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1 ures such as particle-mediated DNA delivery (gene gun).
2 and skin by particle-mediated gene transfer (Gene Gun).
3 293 cells and whole brain using a hand-held gene gun.
4 d organotypic brain slices using a hand-held gene gun.
5 DNA vaccines administered intradermally via gene gun.
6 ary vaccine Ags after single immunization by gene gun.
7 s only in sera of mice inoculated by using a gene gun.
8 rabbit Peyer's patches using a helium-driven gene gun.
9 parate plasmid after codelivery into skin by gene gun.
11 ediated biolistic delivery using a hand-held gene gun, allows non-toxic labeling of multiple cells in
13 nts were delivered to the skin of a mouse by gene gun and IFN-gamma levels were measured at the skin
15 entation may be more significant in clinical Gene Gun applications than in pre-clinical mouse studies
17 psy of the skin target site up to 24 h after gene gun bombardment completely abrogated the Ab respons
18 been studied, including liposomal delivery, gene gun bombardment, and picoinjection into single livi
22 X3C-mut were inoculated into mice by using a gene gun, both plasmids elicited an antibody response de
23 ression vectors simultaneously delivered via gene gun can significantly augment antitumor effects, ev
28 was conducted to investigate whether Accell gene gun coadministration of DNA encoding human interleu
30 vered by a combination of vaccinia virus and gene gun-delivered DNA were effective against SHIV89.6P
32 erologous prime/boost strategy consisting of gene gun-delivered PSCA-cDNA followed by Venezuelan equi
34 y raised immunoglobulin G2a (IgG2a), whereas gene gun deliveries of DNA predominantly raised IgG1.
36 DNA vaccine efficacy by immunizing mice via gene gun delivery and challenging them with live, virule
37 e data suggested that muscle inoculation and gene gun delivery elicited Th1-like and Th2-like respons
40 ually given by intramuscular injection or by gene gun delivery of DNA-coated particles into the epide
41 all, the high levels of protection seen with gene gun delivery of HA-DNA were as good as, if not bett
43 e evaluated a physical gene transfer method (gene gun delivery) for its ability to transfect the epid
46 response with mostly IgG2a anti-H1 Ab, while gene gun DNA immunization produced a predominantly Th2 r
51 ersely, intradermal genetic immunization via gene gun (GG) delivered TcPRAC as an immunogen, generati
54 when these mice were challenged with OVA by gene gun immunization in the contraction phase of the pr
59 We tested the ability of intramuscular and gene gun immunization with DNA expressing influenza viru
60 ed in predominantly IgG2a responses, whereas gene gun immunization yielded a preponderance of IgG1 an
61 ss-presentation in CD8+ T cell priming using gene gun immunization, and indicate that augmentation of
66 cited to the SERA protein following i.m. and Gene Gun immunizations with SERA plasmid DNA was immunog
67 itro skin organ cultures were developed from gene gun immunized mouse ear specimens to obtain LC.
70 ata of in vivo transfection in the rabbit by Gene Gun indicate that reporter gene constructs containi
71 d particles to neuronal preparations with a "gene gun," individual neurons and glia whose membranes a
72 ccinations administered to the skin with the gene gun induced and progressively increased p11C, C-->M
73 epidermis using a hand-held, helium-driven "gene gun" induced beta-gal-specific Ab and lytic respons
76 her gp120 or gp140 DNA vaccines delivered by gene gun inoculation followed by recombinant gp120 prote
77 body responses in mice immunized by a single gene gun inoculation of plasmid expressing the influenza
85 at DNA vaccine with HEV ORF2 administered by gene gun is protective against a heterologous viral chal
86 DNA-based immunizations administered by the gene gun may be an effective method of inducing local im
87 vaccination and demonstrates the efficacy of gene gun-mediated delivery of foreign DNA to a mucosal t
94 y at the skin site receiving DNA transfer by gene gun on days 6, 8, 10, and 12 after tumor implantati
96 radermal administration of nucleic acids via gene gun represents an efficient method for delivering n
98 odes, but not in other lymph nodes, revealed gene gun responses being initiated in the nodes that dra
99 er 4 doses of DNA administered by epidermal (gene gun) route, all guinea pigs developed enzyme-linked
100 munized via the intramuscular and epidermal (gene gun) routes with 100 and 1 micrograms, respectively
103 with a model DNA-based antigen delivered by gene gun technology would induce an antibody response de
105 ow that after immunization of mouse skins by gene gun, the number of antigen-bearing DCs that migrate
107 ermally with high expresser plasmid, using a gene gun to administer three doses at 6-wk intervals.
109 ted with DNA-coated gold micro-projectiles ("Gene Gun") to induce potent cellular and humoral immune
111 cial role in Purkinje cell development using gene gun transfections within intact murine cerebellar c
113 el this mechanism, we examined the impact of gene gun treatment on LC with respect to their activatio
114 we compared immune responses generated after gene gun vaccination of mice with DNA vaccine plasmids d
115 this model, depigmentation was introduced by gene gun vaccination with eukaryotic expression plasmids
118 ntrast, cutaneous DC transfected in situ via gene gun were detected in the draining lymph node at a 2
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