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
a crystalline amino acid containing sulfur; found in most proteins and essential for nutrition

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

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1. 先天性代謝異常：疫学、病因、および臨床的特徴 inborn errors of metabolism epidemiology pathogenesis and clinical features
2. チロシン代謝障害 disorders of tyrosine metabolism
3. ガラクトース血症：臨床的特徴および診断 galactosemia clinical features and diagnosis
4. フェニルケトン尿症の概要 overview of phenylketonuria
5. 食物中の微量ミネラルの概要 overview of dietary trace minerals

Metabolomic analysis revealed glycylglycine accumulation in astrocytes after methionine enkephalin administration exhibiting neuron protective effects.

Zhao C1, Du H2, Xu L3, Wang J4, Tang L4, Cao Y5, Li C5, Wang Q5, Liu Y6, Shan F7, Feng J8, Xu F9, Gao P10.
Journal of pharmaceutical and biomedical analysis.J Pharm Biomed Anal.2015 Nov 10;115:48-54. doi: 10.1016/j.jpba.2015.06.028. Epub 2015 Jun 24.
Owing to its unrevealed etiology, multiple sclerosis lacks specific therapies up to now. Experiential administration of methionine enkephalin (MENK) on mouse model improved disease manifestations to some extent. In order to gain more insight on the significance of MENK application, a capillary elect
PMID 26163404

CX3CR1 is a gatekeeper for intestinal barrier integrity in mice: Limiting steatohepatitis by maintaining intestinal homeostasis.

Schneider KM1, Bieghs V1, Heymann F1, Hu W1, Dreymueller D2, Liao L1, Frissen M1, Ludwig A2, Gassler N3, Pabst O4, Latz E5,6,7, Sellge G1, Penders J8, Tacke F1, Trautwein C1.
Hepatology (Baltimore, Md.).Hepatology.2015 Nov;62(5):1405-16. doi: 10.1002/hep.27982. Epub 2015 Sep 2.
Nonalcoholic fatty liver disease is seen as the hepatic manifestation of the metabolic syndrome and represents the most common liver disease in Western societies. The G protein-coupled chemokine receptor CX3CR1 plays a central role in several metabolic syndrome-related disease manifestations and is
PMID 26178698

Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.

Huemer M1,2,3, Kožich V4, Rinaldo P5, Baumgartner MR6,7, Merinero B8, Pasquini E9, Ribes A10, Blom HJ11.
Journal of inherited metabolic disease.J Inherit Metab Dis.2015 Nov;38(6):1007-19. doi: 10.1007/s10545-015-9830-z. Epub 2015 Mar 12.
Newborn screening (NBS) is justified if early intervention is effective in a disorder generally not detected early in life on a clinical basis, and if sensitive and specific biochemical markers exist. Experience with NBS for homocystinurias and methylation disorders is limited. However, there is rob
PMID 25762406

斎藤芳郎
日本毒性学会学術年会 47.1(0), S4-5, 2020
<p>　必須微量元素であるセレンは反応性が高く、強い毒性を持つ元素であるが、生体はセレンの特性を巧みに取り込み、生体防御に利用している。セレンはセレノシステイン（Sec：システインの硫黄がセレンに置換したアミノ酸）の形で主にタンパク質中に含まれ、過酸化物を還元・無毒化するグルタチオンペルオキシダーゼやレドックス制御因子チオレドキシン還元酵素の活性部位を形成する。セレンは、これらの抗酸化 …
NAID 130007898600

A study of single nucleotide polymorphisms of the SLC19A1/RFC1 gene in subjects with autism spectrum disorder

Al Mahmuda Naila,Yokoyama Shigeru,Huang Jian-Jun,Liu Li,Munesue Toshio,Nakatani Hideo,Hayashi Kenshi,Yagi Kunimasa,Yamagishi Masakazu,Higashida Haruhiro
International Journal of
… Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with complex genetic etiology. … Recent studies have indicated that children with ASD may have altered folate or methionine metabolism, suggesting that the folate-methionine cycle may play a key role in the etiology of ASD. …
NAID 120005774898

The α-tocopherol status and expression of α-tocopherol-related proteins in methionine-choline deficient rats treated with vitamin E

Miyazaki Hiroshi,Takitani Kimitaka,Koh Maki,Yoden Atsushi,Tamai Hiroshi
Ｊｏｕｒｎａｌ　ｏｆ
… Non-alcoholic fatty liver disease is the most common liver disorder in developed countries, and its incidence is increasing in all population groups. … As an antioxidant, vitamin E is effective in the treatment of non-alcoholic fatty liver disease, although the mechanism is still unclear. …
NAID 130004466749