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1 ation site in hDGAT1 was mutated by a single base pair substitution.
2 s particularly sensitive to reversion by DNA base-pair substitution.
3 tocols and facilitate the recovery of single base-pair substitution.
4 ation of the ssODNs enabled effective single-base-pair substitution.
5 imilar but shows a deletion plus a number of base pair substitutions.
6 DNAs that differed from each other by single base pair substitutions.
7                    All six are unique single base pair substitutions.
8 with an increased variant rate of synonymous base pair substitutions.
9 ifically cleaves a site with four contiguous base pair substitutions.
10 ng orientation in response to amino acid and base pair substitutions.
11 ial G4 is a source of mutagenesis leading to base-pair substitutions.
12 onucleotide duplexes containing I.C or other base-pair substitutions.
13 nts occur at only 1/10th the genomic rate of base-pair substitutions.
14 d undetectable with dsOligos carrying single base-pair substitutions.
15 mutations in a chosen gene, typically single base-pair substitutions.
16 mutations in the Mlh1 null cells were due to base-pair substitutions.
17 l as the slow, steady accumulation of single base-pair substitutions.
18 c landscape of these two species than single-base-pair substitution (1.2%).
19 Z.bailii substrate primarily due to a single base-pair substitution (A/T+5 --> T/A+5).
20 he affected patients had an identical single base pair substitution, a G-->A, at the -1 position of t
21 ts, was unexpectedly affected by a 1062/1076 base pair substitution; additional mutations were requir
22  three sister plaques showed only two single-base-pair substitutions after in vitro passage.
23                                              Base pair substitution analysis suggests that the sequen
24 c changes in this region, including a single base pair substitution and deletions of arginine repeats
25 all cells to each other where every call for base pair substitution and indel is classified as either
26 boxylase activity (encoded by pyrF), whereas base pair substitutions and an 18-bp deletion had no eff
27  low and the products comprised a mixture of base pair substitutions and deletions.
28                                          All base pair substitutions and mismatches were examined at
29                               In addition to base pair substitutions and one- or two-base deletions,
30 tent with E. coli DNA polymerase V-generated base-pair substitutions and that matched that of sequenc
31                       Over 22% of all single base-paired substitutions and 30% of all deletions and i
32  intragenic events, which were predominantly base-pairs substitutions, and loss of heterozygosity eve
33 rallels findings of in vivo experiments that base pair substitutions are induced by PdG in the former
34                            Recurrent somatic base-pair substitutions are believed to be less contribu
35              These homologs differ by single base pair substitutions as well as indels in regions cod
36          The mutant allele contains a single base pair substitution at amino acid 510.
37 this study, mutant Ter sites carrying single base pair substitutions at 16 different positions were e
38                                  M1G induced base pair substitutions at comparable frequencies in bot
39       The rank order of effects of canonical base pair substitutions at each position on kcat/Km was
40 n vitro competition assays demonstrated that base pair substitutions at positions 8-19 had significan
41                                              Base pair substitutions at potential CRP binding sites i
42 tation rates orders of magnitude higher than base pair substitutions at single-copy genes.
43 ion sequences, the consequences of analogous base pair substitutions at the same relative positions o
44 ds to partial intron inclusion, and a single base-pair substitution at an acceptor site, which gives
45  induced mutations were deletions and single-base-pair substitutions at or adjacent to the targeted P
46 ites contained symmetrical single and double base-pair substitutions at positions 4 and/or 5 [sequenc
47                                              Base-pair substitutions at positions 5 and 6 in U3 mostl
48 f a specific lamivudine-resistant virus with base-pair substitutions at the YMDD locus of the DNA pol
49 ties are not tightly coupled: individual DNA base-pair substitutions at those positions that signific
50 ngineer mouse strains with reciprocal single base pair substitutions (B6-Cdh23(c.753A>G) and 129S1-Cd
51                        The mutations include base pair substitutions (BPSs) and additions and deletio
52 ts of this reaction, frameshifts outnumbered base pair substitutions by greater than 70-fold.
53  specificity switches for multiple concerted base pair substitutions can be computationally designed,
54 ex (IDI), to more accurately determine which base pair substitutions can potentially occur in conserv
55     We describe how a small number of single-base-pair substitutions can generate hotspots de novo an
56 uch of its target site, such that few single base pair substitutions cause a significant decrease in
57                    The possibility that rRNA base pair substitutions compensate for variants in L11 a
58                       Cloning of BRAF double base-pair substitutions confirmed that both base changes
59 (and both parents heterozygous) for a single base pair substitution converting the codon for Arg-282
60                                       Tandem base-pair substitutions encoding V599R and V599K amino a
61 , can enhance the recovery of precise single base-pair substitution events tenfold.
62 deficient cells exhibited two well-separated base-pair substitution events.
63                        Single amino acid and base-pair substitutions had parallel effects on DNA bend
64 ntaining either 5' deletions or continuous 6-base pair substitutions identified a hyperosmotic stress
65 revealed a missense mutation due to a single base pair substitution in exon 6 in cpfl3.
66     Here, we report that a homozygous single base pair substitution in POLE1 (polymerase epsilon 1),
67 ects on protein levels of an adaptive single-base pair substitution in the coding sequence of a signa
68 inding to the AREs is diminished by a single base pair substitution in the core sequence.
69  likely to be caused by the same mutation, a base pair substitution in the G protein-coupled inwardly
70             The mutant results from a single base pair substitution in the rpoD gene that causes a Gl
71 of mice homozygous for an HDR-mediated three base pair substitution in the Tspan2 CArG box.
72 t of Bxb1 prophage orientation, and a single base pair substitution in the two sites is sufficient to
73 s-linked, consistent with the observation of base pair substitutions in 5'-d(CG) sites in the MDA-ind
74                       Among the six possible base pair substitutions in a lacZ reversion system, the
75  sequence-dependent frameshift mutations and base pair substitutions in bacteria and in mammalian cel
76 moter P1 of the C. crescentus dnaK gene, and base pair substitutions in either the -10 or -35 region
77  patients with a nearly identical cluster of base pair substitutions in exon 23.
78 ot present; instead, we found several single base pair substitutions in exons 2 and 6.
79 ividuals were discovered to have clusters of base pair substitutions in exons 23 and 25.
80 ot detect associations between the number of base pair substitutions in genes and their orientation o
81 binants, rOKAgI-Sp1 and rOKAgI-USF, with two base pair substitutions in Sp1 or USF sites, replicated
82                         We found that single base pair substitutions in the consensus sequence result
83            We examined the effects of single base pair substitutions in the high-affinity GerE bindin
84                                       Single base pair substitutions in this IRE decreased transcript
85  melanoma include a cell line possessing a 2 base-pair substitution in BRAF exon 11 and a case harbor
86 l to SL3 except for the presence of a single-base-pair substitution in each of the two core elements.
87   In a second family, there was a homozygous base-pair substitution in the alternative splice site of
88                                     A single base-pair substitution in the DNA binding sequence reduc
89                                     A single base-pair substitution in the first intron of Btk was id
90                                     A single base-pair substitution in the nieuwkoid/dharma gene resu
91                                   The single-base-pair substitution in the seed region of miR-184 is
92 ion mutation spanning the site of the single-base-pair substitution in trans.
93 gnition, we systematically introduced single base-pair substitutions in an a1-alpha2 DNA-binding site
94 site found at silencers, which contains four base-pair substitutions in comparison to the telomeric b
95  TA step was further tested by making single base-pair substitutions in Fragment 67 and the results r
96 cted novel dinB alleles, generated by single-base-pair substitutions in the dnaE915 strain, indicated
97    Mutant virus LST-4BS contains four single-base-pair substitutions in the ICP4 binding site in the
98                                 Compensatory base pair substitutions incorporated into the helical st
99 analysis of stem 1 hairpins and compensatory base-pair substitutions incorporated into helical stem 2
100                                 Compensatory base-pair substitutions incorporated into helical stems
101 tant alleles with two and occasionally three base-pair substitutions increased when the Pms2 and Mlh1
102 us to detect a variety of spontaneous single-base pair substitutions, insertions, and deletions, and
103 two regions of the TolC protein and included base-pair substitutions, insertions, and deletions.
104 sertion of linear plasmids containing either base-pair substitutions, insertions, or deletions in the
105 o, we have introduced an extensive series of base pair substitutions into an Mcm1 operator site and e
106                                              Base-pair substitutions introduced at these positions in
107                           This clustering of base pair substitutions is unusual and suggests that mut
108 s (LD50 < 900 PFU), although the four single-base-pair substitutions lie outside the coding region fo
109                       The spectrum of single-base-pair substitutions logged in The Human Gene Mutatio
110 cherichia coli and mammalian cells, inducing base-pair substitutions (M(1)dG --> A and M(1)dG --> T)
111 enced by DNA breathing dynamics, we designed base-pair substitutions, mismatch, and methylation modif
112                                  Two base or base pair substitution mutant RNAs which destabilize the
113 and was a compound heterozygote for a single-base-pair-substitution mutation and a novel, approximate
114                              Analysis of the base-pair-substitution mutations induced by recA730 in a
115  Mutations were represented mainly by single base pair substitutions (n = 63) with rare deletions/ins
116            The mutation consists of a single base pair substitution of the gene encoding the G-protei
117 ents of the effects of every possible single base-pair substitution of a consensus sequence, we defin
118     The effects of individual amino acid and base pair substitutions on heterodimer binding orientati
119  promoter by measuring the effects of single base pair substitutions on in vitro promoter activity.
120 nine base are explained by the impact of the base pair substitutions on the delocalized conduction ch
121 t cases the distance separating the multiple base-pair substitutions on a given allele was in excess
122 omain were influenced by the identity of the base pair substitution or mismatch as well as by the sit
123         I-CreI homing site mutants contained base pair substitutions or single base deletions that al
124 nB intragenic mutations examined were either base pair substitutions or those that we inferred to be
125                                     A single base pair substitution outside the sequences contacted i
126 ng an in silico screen, we identified single base-pair substitutions predicted to disrupt binding by
127 are evenly distributed and show a variety of base pair substitutions, predominantly transitions.
128                                              Base-pair substitution rates for the mitochondrial cytoc
129  surrounding DNA sequence on relative single-base-pair substitution rates was observed, which extende
130 ure-sensitive dnaE allele indicated a single base pair substitution resulting in a change from valine
131   In this report we identify a novel, single base pair substitution resulting in an amino acid exchan
132 esions delineated thus far consist of single-base-pair substitutions resulting in nonsense, missense,
133 e specificity of I-MsoI for three contiguous base pair substitutions, resulting in an endonuclease wh
134             Analysis of a series of 7- to 13-base-pair substitutions revealed two regions crucial for
135                                          The base pair substitution specificity and high fidelity for
136 Y955C derivative is 2-fold less accurate for base pair substitutions than wild-type pol gamma despite
137 however, stable alleles contain one to three base pair substitutions that interrupt the TNR tract.
138 e, involved in lignin biosynthesis, showed a base-pair substitution that is associated with decreased
139                             Most were single-base-pair substitutions that identified separate DNA- an
140             For RNA pairs distinguished by a base pair substitution, the deltaDeltaG values were clos
141 l but 6 of the 33 independent mutations were base pair substitutions, the majority of which (17/33; 5
142                              Although single base-pair substitutions throughout the entire DNA target
143 system that allows the rates of all possible base pair substitutions to be measured when the TRP5 loc
144 system could transfer each of 23 nonselected base pair substitutions to the recipient chromosome alon
145 24 with cysteine in TGFBI via ssODN-mediated base-pair substitution using CRISPR/Cas9 technology.
146                     Also, over 59% of single base-paired substitutions versus 20% of deletions and in
147                  In addition, 3.7% of single base-paired substitutions versus 30% of deletions and in
148 ons were large insertions and deletions, but base pair substitutions were also detected.
149 nt and repair-deficient E. coli strains, and base pair substitutions were quantitated by hybridizatio
150                     At each of the specified base pairs, substitutions were found which reduced promo
151 ne pyrimidine dimer, and predominantly makes base pair substitutions when replicating undamaged DNA.
152 icating undamaged DNA, Dpo4 is prone to make base pair substitutions, whereas Dbh predominantly makes
153 dsRBD] is sensitive to specific Watson-Crick base-pair substitutions which also inhibit RNase III.
154 ed DNA oligonucleotides can achieve targeted base-pair substitution with modest efficiency but high p
155 rked resolution enhancement upon GC/AU to GU base pair substitution, with two cases achieving high-re

 
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