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1 data, and validation by whole-genome optical restriction mapping.
2 e genes have been ordered by STS content and restriction mapping.
3 determined by polymerase chain reaction and restriction mapping.
4 ion fragments without necessarily performing restriction mapping.
5 Chimerism of YACs was determined by FISH and restriction mapping.
6 raightening DNA molecules for use in optical restriction mapping.
7 0 kb of D1S214 by YAC content and long-range restriction mapping.
15 tions in ine were localized on cloned DNA by restriction mapping and restriction fragment length poly
21 were constructed correctly as determined by restriction mapping and the absence of relevant protein
22 ility, biochemical tests, ribotyping, genome restriction mapping, and multilocus sequence typing (MLS
24 ficial intelligence techniques for automated restriction mapping, and use them to create a powerful m
29 mapping), which is a high-resolution ordered restriction mapping of a bacterial genome, is a relative
31 reside approximately 200 to 300 bp apart by restriction mapping of cloned genomic regions associated
33 oughput genome-sequence data, and long-range restriction mapping of genomic and cloned DNA by pulsed-
39 lotting, nucleotide sequencing, and detailed restriction mapping of the vbs-containing genomic clones
40 interactions is demonstrated by noncatalytic restriction mapping on a 4-kb DNA with three restriction
46 ned into target DNAs of up to 50 kb in size, restriction mapping showed insertion to be relatively ra
49 from human genomic DNA and characterized by restriction mapping, Southern blot analysis, and nucleot
52 g M6a and M6b and have characterized them by restriction mapping, Southern hybridization with cDNA pr
55 determined by sequence analysis and detailed restriction mapping that G21, previously isolated as a '
58 s homozygous deletion physically, long-range restriction mapping was performed using yeast artificial
60 cleavage is an "Achilles' heel" approach to restriction mapping whereby a RecA-protein-oligodeoxynuc
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