C8欠損症
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English Journal
- Metabolic disturbances and worsening of atherosclerotic lesions in ApoE-/- mice after cola beverages drinking.
- Otero-Losada ME, Loughlin SM, Rodríguez-Granillo G, Müller A, Ottaviano G, Moriondo M, Cutrin JC, Milei J.SourceInstituto de Investigaciones Cardiológicas "Prof, Dr, Alberto C, Taquini" (ININCA), Facultad de Medicina, Universidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina. mol@fmed.uba.ar.
- Cardiovascular diabetology.Cardiovasc Diabetol.2013 Apr 1;12(1):57.
- BACKGROUND: Atherosclerosis is a major health burden. Metabolic disorders had been associated with large consumption of soft drinks. The rising incidence of atherosclerosis and metabolic alterations warrants the study of long-term soft drink consumption' effects on metabolism and atherosclerosis in
- PMID 23547749
- Contribution of the production of quormones to some phenotypic characteristics of Pseudomonas aeruginosa clinical strains.
- Nagant C, Seil M, Nachtergael A, Dulanto SA, Dehaye JP.SourceUniversité libre de Bruxelles.
- Journal of medical microbiology.J Med Microbiol.2013 Mar 28. [Epub ahead of print]
- The contribution of quorum sensing in some phenotypic and pathogenic characteristics of Pseudomonas aeruginosa was studied. The production of acylhomoserine lactones (AHL) by planktonic cultures of 8 clinical and reference strains of P. aeruginosa was evaluated using two biosensors. The adhesion of
- PMID 23538560
Japanese Journal
- 千葉 寛,森本 かおり
- YAKUGAKU ZASSHI 131(2), 247-253, 2011
- … In addition to SLCO1B1, recent studies suggested that variants of genes encoding transporters (ABCG2 and ABCB1) and metabolic enzymes (CYP2C8 and UGT1A3) involved in the disposition of statins, and those involved in the metabolic muscle disease (glycogen storage disorders, carnitine palmitoyl-2 deficiency and myoadenylate deaminase deficiency) are also risk factors of statin-induced myopathy. …
- NAID 130000451459
- Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Yokoi Kyoko,Ito Tetsuya,Maeda Yasuhiro,Nakajima Yoko,Ueta Akihito,Nomura Takayasu,Koyama Norihisa,Kato Ineko,Suzuki Satoshi,Kurono Yukihisa,Sugiyama Naruji,Togari Hajime
- The Tohoku Journal of Experimental Medicine 213(4), 351-359, 2007
- … Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is rare among Asian individuals, and the clinical course and biochemical findings remain unclear. … Our described method with high-performance liquid chromatography/tandem mass spectrometry allows quantification of levels of n-octanoylcarnitine (C8-N) and other isomers (e.g. valproylcarnitine). …
- NAID 130004459642
- 中鎖アシルCoA脱水素酵素欠損症保因者のC8アシルカルニチン値の検討
- 重松 陽介,畑 郁江,田中 幸枝,但馬 剛,佐倉 伸夫
- 日本マス・スクリーニング学会誌 = Journal of Japanese Society for Mass-screening 15(2), 51, 2005-09-27
- NAID 10020472109
Related Links
- Identification of the heterozygotes for deficiency of the beta-subunit of the eighth component of complement by reduced levels of C8 beta and increased amounts of free C8 alpha-gamma. Pediatr Res. 1990 Mar; 27(3):234-8. [Pediatr ...
- C8 beta subunit deficiency in a patient with recurrent neisserial infections. Ric Clin Lab. 1987 Jan-Mar; 17(1):19-25. [Ric Clin Lab. 1987] Inherited deficiency of C8 in a patient with recurrent meningococcal infections: further evidence ...
★リンクテーブル★
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- 英
- C8 deficiency
- 関
- C8
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- 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
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