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pharmacogenet genomics » pharmacogenetics genomics (Expandir a Pesquisa), pharmaco genomics (Expandir a Pesquisa)
A mostrar 681 - 700 resultados de 1,112 para a pesquisa 'Pharmacogenet Genomics', tempo de pesquisa: 0.75seg Refinar resultados
Impact of nonsynonymous single nucleotide polymorphisms on in vitro metabolism of exemestane by hepatic cytosolic reductases
Associations between polymorphisms in target, metabolism, or transport proteins of mycophenolate sodium and therapeutic or adverse effects in kidney transplant patients

Genetic Determinants of Variability in Warfarin Response after the Dose-Titration Phase
Variation in CYP2A6 and nicotine metabolism among two American Indian tribal groups differing in smoking patterns and risk for tobacco-related cancer

Impact of the CYP2C19 Genotype on Voriconazole Exposure in Adults with Invasive Fungal Infections
TPMT, COMT and ACYP2 genetic variants in paediatric cancer patients with cisplatin-induced ototoxicity

Quality of anticoagulation control and hemorrhage risk among African American and European American warfarin users
CYP2D6 haplotypes with enhancer SNP rs5758550 and rs16947 (*2 allele): implications for CYP2D6 genotyping panels

Targeted ultra-deep sequencing of a South African Bantu-speaking cohort to comprehensively map and characterize common and novel variants in 65 pharmacologically-related genes
Influence of CYP2B6 and CYP3A4 polymorphisms on the virologic and immunological responses of patients treated with efavirenz containing regimen

SNP biomarkers of adjuvant anastrozole-induced estrogen suppression in early breast cancer
Association of SLCO1B1 c.521T>C (rs4149056) with Discontinuation of Atorvastatin Due to Statin-Associated Muscle Symptoms

Haplotype and functional analysis of four flavin-containing monooxygenase isoform 2 (FMO2) polymorphisms in Hispanics
CYP2J2 and CYP2C8 polymorphisms and coronary heart disease risk: the Atherosclerosis Risk in Communities (ARIC) study

Genetic variation in N-acetyltransferase 1 (NAT1) and 2 (NAT2) and risk of non-Hodgkin lymphoma
Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1)

Interaction of soy and 17β-HSD1 gene polymorphisms in the risk of endometrial cancer
The discovery of new coding alleles of human CYP26A1 which are potentially defective in the metabolism of all-trans retinoic acid and their assessment in a recombinant cDNA expression system

Absorption of Montelukast is Transporter Mediated: a Common Variant of OATP2B1 is Associated with Reduced Plasma Concentrations and Poor Response
The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13) on the effectiveness of statins: the GenHAT study

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