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1 eakpoints, and by the expression patterns of enhancer traps.
2 ry system for poplar trees based on gene and enhancer traps.
3 be more effective for activation tagging and enhancer trapping.
4 ranscription in Arabidopsis, we used in vivo enhancer trapping.
5 trate that lacZ expression from the dpp(F11) enhancer trap accurately reflects dpp mRNA accumulation
6                                              Enhancer trap analysis of the smi lines indicates that e
7                                        Using enhancer trap and Cre transgenes, our lineage tracing ex
8  knockdown, expression-based screening using enhancer trapping and forward genetic screening using tr
9 ial chromosomes (BACs) were retrofitted with enhancer traps, and expressed as transgenes in zebrafish
10 as insertional mutagenesis screens, gene and enhancer trap applications, and gene therapy.
11                    The results show that the enhancer trap approach can be a productive way of explor
12                             We have taken an enhancer trap approach to identify genes that are expres
13                                   We used an enhancer trap approach to study the adult structure, con
14         Here we report on the utilization of enhancer trap approach toward the identification and ana
15                                    Using the enhancer trapping approach, we identified a new Drosophi
16                              We have used an enhancer-trap approach to begin characterizing the funct
17 e confirmed that the genes detected by these enhancer traps are expressed in patterns similar to thos
18         To address this issue, we devised an enhancer trap assay to systematically screen 1 Mb of DNA
19                            A gal4-containing enhancer-trap called C309 was previously shown to cause
20                                    Our T-DNA enhancer trapping cassette consisted of two principle co
21 aused by the insertion of a DsE transposable enhancer trap element into the 5' untranslated leader of
22                    Finally, I have mapped an enhancer trap element within the 5' region of dFKBP59 wh
23                Here, we report that using an enhancer-trap embryo mutant of Arabidopsis, we identifie
24               Individual lines identified by enhancer trapping exhibit peak transcription rates at ci
25                              This phenotypic enhancer-trap facilitates (i) the isolation of enhancer-
26                                           An enhancer-trap GAL4 line C309 directing shi(ts1) expressi
27 s, we use the MARCM techniques with a set of enhancer-trap GAL4 lines to perform systematical lineage
28                  Transgenic Arabidopsis with enhancer-trapped GAL4 expression in specific cell types
29                                  Finally, an enhancer trap in the sr gene detects the response to Spi
30 contrast to the above model, we find that an enhancer trap inserted near the Dpp target gene, Daughte
31            We screened 1300 lethal P-element enhancer trap insertions on the second chromosome for a
32 pulations because many of the genes and Gal4 enhancer trap insertions that are expressed in the ovary
33                                              Enhancer trap is a powerful approach for identifying tis
34  ubiquitously expressed, suggesting that the enhancer trap is detecting only a subset of its control
35         However, the gene identified by this enhancer trap is ubiquitously expressed, suggesting that
36                                 Using a GAL4 enhancer trap line (201Y) that drives MB-restricted repo
37                                              Enhancer trap line 5580 exhibits expression in young veg
38 s cloned from an Arabidopsis leaf senescence enhancer trap line and functionally characterized.
39 w class of vascular-expressed gene tagged by enhancer trap line cET-1-pop1-145.
40 nt located at chromosomal location 33AB, the enhancer trap line E8-2-46, indicating that a gene near
41 the third segment of the antenna of the 2216 enhancer trap line in Drosophila melanogaster reveals tw
42 sociated genes, we identified an Arabidopsis enhancer trap line in which the reporter gene GUS is up-
43 nidase (GUS) reporter gene expression in the enhancer trap line is observed specifically in all cell
44 ounder cell marker Duf-LacZ, produced by the enhancer trap line rP298LacZ, is coexpressed in numerous
45 hase gene (CS) using an Arabidopsis thaliana enhancer trap line specific to veins.
46                        We also identified an enhancer trap line that exhibits altered morphogenetic f
47 e was isolated by plasmid rescue from a GAL4 enhancer trap line which shows reporter gene expression
48 inally, we have molecularly characterized an enhancer trap line, AE33, that was identified in earlier
49                                           An enhancer trap line, line 5580, contains a T-DNA insertio
50                       Starting from the H214 enhancer trap line, we identified a transcription unit,
51 cell-specific GAL4-green fluorescent protein enhancer trap line.
52 tive chlorophyllase in a guard cell specific enhancer trap line.
53 ctors regulate the expression of bft and the enhancer trap line.
54 hat lie within the expression pattern of the enhancer-trap line c929-Gal4.
55                          We have used a GAL4 enhancer-trap line driving the expression of a lacZ cons
56 g method and have screened 1,300 Arabidopsis enhancer trap lines and have identified 147 lines in whi
57                                     Gene and enhancer trap lines defining genes expressed during prim
58                     We found that 36% of our enhancer trap lines display circadian-regulated transcri
59   In contrast, the expression pattern of the enhancer trap lines during zygotic embryogenesis was mor
60 ify the R2/R5 neuronal sub-type, we screened enhancer trap lines expressed in developing photorecepto
61 ved in follicle cell patterning, we analyzed enhancer trap lines expressed in specific subsets of fol
62 elected a set of 21 frequently used GAL4/UAS enhancer trap lines for detailed characterization of exp
63   We use GAL4 transactivation of aequorin in enhancer trap lines of Arabidopsis (Arabidopsis thaliana
64                                        Using enhancer trap lines targeted to different subsets of Joh
65 ectivity and provides a set of characterized enhancer trap lines that will be valuable for future stu
66 nking genomic sequence was identified for 23 enhancer trap lines to identify clock-controlled genes (
67                 We produced more than 13 000 enhancer trap lines with this cassette and screened T(0)
68 ression patterns were determined for two GFP enhancer trap lines with tissue-specific expression in t
69 al circuits using genetic tools such as GAL4 enhancer trap lines, as Drosophila has been intensively
70 terized by localizing beta-gal expression in enhancer trap lines, as well as with BrdU incorporation
71 lso cloned three SAGs from randomly selected enhancer trap lines, demonstrating that reporter express
72  putative midline-expressed genes, including enhancer trap lines, microarray data, published accounts
73                                     By using enhancer trap lines, we find that the overproliferating
74 o either muscles or motorneurons using Gal-4 enhancer trap lines, we were able to rescue substantiall
75 DN-cadherin and Echinoid, and a set of seven enhancer trap lines.
76  cell identities is a collection of GAL4/UAS enhancer trap lines.
77 l specificity is achieved through the use of enhancer trap lines.
78 ype-specific marker lines and for genotyping enhancer trap lines.
79                                 We show that enhancer-trap lines can transactivate an unlinked pOp-gr
80 abidopsis research, beta-glucuronidase (GUS) enhancer-trap lines have been created and successfully u
81         This library of the Arabidopsis seed enhancer-trap lines is an efficient tool for identifying
82 ression studies, we describe a population of enhancer-trap lines obtained with LhG4AtO in a pOp-GUS b
83                                  Etl4(lacZ) (Enhancer trap locus 4) and Skt(Gt) (Sickle tail) are lac
84                        First, we describe an enhancer trap marker called R32 that specifically reveal
85 ompanied by expression of a different set of enhancer trap markers.
86              We previously reported that the enhancer trap Mlcv1v-nLacZ-24 transgenic mouse strain fu
87                                           An enhancer-trap P element was constructed with the homing
88 heterologous beta-globin gene promoter in an enhancer trap plasmid and of the alpha1(I) collagen gene
89                       Characterization of an enhancer-trap population identified multiple lines that
90                             We identified an enhancer trap probe often producing restricted reporter
91                              Poplar gene and enhancer traps provide a new resource that allows plant
92  method adds two components: a collection of enhancer-trap recombinase, Flippase (ET-FLP), transgenic
93                DPP induces expression of the enhancer trap reporter A359 and represses expression of
94                                          One enhancer trap revealed expression of the gene encoding t
95  fat body-specific green fluorescent protein enhancer trap screen in D. melanogaster and expression p
96                    A gene identified from an enhancer trap screen is shown to encode the Drosophila m
97                                           An enhancer trap screen of synapse-inactivated neural circu
98 sis of events in the margin, we performed an enhancer trap screen to identify genes specifically expr
99                           We present a pilot enhancer trap screen using GAL4 to drive expression of u
100 xpression system, we performed a large-scale enhancer-trap screen for insertions that yielded nervous
101  reporter expression and developed efficient enhancer trap screening with the PiggyBac transposon.
102  gene of Drosophila melanogaster, defined by enhancer trap strain 24B of Brand and Perrimon.
103                                     Using an enhancer trap strain in which white+ gene expression is
104  using a set of Drosophila melanogaster GAL4 enhancer trap strains for an upper-level undergraduate l
105                     P-element-based gene and enhancer trap strategies have provided a wealth of infor
106 n vivo bacterial artificial chromosome (BAC) enhancer-trapping strategy in mice to scan a half-megaba
107                       The Tol2-mediated gene/enhancer trapping system together with UAS transgenic li
108 n generated using a GAL4-dependent bipartite enhancer-trap system confirmed that PPhiB or phytochrome
109                                  H-2Z1 is an enhancer trap transgenic mouse line in which the lacZ re
110                  A collection of Arabidopsis enhancer trap transposants has been identified for use a
111 ant allele caused by the insertion of a GAL4 enhancer trap transposon.
112           In that study, we mobilized a hobo enhancer trap vector and generated two unique alleles of
113 n system to distribute a self-reporting gene/enhancer trap vector efficiently throughout the zebrafis
114        Using a self-reporting Gal4-VP16 gene/enhancer trap vector, we isolated tissue-specific driver
115                    When incorporated into an enhancer-trapping vector, however, LhG4AtO and Lh314 yie
116                                     Gene and enhancer trap vectors carrying the beta-glucuronidase (G
117 specific ectopic expression of the A251-lacZ enhancer trap whereas overexpression of a transgene enco
118                                      We used enhancer trapping with the GAL4 transcriptional activato
119 g vector, however, LhG4AtO and Lh314 yielded enhancer traps with approximately twice the frequency of
120 hancer-trap facilitates (i) the isolation of enhancer-traps with a specific expression pattern, and (

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