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29篇 您的检索式：作者名="CLEMENT RP"

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	题名	作者	年代	出处	被引量
1	The farnesyl protein transferase inhibitor SCH66336 is a potent inhibitor of MDR1 product P-glucoprotein 显示文摘	Wang E Casciano CN Clement RP	2001	Cancer Res2001，61，20：	1
2	HMG-CoA reductase inhibitors (statins)characterized as direct inhibitors of Pglycoprotein显示文摘	WANG E CASCIANO CN CLEMENT RP	2001	Pharm Res2001，18，6：	1
3	Structure-activity relationships of the peptide deformylase inhibitor BB-3497: modification of the metal binding group 显示文摘	Helen KS Beckett RP Clements JM	2002	Bioorg Med Chem Lett2002，12，24：	1
4	Antibiotic activity and haracterization of BB-3497, a novel peptide deformylase inhibitor显示文摘	Clements JM Beckett RP Brown A	2001	Antimicrob Agents Chemother2001，45，2：	1
5	Cholesterol interaction with the daunorubicin binding site of P - glycoprotein 显示文摘	Wang E Casciano CN Clement RP	2000	Biochem Biophys Res Commun2000，276，3：	1
6	Antibiotic activity and characterization of BB-3497,a novel peptide deformylase inhibitor显示文摘	Clements JM Beckett RP Brown A	2001	Antimicrob Agents Chemother2001，45，2：	1
7	Structureactivity relationships of the peptide deformylase inhibitor BB-3497:modification of the metal binding group显示文摘	Smith HK Beckett RP Clements JM	2002	Bioorg Med Chem Lett2002，12，24：	1
8	Antibiotic activity and characterization of BB-3497,a novel peptide deformylase inhibitor显示文摘	Clements MJ Beckett RP Hunter MG	2001	Antimicrob Agents Chemother2001，45，2：	1
9	HMG - CoA reductase inhibitors (stafins) characterized as direct inhibitors of pglycopretein显示文摘	Wang E Caseiano CN Clement RP	2001	Phann Res2001，18，：	1
10	Oral anti-pneumococcal activity and pharmacokinetic profiling of a novel peptide deformylase inhibitor 显示文摘	Gross M Clements J Beckett RP	2004	J Antimicrob Chemother2004，53，3：	1
11	Nurture trumps nature in a longitudinal survey of salivary bacterial communities in twins from early adolescence to early adulthood显示文摘	Stahringer SS Clemente JC Corley RP	2012	Genome Res2012，22，11：	1
12	Antibiotic activity and characterization of BB-3497, a novel peptide deformylase inhibitor 显示文摘	Clements JM Becket RP Hunter MG	2001	Antimicrob Agents Chemother2001，45，2：	1
13	The farnesyl protein transferase inhibitor SCH66336 is a potent inhibitor of MDR1 product P-glycoprotein 显示文摘	Wang E Casciano CN Clement RP	2001	Cancer Res2001，61，20：	1
14	HMG-Co A reductase inhibitors(statins)characterized as direct inhibitors of P-glycoprotein显示文摘	Wang E Casciano CN Clement RP	2001	Pharm Res2001，18，6：	1
15	In Vitro flow eytometry method to quantitatively assess inhibitors of P-glycoprotein显示文摘	Wang EJ Casciano CN Clement RP Johnson WW	2000	Drug Metab Dispos2000，28，：	1
16	Pulmonary surface tension and alveolar stability 显示文摘	Clements JA Hustead RF Johnson RP	1961	J Appl Physiol1961，16，3：	1
17	Identification of human liver cytochrome P450 enzymes that metabolize the nonsedating antihistamine loratadine:Formation of descarboethoxyloratadine by CYP3A4 and CYP2D6显示文摘	Yumibe N Huie K Chen KJ Snow M Clement RP Cayen MN	1996	Biochem Pharmacol1996，51，：	1
18	Antibiotic activity and characterization of BB3497, a novel peptide deformylase inhibitor显示文摘	Clements JM Beckett RP Brown A	2001	Antimicrob Agents Chemother2001，45，2：	1
19	Structure-activity relationships of the peptide deformylase inhibitor 1313-3497:modification of the metal binding group显示文摘	Smith HK Beckett RP Clements J M	2002	Bioorg Med Chem Lett2002，12，24：	1
20	Cholesterol interaction with the daunorubicin binding site of P -glycoprotein显示文摘	Wang EJ Casciano CN Clement RP	2000	Biochem Biophys Res Commun2000，276，：	1

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