WordNet
- (medicine) any disturbance in the functioning of an organ or body part or a disturbance in the functioning of a social group; "erectile dysfunction"; "sexual relationship dysfunction" (同)disfunction
PrepTutorEJDIC
- 機能障害,機能不全
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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. ミトコンドリアミオパシー：治療 mitochondrial myopathies treatment
- 3. ミトコンドリアの構造、機能、および遺伝学 mitochondrial structure function and genetics
- 4. ミトコンドリア細胞症における腎病変 renal involvement in the mitochondrial cytopathies
- 5. 代謝性ミオパチーへのアプローチ approach to the metabolic myopathies
English Journal
- Long-term follow-up of four patients affected by HHH syndrome.
- Kim SZ, Song WJ, Nyhan WL, Ficicioglu C, Mandell R, Shih VE.SourceKorea Genetic Research Center, Cheong Ju, Republic of Korea.
- Clinica chimica acta; international journal of clinical chemistry.Clin Chim Acta.2012 Jul 11;413(13-14):1151-5. Epub 2012 Mar 23.
- BACKGROUND: In hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome, impaired ornithine transport across the mitochondrial membrane causes ornithine accumulation in cytoplasm. The resulting mitochondrial ornithine deficiency leads to reduced clearance of ammonia through the urea cycle.
- PMID 22465082
- Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies.
- Sabatelli P, Palma E, Angelin A, Squarzoni S, Urciuolo A, Pellegrini C, Tiepolo T, Bonaldo P, Gualandi F, Merlini L, Bernardi P, Maraldi NM.SourceCNR-National Research Council of Italy, Institute of Molecular Genetics c/o IOR, Bologna, Italy.
- Journal of cellular physiology.J Cell Physiol.2012 Jul;227(7):2927-35. doi: 10.1002/jcp.23039.
- Collagen VI myopathies (Ullrich congenital muscular dystrophy (UCMD), Bethlem myopathy (BM), and myosclerosis myopathy) share a common pathogenesis, that is, mitochondrial dysfunction due to deregulation of the permeability transition pore (PTP). This effect was first identified in the Col6a1(-/-) m
- PMID 21953374
Japanese Journal
- 抗GAD抗体，抗glycine受容体抗体，抗GM1抗体が陽性のprogressive encephalomyelitis with rigidity and myoclonusの1例
- 小池 佑佳,諏訪部 達也,今野 卓哉,梅田 能生,小宅 睦郎,藤田 信也
- 臨床神経学 55(2), 111-114, 2015
- 症例は1型糖尿病と診断されている62歳の女性である．発熱後，亜急性に両下肢筋力低下，尿閉をきたして入院した．頸部・上肢の筋強剛と上肢ミオクローヌス，感覚性運動失調をみとめた．血清抗GAD抗体，抗TPO抗体，抗ミトコンドリアM2抗体，抗glycine受容体抗体が陽性であり，多腺性自己免疫症候群を背景に発症した，progressive encephalomyelitis with rigidity a …
- NAID 130004921314
- Tacrine, an Oral Acetylcholinesterase Inhibitor, Induced Hepatic Oxidative Damage, Which Was Blocked by Liquiritigenin through GSK3-beta Inhibition
- , , [他], , , , ,
- Biological and Pharmaceutical Bulletin 38(2), 184-192, 2015
- … Fluorescent activated cell sorter (FACS) analysis revealed that LQ inhibited cellular H2O2 production and mitochondrial dysfunction induced by tacrine in HepG2 cells. …
- NAID 130004872247
- Melatonin protects the integrity of granulosa cells by reducing oxidative stress in nuclei, mitochondria, and plasma membranes in mice
- , , , , , , , , ,
- Journal of Reproduction and Development 61(1), 35-41, 2015
- … Mitochondrial function was assessed by the fluorescence intensity of MitoTracker Red probes, which diffuse across the membrane and accumulate in mitochondria with active membrane potentials. … Melatonin reduced oxidative stress-induced DNA damage, mitochondrial dysfunction, lipid peroxidation, and apoptosis in GCs, suggesting that melatonin protects GCs by reducing oxidative stress of cellular components including nuclei, mitochondria, and plasma membranes. …
- NAID 130004774186
Related Links
- Mitochondrial disorders may be caused by mutations, acquired or inherited, in mitochondrial DNA (mtDNA) or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondrial dysfunction due to ...
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★リンクテーブル★
| リンク元 | 「ミトコンドリア機能不全」「ミトコンドリア機能異常」 |
| 関連記事 | 「dysfunction」「mitochondrial」 |
「ミトコンドリア機能不全」
「ミトコンドリア機能異常」
「dysfunction」
- n.
- vi
- 機能不全に陥る
- 関
- barrier、damage、difficulty、disorder、disturbance、foe、functional disorder、functional impairment、hindrance、hypofunction、impair、impairment、impediment、incompetence、insufficiency、lesion、malfunction、obstacle、stun
「mitochondrial」
- adj.
- ミトコンドリアの