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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
16                We also discuss how different selection markers affect vector copy number in transform
17 hod is based on reconstitution of a dominant selection marker after Cre-mediated recombination of Lox
18            Retrofitted fosmid clones carry a selection marker and a phiC31 attB site, which facilitat
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
22                                          The selection marker and reporter (Luc-Ubi-Neo) in the BVDV
23      mfabI expands the limited repertoire of selection markers and allows for more efficient molecula
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
28 on efficiency when antibiotic based dominant selection markers are used.
29           Dual-conditional positive/negative selection markers are versatile genetic tools for manipu
30 when using Lymphocyte Activation Gene-3 as a selection marker, as few as 4,000 cells sufficed.
31 ry site (IRES) sequence followed by a Zeocin selection marker at the 3' end of the env sequence.
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
34                                   Since this selection marker coexisted in trans with the helper viru
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
37                 Our approach utilizes a dual selection marker consisting of the puromycin resistance
38  plants, but very few of these combine plant selection markers, control of expression domains, access
39              We exploited Sox10 reporter and selection markers created by homologous recombination to
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
42                                              Selection markers for B. mallei are limited to Km and Ze
43 onally, there are few well developed counter-selection markers for use in Burkholderia.
44 es currently used, however, will introduce a selection marker gene at the modified site.
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
47 rocess included the removal of a lox-flanked selection marker gene, bar.
48 les of phytochrome B (eYHB) as plant-derived selection marker genes in the model plant Arabidopsis (A
49 (and, at the same time, deletes the original selection/marker genes).
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
52 suggests that IMH3 can be used as a dominant selection marker in C. albicans.
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
55 re no data available for the use of negative selection markers in monocotyledonous species.
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,
58 an CTLA4-Ig, and the dhfr gene as a positive selection marker is described.
59                                     Since no selection marker is used, recombinant clones are identif
60       Here we report the adoption of a novel selection marker, mfabI (mutant fabI) for plasmid propag
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
66 is cassette containing an inverted repeat of selection marker(s) is integrated into the genome.
67                                    Treatment selection markers, sometimes called predictive markers,
68                         The single-gene dual selection marker tetA was translationally fused to green
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
73 omology-directed repair with rates that make selection markers unnecessary.
74 i when a carbenicillin, but not a kanamycin, selection marker was used.
75       Trophoblasts and B cells with separate selection markers were fused with polyethylene glycol.
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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