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1  discovered by subtractive hybridization and chromosome walking.
2 utational analysis, STS content mapping, and chromosome walking.
3 ng significant matches, resulting in virtual chromosome walking.
4 ase has been cloned from S. viridifaciens by chromosome walking.
5                  We cloned the CER2 gene via chromosome walking.
6 assembled into contigs that were extended by chromosome walking.
7  similar but not identical, complicates both chromosome walking and assembly of sequence-ready contig
8                                              Chromosome walking and DNA sequence analysis permitted t
9 e in situ hybridization to chromatin fibres, chromosome walking and DNA sequencing of genomic clones,
10 these two diseases, we used a combination of chromosome walking and expressed sequence tag (EST) scre
11 terized seven prevalent unknown sequences by chromosome walking and find these represent novel microb
12 f multiple BAC mapping strategies, including chromosome walking and multiplex oligonucleotide hybridi
13                             A combination of chromosome walking and sequence-tagged site (STS)-conten
14                            ra2 was cloned by chromosome walking and shown to encode a LATERAL ORGAN B
15             To facilitate map-based cloning, chromosome walking, and genome organization studies of M
16 tly linked molecular markers on LG10 through chromosome walking approach led to the identification of
17                           We first conducted chromosome walking at the S2 locus using BAC clones that
18 ility of this YAC contig map will accelerate chromosome-walking experiments, provide substrates for l
19 i were cloned from Pyrenopeziza brassicae by chromosome walking from a mating type-linked polymerase
20                             Mapping genes by chromosome walking is a widely used technique applicable
21  to clone additional regions of the GGI by a chromosome-walking procedure.
22            These results and our preliminary chromosome walking results suggest that the S locus is a
23 es, we used a method termed 'semi-random PCR chromosome walking' (SRPCW) to walk through a large moti
24                                        Three chromosome walking steps were performed by complete sequ
25 ach combined with a reference sequence-based chromosome walking strategy and high-density mapping pop
26 n of mouse caspase-12 gene by a PCR-mediated chromosome-walking technique, using mouse genomic DNA as
27 n homology search experiments, together with chromosome walking, to build both physical and radiation
28                                              Chromosome walking using clones identified from several
29                                              Chromosome walking was initiated from both markers but w
30 quence tagged site (STS)-content mapping and chromosome walking, we assembled a genomic clone contig
31 the BACs, STS development, and bidirectional chromosome walking yielded 109 markers (100 STS and 9 ge