コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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 28-fold that obtained using single-stranded adeno-associated virus vectors.
5 blastic cells using herpes simplex virus and adeno-associated virus vectors.
6 livered to injured heart tissue by different adeno-associated virus vectors.
7 assemblies, similar to the best recombinant adeno-associated virus vectors.
8 med m.11778G>A mutation, using a recombinant adeno-associated virus vector 2, serotype 2 (rAAV2/2-ND4
9 ty and tolerability of escalated doses of an adeno-associated virus vector (AAV) expressing a normal
13 es simplex virus vector, HSV.CMVlac, and the adeno-associated virus vector, AAV.CMVlac, is affected b
14 very of anti-N-terminal htt scFv-C4 using an adeno-associated virus vector (AAV2/1) significantly red
18 cus aureus) and guide RNA constructs into an adeno-associated virus vector and systemically delivered
19 sfer by nonspecifically bound adenovirus and adeno-associated virus vectors and by a modified adenovi
20 A candidate was overexpressed in hearts with adeno-associated virus vectors and inhibited with antise
21 either singly or in combination by employing adeno-associated virus vectors and then challenged with
23 ession of IkappaBzeta in hepatocytes via the adeno-associated virus vector attenuated liver steatosis
26 erapy approach for Alzheimer's disease using adeno-associated virus vector-based knockdown of CD33 re
27 n delivered in a single, clinically relevant adeno-associated virus vector, can support functional im
28 encies in vivo, we constructed a recombinant adeno-associated virus vector carrying the NDI1 gene (rA
31 the use of a dominant-negative forkhead boxO adeno-associated virus vector delivered directly to the
34 novel treatment strategy with a recombinant adeno-associated virus vector delivering a modified FVII
35 ive vaccination strategy whereby recombinant adeno-associated virus vectored delivery of anti-prion s
38 therapy of CML, we constructed a recombinant adeno-associated virus vector encoding the p210(BCR-ABL)
39 xpression system, we generated a recombinant adeno-associated virus vector encoding the VEGFR2-neutra
41 r the use of DCs transduced with recombinant adeno-associated virus vectors encoding multiepitope imm
42 developed adult brain, we have generated an adeno-associated virus vector expressing a small hairpin
43 was obtained by stereotaxic injection of an adeno-associated virus vector expressing Cre recombinase
44 ingle intraportal injection of a recombinant adeno-associated virus vector expressing factor IX succe
47 directed gene therapy with a single-stranded adeno-associated virus vector expressing human Factor IX
48 uring early AD-like pathology, a recombinant adeno-associated virus vector expressing TNF-alpha was s
50 proach to assess the efficacy of recombinant adeno-associated virus vectors expressing inducible IL-2
51 t NOD scid gamma (NSG) mice by the use of an adeno-associated virus vector, followed by engraftment o
52 is compact enough to be packaged in a single adeno-associated virus vector for persistent in vivo gen
53 ng to minimize its size to fit into a single adeno-associated-virus vector for future application.
54 latory system involving a single recombinant adeno-associated virus vector harboring two expression c
55 atory elements in the context of recombinant adeno-associated virus vectors has enabled cell-type-res
56 we show that expression of these genes from adeno-associated virus vectors in C57BL/6 mice is able t
57 SG -( K(b) D(b)) (null) ( IA(null)) mice via adeno-associated virus vector increased human CD45(+) ce
59 the nuclei of retinal ganglion cells via an adeno-associated virus vector injected into the vitreous
60 e correction mediated by a limited number of adeno-associated virus vector injections in the cat mode
62 he NFAT inhibitor VIVIT to astrocytes, using adeno-associated virus vectors, led to reduced GFAP prom
66 demonstrate that a combined adeno virus and adeno-associated virus vector-mediated gene transfer lea
67 deletion of the cannabinoid receptor-1 or by adeno-associated virus vector-mediated silencing of astr
68 gnaling in a common mouse model of AD, using adeno-associated virus vectors normalized glutamate sign
70 d, we have generated a series of recombinant adeno-associated virus vectors of serotypes 1 and 5 enco
71 ing co-injection of two separate recombinant adeno-associated virus vectors, one encoding an inducibl
74 ing either gene replacement strategies using adeno-associated virus vectors or gene editing strategie
80 receptor retargeting.IMPORTANCE Recombinant adeno-associated virus vectors (rAAVs), based on AAV8 an
81 F21 by administration of an FGF21-expressing adeno-associated virus vector recapitulated these compli
82 yte-selective overexpression of p21 using an adeno-associated virus vector reduced long-term patholog
83 acerebral administration of a Ngb-expressing adeno-associated virus vector reduces infarct size and i
84 mophilia A in dogs, and that double-stranded adeno-associated virus vectors resulted in expression of
85 of mice, by using a replication-incompetent adeno-associated virus vector, results in tumours with a
86 human patients, and gene augmentation using adeno-associated virus vectors robustly sustained the re
87 ubpial dorsal horn-targeted delivery of AAV (adeno-associated virus) vector(s) encoding GABA (gamma-a
91 In contrast to other gene delivery systems, adeno-associated virus vectors show long term gene expre
92 liver as a key target for gene therapy, with adeno-associated virus vectors showing long-term effecti
93 In vivo knockdown of IFITM1 using an AAV (adeno-associated virus) vector significantly attenuated
95 ts within the packaging limit of recombinant adeno-associated virus vectors that have been shown to b
96 timized parameters and methods for injecting adeno-associated virus vectors through the cranial imagi
98 acerebral antibody delivery, we developed an adeno-associated virus vector to drive neuronal expressi
99 -deleted factor VIII coding sequence with an adeno-associated virus vector to prevent bleeding in per
102 nzymatically inactive HEXA(R178H) mutant, or adeno-associated virus vectors to induce hepatocyte-spec
103 Delivery of this isoform using a recombinant adeno-associated virus vector type 9 resulted in amelior
106 o circumvent this toxicity, we developed new adeno-associated virus vectors with skeletal muscle-rest
107 review the main molecular characteristics of adeno-associated virus vectors, with a particular view t