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		题名	作者	年代	出处	被引量
	1	显示文摘	陈仕国(ChenSG) 郭玉娟(GuoYJ) 陈少军(ChenSJ) 戈早川(GeZC)		材料导报A综述篇0，，：	1
	2	The application of power- based transfer path analysis to passenger car structure borne noise显示文摘	Han X GuoYJ Zhao Y E	2008	Journal of Automobile Engineering2008，222，11：	1
	3	Clinicalobservationonthetreatmentofchronicdermatitis-eczemabyebastine显示文摘	GUOYJ HANXP	2010	临床皮肤科杂志2010，39，1：	1
	4	StudiesonchemicalconstituentsofPhyllanthusurinariaL显示文摘	ZhangLZ(张兰珍) GuoYJ(郭亚键) TuGZ(涂光忠)		中国中药杂志0，，：	1
	5	Localimmuneresponseinhepatobiliary malignance and its clinical significance显示文摘	WuMC KongXT etal	1986	JMed Colle PLA1986，1，：	1
	6	CorilaginProtectsAgainstHSV1EncephalitisThroughInhibitingtheTLR2SignalingPathwaysInVivoandInVitro显示文摘	GuoYJ LuoT WuF etal	2015	MolNeurobiol2015，52，3：	1
	7	Dosimetricdifferencesamongvolumetricmodulatedarcradiotherapy(RapidArc)plansbasedondifferenttargetvolumesinradiotherapyofhepatocellularcarcinoma显示文摘	GongGZ YinY GuoYJ etal	2013	JournalofRadiationResearch2013，54，18：	1
	8	Characterization of the pathogenicity of members of the newly established H9N2 influenza virus lineages in Asia 显示文摘	GuoYJ Krauss S Senne DA	2000	Virology2000，267，：	1
	9	Decreased expression of serotonin 1A receptor in the dentate gyrus in association with chronic mild stress: a rat model of post-stroke depression 显示文摘	Wang SH Zhang ZJ GuoYJ	2009	Psychiatry Res2009，170，23：	1
	10	Non-fusion expression in Escherichia coli, purification, and characterization of a novel Ca^2+- and phospho-lipid-binding protein annexin B1显示文摘Annexin B1 is a novel member of the annexin family of Ca^2+- and phospholipid-binding proteins from Cysticercus cellulosae. To obtain high quality annexin B1 for biochemical and biophysical analyses, its cDNA was cloned into the prokaryotic expression vector pJLA503 and the translation initiation codon was immediately under the control of the inducible bacteriophage lambda promoters P(R) and P(L). Alter induction by shifting temperature, large amounts of non-fusion protein were produced in Escherichia coli in a soluble form. The recombinant protein was purified to homogeneity by means of two subsequent ion-exchange chromatographic steps. The final yield was about 25 mg/L bacterial culture.	ZhangY GuoYJ SunSH YanHL HeY	2005	第二军医大学学报2005，26，5：	0

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