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1 ats using short interfering RNA delivered by recombinant adenovirus.
2 y overexpression of superoxide dismutase via recombinant adenovirus.
3 erexpressed in PA myocytes with the use of a recombinant adenovirus.
4 and CYP7A1 were mediated via infection with recombinant adenoviruses.
6 limb ischemia after intravenous injection of recombinant adenoviruses (10(9) plaque-forming units) en
7 luated the ability of an enteric adenovirus, recombinant adenovirus 41 (rAd41), to elicit intestinal
9 the rBCG-primed monkeys after boosting with recombinant adenovirus 5 (rAd5) expressing the SIV antig
10 ) 505 was a phase 2b efficacy trial of a DNA/recombinant adenovirus 5 (rAd5) HIV vaccine regimen.
11 ta from the HVTN 505 efficacy trial of a DNA/recombinant adenovirus 5 (rAd5) vaccine regimen, we foun
13 hesized that the efficacy of a DNA prime and recombinant adenovirus 5 boost vaccination regimen (DNA/
14 vaccinia HIV clade B (NYVAC-B) vaccine and a recombinant adenovirus 5-vectored (rAd5-vectored) vaccin
16 is study, we examined whether infection with recombinant adenovirus (Ad) encoding CD154 and/or treatm
17 expressed in lung cancer cell lines through recombinant adenovirus (Ad) infection (Ad-WWOX), and thr
23 of 'smart' nanoparticles that are based upon recombinant adenovirus (Ad) vectors and that combine mul
24 he widespread use of replication-incompetent recombinant adenovirus (Ad) vectors as candidate vaccine
28 protein in primary CD4(+) cells by use of a recombinant adenovirus (Ad5/Delta32) was able to down-re
30 was induced by infection of myocytes with a recombinant adenovirus (AdPak1) containing cDNA for a co
32 catenin/Tcf4 pathway is activated by using a recombinant adenovirus AdTOP-CMV-TK, which carries a her
35 arby canine kidney cells, were packaged into recombinant adenovirus and delivered to WIF-B cells in v
36 In chimpanzees successfully vaccinated with recombinant adenovirus and DNA against HCV NS3-5, HCV-sp
37 manipulated by using dominant-negative STAT3 recombinant adenoviruses and a specific inhibitor of MAP
38 ppocampal neurons using nuclear injection or recombinant adenoviruses and examined modulation of ion
39 oned into tetracycline-regulated vectors and recombinant adenoviruses and then studied in colorectal
40 different immunogens--recombinant vaccinia, recombinant adenovirus, and plasmid DNA--on the generati
42 Animals primed by intranasal delivery of recombinant adenoviruses, and boosted by intramuscular i
45 ther hand, infection with wild-type GSK3beta recombinant adenovirus-associated virus increased activi
46 production and subsequent administration of recombinant adenovirus-based vaccines to both birds and
47 g with a new technique for labeling axons, a recombinant adenovirus bearing the gene for green fluore
49 of mitochondrial superoxide dismutase using recombinant adenovirus blunted lipid peroxidation and at
51 A prime, protein boost as well as DNA prime, recombinant adenovirus boost regimens expressing these a
52 Rhesus monkeys were immunized with DNA prime-recombinant adenovirus boost vaccines encoding a Gag-Pol
53 ly shown that survival in plasmid DNA-primed/recombinant adenovirus-boosted rhesus monkeys that are c
55 r system to generate a replication-deficient recombinant adenovirus capable of simultaneously express
56 A polymerase II and III in cells infected by recombinant adenoviruses carrying ectopic E2E-CAT (chlor
57 tly bound the phosphate moiety, we generated recombinant adenoviruses carrying G6Pase wild type and a
59 ganelle level during viral infection using a recombinant adenovirus coding for a mitochondrial tracer
62 f PC in beta-cell function, we constructed a recombinant adenovirus containing a small interfering RN
63 s were infected with a replication-defective recombinant adenovirus containing an inducible KLF4 and
64 r 4 x 10(9) plaque-forming units of E1a-/E3- recombinant adenovirus containing either a rat beta1 Na,
65 cker diabetic fatty (ZDF) (fa/fa) rats, with recombinant adenovirus containing insig-1 or -2 cDNA.
70 slets with a cytomegalovirus promoter-driven recombinant adenovirus containing the Nkx6.1 cDNA (AdCMV
72 osite termination sequence CT were tested in recombinant adenoviruses containing luciferase reporters
73 s were individually expressed in EC by using recombinant adenoviruses, cultured BL cells adhered excl
75 inoculation of BALB/cByJ mice with tcMCMV or recombinant adenoviruses differentially activates T help
77 CypD would alter mPTP in vivo, we injected a recombinant adenovirus encoding C203S-CypD or WT CypD in
79 n contrast, transduction of pericytes with a recombinant adenovirus encoding dominant-negative T-cell
80 extracts confirmed that HAECs treated with a recombinant adenovirus encoding E2F-1 failed to associat
81 irect intramyocardial injections of either a recombinant adenovirus encoding for SCF (Ad.SCF, n=9) or
83 , murine CD11c(+) DCs were transduced with a recombinant adenovirus encoding full-length murine T-bet
85 yocardial injection of replication-deficient recombinant adenovirus encoding HGF (n=10) or empty null
87 metabolism in vivo, 1 x 1011 particles of a recombinant adenovirus encoding human EL (AdEL), catalyt
94 eys through vaccination with plasmid DNA and recombinant adenovirus encoding simian-human immunodefic
95 For functional characterization of Smad4, a recombinant adenovirus encoding Smad4 (Ad-Smad4) was gen
96 ERK1/2 inhibitor PD98059, or infection of a recombinant adenovirus encoding the dominant-negative fo
99 1 mouse pancreatic islets were infected with recombinant adenoviruses encoding enhanced green fluores
100 oxycycline-repressible replication-defective recombinant adenoviruses encoding individual epitope-tag
103 that overexpression of wild-type Axl, using recombinant adenoviruses, enhances Axl phosphorylation a
104 largely overcome by prior immunization with recombinant adenovirus, especially for adjuvants that ar
106 ial injury 1 day after systemic injection of recombinant adenovirus expressing (1) VEGF, (2) VEGF-tra
109 uced the embryonic chicken heart in ovo with recombinant adenovirus expressing a death (FasL) ligand.
111 marrow-derived DCs transduced with Ad.Neu, a recombinant adenovirus expressing a truncated neu oncopr
114 Using a single intrabursal administration of recombinant adenovirus expressing Cre, we demonstrate th
115 arrow-derived macrophages (BMDMs) by using a recombinant adenovirus expressing dominant-negative Ikap
116 23, transduction of IL-12p40(-/-) DCs with a recombinant adenovirus expressing functional IL-23 resto
119 s rapidly expanded following boosting with a recombinant adenovirus expressing HIV-1 Env to gp120-spe
120 ury, we used mouse tail vein injections with recombinant adenovirus expressing HNF-6 complementary DN
122 pidemia was corrected by co-infection with a recombinant adenovirus expressing human lipoprotein lipa
123 udy we have transfected rat macrophages with recombinant adenovirus expressing IL-4 (Ad-IL4) and demo
125 ic potential of MBP-1, replication-deficient recombinant adenovirus expressing MBP-1 was given intrat
126 model, we induced plasma APN levels using a recombinant adenovirus expressing mouse APN (AdAPN) and
128 Microarray analysis of cells infected with a recombinant adenovirus expressing ORF63 showed that tran
129 ly, infection of cultured HepG2 cells with a recombinant adenovirus expressing PGC-1alpha directly ac
131 By infecting pre-fusion osteoclasts using recombinant adenovirus expressing PYK2 and its mutants,
132 rradiated Plasmodium yoelii sporozoites or a recombinant adenovirus expressing the P. yoelii circumsp
136 osteosarcoma cells after their exposure to a recombinant adenovirus expressing wild type BRCA1 (Ad.BR
138 ells transduced with a replication-deficient recombinant adenovirus expressing Z (rAd-Z) are resistan
140 density lipoprotein (HDL), we have generated recombinant adenoviruses expressing apolipoprotein A-I (
142 oping and testing tetracycline-regulated and recombinant adenoviruses expressing dominant negative re
143 dothelial cell networks with C3 exoenzyme or recombinant adenoviruses expressing dominant negative Rh
144 d be induced in the absence of IGF action by recombinant adenoviruses expressing MyoD or myogenin, bu
145 an effect that is rescued by infection with recombinant adenoviruses expressing SOD2 and Catalase1.
146 yes were infected with replication-deficient recombinant adenoviruses expressing the beta-galactosida
147 ia was corrected by coinfection of mice with recombinant adenoviruses expressing the mutant apoA-I an
148 obtained by using C57BL/6 mice infected with recombinant adenoviruses expressing the replicating HBV
149 es 261 and 283 were mutated to alanines, and recombinant adenoviruses expressing these apoE mutants w
150 produce mda-7/IL-24 following infection with recombinant adenoviruses expressing this cytokine secret
152 To initiate our studies, we generated three recombinant adenoviruses expressing wild type, constitut
153 3-null H1299 human lung carcinoma cells with recombinant adenoviruses expressing WT p53, p73 or beta-
154 ells were infected with a dominant-negative, recombinant adenovirus, expressing E-cadherin lacking an
155 ent femoral arterial denudation and received recombinant adenovirus, expressing either murine endosta
159 rate cohorts also received i.v. injection of recombinant adenovirus-expressing murine GM-CSF (AdGMCSF
160 ransfection, and fibroblasts infected with a recombinant adenovirus-expressing UL142, were used to sc
161 d inside cells using a replication-deficient recombinant adenovirus expression system inhibited LCMV
162 transduction with the replication-deficient recombinant adenovirus expression system to Z and L effe
163 review recent studies combining the tools of recombinant adenovirus for gene delivery, the developmen
165 (rAd-IFNalpha/Syn3), a replication-deficient recombinant adenovirus gene transfer vector, for patient
166 se important properties of Vpr, we created a recombinant adenovirus H5.010CMV-vpr (adCMV-vpr) as a to
169 rials for cystic fibrosis lung disease using recombinant adenovirus in the early 1990s, the field has
170 as precursors to DCs and also for the use of recombinant adenovirus in vaccines or gene therapy.
171 ular microarrays on a micropillar chip using recombinant adenoviruses in a complementary microwell ch
174 Here we show that WT TAg expressed from recombinant adenoviruses in U2OS cells induced the phosp
175 an, and restoring iPLA(2)betaexpression with recombinant adenovirus increases apoptosis toward WT lev
176 transduced ex vivo by BMP cDNA delivered by recombinant adenoviruses induce bone formation and conve
179 transgenic mice (transthyretin HNF-3beta) or recombinant adenovirus infection (AdHNF3beta), and obser
180 previous studies we used transgenic mice or recombinant adenovirus infection to increase hepatic exp
182 Overexpression of LAT1 in T24 cells using recombinant adenoviruses led to increased uptake of L-CS
184 and apoptosis in human lung cancer cells by recombinant adenovirus-mediated gene transfer in vitro a
186 rogen-independent prostate cancer cells upon recombinant adenovirus-mediated introduction of MBP-1.
187 infection, suggesting that L1 expressed from recombinant adenoviruses might provide protective immuni
188 erexpression of DGAT1 mRNA by >20-fold via a recombinant adenovirus only resulted in approximately 2-
189 e antiviral signals following infection with recombinant adenovirus or by direct nucleic acid transfe
191 demonstrated that intratumoral injections of recombinant adenovirus overexpressing p27Kip1 (Adp27) re
194 , followed by two mucosal boosts with either recombinant adenovirus (rAd) or fowlpox virus (rFWPV) ex
195 dminister AERAS-402, a replication-defective recombinant adenovirus (rAd) type 35 expressing Mycobact
197 t contribute to the potent immunogenicity of recombinant adenovirus (rAd) vaccine vectors remain larg
198 e that single intranasal immunization with a recombinant adenovirus (rAd) vector encoding both HA of
202 an populations has led to the development of recombinant adenovirus (rAd) vectors derived from rare A
204 at intramuscular injection of nonreplicating recombinant adenovirus (rAd) vectors into rhesus monkeys
206 modified for optimal antigen expression and recombinant adenovirus (rAd) vectors, all encoding the g
207 tilizing intramuscularly (i.m.) administered recombinant adenovirus (rAd)-based vectors can induce po
208 vaccines suggest that replication-competent recombinant adenoviruses (rAds) could serve as effective
213 ertk to cultured RCS RPE cells by means of a recombinant adenovirus restored the cells to complete ph
214 ion of primary oligodendrocyte cultures with recombinant adenovirus revealed that expression of Fyn o
215 that therapeutic vaccination with Ad26/MVA (recombinant adenovirus serotype 26 (Ad26) prime, modifie
216 CD8(+) T lymphocyte responses elicited by a recombinant adenovirus serotype 26 (rAd26) vector expres
217 of recombinant adenovirus serotype 5 (rAd5), recombinant adenovirus serotype 28 (rAd28), and recombin
219 ombinant adenovirus serotype 28 (rAd28), and recombinant adenovirus serotype 35 (rAd35) in associatio
220 tective efficacy of replication-incompetent, recombinant adenovirus serotype 35 (rAd35) vectors expre
223 ly increases the immunogenicity of DNA prime-recombinant adenovirus serotype 5 (rAd5) boost and DNA p
224 eutralizing antibodies elicited by DNA prime-recombinant adenovirus serotype 5 (rAd5) boost vaccinati
225 g HIV-1-infected participants who received a recombinant adenovirus serotype 5 (rAd5) HIV-1 gag vacci
226 ccine efficacy trial testing DNA followed by recombinant adenovirus serotype 5 (rAd5) in circumcised,
228 l activation during the first 2 months after recombinant adenovirus serotype 5 (rAd5) prime or boost
230 lication deficient and requires the parental recombinant adenovirus serotype 5 (rAd5) vector for repl
231 nd immunogenicity of a replication-defective recombinant adenovirus serotype 5 (rAd5) vector HIV-1 ca
235 infectivity and cell stimulatory capacity of recombinant adenovirus serotype 5 (rAd5), recombinant ad
236 ysis of the phase 2b Step study evaluating a recombinant adenovirus serotype 5 (rAd5)-based HIV-1 vac
238 he monkeys were boosted a second time with a recombinant Adenovirus serotype 5 vector containing matc
239 othesis in a relevant primate model, we used recombinant adenovirus serotype 5 vectors expressing SIV
240 When apoM(Q22A) was expressed in vivo, using recombinant adenoviruses, smaller plasma HDL particles a
241 Similarly, treatment of 832/13 cells with a recombinant adenovirus specific to FAS (Ad-siFAS) reduce
243 cells were pulsed with CFP10 expressed in a recombinant adenovirus, surface adsorbed to microspheres
244 ast carcinoma cell line MDA-MB-468 using the recombinant adenovirus, TGF-beta signaling was restored
245 as rAd-IFNa/Syn3) is a replication-deficient recombinant adenovirus that delivers human interferon al
248 cells fromnormal human breast tissue using a recombinant adenovirus that expresses green fluorescence
249 This article describes a method for making recombinant adenoviruses that efficiently drive expressi
251 n-specific T(CD8(+)) after immunization with recombinant adenoviruses that express antigen driven by
254 ng neonatal rat cardiomyocytes infected with recombinant adenovirus to overexpress tropomodulin.
255 row-derived dendritic cells engineered using recombinant adenovirus to secrete high levels of IL-12p7
256 and granzyme B cleavage sites, and utilized recombinant adenoviruses to express this protein in hepa
257 ide-binding domains (NBD) of G5 and G8 using recombinant adenoviruses to reconstitute biliary sterol
258 accine constructs: (i) replication-defective recombinant adenovirus type 5 (Ad5) expressing human imm
261 1 Env and Gag-Pol by DNA priming followed by recombinant adenovirus type 5 (rAd5) boosting elicited C
262 me-boost immunization regimens revealed that recombinant adenovirus type 5 (rAd5) prime followed by r
263 f a T-cell-based AIDS vaccine delivered with recombinant adenovirus type 5 (rAd5) vectors showed no e
264 iciency virus (SIV) vaccine trial (DNA prime/recombinant adenovirus type 5 [rAd5] boost) (VRC-10-332)
266 s were vaccinated via three DNA primes and a recombinant adenovirus type 5 boost (weeks 0, 4, 8, and
267 ium cell line (ARPE-19) were transduced with recombinant adenovirus type 5 carrying mouse Elovl4 and
268 ies such dynamics, using a newly constructed recombinant adenovirus type-5 (Ad5) that expresses enhan
270 This study assesses the hypothesis that a recombinant adenovirus vaccine based on the nonhuman pri
275 with dendritic cells expressing mEGP from a recombinant adenovirus vector exhibited a muted anti-ade
277 tic levels of HNF-6 either by infection with recombinant adenovirus vector expressing HNF-6 cDNA by g
278 tegy to bypass this escape mechanism using a recombinant adenovirus vector expressing interleukin-12
279 in vivo priming with a replication-defective recombinant adenovirus vector expressing the lymphocytic
280 f ZTA in cell cycle arrest, we constructed a recombinant adenovirus vector expressing ZTA (Ad-ZTA), w
283 either naive or had been vaccinated using a recombinant, adenovirus-vectored vaccine 2 weeks before
284 ally, we demonstrated that immunization with recombinant adenovirus vectors expressing NP and M2 sign
286 protection conferred by a highly protective recombinant adenovirus virus serotype 5 (rAd5) encoding
287 multiclade (A, B, and C) envelope (Env) DNA/recombinant adenovirus virus type 5 (rAd5) vaccine studi
291 get the apoptosis of the OFT cardiomyocytes, recombinant adenovirus was used to express the X-linked