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Brian Houston

Showing results (81-90 of 156) with videos related to

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 14, 2018
Simultaneous Assessment In Vitro of Transporter and Metabolic Processes in Hepatic Drug Clearance: Use of a Media Loss ApproachJames Harrison, Tom De Bruyn, Adam S Darwich, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 7, 2009
Evaluation of recombinant cytochrome P450 enzymes as an in vitro system for metabolic clearance predictionsRowan A Stringer, Claire Strain-Damerell, Paul Nicklin, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 15, 2003
Generation and evaluation of a CYP2C9 heteroactivation pharmacophoreAnn-Charlotte Egnell, Cecilia Eriksson, Nan Albertson, et al.
International Journal of Emergency Mental Health|February 25, 2014
Children of National Guard troops: a pilot study of deployment, patriotism, and media coverageBetty Pfefferbaum, Haekyung Jeon-Slaughter, Anne K Jacobs, et al.
The Journal of the Acoustical Society of America|July 12, 2012
Surface decomposition method for near-field acoustic holographyNicolas P Valdivia, Earl G Williams, Peter C Herdic, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 18, 2010
Comparative use of isolated hepatocytes and hepatic microsomes for cytochrome P450 inhibition studies: transporter-enzyme interplayHayley S Brown, Alison J Wilby, Jane Alder, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 21, 2002
Incorporating measures of variability and uncertainty into the prediction of in vivo hepatic clearance from in vitro dataIvan Nestorov, Ivelina Gueorguieva, Hannah M Jones, et al.
Pharmaceutical Research|March 14, 2014
Reduced physiologically-based pharmacokinetic model of repaglinide: impact of OATP1B1 and CYP2C8 genotype and source of in vitro data on the prediction of drug-drug interaction riskMichael Gertz, Nikolaos Tsamandouras, Carolina Säll, et al.
Biochemical Pharmacology|February 4, 2006
In vitro-in vivo correlation for drugs and other compounds eliminated by glucuronidation in humans: pitfalls and promisesJohn O Miners, Kathleen M Knights, J Brian Houston, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 4, 2008
Prediction of drug clearance by glucuronidation from in vitro data: use of combined cytochrome P450 and UDP-glucuronosyltransferase cofactors in alamethicin-activated human liver microsomesPeter J Kilford, Rowan Stringer, Bindi Sohal, et al.
Pageof 16

Showing results (81-90 of 156) with videos related to

Sort By:
Pageof 16
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 14, 2018
Simultaneous Assessment In Vitro of Transporter and Metabolic Processes in Hepatic Drug Clearance: Use of a Media Loss ApproachJames Harrison, Tom De Bruyn, Adam S Darwich, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 7, 2009
Evaluation of recombinant cytochrome P450 enzymes as an in vitro system for metabolic clearance predictionsRowan A Stringer, Claire Strain-Damerell, Paul Nicklin, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 15, 2003
Generation and evaluation of a CYP2C9 heteroactivation pharmacophoreAnn-Charlotte Egnell, Cecilia Eriksson, Nan Albertson, et al.
International Journal of Emergency Mental Health|February 25, 2014
Children of National Guard troops: a pilot study of deployment, patriotism, and media coverageBetty Pfefferbaum, Haekyung Jeon-Slaughter, Anne K Jacobs, et al.
The Journal of the Acoustical Society of America|July 12, 2012
Surface decomposition method for near-field acoustic holographyNicolas P Valdivia, Earl G Williams, Peter C Herdic, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 18, 2010
Comparative use of isolated hepatocytes and hepatic microsomes for cytochrome P450 inhibition studies: transporter-enzyme interplayHayley S Brown, Alison J Wilby, Jane Alder, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 21, 2002
Incorporating measures of variability and uncertainty into the prediction of in vivo hepatic clearance from in vitro dataIvan Nestorov, Ivelina Gueorguieva, Hannah M Jones, et al.
Pharmaceutical Research|March 14, 2014
Reduced physiologically-based pharmacokinetic model of repaglinide: impact of OATP1B1 and CYP2C8 genotype and source of in vitro data on the prediction of drug-drug interaction riskMichael Gertz, Nikolaos Tsamandouras, Carolina Säll, et al.
Biochemical Pharmacology|February 4, 2006
In vitro-in vivo correlation for drugs and other compounds eliminated by glucuronidation in humans: pitfalls and promisesJohn O Miners, Kathleen M Knights, J Brian Houston, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 4, 2008
Prediction of drug clearance by glucuronidation from in vitro data: use of combined cytochrome P450 and UDP-glucuronosyltransferase cofactors in alamethicin-activated human liver microsomesPeter J Kilford, Rowan Stringer, Bindi Sohal, et al.
Pageof 16