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The Journal of Antimicrobial Chemotherapy
|
March 29, 2011
Integration of population pharmacokinetics and pharmacogenetics: an aid to optimal nevirapine dose selection in HIV-infected individuals
Alessandro Schipani, Christoph Wyen, Tabitha Mahungu, et al.
Pharmacogenetics and Genomics
|
January 7, 2010
HIV protease inhibitors are substrates for OATP1A2, OATP1B1 and OATP1B3 and lopinavir plasma concentrations are influenced by SLCO1B1 polymorphisms
Ruben C Hartkoorn, Wai San Kwan, Victoria Shallcross, et al.
Clinical Pharmacokinetics
|
September 10, 2004
Effect of mycophenolate mofetil on the pharmacokinetics of antiretroviral drugs and on intracellular nucleoside triphosphate pools
Sanjay U C Sankatsing, Patrick G Hoggard, Alwin D R Huitema, et al.
Antimicrobial Agents and Chemotherapy
|
September 18, 2002
Intracellular accumulation of human immunodeficiency virus protease inhibitors
Saye H Khoo, Patrick G Hoggard, Ian Williams, et al.
Lancet (London, England)
|
January 26, 2002
Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study
Jacques Fellay, Catia Marzolini, Emma R Meaden, et al.
The Journal of Antimicrobial Chemotherapy
|
February 19, 2008
Impact of CYP2B6 983T>C polymorphism on non-nucleoside reverse transcriptase inhibitor plasma concentrations in HIV-infected patients
Christoph Wyen, Heidy Hendra, Martin Vogel, et al.
Antimicrobial Agents and Chemotherapy
|
October 6, 2010
Population pharmacokinetic modeling of the association between 63396C->T pregnane X receptor polymorphism and unboosted atazanavir clearance
Alessandro Schipani, Marco Siccardi, Antonio D'Avolio, et al.
The Journal of Antimicrobial Chemotherapy
|
July 1, 2011
Cytochrome P450 2B6 (CYP2B6) and constitutive androstane receptor (CAR) polymorphisms are associated with early discontinuation of efavirenz-containing regimens
Christoph Wyen, Heidy Hendra, Marco Siccardi, et al.
Clinical Pharmacology and Therapeutics
|
May 22, 2020
Prioritization of Anti-SARS-Cov-2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics
Usman Arshad, Henry Pertinez, Helen Box, et al.
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Search research articles
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Showing results (91-100 of 99) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 99 results.
The Journal of Antimicrobial Chemotherapy
|
March 29, 2011
Integration of population pharmacokinetics and pharmacogenetics: an aid to optimal nevirapine dose selection in HIV-infected individuals
Alessandro Schipani, Christoph Wyen, Tabitha Mahungu, et al.
Pharmacogenetics and Genomics
|
January 7, 2010
HIV protease inhibitors are substrates for OATP1A2, OATP1B1 and OATP1B3 and lopinavir plasma concentrations are influenced by SLCO1B1 polymorphisms
Ruben C Hartkoorn, Wai San Kwan, Victoria Shallcross, et al.
Clinical Pharmacokinetics
|
September 10, 2004
Effect of mycophenolate mofetil on the pharmacokinetics of antiretroviral drugs and on intracellular nucleoside triphosphate pools
Sanjay U C Sankatsing, Patrick G Hoggard, Alwin D R Huitema, et al.
Antimicrobial Agents and Chemotherapy
|
September 18, 2002
Intracellular accumulation of human immunodeficiency virus protease inhibitors
Saye H Khoo, Patrick G Hoggard, Ian Williams, et al.
Lancet (London, England)
|
January 26, 2002
Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study
Jacques Fellay, Catia Marzolini, Emma R Meaden, et al.
The Journal of Antimicrobial Chemotherapy
|
February 19, 2008
Impact of CYP2B6 983T>C polymorphism on non-nucleoside reverse transcriptase inhibitor plasma concentrations in HIV-infected patients
Christoph Wyen, Heidy Hendra, Martin Vogel, et al.
Antimicrobial Agents and Chemotherapy
|
October 6, 2010
Population pharmacokinetic modeling of the association between 63396C->T pregnane X receptor polymorphism and unboosted atazanavir clearance
Alessandro Schipani, Marco Siccardi, Antonio D'Avolio, et al.
The Journal of Antimicrobial Chemotherapy
|
July 1, 2011
Cytochrome P450 2B6 (CYP2B6) and constitutive androstane receptor (CAR) polymorphisms are associated with early discontinuation of efavirenz-containing regimens
Christoph Wyen, Heidy Hendra, Marco Siccardi, et al.
Clinical Pharmacology and Therapeutics
|
May 22, 2020
Prioritization of Anti-SARS-Cov-2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics
Usman Arshad, Henry Pertinez, Helen Box, et al.
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of 10