WordNet

the 4th letter of the Roman alphabet (同)d

PrepTutorEJDIC

deuteriumの化学記号
dishonorable discharge

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/01/05 14:38:06」(JST)

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1. 心臓ペーシングのモード：名称および選択 modes of cardiac pacing nomenclature and selection
2. HIV抗レトロウイルス療法に関する臨床試験：3剤療法と4剤療法の比較 clinical trials of hiv antiretroviral therapy three versus four drug regimens
3. HIV感染患者におけるミトコンドリア毒性の治療および予防 treatment and prevention of mitochondrial toxicity in hiv infected patients
4. HIV抗レトロウイルス療法に関する臨床試験：ヌクレオシド系逆転写酵素阻害剤を使用した3剤療法 clinical trials of hiv antiretroviral therapy triple regimens using nucleoside reverse transcriptase inhibitors
5. HIVヌクレオシド系逆転写酵素阻害剤のミトコンドリア毒性 mitochondrial toxicity of hiv nucleoside reverse transcriptase inhibitors

English Journal

Application of an LC-MS/MS method for the simultaneous quantification of human intestinal transporter proteins absolute abundance using a QconCAT technique.

Harwood MD1, Achour B2, Russell MR2, Carlson GL3, Warhurst G3, Rostami-Hodjegan A4.
Journal of pharmaceutical and biomedical analysis.J Pharm Biomed Anal.2015 Jun 10;110:27-33. doi: 10.1016/j.jpba.2015.02.043. Epub 2015 Feb 28.
Transporter proteins expressed in the gastrointestinal tract play a major role in the oral absorption of some drugs, and their involvement may lead to drug-drug interaction (DDI) susceptibility when given in combination with drugs known to inhibit gut wall transporters. Anticipating such liabilities
PMID 25796981

Evaluation of cynomolgus monkeys for the identification of endogenous biomarkers for hepatic transporter inhibition and as a translatable model to predict pharmacokinetic interactions with statins in humans.

Chu X1, Shih SJ2, Shaw R2, Hentze H2, Chan GH2, Owens K2, Wang S2, Cai X2, Newton D2, Castro-Perez J2, Salituro G2, Palamanda J2, Fernandis A2, Ng CK2, Liaw A2, Savage MJ2, Evers R2.
Drug metabolism and disposition: the biological fate of chemicals.Drug Metab Dispos.2015 Jun;43(6):851-63. doi: 10.1124/dmd.115.063347. Epub 2015 Mar 26.
Inhibition of hepatic transporters such as organic anion transporting polypeptides (OATPs) 1B can cause drug-drug interactions (DDIs). Determining the impact of perpetrator drugs on the plasma exposure of endogenous substrates for OATP1B could be valuable to assess the risk for DDIs early in drug de
PMID 25813937

Japanese Journal

製薬ビジネス激変時代のタレントマネジメント(第1回)DDI調査にみる人材開発の課題

ミクス 44(3), 63-65, 2016-03
NAID 40020746719

Requirements for human iPS cell-derived hepatocytes as an alternative to primary human hepatocytes for assessing absorption, distribution, metabolism, excretion and toxicity of pharmaceuticals

Fundamental Toxicological Sciences 3(3), 89-99, 2016
NAID 130005144692

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