Search Results - "SUKRI, Norita"

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    Genotype of human carbonyl reductase CBR3 correlates with doxorubicin disposition and toxicity by Fan, Lu, Goh, Boon-Cher, Wong, Chiung-Ing, Sukri, Norita, Lim, Siew-Eng, Tan, Sing-Huang, Guo, Jia-Yi, Lim, Robert, Yap, Hui-Ling, Khoo, Yok-Moi, Iau, Philip, Lee, How-Sung, Lee, Soo-Chin

    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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    Journal Article
  3. 3

    Chemotherapy-induced tumor gene expression changes in human breast cancers by Lee, Soo-Chin, Xu, Xin, Lim, Yi-Wan, Iau, Philip, Sukri, Norita, Lim, Siew-Eng, Yap, Hui Ling, Yeo, Wee-Lee, Tan, Patrick, Tan, Sing-Huang, McLeod, Howard, Goh, Boon-Cher

    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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  4. 4

    A comparative study of dynamic contrast-enhanced MRI parameters as biomarkers for anti-angiogenic drug therapy by Koh, Tong San, Thng, Choon Hua, Hartono, Septian, Tai, Bee Choo, Rumpel, Helmut, Ong, Ai Bee, Sukri, Norita, Soo, Ross A., Wong, Chuing Ing, Low, Albert S. C., Humerickhouse, Rod A., Goh, Boon Cher

    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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    A phase I study of docetaxel with ketoconazole modulation in patients with advanced cancers by Yong, Wei-Peng, Wang, Ling-Zhi, Tham, Lai-San, Wong, Chiung-Ing, Lee, Soo-Chin, Soo, Ross, Sukri, Norita, Lee, How-Sung, Goh, Boon-Cher

    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 by THAM, Lai-San, LEE, How-Sung, LINGZHI WANG, YONG, Wei-Peng, LU FAN, ONG, Ai-Bee, SUKRI, Norita, SOO, Ross, LEE, Soo-Chin, GOH, Boon-Cher

    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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