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1 or forming what has been called a 'satellite DNA library'.
2 or random clones from a small insert genomic DNA library.
3 and used to a probe a P. funiculosum genomic DNA library.
4 nding sequence from a human single-copy (sc) DNA library.
5  but one of these classes from a chromosomal DNA library.
6 eta, were isolated from a Paramecium genomic DNA library.
7 eening a recombinant M. tuberculosis genomic DNA library.
8 ruct, screen and finally clone a gene from a DNA library.
9 a1 gene was isolated from a human P1 genomic DNA library.
10 f strain AG84-3, was isolated from a genomic DNA library.
11 oding gene was isolated from a human genomic DNA library.
12 ces in GenBank and from inserts in a genomic DNA library.
13 with next-generation sequencing of a genomic DNA library.
14 nd-read drop-IVT2H method to screen a random DNA library.
15 organs, and used to generate a complementary DNA library.
16 ed fluorescence compared with the unselected DNA library.
17 using fosmids selected from a total cellular DNA library.
18 tilize nucleotide content changes to produce DNA libraries.
19 ubtracted thymus cDNA library and in genomic DNA libraries.
20  total DNA instead of cloning fragments from DNA libraries.
21 able elements to be present in complementary DNA libraries.
22 ication by extensive screening of randomized DNA libraries.
23 e discovered within 3 days using preselected DNA libraries.
24 ust techniques for enhanced amplification of DNA libraries.
25 , using it to deplete unwanted sequence from DNA libraries.
26 ement to use global mutagenesis or introduce DNA libraries.
27 nd provides a way to preserve the quality of DNA libraries.
28 ly 3 d from flow cytometry to sequence-ready DNA libraries.
29 ired-end sequences derived from large-insert DNA libraries.
30 oxyl radical cleavage data produced from two DNA libraries.
31 Escherichia coli carrying a soil metagenomic DNA library(3) with the lytic coliphage T4 to isolate cl
32           From an H. ducreyi 35000HP genomic DNA library, a clone complementing the defect in A77 was
33 s of other groups using the same recombinant DNA library, a comprehensive map was constructed that in
34                           We selected from a DNA library an aptamer specifically recognizing human ep
35 -generation sequencing analysis of mate-pair DNA libraries and applied these tools to 16 PTCL patient
36 phage and P1 phage clones from human genomic DNA libraries and characterized by Southern blot and nuc
37 anism to clone biosynthesis genes from large DNA libraries and greatly facilitate the exploration of
38   We demonstrate the stability of conjugated DNA libraries and related sequencing results over the co
39 w approach could be applied in the design of DNA libraries and result in a more efficient and faster
40 es were prepared into reduced representation DNA libraries and sequenced to identify genomic regions
41 l three assays on a common set of 27 ancient DNA libraries and show that all three are effective at e
42 acterial artificial chromosome mouse genomic DNA library and characterized by polymerase chain reacti
43 se (ADH) was cloned from a Caucasian genomic DNA library and characterized.
44                      Also, by using a cosmid DNA library and genomic fractions as hybridization probe
45       Serologic screening of a complementary DNA library and Northern blotting were used to clone the
46 e was transformed with a C. albicans genomic DNA library and screened for the production of active al
47  lysozyme c group were cloned from a genomic DNA library and sequenced.
48 ow-copy sequences were isolated from a human DNA library and tested for their ability to detect restr
49 li strain CS89 was transformed with the same DNA library and then screened for Asp-tRNA(Asp) formatio
50  by sequencing inserts from a CB4856 genomic DNA library and using an informatics pipeline to compare
51 tor of neutrophil elastase into a randomized DNA library and, using the SELEX process, iteratively se
52      We establish methods for barcoding CAGE DNA libraries, and apply them to measure persistence of
53 isms was identified by screening chromosomal DNA libraries, and cloned.
54 in situ hybridization of chromosome-specific DNA libraries, and mapped >2,000 sites of recombination
55  microfluidics workflow for screening random DNA libraries, and represents a novel alternative method
56  cloning complex individual or combinatorial DNA libraries, and routine or high-throughput cloning of
57 t was used to screen a lambda ZAP II genomic DNA library, and an open reading frame expressing a 28-k
58 shortcomings, we have devised a method where DNA libraries are constructed on the surface of microbea
59                                              DNA libraries are constructed using native genomic DNA f
60 d genes in this region by directly screening DNA libraries as well as by database searching for ESTs.
61 ers, SVCT1 and SVCT2, from rat complementary DNA libraries, as the first step in investigating the im
62 ector ideal for cloning PCR products, making DNA libraries, as well as routine cloning and bacterial
63 d DNA sequencing, hybridization screening of DNA libraries, assembly of gene cassettes, run-off trans
64 s the generation of eukaryotic and bacterial DNA libraries at eukaryotic single-cell level resolution
65 .5.1.9) from an Arabidopsis thaliana genomic DNA library based on the homology between the yeast bios
66 rmation in real time and within minutes of a DNA library being loaded.
67 leavage of a phosphodiester bond in RNA than DNA libraries built from a standard four-nucleotide alph
68 has been cloned from adaptor-ligated genomic DNA libraries by polymerase chain reaction.
69  cloned and used to probe a wild-type Xa23R1 DNA library by colony hybridization.
70       The genes were isolated from a genomic DNA library by complementation of a lipase-deficient tra
71 tein) by screening a HeLa cell complementary DNA library by using the yeast two-hybrid system.
72 e-tag-guided screening of soil environmental DNA libraries can be used to guide the discovery of new
73                                Complementary DNA libraries can define the genetic constituents of spe
74 oylphenylalanine, Bpa) amino acids, a single DNA library can be used to incorporate different amino a
75 TF-DNA interactions using mixtures of random DNA libraries carrying different epigenetic modification
76 designed for the propagation of large insert DNA library clones.
77 ed technology that entails construction of a DNA library comprising up to at least 4(7) ( approximate
78                              Sequencing of a DNA library constructed from circular plasmid fragments
79 ntaining clones were isolated from a genomic DNA library constructed in our lVET promoter trap vector
80 ms of high molecular weight DNA suitable for DNA library construction and Sanger sequencing.
81                                              DNA library construction and sequencing were performed u
82                               Using improved DNA library construction methods that enrich for DNA fra
83 ery, the currently widely used complementary DNA library construction protocol generates biased seque
84 ng ALK translocations, we combined mate-pair DNA library construction, massively parallel ("Next Gene
85 cations in nanotechnology, gene editing, and DNA library construction.
86                                Environmental DNA libraries contain large reservoirs of bacterial gene
87          Two cosmids from an E. coli O157:H7 DNA library contain an adherence-conferring chromosomal
88 of IL-6 SOMAmers were isolated from modified DNA libraries containing 40 random positions and either
89                                              DNA libraries containing exome sequences tagged with uni
90 ctural families using chemically synthesized DNA libraries containing position-specific 5-methylcytos
91 ctivity, we deep-sequenced the products of a DNA library containing 10 random base-pairs on each side
92                                    A hairpin DNA library containing an 8-base pair sequence-randomize
93                                            A DNA library containing DNA-DNA mismatches at PAM + 1 to
94 quencing small fragments of a random genomic DNA library containing one or more modular PKS gene clus
95                                 Notably, our DNA library contains the genome of a bacterium within th
96 bidopsis thaliana, and man, (3) large-insert DNA libraries: cosmid, YAC and BAC, and genome physical
97 d in a macroarray format to analyze chimeric DNA libraries created by DNA shuffling.
98 ened over one million clones from metagenome DNA libraries derived from sixteen different environment
99                                      Complex DNA libraries derived from the host-symbiont population
100 roviral clone, pJSRV21, from a tumor genomic DNA library derived from a natural case of SPA.
101 ce within the equilibrium mixture of masking DNA, library DNA, and target cells.
102            Five cosmids from N. meningitidis DNA library enabled a heme-requiring (hemA), HmbR-expres
103 tion gene homologs found within a large soil DNA library enabled the identification and recovery of a
104 eriments were carried out on circular 103-nt DNA libraries encoding 40-nt randomized sequences as wel
105 d shotgun scanning glycomutagenesis in which DNA libraries encoding all possible glycosylation site v
106 a systematic approach in which combinatorial DNA libraries encoding large numbers of random mutations
107                                            A DNA library encoding potential peptide binders was encap
108 lecules result in the establishment of oligo DNA libraries enriched in DNA molecules containing speci
109 gate amplification mechanisms: sequencing of DNA libraries enriched with tumor-derived palindromic DN
110 ent within GCs, we constructed a recombinant DNA library enriched for cDNAs derived from human genes
111 n 8,000-3,000 years ago by enriching ancient DNA libraries for a target set of almost 400,000 polymor
112                       We constructed genomic DNA libraries for AFGP-bearing and AFGP-lacking species
113 fluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing.
114 ling of bacterial samples and preparation of DNA libraries for next-generation sequencing.
115  inhibit splicing, we searched human genomic DNA libraries for sequences that would inhibit the inclu
116 linking a drug-pharmacophore to a degenerate DNA library for use in cell- and whole-animal systematic
117  harboring members of an F. novicida genomic DNA library, for 4'-phosphatase activity.
118 M-seq method successfully generated reliable DNA libraries from 1-25 ng of mouse and human DNA.
119                     Subtracted complementary DNA libraries from highly purified murine fetal liver st
120              We compared human complementary DNA libraries from OA-affected and normal cartilage and
121 re, we constructed directional complementary DNA libraries from plaque-periplaque messenger RNA and a
122                                     A cosmid DNA library from a PAK strain deleted for xcpP-Z was tes
123 pathway in tea, we generated a complementary DNA library from leaf tissue of the blister blight-resis
124                      Analysis of single-cell DNA libraries generated by different technologies reveal
125  are accelerated by integrating high-quality DNA library generation with an ultra-high throughput pro
126  screening an ordered S. typhimurium genomic DNA library, harbored in Escherichia coli K-12, for expr
127 ectors, with which several very large-insert DNA libraries have been developed.
128 the p79 gene as the bait and a yeast genomic DNA library, identified two independent groups of positi
129 vo synthesis and cell-free cloning of custom DNA libraries in sub-microliter reaction droplets using
130 ies using only a single, long-insert shotgun DNA library in conjunction with Single Molecule, Real-Ti
131 was isolated by activity screening a genomic DNA library in Streptomyces lividans TK24.
132  colonies of a R. leguminosarum 3841 genomic DNA library in the host strain R. etli CE3.
133 colonies of an R. leguminosarum 3841 genomic DNA library in the host strain S. meliloti 1021.
134 lection and evolution of proteins encoded by DNA libraries, in which individual nascent proteins (phe
135 egy that combines a synthetically engineered DNA library inserted in each run and a new computational
136  We developed quantitative gene assembly and DNA library insertion into the Saccharomyces cerevisiae
137 sed method of highly efficient site-specific DNA library integration.
138       By transferring an F. novicida genomic DNA library into E. coli and selecting for low level pol
139 niform amplification of complex templates in DNA libraries, introducing unwanted biases.
140 High-throughput transgenesis using synthetic DNA libraries is a powerful method for systematically ex
141 randomization and screening of combinatorial DNA libraries is a powerful technique for understanding
142 ology-based screening of large environmental DNA libraries is likely to permit the directed discovery
143                                The resulting DNA library is incubated with an affinity-tagged in vitr
144 ast method for introduction of barcodes into DNA libraries made from 5 ng of DNA.
145 hroughput screening of complex environmental DNA libraries more than 40 novel microbial pectate lyase
146 ternative for construction of small-fragment DNA libraries of defined sequences.
147 pA protein, its gene was cloned from genomic DNA libraries of T. denticola.
148  designated chsC and chsG were isolated from DNA libraries of the opportunistic fungal pathogen, Aspe
149 ere selected in vitro from a single-stranded DNA library of 1.8 x 10(15) oligonucleotides showing dis
150    We have designed an effective search of a DNA library of approximately 10(60) in size, and have id
151 st for relapsing fever, we created a genomic DNA library of B. hermsii, screened transformed Escheric
152                            A partial genomic DNA library of Chlamydomonas reinhardtii was screened wi
153                                            A DNA library of F. nucleatum FDC 364 was constructed by p
154  clone these immunogenic antigens, a genomic DNA library of Nine Mile phase I was screened with conva
155  this sequence were used to screen a genomic DNA library of PG31.
156                                            A DNA library of pRJ28, a large linear plasmid encoding me
157  to the N terminus of the enzyme to screen a DNA library of Pseudomonas sp. MA-1.
158 , arsA and arsB were isolated from a genomic DNA library of S. ovata.
159 erovar Enteritidis, we transformed a genomic DNA library of SE2472 into SE8743.
160  and cobalt ions was isolated from a genomic DNA library of Staphylococcus aureus RN450.
161               Using tpgR1 to probe a genomic DNA library of Streptomyces lividans ZX7, whose linear c
162                                  For each, a DNA library of V3 region of bacterial 16S ribosomal RNA
163 dCHS2 was isolated by screening a subgenomic DNA library of Wangiella dermatitidis by using a 0.6-kb
164  preserve RNA structure and to limit all RNA-DNA library oligonucleotide interactions to 1:1 stoichio
165                       By sequencing a common DNA library on different sequencers, we demonstrate that
166 nsformants harboring a Campylobacter genomic DNA library, one recombinant plasmid that encoded a heat
167 t and economical strategies to clone complex DNA libraries or variants of biological modules.
168                     Single and multiorganism DNA libraries originating from various environments were
169 omain amplicons derived from saturating soil DNA libraries, our analysis pipeline led to the recovery
170 amplification, and the use of the Nextera XT DNA library preparation kit produced significantly bette
171 atic cleavage-based approach, the Nextera XT DNA library preparation kit, for library preparation.
172 es fast and reliable targeted single-nucleus DNA library preparation of 38 samples from 16 pancreatic
173  This method can be easily added to existing DNA library preparation techniques and can improve the a
174 ped a methodology integrating cost-effective DNA library preparation with nanopore sequencing, reduci
175          In combination with single-stranded DNA library preparation, this method enabled us to recon
176 on data, which are routinely acquired during DNA library preparation, to annotate output sequence dat
177 es accessibility and methylation from single DNA library preparations.
178 use WEHI-3 monocytic cell line and a genomic DNA library prepared from 129/SvJ mouse tissue.
179                                    A genomic DNA library prepared from a benomyl resistant strain of
180 have cloned its gene, gngC, from the genomic DNA library prepared from C. perfringens ATCC10543.
181 , we isolated 14 clones from a complementary DNA library prepared with total RNA extracted from the s
182                  Two members of a 10-hairpin DNA library previously found to bind most tightly to the
183                                  We utilized DNA libraries produced from Mycobacterium tuberculosis c
184                                 From genomic DNA library production to base-called sequences, this pr
185         While many methods are available for DNA library quantification, there is no unambiguous gold
186                                         Soil DNA libraries represent large reservoirs of biosynthetic
187 D46 and GTKO porcine aortic EC complementary DNA libraries, respectively.
188    Remarkably, selections employing modified DNA libraries resulted in the first successful isolation
189 genetic information has been 'fished out' of DNA libraries resulting in the discovery of new natural
190 eration sequencing analysis of the assembled DNA library revealed that ligation was accurate, directi
191                        Using a complementary DNA library screen, we identified the transcriptional re
192 nesis, mutation detection, DNA modification, DNA library screening and circular DNA production.
193 re we show, using an iterative complementary DNA library screening approach, that human occludin (OCL
194 study, we used a phage display complementary DNA library screening strategy to identify P falciparum
195 t the depth-of-coverage yield of single-cell DNA libraries sequenced at arbitrary depths.
196 nterlacing of multiple messages on synthetic DNA libraries showcases the potential of chemical reacti
197 t to screen a yeast two-hybrid complementary DNA library specific for regenerating livers with massiv
198 rotected mRNA fragments are converted into a DNA library suitable for deep sequencing using a strateg
199 titative conversion of the RNA sample into a DNA library suitable for sequencing.
200  In this study, we look at the error rate of DNA libraries synthesized by photolithography and dissec
201 the form of adapter-ligated, short-fragment, DNA libraries that may be amplified by polymerase chain
202 tion, we conducted a screen of an M. marinum DNA library that provides 2.6-fold coverage of the entir
203 ing radiation, was constructed without using DNA libraries, the polymerase chain reaction, or electro
204 n-for a large randomly generated recombinant DNA library, there exists a staircase of DNA fragments a
205 ce the effective depth of synthesized vector DNA libraries, thereby raising the discovery cost of nov
206  screen several heterologous and metagenomic DNA libraries, thus enlarging the genomic space that can
207 224,180 Illumina reads from 12 complementary DNA libraries to build what is to our knowledge the firs
208 inaceous transdominant inhibitors encoded by DNA libraries to cause mutant phenocopies may facilitate
209           Most techniques use PCR to amplify DNA libraries to obtain sufficient quantities for optica
210 gainst standard and normalized complementary DNA libraries to produce a draft map of 7048 proteins an
211             DNA aptamers are selected from a DNA library to bind intact infectious, but not noninfect
212 f aptamers have been evolved from an initial DNA library to characterize target cells at the molecula
213 A-approved drug Pluvicto to a degenerate N40-DNA library to direct the selection of aptamers against
214 : 1) in an aptamer evolved from a six-letter DNA library to selectively bind liver cancer cells; and
215 A), short barcodes are counted by sequencing DNA libraries transfected into cells and the cell's outp
216 of human PAX6 from single-copy human genomic DNA libraries using cyclic amplification of protein bind
217 with subnanomolar affinity from a randomized DNA library using in vitro selection.
218 ected a few DNA aptamers by immobilizing the DNA library using oxytetracycline as the target.
219            The screening of an archived soil DNA library using primers designed to target oxytryptoph
220       High throughput screening of microbial DNA libraries was used to identify alpha-amylases with p
221                    An A. salmonicida genomic DNA library was constructed by using lambda GEM-11 and r
222 n of the crab MIH and MO-IH genes, a genomic DNA library was constructed from DNA of an individual fe
223                                 An H. pylori DNA library was cotransformed into SE5000 (pHP8080) and
224          A large-insert domestic cat genomic DNA library was developed using a P1 artificial chromoso
225 ed from a P. radiata (Monterey pine) genomic DNA library was found to possess all of the sequence fea
226                                     A fosmid DNA library was prepared from a marine picoplankton asse
227                      A lambda ZAP II genomic DNA library was screened with the pool of antisera to or
228                                A new hairpin DNA library was selected based on affinity for immobiliz
229 OD gene isolated from a normal human genomic DNA library was used to determine the DNA sequence of Mn
230 tinylated RNA baits transcribed from genomic DNA libraries, we are able to capture DNA fragments from
231              By rational design of synthetic DNA libraries, we first evolve neurotensin receptor 1 fo
232 functional screen of mammalian complementary DNA libraries, we identified moesin as a novel gene whos
233 ing of a murine choroid plexus complementary DNA library, we identified a new chemokine, designated n
234              From an N. coriiceps testicular DNA library, we isolated a 13.8-kilobase pair genomic cl
235 ter 15 rounds of selection with a structured DNA library, we were able to isolate SRAs that possess l
236 igonucleotide sequences of a full complexity DNA library well below the value for the dissociation co
237 hese painting probes and their corresponding DNA libraries were developed by chromosome micromanipula
238                                      Genomic DNA libraries were generated from one miniature swine th
239                   Woodchuck cDNA and genomic DNA libraries were screened with woodchuck-specific DNA
240                                Complementary DNA libraries were sequenced by Solexa.
241  the RRBS method failed to generate reliable DNA libraries when using <2 ng of DNA, the RREM-seq meth
242 h to interrogate Sox2/Pax6 dimerization on a DNA library where five positions of the Pax6 half-site w
243  typically requires screening sizable random DNA libraries, which limits the designs to span merely a
244 ts from comparative experiments suggest that DNA libraries with increased chemical diversity, higher
245 ing data for both human and Escherichia coli DNA libraries with negligible coverage bias compared to
246 ermore, by constructing and screening random DNA libraries with the tet expression shuttle system, 78
247             Probing of a human complementary DNA library with anti-Ma serum resulted in the cloning o
248 uffling method to create a customized random DNA library with flexible sequence design and length.
249                   The screening of a genomic DNA library with polyclonal antisera raised against nati
250 nnewicki was isolated by screening a genomic DNA library with serum from a mare that had recently abo
251 liformis was isolated by screening a genomic DNA library with serum from a patient with the chronic v

 
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