WordNet

bring disorder to (同)disarray
a physical condition in which there is a disturbance of normal functioning; "the doctor prescribed some medicine for the disorder"; "everyone gets stomach upsets from time to time" (同)upset
a disturbance of the peace or of public order
the organic processes (in a cell or organism) that are necessary for life (同)metabolic_process
an essential amino acid found in proteins that is important for the growth and repair of tissue

PrepTutorEJDIC

〈U〉『無秩序』,混乱,乱雑(confusion) / 《しばしば複数形で》(社会的・政治的な)粉争,騒動 / 〈C〉(肉体的・精神的な)不調,異常,障害 / …‘の'秩序を乱す / 〈心身〉‘に'異常を起こさせる
《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
新陳代謝,物質交代
OLD French古[代]フランス語

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 先天性代謝異常：分類 inborn errors of metabolism classification
2. 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
3. 代謝性ミオパチーへのアプローチ approach to the metabolic myopathies
4. クレアチン代謝の先天性疾患 congenital disorders of creatine metabolism
5. 先天性代謝異常：代謝性救急疾患 inborn errors of metabolism metabolic emergencies

Peters V1, Klessens CQ, Baelde HJ, Singler B, Veraar KA, Zutinic A, Drozak J, Zschocke J, Schmitt CP, de Heer E.
Amino acids.Amino Acids.2015 Jul 24. [Epub ahead of print]
Histidine-containing dipeptides like carnosine and anserine have protective functions in both health and disease. Animal studies suggest that carnosine can be metabolized within the kidney. The goal of this study was to obtain evidence of carnosine metabolism in the human kidney and to provide insig
PMID 26206726

(1)H nuclear magnetic resonance spectroscopy-based metabonomic study in patients with cirrhosis and hepatic encephalopathy.

Dabos KJ1, Parkinson JA1, Sadler IH1, Plevris JN1, Hayes PC1.
World journal of hepatology.World J Hepatol.2015 Jun 28;7(12):1701-7. doi: 10.4254/wjh.v7.i12.1701.
AIM: To identify plasma metabolites used as biomarkers in order to distinguish cirrhotics from controls and encephalopathics.METHODS: A clinical study involving stable cirrhotic patients with and without overt hepatic encephalopathy was designed. A control group of healthy volunteers was used. Plasm
PMID 26140090

Possible peroxidase active site environment in amyloidogenic proteins: Native monomer or misfolded-oligomer; which one is susceptible to the enzymatic activity, with contribution of heme?

Khodarahmi R1, Ashrafi-Kooshk MR2, Khodarahmi S2, Ghadami SA3, Mostafaie A2.
International journal of biological macromolecules.Int J Biol Macromol.2015 Jun 26;80:293-301. doi: 10.1016/j.ijbiomac.2015.06.020. [Epub ahead of print]
Amyloid states of many proteins complex with heme and exhibit significant non-specific peroxidase activity, compared to free heme. Neurotransmitter deficiency, generation of neurotoxins, altered activity/metabolism of key enzymes and cellular DNA damage are possible evidences highlighting the import
PMID 26123814

, , [他],
Biomedical research on trace elements 18(3), 249-254, 2007-09-01
… Genetic disorders of copper metabolism are reviewed, particularly in Menkes disease and Wilson's disease. … However, the pathology of Menkes disease is completely different from that of Wilson's disease, with Menkes disease characterized by a copper deficiency and Wilson's disease by a toxic excess of copper. …
NAID 10019766046

岩垣博巳
全日本鍼灸学会雑誌 57(5), 613-620, 2007
担癌悪液質モデルマウスを用いて、脳内モノアミン神経活動、末梢ヒスタミン代謝、消化管セロトニン代謝について解析した。非担癌マウスに比し、悪液質マウスの脳内モノアミン代謝は、ドーパミンについては低下、セロトニン、ヒスタミンについては有意に増加し、それぞれ、運動量の低下、うつ的傾向、食欲不振に関与していることが示唆される。また、癌悪液質マウスでは、非肥満細胞におけるヒスチジン脱炭酸酵素が強く誘導されてお …
NAID 130004513374

Simultaneous determination of urinary creatinine and UV-absorbing amino acids using a novel low-capacity cation-exchange chromatography for the screening of inborn errors of metabolism

YOKOYAMA Yukio,YAMASAKI Keiko,SATO Hisakuni
Journal of
… A simple and versatile low-capacity cation-exchange chromatography system for the simultaneous determination of creatinine and UV-absorbing amino acids was developed. … Urinary creatinine, creatine, tyrosine, histidine, phenylalanine, and tryptophan were simultaneously separated and determined by an isocratic elution with phosphate/acetonitrile eluent in 25 min. Relative standard deviations (R.S.D.) of the retention times for the analytes were between 0.28 and 1.06 %. …
NAID 120000920844