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12篇 您的检索式：作者名="PELEMANS H"

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		题名	作者	年代	出处	被引量
	1	Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors显示文摘	PELEMANS H ESNOUF R DE CLERCQ E	2000	Mol Pharmacol2000，57，5：	1
	2	Retention of marked sensitivity to HBY097 in the combined presence of quinoxaline HBY097 and lamivudine 显示文摘	Balzarini J Pelemans H Riess G	1998	Biochem Pharmacol1998，55，5：	1
	3	AFLP a new technique for DNA fingerprinting 显示文摘	Vos P Hogers R Bleeker M Reijans M van de Lee T Hornes M Frijters A Pot H Peleman J Kuiper M Zabeau M	1995	Nucleic Acids Research1995，23，：	1
	4	Acute intestinal obstruction in an elderly patient 显示文摘	Linthoudt H Filez L and Pelemans W	1996	Tijdschr Gerontol Geriatr1996，27，6：	1
	5	Presence of 2′,5′ - Bis- O - ( tert- butyldimethylsilyl) - 3′ - spiro- 5′ - ( 4′ - amino- 1′,2′ - oxath iole - 2′,2′ - dioxide) ( TS- AO) - resistant virus strains in TSAO- inexperienced H- IV patients显示文摘	Schmit JC Pelemans H	2000	AIDS Res Hum Retroviruses2000，16，9：	1
	6	Characteristics of the Pro225His mutation in human immunodeficiency virus type 1 ( HIV- 1) reverse transcriptase that appears under selective pressure of dose-escalating quinoxaline treatment of HIV-1显示文摘	Pelemans H Esnuof R Dunkler A	1997	J Virol1997，71，：	1
	7	Mutations at amino acid positions 63,189 ,and 396 of human immunodeficiency virus type 1 reverse transcriptase(RT) partially restore the DNA polymerase activity of a Trp229Tyr mutant RT 显示文摘	PELEMANS H ESNOUF R MINK L	2001	Virology2001，287，1：	1
	8	A novel mutation (F227L)arises in the reverse transcriptase of human immunodeficiency virus type 1 on dose-escalating treatment of HIV type 1-infected cell cultures with the nonnucleoside reverse transcriptase inhibitor thiocarboxanilide UC-781显示文摘	Balzarini J Pelemans H Esnouf R	1998	AIDS Res Hum Retrovir Uses1998，14，：	1
	9	Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase ( RT ) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors 显示文摘	PELEMANS H ESNOUF R de CLERCQ E	2000	Mol Pharmacol2000，57，5：	1
	10	Highly favorable antiviral activity and resistance profile of the novel thiocarboxanilide pentenyloxy ether derivatives UC-781 and UC-82 as inhibitors of human immunodeficiency virus type 1 replication显示文摘	Balzarini J Pelemans H Aquaro S	1996	Mol Pharmacol1996，50，：	1
	11	Zidovudine-resistant human immunodeficiency virus type 1 strains subcultured in the presence of both lamivudine and quinoxaline HBY 097 retain markedsensitivity to HBY 097 but not to lamivudine显示文摘	BALZARINI J PELEMANS H RIESS G	1997	J Infect Dis1997，176，5：	1
	12	Characteristics of the Pro225His mutation in human immunodeficiency virus type 1 (HIV-1) reverse transcriptase that appears under selective pressure of dose-escalating quinoxaline treatment of HIV-1 显示文摘	Pelemans H Esnouf R Dunkler A	1997	J Virol1997，71，：	1

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