Search Results - "SUKRI, Norita"
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Phase I and Biomarker Study of ABT-869, a Multiple Receptor Tyrosine Kinase Inhibitor, in Patients With Refractory Solid Malignancies
Published in Journal of clinical oncology (01-10-2009)“…To determine the safety and tolerability of ABT-869 at escalating doses and its effects on biomarkers relevant for antiangiogenic activity in patients with…”
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2
Genotype of human carbonyl reductase CBR3 correlates with doxorubicin disposition and toxicity
Published in Pharmacogenetics and genomics (01-07-2008)“…OBJECTIVESDoxorubicin is a cytotoxic drug with potential for severe myelosuppression that is highly variable and poorly predictable. METHODSWe correlated CBR1…”
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Chemotherapy-induced tumor gene expression changes in human breast cancers
Published in Pharmacogenetics and genomics (01-03-2009)“…OBJECTIVEStudying chemotherapy-induced gene expression changes in vivo, which could provide insights into mechanisms of chemotherapy resistance. METHODSWe…”
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A comparative study of dynamic contrast-enhanced MRI parameters as biomarkers for anti-angiogenic drug therapy
Published in NMR in biomedicine (01-11-2011)“…The aim of the present study was to compare three tracer kinetics methods for the analysis of dynamic contrast‐enhanced (DCE) MRI data, namely the generalized…”
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Post-treatment tumor gene expression signatures are more predictive of treatment outcomes than baseline signatures in breast cancer
Published in Pharmacogenetics and genomics (01-11-2009)“…OBJECTIVETumor gene expression signatures have been used to classify, prognosticate, and predict chemotherapy sensitivity in breast cancer, although almost all…”
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A phase I study of docetaxel with ketoconazole modulation in patients with advanced cancers
Published in Cancer chemotherapy and pharmacology (01-07-2008)“…Purpose The aims were to determine the maximum tolerable dose (MTD) of docetaxel with CYP3A inhibition by ketoconazole, and to correlate the pharmacokinetics…”
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Ketoconazole renders poor CYP3A phenotype status with midazolam as probe drug
Published in Therapeutic drug monitoring (01-04-2006)“…Drugs metabolized by cytochrome CYP3A isoenzymes have wide interindividual variability and normally distributed plasma clearance distributions. This makes…”
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