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1 by generating chimeras with hASNase1 through DNA shuffling.
2 y from a cellulase library created by family DNA shuffling.
3 d on in vitro recombination methods, such as DNA shuffling.
4 dely used in vitro DNA recombination method, DNA shuffling.
5 dition to library generation methods such as DNA shuffling.
6 to analyze chimeric DNA libraries created by DNA shuffling.
7 ent protein was subjected to mutagenesis and DNA shuffling.
8 ation for the creation of hybrid enzymes and DNA shuffling.
9 crossover statistics and draws contrast with DNA shuffling.
10 eling a specific DNA recombination protocol, DNA shuffling.
11 roteins and enzymes have been improved using DNA shuffling.
12 ropic murine leukemia virus (MLV) strains by DNA shuffling.
13 qual to the activity of the hybrids found by DNA shuffling.
14 This mutagenesis approach is called DNA shuffling.
15 hniques such as directed evolution including DNA shuffling, a great number of BBB-crossing AAVs have
16 r multiple rounds of cycling mutagenesis and DNA shuffling, a more efficient nuclease variant (Sharke
18 iscipline was galvanized by the invention of DNA shuffling, a procedure that randomly recombines poin
20 other into extinction (clonal interference); DNA shuffling and combinatorial cassette mutagenesis led
23 erent PRRSV strains were molecularly bred by DNA shuffling and iteration of the process, and the shuf
28 in vivo capsid evolution through sequential DNA shuffling and peptide library screening in a NF1 xen
29 een altered by stochastic mutations based on DNA shuffling and rationally tailored by structure-based
30 utant, TG-15, was subjected to iterations of DNA shuffling and screened for enzyme variants with up-r
32 oped a more potent version of IL-12 by using DNA shuffling and screening to improve its expression in
33 among 32 clones isolated in three rounds of DNA shuffling and screening were mapped to the active si
34 s in specificity and activity by reiterative DNA shuffling and screening, even for an enzyme of 109 k
39 ies, requires fewer PCR cycles than in vitro DNA shuffling and, unlike site-specific recombination me
40 tion to existing DNA recombination methods ('DNA shuffling') and should be particularly useful for re
41 f enzymes resulting from random mutagenesis, DNA shuffling, and combinatorial saturation mutagenesis
42 on of error-prone polymerase chain reaction, DNA shuffling, and multiple-site-directed mutagenesis to
44 nzymes, including site-directed mutagenesis, DNA shuffling, and site-saturation mutagenesis, among ot
48 eric Pgp with an altered resistance profile, DNA shuffling between the homologous but not identical d
52 of improved variants from the two rounds of DNA shuffling confirmed important features of the recomb
53 High fidelity in vitro gene recombination ("DNA shuffling") coupled with sequence analysis of a smal
56 odon usage and performed recursive cycles of DNA shuffling followed by screening for the brightest E.
57 s resource-intensive and more effective than DNA shuffling for this particular evolutionary pathway.
58 An efficient beta-fucosidase was evolved by DNA shuffling from the Escherichia coli lacZ beta-galact
61 m mutagenesis, site-directed mutagenesis and DNA shuffling, have been widely used to generate variant
65 These studies demonstrate the utility of DNA shuffling in breeding viral strains with improved ch
66 c resistance operon has been accomplished by DNA shuffling, involving multiple rounds of in vitro rec
72 DNA sequences for recombination, we combined DNA shuffling mutagenesis and a forward selection strate
75 th in vitro and in vivo, indicating that the DNA shuffling of GP4 and M genes did not significantly i
79 this study we molecularly bred PRRSV through DNA shuffling of the GP4 and M genes, separately, from s
82 n of the virus was achieved in this study by DNA shuffling of the viral envelope genes from multiple
83 this study reveals a unique approach through DNA shuffling of viral envelope genes to attenuate a pos
84 ified as beneficial by random mutagenesis or DNA shuffling or seen in any of the naturally occurring
85 of hGSTT1-1 constructed by error-prone PCR, DNA shuffling, or saturation mutagenesis were screened f
86 etween phenotypes and variation generated by DNA shuffling paralleled natural variation observed betw
88 ed chimeric sections are then subjected to a DNA shuffling process generating an enhanced crossover S
91 t diversity targets are investigated for the DNA shuffling protocol to showcase the utility of the eC
95 ned sequence; (ii) minimizing bias in family DNA shuffling so that each of the parental sequence pair
96 his artificial family is then subjected to a DNA-shuffling step to augment the number of crossovers.
99 enesis of cloned genes by error-prone PCR or DNA shuffling that eliminates the need for post-amplific
100 the protein engineer with a new approach to DNA shuffling that supports substantially more diverse p
104 nts efficient methods to extend the scope of DNA shuffling to handle significantly more diverse paren
106 te spectrum, we used rounds of selection and DNA shuffling to obtain GroEL/S variants that dramatical
107 ed iterative site-saturation mutagenesis and DNA shuffling to screen precise gene-variant yeast displ
108 oduce a method of in vitro recombination or "DNA shuffling" to generate libraries of evolved enzymes.
110 tion mutagenesis and in vitro recombination (DNA shuffling) was used to generate mutant libraries, wh
111 combinatorial random mutagenesis technique (DNA shuffling), we have isolated an IE(ME)-specific hype
112 xplore whether there might be limits to such DNA shuffling, we have mapped the termini of mitochondri
114 antage of multi-parental crossing allowed by DNA shuffling with the recombination of entire genomes n
115 nt cln2-KAEA, but additional mutagenesis and DNA shuffling yielded multiply mutant CDC28-BYC alleles