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1 n be used to generate a partially randomized gene library.
2  Escherichia coli from a randomly fragmented gene library.
3 imal false positives using a compact 5 sgRNA/gene library.
4 70 homolog was isolated and sequenced from a gene library.
5 ere selected from a random pentapeptide mini-gene library.
6 lterations in an E. coli DNA damage-inducing gene library.
7 cing after construction of 16S ribosomal RNA gene libraries.
8 reated pigs using pyrosequencing of 16S rRNA gene libraries.
9 n to 3 h, depending on the complexity of the gene libraries.
10 key step is the creation of suitably diverse gene libraries.
11  ESTs representing 21 neural crest-expressed genes (library 198).
12 NanoFLUID-mediated in vivo transfection of a gene library also enabled efficient screening of essenti
13                       Additionally, SSU rRNA gene libraries and shotgun metagenomes showed reduced re
14 on in directed evolution for the assembly of gene libraries and the regeneration of linear DNA templa
15 e assembled Nematostella genome, a confirmed gene library, and a predicted genome using both keyword
16 , a low-cost, multiplexed method that builds gene libraries by compartmentalizing and assembling micr
17                               The calculated gene library can be readily used in the context of stand
18 solated by immunoscreening of a B. forsythus gene library constructed in a lambda ZAP II vector.
19 oclonal autoantibodies from combinatorial Ig-gene libraries derived from autoimmune thyroiditis patie
20 he high-throughput screening of NAAAR mutant gene libraries directly from cell lysates.
21 system provides a way to recombine VH and VL gene libraries efficiently in vivo to make extremely lar
22                     We generated IgM and IgG gene libraries established from lymphocytes of patients
23 ble, however, on the composition of shuffled gene libraries, from which one could assess the efficien
24                       Complementary chimeric gene libraries generated by incremental truncation (ITCH
25    However, selecting improved variants from gene libraries in living cells requires plasmid expressi
26 generates a library of mutants (a randomised gene library) in a single experiment.
27 , we constructed a membrane protein-encoding gene library of B. miyamotoi using Borrelia garinii stra
28  protective cell-mediated immune response, a gene library of Brucella abortus 2308 was screened for t
29 body screen designed to identify clones in a gene library of L. interrogans serovar Pomona expressing
30       In vivo screening of six combinatorial gene libraries provided 158 functional variants of the E
31 pylori and Helicobacter felis were cloned by gene library screening.
32 terial DNA was isolated and 16S ribsomal RNA gene libraries sequenced using 454-pyrosequencing target
33 ameters required for robust in vivo screens: gene library size, cell transfer quantity, and number of
34                       Numerous environmental gene library studies have shown that eukaryote microbial
35 n we have rapidly constructed 60 overlapping gene libraries that encode zinc finger proteins, randomi
36 20 kDa) and highly soluble SynIDPs from this gene library that lack secondary structure and have high
37                 Screening of a 21-codon mini-gene library (the general structure ATG (NNN)20 TAA) dem
38 y strategy based on designed combinatorial V gene libraries, the humanization of mouse monoclonal ant
39 ely heavily upon the screening of randomized gene libraries, there is surprisingly little information
40 ng of the immunoglobulin and T cell receptor gene libraries to the genome, which are largely absent i
41 f partially randomized genes, expressing the gene library to generate the proteins the library encode
42 ystem based on a randomized hairpin ribozyme gene library to identify cellular factors involved in HC
43                         By fusing the hybrid gene library to the gene for chloramphenicol acetyl tran
44 ned the Escherichia coli ASKA overexpression gene library using the Differential Radial Capillary Act
45 y highly soluble SynIDPs, we create a pooled gene-library utilizing a one-pot gene synthesis technolo
46 ics" approach based on a randomized ribozyme gene library was applied to identify cellular genes regu
47                                            A gene library was constructed coding for all possible var
48                          A random five-codon gene library was used to isolate minigenes whose express
49 f pet, 10 cosmid clones of an E. coli CFT073 gene library were positive for hybridization.
50                       The shuffled GP4 and M genes libraries were each cloned into the backbone of PR
51 anning (ACS) strategy that creates a defined gene library wherein each individual codon within a spec
52  techniques are now available for generating gene libraries with different characteristics.
53                                   A ribozyme gene library with randomized target recognition sequence
54  for functional genomics, a hairpin ribozyme gene library with randomized target recognition sequence
55                                     The 2100 gene library yielded 97% coverage of all targeted CpGs a