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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
8                        We used a recombinant adeno-associated virus vector (AAV) to deliver a foreign
9                                  Recombinant adeno-associated virus vectors (AAV) were prepared in hi
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
12                                           An adeno-associated virus vector (AAV9) for alpha-synuclein
13 protein tau to the substantia nigra using an adeno-associated virus vector (AAV9).
14      Apart from their therapeutic potential, adeno-associated virus vectors also represent outstandin
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
18                                  Recombinant adeno-associated virus vectors based on serotype 2 (rAAV
19                                  Recombinant adeno-associated virus vectors based on serotype 6 (rAAV
20 encies in vivo, we constructed a recombinant adeno-associated virus vector carrying the NDI1 gene (rA
21       Administration of rTMD1 or recombinant adeno-associated virus vector carrying TMD1 could be a p
22               Intrahippocampal injections of adeno-associated virus vectors containing the astrocyte-
23 the use of a dominant-negative forkhead boxO adeno-associated virus vector delivered directly to the
24                                      We used adeno-associated virus vector-delivered siRNAs to select
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
27                                A recombinant adeno-associated virus vector encoding human delta-sarco
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
33       Administration of a self-complementary Adeno-Associated Virus vector expressing full-length SMN
34      We transduced NAcore astrocytes with an adeno-associated virus vector expressing hM3D designer r
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
41            Clenbuterol along with a low-dose adeno-associated virus vector increased Rotarod latency
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
44              These observations suggest that adeno-associated virus vectors may be used to modify tro
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
49                             A mixture of two adeno-associated virus vectors, one expressing the trans
50         This is achieved using a specialized adeno-associated virus vector optimized for the producti
51                    We introduced recombinant adeno-associated virus vector (rAAV) carrying a lacZ rep
52                                  Recombinant adeno-associated virus vector (rAAV) incorporating a con
53                                  Recombinant adeno-associated virus vectors (rAAV) show promise in pr
54 tically enhances transduction by recombinant adeno-associated virus vectors (rAAV).
55 through delivery of a serotype-1 recombinant adeno-associated virus vector (rAAV1-IFNgamma).
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
62                                   We used an adeno-associated virus vector to achieve targeted insert
63                           Here, we have used adeno-associated virus vectors to disrupt dominant-negat
64                                   The use of adeno-associated virus vectors to express short-hairpin
65               Using an inducible recombinant adeno-associated virus vector, we investigated the effec
66               Here we compare the effects of adeno-associated virus vectors with neurotrophin gene in
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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