Results 81 to 90 of about 4,935 (109)

Application of a mouse model humanized for cytochrome P450-mediated drug metabolism to predict drug-drug interactions between a peptide and small molecule drugs. [PDF]

open access: yesDrug Metab Dispos
Kapelyukh Y   +10 more
europepmc   +1 more source

A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile.

open access: yesJ Clin Endocrinol Metab
Rojas Velazquez MN   +16 more
europepmc   +1 more source

In vitro and clinical data demonstrate negligible risk of drug-drug interactions with opelconazole, a novel inhaled antifungal agent. [PDF]

open access: yesJ Antimicrob Chemother
Cass LMR   +7 more
europepmc   +1 more source

Prevalence of actionable pharmacogenomic variants in Brazilian patients with cancer. [PDF]

open access: yesFront Pharmacol
Schuch JB   +28 more
europepmc   +1 more source

The effect of salidroside, an active component of Rhodiola rosea, on the metabolic activity of rat and human cytochromes P450 in preclinical studies. [PDF]

open access: yesPharmacol Rep
Klaskova E   +9 more
europepmc   +1 more source

Influence of cytochrome P-450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment

Blood, 2000
Abstract Cytochrome P-450 2C9 is the principle enzyme that terminates the anticoagulant effect of warfarin. Genetic polymorphisms inCYP2C9 producing variants with altered catalytic properties have been identified. Patients (n = 561) with a target international normalized ratio (INR) of 2.5 who had been treated with warfarin for more than
J, Taube, D, Halsall, T, Baglin
exaly   +3 more sources

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