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1 odification (e.g. the addition or removal of restriction sites).
2 nto unit-length genomes when cut at a unique restriction site.
3 istribution of ApaI conformations around the restriction site.
4 and catalytic activity and abrogates a DraI restriction site.
5 model for a DNA decamer containing the EcoRI restriction site.
6 he opposite strand just outside of the PvuII restriction site.
7 ible for the presence or absence of the PstI restriction site.
8 ve; all were due to point mutations within a restriction site.
9 d by O6-methylguanine, positioned within the restriction site.
10 DR method requires the introduction of a new restriction site.
11 vivo compared with individuals lacking this restriction site.
12 ase I-SceI that recognizes and cuts an 18-bp restriction site.
13 cific bases in a sequence and generate a new restriction site.
14 indexing sequence located juxtaposed to the restriction site.
15 -2, which causes a gain or loss of an NlaIII restriction site.
16 ragments that do not have a common or unique restriction site.
17 l tags that can be derived from a predefined restriction site.
18 108, 310 and 350pb), due to a conserved BsaI restriction site.
19 281 bp) due to a 16 S rDNA conserved Hinf I restriction site.
20 npredicted HinfI RFLP, resulting in an EcoRI restriction site.
21 wed absence of the conserved 16 S rDNA HinfI restriction site.
22 ctinomycin (Spc) and causes loss of one HpaI restriction site.
23 le changes typically involve the revision of restriction sites.
24 re facilitated by a repeated set of flanking restriction sites.
25 y cut lambda-phage DNA molecules at specific restriction sites.
26 ed a duplicated sgp region flanked by marker restriction sites.
27 h A and D genomes but differently flanked by restriction sites.
28 to digestion since it does not contain these restriction sites.
29 ion-PCR followed by digestion at polymorphic restriction sites.
30 ng recombinant molecules without reliance on restriction sites.
31 lity of the different nucleotides within the restriction sites.
32 d SVs with or without creating or destroying restriction sites.
33 into the PCR product to protect most of the restriction sites.
34 gene construction in the absence of suitable restriction sites.
35 ithout the limitation of naturally occurring restriction sites.
36 tifies genomes encoding systems with similar restriction sites.
37 such a family uses a specific combination of restriction sites.
38 on the creation of novel (SfiI) and (BstUI) restriction sites.
39 5-hmC at single base pair resolution at MspI restriction sites.
40 enic region that contains many commonly used restriction sites.
41 d by the limited availability of appropriate restriction sites.
42 a coli without dependence on suitably placed restriction sites.
43 vectors multiple cloning site with 10 unique restriction sites, (4) an oriT for conjugation-mediated
44 ions do not always occur within pre-existing restriction sites, a generalized PCR/RE/LDR method requi
45 solubility' mutations) flanked by convenient restriction sites, a translational enhancer, and a conse
46 ds and an antagonist showed that increase in restriction site accessibility correlates with transcrip
49 fficient algorithm to minimize the number of restriction sites against sets of cutter sequences, and
50 parative macrorestriction mapping using rare-restriction-site alleles (made with the Tn10dRCP2 family
52 ated in order to evenly distribute 25 unique restriction sites along the length of the gene while ret
56 ng the sequence complementary to the cleaved restriction site and a 4-nucleotide 'indexing sequence.'
58 causes skipping of exon 5, deleting an RsaI restriction site and decreasing the amounts of mRNA foun
60 the oligonucleotide and the template at the restriction site and sufficient complementarity overall
61 I was exchanged for that of mBE I at a BspHI restriction site and was purified to homogeneity and cha
62 that now contains the NotI, AscI, and EcoRV restriction sites and allows the rapid cloning of NotI-E
64 In addition, for each possible target site, restriction sites and primer candidates are visualized,
66 promoter type, restriction enzyme, number of restriction sites and with a noted exception, cell line.
67 e chain reaction primers containing internal restriction sites, and cloned into the phagemid pCOMB3H
68 d by the distribution of naturally occurring restriction sites, and requires minimal DNA sequencing.
69 3A26 hybrids were generated using convenient restriction sites, and site-directed mutagenesis was use
70 sequences lying adjacent to a given Type IIS restriction site are ligated between two DNA adapters.
72 chromosome size, gene order, and some of the restriction sites are conserved between the two phage gr
73 loped a novel physical assay in which HaeIII restriction sites are positioned within the telomeric tr
75 The spacer sequences between the nicking and restriction sites are tailored to create ss extensions o
77 It was concluded that point mutations at restriction sites are unlikely to account for the restri
79 ion sites, whereas R recognizes unmethylated restriction sites as non-self and introduces a double-st
83 ale biological sampling and phenotyping with restriction site associated DNA sequencing (RAD-Seq) dat
85 worldwide collections of P. triticina using restriction site associated genotyping by sequencing.
86 We tested the potential of double digested restriction-site associated DNA (ddRAD) sequencing for d
88 gant analysis (BSA) version of double-digest restriction-site associated DNA sequencing (BSA-ddRADseq
93 nation of flow cytometry and high-throughput restriction-site associated DNA tag sequencing, we show
94 , and eastern) via analysis of double digest restriction-site associated DNA using Next Generation Se
96 l wing-pattern variants, we used genome-wide restriction site-associated DNA (RAD) genotyping, tradit
100 gle-nucleotide variants (SNVs) by sequencing restriction site-associated DNA (RAD) tags in 138 Micant
101 gle-nucleotide variants (SNVs) by sequencing restriction site-associated DNA (RAD) tags in 138 Micant
102 We use quantitative trait loci analysis of restriction site-associated DNA -tag single nucleotide p
103 enerated and analyzed nuclear (double-digest restriction site-associated DNA fragment procedure [ddRA
104 pen source tool for assembling and analyzing restriction site-associated DNA sequence datasets using
106 sity genetic maps of Zoysia japonica using a restriction site-associated DNA sequencing (RAD-Seq) app
107 ed out a genome-wide association study using restriction site-associated DNA sequencing (RAD-seq) of
108 types from more than 1,000 individuals using restriction site-associated DNA sequencing (RAD-seq).
112 otide polymorphism data were produced from a restriction site-associated DNA sequencing protocol for
113 lizing PacBio long reads in combination with restriction site-associated DNA sequencing, and for dipl
116 h as pooled barcoded amplicon sequencing and restriction site-associated DNA tags, should be used to
117 Neurospora, we have adapted microarray-based restriction-site-associated DNA (RAD) mapping for use wi
118 t of RILs from a dense set of semicodominant restriction-site-associated DNA (RAD) markers and use si
119 Then, twenty of the offspring were used for Restriction-site-Associated DNA Sequencing (RAD-Seq) to
123 of 31 mayfly (Ephemeroptera) communities and restriction-site-associated-DNA sequencing in the four m
125 lion base pairs in length and used to insert restriction sites at any given nucleotide in a microbial
129 i and find that, in agreement with levels of restriction site avoidance, EcoRI, but not EcoRV, cleave
131 enoviral expression vector containing unique restriction sites between the human CMV-IE promoter and
135 35-fold-repetitive B1 locus identified three restriction sites capable of discriminating type I (mous
137 Using a combination of haplogroup-specific restriction site changes and control region nucleotide s
138 , including very high G+C content and enzyme restriction sites characteristic of an HTF-island, no TA
139 ed, six of which were identical for numerous restriction site characters to plastome types found amon
141 s approach facilitates cloning regardless of restriction site compatibility and overcomes an importan
143 etic resolution within the prior plastid DNA restriction site data, highlight plastid/nuclear incongr
145 ged constructs with no undesirable vector or restriction-site-derived amino acids added to the expres
146 lution has failed to eliminate many possible restriction sites despite selective pressure, thus motiv
148 A amplification products resolved diagnostic restriction site differences for I. fulva and I. hexagon
149 126 strains were obtained at 16 polymorphic restriction sites distributed on nine PCR fragments.
150 uction was verified by detection of a unique restriction site engineered into the SHRV genome between
152 I should facilitate the automation of cosmid restriction site fingerprinting needed for large-scale m
157 ng (a) a finely spaced DNA ladder carrying a restriction site for BamHI, (b) RNA translocation by DEx
159 gle alpha-factor repeat was constructed with restriction sites for cassette mutagenesis flanking the
160 A borders without compromising the choice of restriction sites for cloning, since the pGreen cloning
161 , and, in some cases, identifying endogenous restriction sites for downstream molecular genetic appli
162 ion was performed using primers that amplify restriction sites for MspAI (A2 polymorphism-CYP17) and
163 onsensus sequence upstream of the undigested restriction sites for possible methyltransferase recogni
164 by PCR using primers containing appropriate restriction sites for subcloning into pTETnirB, which co
166 s quantitated as a function of the number of restriction sites for the restriction enzymes carried by
167 oxynucleotide complex protects an individual restriction site from methylation, thus limiting subsequ
168 y EcoRI and DraI enzymes at their respective restriction sites, G downward arrow AATTC and TTT downwa
171 hetic vector arms from which the undesirable restriction sites have been removed by point mutations.
173 d mutation, TER1-Bcl, which generates a BclI restriction site in newly synthesized telomeric repeats,
179 This sequence alteration introduces a PleI restriction site in the nonsyphilis strains and thus all
181 e substitution abolished the conserved HinfI restriction site in the two PCR fragments with unpredict
183 The specific protection of only one of many restriction sites in a genome from inactivation by a cog
186 kelihood analysis of independent polymorphic restriction sites in humans reveals a decrease in effect
188 y is based on the deprotection of methylated restriction sites in synthetic oligonucleotides and can
189 ocations of the EcoRI, SacII, EagI, and NotI restriction sites in the clones, resulting in a high-res
192 o the appearance of PstI and loss of HindIII restriction sites in the pol region as a result of sever
193 he constant regions and 47% of the potential restriction sites in the variable regions were present i
194 codon optimization for any expression host, restriction site inclusion and exclusion, separation of
195 representing both minor gene editing events (restriction site insertion) to mimic gene correction, or
200 ifier: through additional silent mutations a restriction site is included or a previous one removed w
203 ic H1 gene (H1d) by introduction of suitable restriction sites just 5' of the TATA box and 3' of the
210 of locations at which RT switched templates, restriction site markers were introduced to divide the d
213 odified HIV-1 (NL-Mme) containing a type IIS restriction site, MmeI, at the right end of viral DNA.
214 oligomer-based library with minimal need for restriction site modification of sequences in the target
217 , the YAC clones revealed several additional restriction sites not previously detected in genomic DNA
218 single copy of Tn551 in the same chromosomal restriction site of both ISP479R and tPMPr transductants
219 ide duplex containing the iterated CG repeat restriction site of the NarI endonuclease has been deter
220 , we have developed protocols using the Notl restriction sites of any PAC or BAC clone to introduce a
221 Our analysis of DNA methylation-sensitive restriction sites of the 3' RR has revealed a similar mo
224 drug resistance genes and of several unique restriction sites on the plasmids enabled rigorous genet
225 o either ineffective cleavage at the cognate restriction site or relaxed specificity allowing cleavag
227 restriction enzymes, mutagenesis of internal restriction sites, or reamplification to add end homolog
228 limited by the presence of mutation-specific restriction sites, patients with neuropathy, ataxia and
230 d using genomic data generated by infrequent restriction site PCR and gene sequence analysis of the f
231 agment length polymorphism analysis, genomic restriction site polymorphism analysis, and plasmid cont
232 plogroups was surveyed through the published restriction site polymorphism and control region sequenc
238 sample of 31 Australian isolates by assaying restriction site polymorphisms from 11 protein encoding
239 detect an unprecedented number of genomewide restriction site polymorphisms from two N. crassa strain
243 DNA (400 bp of hypervariable region 1 and 14 restriction site polymorphisms) and Y-chromosome (20 bia
244 f 301 polymorphic markers, consisting of 228 restriction site polymorphisms, 63 microsatellites, two
246 Variation is assessed by use of 30 autosomal restriction-site polymorphisms (RSPs), 60 autosomal shor
249 mages and data are presented that locate six restriction sites, predicted from gel electrophoresis, o
250 performs the following tasks in gene design: restriction site prediction, codon optimization for any
252 lly silent single-base mutations that create restriction sites (restriction fragment length polymorph
254 the two alleles based on a polymorphic EarI restriction site showed that the Lys and Arg alleles had
256 relatively inexpensive method called nested restriction site-specific PCR (RSS-PCR) that generates a
257 CR-mediated generation of an artificial AluI restriction site specifically with the CRM197 DNA templa
262 it, as the T8399G mutation creates a unique restriction site that is not present in wild-type human
263 A probe and target DNA anneal to create a restriction site that is recognized by a strand-specific
265 tial fraction of subtelomeric DNA containing restriction sites that is not digested with enzymes such
266 nce of a variable methylation pattern at the restriction sites that prevented proper enzyme cleavage
267 ively demonstrating the marker mutations and restriction sites that were engineered into the componen
268 r sequence motifs besides the canonical GATC restriction sites, thereby expanding the utility of this
269 se H1 digests RNA that occludes the relevant restriction sites, thus preventing detection of these lo
270 (less than 3 kb); (ii) possess eleven unique restriction site to facilitate directional cloning; (iii
272 utation sites sometimes present some natural restriction sites to differentiate the wild-type and mut
273 applying it to data from a recent survey of restriction site variation in the chloroplast genome of
275 l mys subfamilies identified on the basis of restriction site variation occur in more than one specie
276 so enhanced integration events at random non-restriction sites via microhomology-mediated recombinati
277 nd methylation of a previously reported NotI restriction site was associated with dense CpG methylati
278 human motilin receptor containing 33 unique restriction sites was designed and stably coexpressed in
283 m the rates of recombination between the two restriction sites were 1 and 7% using Taq and Vent polym
284 P analysis also disclosed that the same AFLP restriction sites were digested in all of the fecal isol
285 the plasmids and because a number of unique restriction sites were present in the vector, studies we
286 , 8 affecting chromosome size and 3 altering restriction sites, were observed in these populations, w
287 s was constructed and five SNPs, residing in restriction sites, were selected for the development of
288 hylating short specific DNA sequences called restriction sites, whereas R recognizes unmethylated res
290 lted from the occurrence in the VL cDNA of a restriction site, which was cleaved during construction
291 s of DNA sequence polymorphisms that disrupt restriction sites, which allows RAD tags to serve as gen
292 he triplet code to design genomes that avoid restriction sites while producing the same proteins as w
293 d have been able to measure the positions of restriction sites with a precision of approximately 1.5
294 gene were characterized at eight polymorphic restriction sites within the beta-globin gene cluster.
300 pairs O6-methylguanine; PvuII cleaves at its restriction site, yielding a blunt-ended double strand,