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24篇 您的检索式:作者名="Beumer JH"
    题名 作者 年代 出处 被引量
1Hair as a biological specimen for therapeutic drug monitoring显示文摘Beumer JH Bosman IJ Maes RA 2001International Journal of Clinical Practice2001,55,6:1
2In vitro eytotoxieity, pharmacokinetics, tissue distribution, and metabolism of small- molecule protein kinase D inhibitors, kb-NB142-70 and kb- NB165-09, in mice bearing human cancer xenografts显示文摘Guo J Clansen DM Beumer JH 2013Cancer Chemother Pharmacol2013,71,2:1
3Trabectedin (ET-743, Yondelis) is a substrate for P-glycoprotein, but only high expression of P-glycoprotein confers the multidrug resistance phenotype 显示文摘Beumer JH Buckle T Ouwehand M 2007Invest New Drugs2007,25,:1
4Safety and efficacy of decitabine in combination with temozolomide in metastatic melanoma:a phaseⅠ/Ⅱstudy and pharmacokinetic analysis显示文摘Tawbi HA Beumer JH Tarhini AA 2013Ann Oncol2013,24,4:1
5Phase Ⅰ pharmacokinetic study of the vascular endothelial growth factor receptor tyrosine kinase in- hibitor vatalanib (PTK787) plus imatinib and hydroxyurea for malignant glioma显示文摘Reardon DA Egorin M J Desjardins A Vredenburgh J J Beumer JH Lagattuta TF 2009Cancer2009,115,10:1
6Safety and effi- cacy of decitabine in combination with temozolomide in metastatic melanoma: A phase Ⅰ/ Ⅱ study and pharma- cokinetic analysis显示文摘Tawbi HA Beumer JH Tarhini AA 2013Ann Oncol2013,24,4:1
7Role of PARP inhibi- tors in cancer biology and therapy 显示文摘Davar D Beumer JH Hamieh L etal 2012Curr Med Chem2012,19,23:1
8A mass balance and disposition study of the DNA methyhransferase inhibitor ze- bularine (NSC 309132) and three of its metabolites in mice 显示文摘BEUMER JH JOSEPH E EGORIN MJ 2006Clin Cancer Res2006,12,19:1
9Concentra- tions of the DNA methyltransferase inhibitor 5-fluoro-2'- deoxycytidine (FdCyd) and its cytotoxic metabolites in plasma of patients treated with FdCyd and tetrahydrouri- dine (THU) 显示文摘Beumer JH Parise RA Newman EM 2008Cancer Chemother Pharmacol2008,62,2:1
10Evaluation of human plasma protein binding of trabeetedin(Yondelis,ET-743)显示文摘Beumer JH Lopez-Lazaro L ScheJlens JH 2009Curr Clin Pharmacol2009,4,1:1
11Role of PARP inhibitors in cancer biology and therapy显示文摘Davar D Beumer JH Hamieh L 0,,23:1
12A liquid chromatography-electrospray ionization tandem mass spectrometric assay for quantitation of the histone deacetylase inhibitor,vorinostat(suberoylanilide hydroxamicacid,SAHA),and its metabolites in human serum显示文摘Parise RA Holleran JL Beumer JH 2006J Chromatogr B2006,840,2:1
13Safety and efficacy of decitabine in combination with temozolomide in metastatic melanoma:a phaseⅠ/Ⅱstudy and pharmacokinetic analysis显示文摘Tawbi HA Beumer JH Tarhini AA 2013Ann Oncol2013,24,4:1
14A liquid chromatography-electrospray ionization tandem mass spectrometric assay for quantitation of the histone deacetylase inhibitor,vorinostat (suberoylanilide hydroxamicacid,SAHA),and its metabolites in human serum显示文摘Parise RA Holleran JL Beumer JH 2006J Chromatogr B Analyt Technol Biomed Life Sci2006,840,2:1
15Mass balance studies,with a focus on anticancer drugs显示文摘Beumer JH Beijnen JH Schellens JH 2006Clin Pharmacokinet2006,45,1:1
16Trabectedin (ET-743, Yondelis) is a substrate for P-glycoprotein, but only high expression of P-glycoprotein confers the multidrug resistance phenotype 显示文摘Beumer JH Buckle T Ouwehand M 2007Invest New Drugs2007,25,1:1
17Body-surface area-based chemo- therapy dosing:appropriate in the 21st century? 显示文摘Beumer JH Chu E Salamone SJ 2012J Clin Oncol2012,30,31:1
18A liquid ehromatography-eleetrospray ionization tandem mass spectro- metric assay for quantitation of the histone deaeetylase inhibitor, vorinostat ( suberoylanilide hydroxamieaeid, SAHA ) , and its metabolites in human serum显示文摘PARISE RA HOLLERAN JL BEUMER JH 2006J Chromatogr B2006,840,2:1
19Plas- ma pharmacokinetics and oral hioavailahility of the 3, 4, 5, 6-tetrahydrouridine (THU) prodrug, tri acetyl-THU(taTHU), in mice 显示文摘Beumer JH Eisesman JL Gilbert JA 2011Cancer Che- mother Pharmacol2011,67,2:1
20Therapeutic drug monitoring of 5-flu- orouracil显示文摘Lee J J Beumer JH Chu E 2016Cancer Chemother Pharmaco12016,20,:1
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