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1 imal false positives using a compact 5 sgRNA/gene library.
2 n be used to generate a partially randomized gene library.
3 Escherichia coli from a randomly fragmented gene library.
4 70 homolog was isolated and sequenced from a gene library.
5 ere selected from a random pentapeptide mini-gene library.
6 cing after construction of 16S ribosomal RNA gene libraries.
7 n to 3 h, depending on the complexity of the gene libraries.
8 key step is the creation of suitably diverse gene libraries.
9 reated pigs using pyrosequencing of 16S rRNA gene libraries.
12 on in directed evolution for the assembly of gene libraries and the regeneration of linear DNA templa
13 e assembled Nematostella genome, a confirmed gene library, and a predicted genome using both keyword
16 oclonal autoantibodies from combinatorial Ig-gene libraries derived from autoimmune thyroiditis patie
18 system provides a way to recombine VH and VL gene libraries efficiently in vivo to make extremely lar
20 ble, however, on the composition of shuffled gene libraries, from which one could assess the efficien
22 However, selecting improved variants from gene libraries in living cells requires plasmid expressi
24 protective cell-mediated immune response, a gene library of Brucella abortus 2308 was screened for t
25 body screen designed to identify clones in a gene library of L. interrogans serovar Pomona expressing
28 terial DNA was isolated and 16S ribsomal RNA gene libraries sequenced using 454-pyrosequencing target
30 n we have rapidly constructed 60 overlapping gene libraries that encode zinc finger proteins, randomi
32 y strategy based on designed combinatorial V gene libraries, the humanization of mouse monoclonal ant
33 ely heavily upon the screening of randomized gene libraries, there is surprisingly little information
34 ng of the immunoglobulin and T cell receptor gene libraries to the genome, which are largely absent i
35 f partially randomized genes, expressing the gene library to generate the proteins the library encode
36 ystem based on a randomized hairpin ribozyme gene library to identify cellular factors involved in HC
38 ned the Escherichia coli ASKA overexpression gene library using the Differential Radial Capillary Act
39 ics" approach based on a randomized ribozyme gene library was applied to identify cellular genes regu
44 anning (ACS) strategy that creates a defined gene library wherein each individual codon within a spec
47 for functional genomics, a hairpin ribozyme gene library with randomized target recognition sequence
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