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18篇 您的检索式：作者名="Parniak"

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		题名	作者	年代	出处	被引量
	1	A fluorescencebased high-throughput screening assay for inhibitors of human immunodeficiency virus-1 reverse transcriptase-associated ribonuelease H activity显示文摘	PARNIAK M A MIN K L BUDIHAS S R	2005	Biochemistry2005，322，1：	1
	2	The thiocarboxanilidenonnucleoside UC781 is a tight-binding inhibitor of HIV-1 reverse transcriptase显示文摘	Barnard J Borkow G Parniak M A	1997	Biochemistry1997，36，：	1
	3	A tight-binding mode of inhibi-tion is essential for anti-human immunodeficiency virustype 1 virucidal activity of nonnucleoside reverse tran-scriptase inhibitors显示文摘	Motakis D Parniak M A	2002	Antimicrob Agents Chemother2002，46，：	1
	4	A fluorescence-based high-throughput screening assay for inhibitors of human immunodeficiency virus- 1 reverse transcriptase-associated ribonuclease H activity显示文摘	Parniak MA Min KL Budihas SR	2003	Anal Biochem2003，322，1：	1
	5	Development and Character-ization of a Vaginal Film Containing Dapivirine, a Non- nucleoside Re-verse Transcriptase Inhibitor (NNRTI),for prevention of HIV-1 sexualtransmission 显示文摘	Akil A Parniak MA Dezzuitti CS	2011	Drug Deliv Transl Res2011，1，3：	1
	6	Mechanism of inhibition of HIV - 1 infection in vitro by purified extract of Prunella vulgaris显示文摘	Yao XJ Wainberg MA Parniak MA	1992	Virology1992，187，1：	1
	7	Inhibitors of HIV-1 reverse transcriptase 显示文摘	ILINA T PARNIAK M A	2008	Adv Pharmacol2008，56，：	1
	8	Mechanism by which phosphonoformic acid resistance mutations restore 3'-azido-3'-deoxythymidine(AZT)显示文摘	Arion D Cremer N S Parniak M A	2000	J Biol Chem2000，275，13：	1
	9	A tight-binding mode of inhibition is essential for anti-human immunodeficiency virus type 1 virucidal activity of non- nucleoside reverse transcriptase inhibitors 显示文摘	MOTAKIS D PARNIAK M A	2002	Antimicrob Agents Chemother2002，46，6：	1
	10	The effects of RNase H inhibitors and nevirapine on the susceptibility of HIV-1 to AZT and 3TC显示文摘	Davis C A Parniak M A Hughes S H		0，，02：	1
	11	Inhibition of carboxypeptidase a by N-(4-t-butylbenzoyl)- 2-hydroxy-1-naphthaldehyde hydrazone显示文摘	Lanthier C M Parniak M A Dmitrienko G I	1997	Bioorg Med Chem Lett1997，7，12：	1
	12	The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue of chain-terminated DNA synthesis显示文摘	Gotte M Arion D Parniak M A	2000	J Virol2000，74，8：	1
	13	Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors 显示文摘	Sluis-Cremer N Arion D Parniak MA	2002	Mol Pharmacol2002，62，：	1
	14	The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2', 3' dideoxyinosine and 2', 3' dideoxycytidine confers high-level resistance to the (-) enantiomer of 2' ,3'-dideoxy-thiacytidine显示文摘	GAO Q GU Z PARNIAK M A	1993	Antimicrob Agents Chemother1993，37，6：	1
	15	Mechanism of Prunella vulgaris 显示文摘	XJ Yao Wainberg MA Parniak MA	1992	Virology1992，187，1：	1
	16	Inhibition of carboxypeptidase A by N-( 4-t-butylbenzoyl)-2-hydroxy-1- naphthaldehyde hydrazone 显示文摘	Lanthier C M Parniak M A Drnitrienko G I	1997	Bioorganic & Medicinal Chemistry Letters1997，7，12：	1
	17	Mechanism of inhibition of HIV-1 infection in vitro by purified extract of Prunellavulgaris显示文摘	Yao XJ Wainberg MA Parniak MA	1992	Virology1992，187，1：	1
	18	碱性pH对鼠肝脏苯丙氨酸羟化酶的影响显示文摘鼠肝脏苯丙氨酸羟化酶的最适PH是由其所用辅助因子的结构及酶的活化状态决定的。以四氢生物蝶呤为辅助因子的天然苯丙氨酸轻化酶的最适pH约为8.5,而以6,7—二甲基四氢蝶呤为辅助因子的苯丙氨酸羟化酶在pH7.0时活性最高。	Michael A Parniak Michael D Davis Seymour Kaufman 毛歆	1992	氨基酸杂志1992，，2：	0

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