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

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