATPase-defective mutant of Corynebacterium glutamicum
- Sawada Kazunori,Kato Yui,Imai Keita [他],Li Liyuan,Wada Masaru,Matsushita Kazunobu,Yokota Atsushi
- Journal of bioscience and bioengineering 113(4), 467-473, 2012-04
- … In addition, the transcriptional level of cytochrome bd oxidase, but not cytochrome bc_1-aa_3, also increased, which may help prevent the excess pmf generation caused by enhanced respiration. …
- NAID 110009444552
- Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiency
- Sacconi Sabrina,Salviati Leonardo,Trevisson Eva
- Journal of human genetics 54(7), 419-421, 2009-07-01
- NAID 10030731133
Related Links
- Cytochrome C Oxidase deficiency is a very rare inherited metabolic disorder characterized by deficiency of the enzyme cytochrome C oxidase (COX), or Complex IV, an essential enzyme that is active in the subcellular structures that help to ...
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★リンクテーブル★
| リンク元 | 「チトクロム酸化酵素欠乏症」「チトクロム酸化酵素欠乏」「cytochrome c oxidase deficiency」「チトクロム酸化酵素欠損症」 |
| 関連記事 | 「deficiency」「cytochrome oxidase」 |
「チトクロム酸化酵素欠乏症」
「チトクロム酸化酵素欠乏」
「cytochrome c oxidase deficiency」
「チトクロム酸化酵素欠損症」
「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