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1 lsulfatase-encoding ARYLSULFATASE2 gene as a selection marker.
2 of DNA and simultaneously insert a positive selection marker.
3 ce antigen and a gene encoding the kanamycin selection marker.
4 -DNA with the I-SceI site and an integration selection marker.
5 rylase subunit ApL3 were fused to a negative selection marker.
6 tion despite selection for the cotransfected selection marker.
7 ansfected with a separate plasmid encoding a selection marker.
8 ining the cDNA encoding myoD and a puromycin selection marker.
9 eletion and the hygromycin-resistant gene as selection marker.
10 ators of the rrnB operon, and a tetracycline selection marker.
11 elements together with fluorescent and drug selection markers.
12 frequencies >1%, thus obviating the need for selection markers.
13 a patients, flanked by positive and negative selection markers.
14 loci and avoid untoward effects of retained selection markers.
15 c library we have constructed has a negative selection marker adjacent to the genomic insert, REC scr
17 hod is based on reconstitution of a dominant selection marker after Cre-mediated recombination of Lox
19 ng the mouse genome using the HPRT gene as a selection marker and for transmission at a high frequenc
20 s; this involved using unc-119 as a positive-selection marker and GFP as a counter-selection marker w
21 usly designed for Cre, containing a positive selection marker and PhiC31 driven by a testis-specific
24 We designed a selection scheme with drug selection markers and Cre/loxP technology which allows s
25 the resulting engineered strain requires no selection markers and is unaffected by plasmid instabili
26 of prokaryotic origin like vector sequences, selection marker, and reporter genes have been shown to
27 -agent regulations, the number of antibiotic selection markers approved for use in these bacteria is
32 that mfabI is not only an efficient plasmid selection marker, but it also possesses unique activity
33 rom hiPS cells using a triple combination of selection markers--CD34, neuropilin 1, and human kinase
35 methods associated with the use of nutrient selection markers, complicated reporter analysis methods
36 luorescent protein (GFPuv) were constructed; selection markers comprised either mchI, conferring immu
38 plants, but very few of these combine plant selection markers, control of expression domains, access
40 e incorporation of a red fluorescent protein selection marker enables combined utilization with widel
41 fetal gonads and can be used as an effective selection marker for germ cell enrichment from different
45 ous recombination followed by removal of the selection marker gene by Cre-loxP-mediated site-specific
46 T-overhang after digestion and the negative selection marker gene ccdB to eliminate the self-ligatio
48 les of phytochrome B (eYHB) as plant-derived selection marker genes in the model plant Arabidopsis (A
50 nti-EGFR antibodies in mCRC, their role as a selection marker has not been established in randomized
51 limited availability of heterologous counter-selection markers, here we explore novel DNA integration
53 drial Alternative oxidase1a gene without HPT selection marker in rice enhanced tolerance to Hyg and a
54 the genetic background or the presence of a selection marker in the mutant mice could influence the
56 ilised Flp recombinase to remove the unc-119 selection marker, in somatic cells, producing clean knoc
57 atistical methods for evaluating a treatment selection marker include assessing its prognostic value,
61 method depends on a thermostable endogenous selection marker operating at high temperatures combined
62 However, the existing assays use antibiotic selection markers or fluorescent proteins as reporters;
63 diated excision of the antibiotic-resistance selection marker present on the chromosomally integrated
64 diated excision of the antibiotic-resistance selection marker present on the chromosomally integrated
65 refinements in gene-transfer techniques, new selection markers, reliable reporter fusions and success
69 d fly stocks and introduced a novel negative selection marker that drastically reduced the frequency
70 ecombinase target sites, a positive/negative selection marker that preserves the germline capacity of
71 Therefore Csf2rb can be used as a negative selection marker to enrich preleukemic progenitor cells
72 t BAC or PAC vectors do not have a mammalian selection marker, transfecting mammalian cells with gene
76 sitive-selection marker and GFP as a counter-selection marker which is lost during homologous recombi
77 tep is monitored using positive and negative selection markers, which are the Kanamycin-resistance ge
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