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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.
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
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
30 tent with E. coli DNA polymerase V-generated base-pair substitutions and that matched that of sequenc
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
37 this study, mutant Ter sites carrying single base pair substitutions at 16 different positions were e
40 n vitro competition assays demonstrated that base pair substitutions at positions 8-19 had significan
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
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
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
59 (and both parents heterozygous) for a single base pair substitution converting the codon for Arg-282
64 ntaining either 5' deletions or continuous 6-base pair substitutions identified a hyperosmotic stress
67 ects on protein levels of an adaptive single-base pair substitution in the coding sequence of a signa
69 likely to be caused by the same mutation, a base pair substitution in the G protein-coupled inwardly
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
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
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
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
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
99 analysis of stem 1 hairpins and compensatory base-pair substitutions incorporated into helical stem 2
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
108 s (LD50 < 900 PFU), although the four single-base-pair substitutions lie outside the coding region fo
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
113 and was a compound heterozygote for a single-base-pair-substitution mutation and a novel, approximate
115 Mutations were represented mainly by single base pair substitutions (n = 63) with rare deletions/ins
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
124 nB intragenic mutations examined were either base pair substitutions or those that we inferred to be
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.
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
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
141 l but 6 of the 33 independent mutations were base pair substitutions, the majority of which (17/33; 5
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.
149 nt and repair-deficient E. coli strains, and base pair substitutions were quantitated by hybridizatio
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