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32篇 您的检索式：作者名="High KA"

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	题名	作者	年代	出处	被引量
1	Haemophilia B : database of point mutations and short additions and deletions--third edition, 1992 显示文摘	Giannelli F Green PM High KA	1992	Nucleic Acids Res1992，201，：	1
2	Gene thansfer as an approach to treating hemophilia显示文摘	High KA	2001	Circ Res2001，88，2：	1
3	Haemophilia B:database of point mutations and short additions and dele-tions-third edition显示文摘	Giannelli F Green PM High KA	1992	Nucleic Acids Res1992，，：	1
4	Viral vector - mediated RNA interference 显示文摘	Couto LB High KA	2010	Curr Opin Pharmacol2010，10，5：	1
5	Age-dependent effects of RPE65 gene therapy for Leb- er' s congenital amaurosis: a phase 1 dose-escalation trial显示文摘	Maguire AM High KA Auricchio A Wright JF Pierce EA Testa F et ol	2009	Lancet2009，374，9701：	1
6	Clinical gene transfer studies for hemophilia B显示文摘	High KA	2004	Semin Thromb Hemost2004，30，2：	1
7	Isolation, cDNA Sequences, and Biochemical Characterization of the Major Cyclosporine-binding Proteins of Toxoplasma gondii显示文摘	High KP Joiner KA Robert EH	1994	J Biological Chemistry1994，269，12：	1
8	Viral vector-mediated RNA interference显示文摘	Couto LB High KA	2010	Curr Opin Pharmacol2010，10，5：	1
9	Therapeutic in vivo gene transfer for geneticdisease using AAV: progress and challenges显示文摘	Mingozzi F High KA	2011	Nat Rev Genet2011，12，5：	1
10	Immune responses to AAV in clinical trials显示文摘	Mingozzi F High KA	2011	Current gene therapy2011，11，4：	1
11	Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis:a phase 1 dose- escalation trial显示文摘	Maguire AM High KA Auricchio A	2009	Lancet2009，374，：	1
12	AAV-mediated gene transfer for hemophilia 显示文摘	High KA Theodore E	2003	Am Clin Climatol Assoc2003，114，：	1
13	Adeno-associated virus-mediated gene transfer for hemophilia B显示文摘	High KA	2002	Int J Hematol2002，76，：	1
14	Manufacturing and regulatorystrategies for clinical AAV2-hRPE65 显示文摘	Wright JF Wellman J High KA	2010	Curr Gene Ther2010，10，5：	1
15	Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis:a phase 1 dose- escalation trial 显示文摘	Maguire AM High KA Auricchio A et a\|	2009	Lancet2009，374，：	1
16	Therapeutic in vivo gene transfer for genetic disease using AAV:progress and challenges显示文摘	Mingozzi F High KA		0，，05：	1
17	A retrospective computed tomography in the assessment of cochlear Implant patients 显示文摘	Nair SB Abouelhamd analysis of high resolution KA Hawthorne M	2000	Clin Otolaryngol2000，25，：	1
18	Viral vector--mediated RNA interfer- ence 显示文摘	Couto LB High KA	2010	Curr Opin Pharmacol2010，10，：	1
19	Immune responses to AAV vectors~ overcoming barriers to successful gene therapy 显示文摘	Mingozzi P High KA	2013	Blood2013，122，1：	1
20	Viral vector-mediated RNA interference 显示文摘	Couto LB High KA	2010	Curr Opin Pharmacol2010，10，：	1

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