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10篇 您的检索式:作者名="Kevyn"
    题名 作者 年代 出处 被引量
1A review on phase change materials integrated in building walls显示文摘Frédéric Kuznik Damien David Kevyn Johannes Jean-Jacques Roux 2010Renewable and Sustainable Energy Reviews2010,,1:2
2Organic matter added to bareroot nursery beds influences soil properties and morphology of Fraxinus pennsylvanica and Quercus rubra seedlings 显示文摘Davis A S Jaeobs D F Kevyn E W 2006New Forests2006,26,31:1
3A review on phase change materials integrated in building walls显示文摘FR(E)D(E)RIC K DAMIEN D KEVYN J 2011Renewable and Sustainable Energy Reviews2011,15,1:1
4A Language Modeling Approach to Predicting Reading Difficulty 显示文摘Kevyn Collins-Thompson and Jamie CaUan 2004In Proceedings of the HLT/NAACL 2004 Conference Boston2004,,:1
5Development and val- idation of a new TRNSYS type for the simulation of ex- ternal building walls containing PCM 显示文摘Frederic K Joseph V Kevyn J 2010Energy and Buildings2010,42,7:1
6Development and validation of a new TRNSYS type for the simulation of external building walls containing PCM显示文摘Frederic K Joseph V Kevyn J 2010Energy and Buildings2010,42,7:1
7Rview on phase change materials integrated in building waUs显示文摘Frederic Kuznik Damien David Kevyn Johannes Jean Jacques Roux 2011Renewable and Sustainable Energy Reviews2011,,15:1
8A review on phase change materials integrated in building walls 显示文摘Fr e d e ric Kuznik Damien David Kevyn Johannes Jean-Jacques Roux 2010Renewable and Sustainable Energy Reviews2010,15,1:1
9Management and monitoring of public buildings through ICT based systems: Control rules for energy saving with lighting and HVAC services显示文摘C. Aghemoa J. Virsone G.V. Fracastoro A. Pellegrino L. Blaso J. Savoyat Kevyn Johannes 2013Frontiers of Architectural Research2013,2,2:1
10Altered cisplatin pharmacokinetics during nonalcoholic steatohepatitis contributes to reduced nephrotoxicity显示文摘Disease-mediated alterations to drug disposition constitute a significant source of adverse drug reactions.Cisplatin(CDDP)elicits nephrotoxicity due to exposure in proximal tubule cells during renal secretion.Alterations to renal drug transporter expression have been discovered during nonalcoholic steatohepatitis(NASH),however,associated changes to substrate toxicity is unknown.To test this,a methionine-and choline-deficient diet-induced rat model was used to evaluate NASH-associated changes to CDDP pharmacokinetics,transporter expression,and toxicity.NASH rats administered CDDP(6 mg/kg,i.p.)displayed 20%less nephrotoxicity than healthy rats.Likewise,CDDP renal clearance decreased in NASH rats from 7.39 to 3.83 mL/min,renal secretion decreased from 6.23 to 2.80 mL/min,and renal CDDP accumulation decreased by 15%,relative to healthy rats.Renal copper transporter-1 expression decreased,and organic cation transporter-2 and ATPase copper transporting protein-7 b increased slightly,reducing CDDP secretion.Hepatic CDDP accumulation increased 250%in NASH rats relative to healthy rats.Hepatic organic cation transporter-1 induction and multidrug and toxin extrusion protein-1 and multidrug resistance-associated protein-4 reduction may contribute to hepatic CDDP sequestration in NASH rats,although no drug-related toxicity was observed.These data provide a link between NASH-induced hepatic and renal transporter expression changes and CDDP renal clearance,which may alter nephrotoxicity.Joseph L.Jilek Kayla L.Frost Kevyn A.Jacobus Wenxi He Erica L.Toth Michael Goedken Nathan J.Cherrington 2021Acta Pharmaceutica Sinica B2021,11,12:1
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