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1 15% DNA divergence did not prevent efficient gene isolation.
2 icum aestivum), with reference to methods of gene isolation.
3  BAC into a TAR vector, thus allowing direct gene isolation.
4 e vectors that are suboptimal substrates for gene isolation.
5  designer that implements a new strategy for gene isolation.
6 d DNA for more detailed physical mapping and gene isolation.
7                                              Gene isolation, amplification, or ligation is not necess
8        To devise a method for function-based gene isolation and characterization in barley, we create
9 assist in genome sequence assembly, targeted gene isolation and comparative genomic analyses among gr
10 ribflies and will be a valuable resource for gene isolation and genomic studies in tephritid insects.
11 cting chromosomal rearrangements, for use in gene isolation, and as a framework for physical mapping.
12  in a vector is a prerequisite for efficient gene isolation by TAR cloning.
13 mal length of a unique sequence required for gene isolation by TAR is approximately 60 bp.
14 ed into a sorghum physical map for map-based gene isolation, comparative genome analysis, and as a so
15 olving dense genetic maps, physical mapping, gene isolation, comparative genomics, analysis of quanti
16                              Although recent gene isolation efforts and metabolic engineering have pr
17  affinity method that is uniquely suited for gene isolation from a highly degenerate collection of nu
18 gion with DNA markers, TRS should facilitate gene isolation from diverse organisms and accelerate the
19 nd the implications of such conservation for gene isolation from the major cereal crops.
20    Current genetic detection methods require gene isolation, gene amplification and detection with a
21 s from stool in < 40 min without the need of gene isolation, gene amplification, or expensive fluores
22 nous transposable elements, useful tools for gene isolation, have not been reported from any legume s
23 vide new ways to accelerate fine-mapping and gene isolation in crops.
24      Clones from this contig will facilitate gene isolation in the region and can be used directly as
25                 The final stage of map-based gene isolation is complementation of the mutant phenotyp
26                                              Gene isolation may exploit the small genome of rice in m
27                                              Gene isolation methods used during positional cloning re
28 arker-assisted trait selection and map-based gene isolation necessary for cowpea improvement.
29                                   Because no gene isolation or amplification is required for sequenci
30                        Using two independent gene-isolation procedures, we isolated a new catenin fam
31           We used virtual subtraction, a new gene isolation strategy, to isolate several genes of int
32                    Because of the variety of gene isolation techniques used, this result is unlikely
33 gs highlight the importance of developmental gene isolation through chromosomal folding structures as
34 is transposon could prove to be an efficient gene isolation tool in sorghum.
35 minimal size of a specific hook required for gene isolation utilizing the Tg.AC mouse transgene as a
36 bination of positional cloning and candidate-gene isolation, we have identified the HY1 gene and foun
37 jannaschii can serve as a starting point for gene isolation, while in vivo genetics in the mesophilic
38 d of the rice genome as a tool to facilitate gene isolation will differ from one region to the next,