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1 y and sufficient for the targeting of hybrid neomycin phosphotransferase.
2 constructed vectors based on HFV that encode neomycin phosphotransferase and alkaline phosphatase.
3 ydrogenase gene as homologous sequences, and neomycin phosphotransferase and cytosine deaminase as po
4 ene trap integration of a beta-galactosidase-neomycin phosphotransferase (betageo) cassette into the
5 coding beta-galactosidase, and neo, encoding neomycin phosphotransferase, for selection by the antibi
7 bacterial beta-galactosidase (beta-gal) and neomycin phosphotransferase fusion protein (betageo) und
8 tabolism by expressing a phosphoribulokinase-neomycin phosphotransferase fusion protein to produce a
11 mia virus (MLV)-based vectors containing the neomycin phosphotransferase gene (neo) and the hygromyci
12 a promoter or the gamma promoter driving the neomycin phosphotransferase gene and enhancer activity w
13 pheral blood lymphocytes transduced with the neomycin phosphotransferase gene between syngeneic twin
14 himeric oligonucleotides to correct a mutant neomycin phosphotransferase gene in a human cell-free ex
15 the env, tat, and vif genes and carrying the neomycin phosphotransferase gene in the vif-tat region w
16 emonstrated unique integration sites for the neomycin phosphotransferase gene into genomic DNA in clo
17 l) or therapeutic genes, with the selectable neomycin phosphotransferase gene under the control of th
18 hosphoglycerate kinase I promoter drives the neomycin phosphotransferase gene) in targeted loci can c
19 codons 1-10 that, when fused in frame to the neomycin phosphotransferase gene, is sufficient to promo
22 r the enhanced green fluorescent protein and neomycin phosphotransferase genes or the hygromycin phos
23 novel retrovirus vector expressing an HBcAg-neomycin phosphotransferase II (HBc-Neo) fusion protein
24 se of Aspergillus terreus, and NEO, encoding neomycin phosphotransferase II from transposon Tn 5, wer
26 -specific ribozyme and the selectable marker neomycin phosphotransferase in the presence of bone marr
27 o detect engraftment of cells expressing the neomycin phosphotransferase marker gene suggested the po
28 developed a cultured cell assay that uses a neomycin phosphotransferase ( neo ) retrotransposition c
30 to obtain selectable transformants uses the neomycin phosphotransferase (neo) gene as the selectable
33 al locations and containing mutations in the neomycin phosphotransferase (neo) gene were corrected by
34 V-1 vector that contains a cassette with the neomycin phosphotransferase (neo) gene, a bacterial orig
35 ial stem cells with a plasmid containing the neomycin phosphotransferase (neo) selectable marker resu
36 cent protein (GFP) and the selectable marker neomycin phosphotransferase (neo), but does not contain
37 enes, encoding Renilla luciferase (Rluc) and neomycin phosphotransferase (Neo), were engineered into
39 ansduced to express both SLA class II DR and neomycin phosphotransferase (NeoR) genes, or the NeoR ge
40 of yopE, when fused to the reporter protein neomycin phosphotransferase (Npt), are sufficient for th
42 anslation efficiency was tested by measuring neomycin phosphotransferase (NPTII) accumulation in toba
43 ed for bombardment contained a gene encoding neomycin phosphotransferase (nptII) and a gene encoding
44 em consisted of a positive selection for the neomycin phosphotransferase (nptII) gene positioned with
45 mediating translation of a bacterial protein neomycin phosphotransferase (NPTII) in tobacco (Nicotian
46 enic approach, measuring accumulation of the neomycin phosphotransferase (NPTII) reporter enzyme tran
47 HIV type 1 (HIV-1) reporter vectors carrying neomycin phosphotransferase or mouse heat stable antigen
48 n of a herpes simplex virus thymidine kinase neomycin phosphotransferase reporter gene (HSV-TKNeo) at
49 C-terminal fusions of YscM1 and YscM2 to the neomycin phosphotransferase reporter revealed sequences
50 d yopE gene fusion experiments with the npt (neomycin phosphotransferase) reporter suggest that yscM1
52 sduction) system could deliver enzymes (Cre, neomycin phosphotransferase), transcription factors (NAN
53 able markers of bacterial origin such as the neomycin phosphotransferase type II gene, which can conf
55 use heat-stable antigen (HSA), and bacterial neomycin phosphotransferase were used as models whose ex
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