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1 in cells transfected with a GKLF-expressing plasmid construct.
2 ular mass of 33-34 kDa, as expected from the plasmid construct.
3 ortened form of the tyrR gene via a specific plasmid construct.
4 flexibility not available in genomic DNA or plasmid constructs.
5 various pharmacologic enzyme inhibitors and plasmid constructs.
6 ted with the wt MDR1 promoter DNA/pGL3-basic plasmid constructs.
7 ouse myeloma with the VH gene DNA in various plasmid constructs.
8 ietic progenitor cells compared with smaller plasmid constructs.
9 c myocytes were transiently transfected with plasmid constructs.
10 s lack integration potency compared to wtAAV plasmid constructs (10- to 100-fold differences) was une
11 ine kinase promoter-luciferase reporter gene plasmid construct and determining reporter gene expressi
13 y employed transfection of p53 or HIF-1alpha plasmid constructs and/or p53 and HIF-1alpha reporter co
14 , transfected with small interfering RNA and plasmid constructs, and analyzed by immunocytochemistry.
15 l dipeptidyl-peptidase-like protein-6 (DPPX) plasmid constructs, and comparative brain immunostaining
16 rp3 and hrp2 sequences that were used in the plasmid constructs as gene control regions (chromosomes
19 estabilization can be dramatic; certain parS-plasmid constructs cannot even be maintained in the pres
21 the likelihood of in vivo instability of the plasmid constructs caused by constitutive hyperexpressio
22 have hydrodynamically transfected mice with plasmid constructs composed of a murine hepcidin 1 promo
23 ransformation of M. smegmatis with inhA on a plasmid construct conferred high-level resistance to INH
25 fragment contained a functional promoter, a plasmid construct containing 2433 base pairs of the gp13
26 MCF-7 and MCF-7/Adr cells with a pGL3-Basic plasmid construct containing a CAAT-deleted MDR1 promote
29 sus octamer sequence in the TOP2 5' UTR in a plasmid construct containing only a single consensus oct
30 ated transfection of EC was performed with a plasmid construct containing the gene encoding eNOS.
32 effect mediated by topical application of a plasmid construct containing the murine IFN-alpha 1 tran
33 for 8 weeks, followed by immunization with a plasmid construct containing the pre-S2/S gene that enco
35 08-15 cells was altered by transfection with plasmid constructs containing a full length cDNA of huma
36 ncrease in luciferase activity compared with plasmid constructs containing CAAT-deleted, GC-box, and
40 UVECS were then transiently transfected with plasmid constructs containing ICAM-1 and HCMV immediate
42 transfection experiments were conducted with plasmid constructs containing serial deletions of the ap
43 tional analysis by transient transfection of plasmid constructs containing site-specific mutations in
44 NFKB1 promoter/exon 1 luciferase reporter plasmid constructs containing the -94delATTG allele and
45 both DeltaNotI replicons and RUB replicon or plasmid constructs containing the C gene resulted in rep
46 ndent transcriptional activation of reporter plasmid constructs containing the consensus element.
47 transfections of A549 cells with pGL3-Basic plasmid constructs containing the functional hTERT promo
48 enotype of these mutants was complemented by plasmid constructs containing the wild-type o359 allele,
51 ed with QR-chloramphenicol acetyltransferase plasmid constructs containing various portions of the 5'
52 sitions of PE I and II sequences in reporter plasmid constructs (containing chloramphenicol acetyltra
54 ctivation and dominant positive and negative plasmid constructs demonstrated that high RhoA activity
60 of the genes for uPA and uPAR using a single plasmid construct expressing shRNAs for both uPA and uPA
61 strated that intratumoral injection with the plasmid construct expressing shRNAs for uPA and uPAR alm
63 ear localization signal was identified using plasmid constructs expressing truncation mutants of the
65 splicing of these modified oligomers into a plasmid construct followed by transfection into mouse em
68 Transient cell transfection assays, using plasmid constructs harboring the perlecan promoter linke
69 ng reporter genes in transiently transfected plasmid constructs implicated a conserved intron found i
70 co-expressed with an MT2a promoter-reporter plasmid construct in human intestinal Caco-2 cells, indi
72 Using a series of transiently transfected plasmid constructs in which gene segments of the prothro
73 Transient cell transfection experiments with plasmid constructs in which the potential AP-1-binding s
75 ells that expressed AQP2 promoter-luciferase plasmid constructs, indicating that TonEBP influences AQ
76 of Agrobacterium cells carrying appropriate plasmid constructs into tobacco leaves in planta, reprod
77 sion results from hybrid and chimeric enzyme plasmid constructs, made with large and small subunit ge
78 cts from clostridial transformants harboring plasmid constructs of thlP-sNTR and abrBP-sNTR showed th
80 btained following transfection with a hybrid plasmid construct (pAP-R2) containing the Neo resistance
81 ealed by transient transfection studies with plasmid constructs (pDTD-1097CAT, XRE-CAT, and ARE-CAT)
82 -198 to +43 region) DNA fragment/pGL3-basic plasmid construct resulted in about 6-fold increased luc
84 hat tumor cells stably transfected with this plasmid construct secrete beta-hCG in response to hypoxi
85 a rat hepatocyte iNOS promoter-reporter gene plasmid construct showed that IL-1beta-induced promoter
86 ction of an OPN promoter-luciferase reporter plasmid construct showed that promoter activity is incre
88 sulted in homologous integration of a pAN7.1 plasmid construct that contained a 1.1-kb fragment of th
89 ion with ParC in Escherichia coli by using a plasmid construct that contained the parC and parB genes
91 n factor-binding sites on the replication of plasmid constructs that contain the SV40 origin of repli
94 e deleted were independently introduced into plasmid constructs that express the complete NSP-ORF.
97 ol acetyltransferase (CAT) reporter gene and plasmid constructs that were stably maintained in Escher
98 on constants by inhibiting the cleavage of a plasmid constructed to contain a target sequence for the
100 f the entire bacterial vector sequences from plasmid constructs to create supercoiled gene expression
106 oramphenicol acetyltransferase reporter gene plasmid constructs, we determined that the region betwee
111 tudied in a series of simian virus 40 (SV40) plasmid constructs whose relative replication efficiency
113 d immunosorbent assay and was highest in the plasmid construct with stxB1 under the control of the ta
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