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1 interference (RNAi) cassette delivered by an adeno-associated virus vector.
2 nly in hepatocytes, due to infection with an adeno-associated virus vector.
3 oloney murine leukemia virus, adenovirus, or adeno-associated virus vector.
4 assemblies, similar to the best recombinant adeno-associated virus vectors.
5 28-fold that obtained using single-stranded adeno-associated virus vectors.
6 blastic cells using herpes simplex virus and adeno-associated virus vectors.
7 ty and tolerability of escalated doses of an adeno-associated virus vector (AAV) expressing a normal
10 es simplex virus vector, HSV.CMVlac, and the adeno-associated virus vector, AAV.CMVlac, is affected b
11 very of anti-N-terminal htt scFv-C4 using an adeno-associated virus vector (AAV2/1) significantly red
15 cus aureus) and guide RNA constructs into an adeno-associated virus vector and systemically delivered
16 sfer by nonspecifically bound adenovirus and adeno-associated virus vectors and by a modified adenovi
17 either singly or in combination by employing adeno-associated virus vectors and then challenged with
20 encies in vivo, we constructed a recombinant adeno-associated virus vector carrying the NDI1 gene (rA
23 the use of a dominant-negative forkhead boxO adeno-associated virus vector delivered directly to the
25 novel treatment strategy with a recombinant adeno-associated virus vector delivering a modified FVII
26 ive vaccination strategy whereby recombinant adeno-associated virus vectored delivery of anti-prion s
28 therapy of CML, we constructed a recombinant adeno-associated virus vector encoding the p210(BCR-ABL)
29 xpression system, we generated a recombinant adeno-associated virus vector encoding the VEGFR2-neutra
30 r the use of DCs transduced with recombinant adeno-associated virus vectors encoding multiepitope imm
31 developed adult brain, we have generated an adeno-associated virus vector expressing a small hairpin
32 ingle intraportal injection of a recombinant adeno-associated virus vector expressing factor IX succe
35 directed gene therapy with a single-stranded adeno-associated virus vector expressing human Factor IX
36 uring early AD-like pathology, a recombinant adeno-associated virus vector expressing TNF-alpha was s
37 proach to assess the efficacy of recombinant adeno-associated virus vectors expressing inducible IL-2
38 t NOD scid gamma (NSG) mice by the use of an adeno-associated virus vector, followed by engraftment o
39 latory system involving a single recombinant adeno-associated virus vector harboring two expression c
40 we show that expression of these genes from adeno-associated virus vectors in C57BL/6 mice is able t
42 the nuclei of retinal ganglion cells via an adeno-associated virus vector injected into the vitreous
43 e correction mediated by a limited number of adeno-associated virus vector injections in the cat mode
45 demonstrate that a combined adeno virus and adeno-associated virus vector-mediated gene transfer lea
46 gnaling in a common mouse model of AD, using adeno-associated virus vectors normalized glutamate sign
47 d, we have generated a series of recombinant adeno-associated virus vectors of serotypes 1 and 5 enco
48 ing co-injection of two separate recombinant adeno-associated virus vectors, one encoding an inducibl
56 acerebral administration of a Ngb-expressing adeno-associated virus vector reduces infarct size and i
57 mophilia A in dogs, and that double-stranded adeno-associated virus vectors resulted in expression of
58 of mice, by using a replication-incompetent adeno-associated virus vector, results in tumours with a
59 human patients, and gene augmentation using adeno-associated virus vectors robustly sustained the re
60 In contrast to other gene delivery systems, adeno-associated virus vectors show long term gene expre
61 ts within the packaging limit of recombinant adeno-associated virus vectors that have been shown to b
67 o circumvent this toxicity, we developed new adeno-associated virus vectors with skeletal muscle-rest
68 review the main molecular characteristics of adeno-associated virus vectors, with a particular view t
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