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1 ia inter- and intragenomic recombination and spontaneous mutation.
2 reby limiting illegitimate recombination and spontaneous mutation.
3 integrity and do so, in part, by suppressing spontaneous mutation.
4 imply a role for yafN, yafO, and/or yafP in spontaneous mutation.
5 f Min 2 (Mom2) locus that is the result of a spontaneous mutation.
6 coli pol IV, which enhances the frequency of spontaneous mutation.
7 uivalent to approximately 100 generations of spontaneous mutation.
8 geting the pcaHG genes of A. tumefaciens for spontaneous mutation.
9 alleles appear in populations through random spontaneous mutation.
10 ern, though the condition has a high rate of spontaneous mutation.
11 that cells usually use and a major source of spontaneous mutation.
12 gnificantly different initial frequencies of spontaneous mutations.
13 arental origin trends for different types of spontaneous mutations.
14 mismatch repair (MMR) increases the risk of spontaneous mutations.
15 y involving pharmaceutical manipulations and spontaneous mutations.
16 out an accompanied increased accumulation of spontaneous mutations.
17 tuitous repair may be an important source of spontaneous mutations.
18 rotective mechanisms have elevated levels of spontaneous mutations.
19 t significantly increase the accumulation of spontaneous mutations.
20 Two sites showed selective enrichment of spontaneous mutations.
21 tiology composed of dominant-acting de novo (spontaneous) mutations.
23 s of PilC-mediated pilus phase variation and spontaneous mutation, a finding consistent with a role f
26 phenotype in such mice is due to accelerated spontaneous mutation accumulation, we crossed these muta
31 entation to deficiencies to map QTL at which spontaneous mutations affecting Drosophila abdominal and
34 ia coli results in an increased frequency of spontaneous mutation and an imbalance in dNTP pool level
36 2 protein functions in a process that avoids spontaneous mutation and insures faithful meiotic chromo
37 yp-resistant Mom2R phenotype resulted from a spontaneous mutation and linkage analysis localized Mom2
38 tandard approach for inferring properties of spontaneous mutation and necessitates further developmen
39 data provide a better understanding of EBOV spontaneous mutation and suggest that ribavirin may have
40 ation of nuclease activities led to frequent spontaneous mutations and accumulation of incompletely d
41 potential for epistatic interactions between spontaneous mutations and QTL affecting bristle number o
43 uency ( approximately 10(-2) to 10(-4)) than spontaneous mutations, and all phenotypes were reversibl
46 ble, error-prone DNA polymerase IV (DinB) in spontaneous mutation are resolved by the finding that mu
49 mmonium are in AMT4 and a high proportion of spontaneous mutations are caused by transposon-related e
50 Using data on older donors, we show that spontaneous mutations are not uniformly distributed thro
55 E. coli nfi(-)alkA(-) strain protected from spontaneous mutations arising in saturated cultures and
56 In this study, we present evidence for two spontaneous mutations as the molecular basis for this SC
61 ng cells, like other cells, probably undergo spontaneous mutation at a rate of 10(-9) per nucleotide.
62 , mutS60, results in almost normal levels of spontaneous mutations at 37 degrees C but above this tem
65 ty to select directly strains that contain a spontaneous mutation blocking the beta-ketoadipate pathw
66 select for Acinetobacter strains containing spontaneous mutations blocking expression of pcaH or -G,
73 y, as demonstrated by increased frequency of spontaneous mutations, chromosome nondisjunction, and te
74 to demonstrate that the measured effects of spontaneous mutations, combined with stabilizing selecti
75 oximately a 100-fold increase in the rate of spontaneous mutation compared with prophage-free strains
80 e-genome sequencing to identify nearly 1,000 spontaneous mutation events accumulated over approximate
81 were conducted to examine recombination and spontaneous mutation events within clusters of resistanc
83 inbred lines that were allowed to accumulate spontaneous mutations for 10, 19, and 47 generations.
85 ls deficient in MMR are grown anaerobically, spontaneous mutation frequencies are reduced compared wi
87 lementation of the JP26 mutY mutant restored spontaneous mutation frequencies to wild-type levels.
89 Strains lacking MutS exhibited increased spontaneous mutation frequencies, and reversion assays d
90 treated with DEA/NO had significantly higher spontaneous mutation frequencies, increased numbers of A
91 functional Fpg, MutY or Smn showed elevated spontaneous mutation frequencies; and, these mutator phe
93 howed that MmuNeil3 greatly reduced both the spontaneous mutation frequency and the level of FapyG in
94 ency, additional loss of Mbd4 does not alter spontaneous mutation frequency at the endogenous Dlb-1b
95 iability and no growth defects or changes in spontaneous mutation frequency but had increased sensiti
97 if the lack of poleta significantly elevates spontaneous mutation frequency in various organs and tis
100 2 cells results in an 8-fold increase in the spontaneous mutation frequency of lambdacII mutants comp
103 e are viable and do not show the increase in spontaneous mutation frequency or cancer incidence that
105 These results demonstrate that EBOV has a spontaneous mutation frequency similar to those of other
107 urther, and the mutant had a slightly higher spontaneous mutation frequency than the wild type in the
109 king both of these activities exhibit a high spontaneous mutation frequency, and here we show that al
110 osatellite instability (MSI) and an elevated spontaneous mutation frequency, characteristic of MMR-de
114 d not only strain-dependent increases in the spontaneous-mutation frequency but also shifts in mutati
115 estimates of the rate and fitness effect of spontaneous mutations generated by mutation accumulation
119 evealed that the underlying genes of natural spontaneous mutations high pigment 1 (hp1), high pigment
124 ecombination could be an important source of spontaneous mutation in cells that are not proliferating
125 y reported that in the Nuc1 rat, which has a spontaneous mutation in Cryba1 (the gene encoding betaA3
126 letions appear to play a much larger role in spontaneous mutation in D. melanogaster than in H. sapie
127 s of retinal amacrine cells from mice with a spontaneous mutation in Down syndrome cell adhesion mole
128 investigate the molecular nature and rate of spontaneous mutation in Drosophila melanogaster, we scre
132 esults reveal that ZIKV evolved to acquire a spontaneous mutation in its NS1 protein, resulting in in
137 r these conditions, the bacterium acquires a spontaneous mutation in the putative promoter region of
140 rophages, macrophages from mice that carry a spontaneous mutation in TLR4 (P712H) were hyporesponsive
141 (sw/sw)) mice previously reported to carry a spontaneous mutation in Wnt1 share major features of OI
142 p a high-resolution picture of the effect of spontaneous mutations in a hypermutator (DeltamutS) stra
143 y serotype M1 GAS strains have high rates of spontaneous mutations in covS during invasive GAS infect
147 y and mismatch repair, we accumulated 40,000 spontaneous mutations in eight diploid yeast strains in
151 ontribute significantly to the appearance of spontaneous mutations in microorganisms and in human dis
153 nthesis, our work identified the spectrum of spontaneous mutations in plastids and reveals that this
154 -lamp biomicroscopy, and ERG to discover new spontaneous mutations in strains from the Genetic Resour
158 far been described for these proteoglycans, spontaneous mutations in the human and induced deletions
163 e and a description of the properties of new spontaneous mutations in the unicellular green alga Chla
167 )Ink4a/Arf(-/-) mNSC-derived tumors revealed spontaneous mutations in Tp53 in vivo with subsequent do
168 opportunity to investigate the formation of spontaneous mutations in vaccinia virus, which encodes i
171 stigation had shown that a large fraction of spontaneous mutations inactivating Acinetobacter protoca
174 If so, our data imply that one generation of spontaneous mutation increases the developmental time by
175 major forces are postulated to contribute to spontaneous mutations: intrinsic DNA polymerase errors,
178 ave a mutator phenotype in which the rate of spontaneous mutation is greatly elevated, and they frequ
179 These results suggest that the site(s) of spontaneous mutation is in a gene(s) which lies upstream
182 most direct and unbiased method of studying spontaneous mutations is via mutation accumulation (MA)
183 ce of a resistant subclone that has acquired spontaneous mutations largely independent of initial the
184 n serum transferrin (Trf) as the result of a spontaneous mutation linked to the murine Trf locus.
185 uble helix, Watson and Crick suggested that "spontaneous mutation may be due to a base occasionally o
187 ur results show that much of the increase in spontaneous mutation observed in an exo1Delta strain is
190 P) degradation of RNA is responsible for the spontaneous mutations observed in an MMR-deficient backg
191 urable effect, suggesting that a fraction of spontaneous mutations occur as a result of dinB polymera
192 lly very low, and it is widely accepted that spontaneous mutations occur at defined, but different, r
193 urs while phage DNA is outside the host, and spontaneous mutations occur during phage DNA replication
195 --> T transitions, which are the most common spontaneous mutations occurring in living organisms and
196 rial cells varies widely depending on when a spontaneous mutation occurs during growth of the culture
197 udies, a synergistic increase in the rate of spontaneous mutations occurs in the absence of POLeta in
202 ombinant inbred congenic strain HcB-19 has a spontaneous mutation of the Txnip gene, and we now show
203 emains stable under cultural drift, i.e. the spontaneous mutation of traits in the population, still
207 arge experiment that examined the effects of spontaneous mutations on age-specific mortality rates in
210 ns in pcaH or -G were suppressed either by a spontaneous mutation or by a PCR-generated random mutati
211 , E2f2-, and E2f3-deficient cells, either by spontaneous mutation or by conditional gene ablation, pr
214 inase mutants have an increased frequency of spontaneous mutation, possibly due to uracil misincorpor
218 stood about the genome-wide impact of MMR on spontaneous mutation processes and the extent to which M
219 or MMR exhibit a 10- to 100-fold increase in spontaneous mutation rate (mutator phenotype), and inact
220 rains exhibited comparable increases in both spontaneous mutation rate and chromosome aberrations.
222 on of recD2 confers a modest increase in the spontaneous mutation rate and that the mutational signat
229 an explain why cancers arise even though the spontaneous mutation rate of differentiated mammalian ce
231 balance probably contributes toward the high spontaneous mutation rate of the mitochondrial genome.
232 3-L612M S. cerevisiae strain has an elevated spontaneous mutation rate that is likely due to reduced
234 -patch repair synthesis might lead to a high spontaneous mutation rate, unless subsequent steps in th
236 ation of ETH1 in apn1 strains also increased spontaneous mutation rates 9- or 31-fold compared to the
237 e, reduces DNA binding in vitro and elevates spontaneous mutation rates and resistance to MNNG treatm
238 processes requires that factors determining spontaneous mutation rates and spectra be identified and
239 NA backbone or mismatched base have elevated spontaneous mutation rates consistent with defective mis
240 A polymerases can also give rise to elevated spontaneous mutation rates if they are allowed to replic
242 Dm mutants were identified corresponding to spontaneous mutation rates of 10(-3) to 10(-4) per gener
243 siae was identified on the basis of elevated spontaneous mutation rates of haploid cells deleted for
245 decreasing SAM levels significantly affected spontaneous mutation rates, leading us to conclude that
247 narily conserved inhibitor of p53, caused by spontaneous mutation recently has been associated with a
248 was found to suppress the increased rates of spontaneous mutation, recombination, and chromosome loss
254 time appears critical to the suppression of spontaneous mutation; second, 3 weeks following exposure
255 these organisms exhibit rates and spectra of spontaneous mutations similar to MMR-bearing species, su
256 ains deficient in RNH35 displayed a distinct spontaneous mutation spectrum of deletions characterized
258 port provides experimental evidence that the spontaneous mutation T544I is a tissue culture adaptatio
259 evidence showing that it is the result of a spontaneous mutation (T544I) specific to tissue culture
260 icate two-to threefold higher frequencies of spontaneous mutations than in the mouse, with most of th
262 the molecular basis for high growth (hg), a spontaneous mutation that causes a 30-50% increase in po
264 in a region containing blind-sterile (bs), a spontaneous mutation that causes spermatogenic defects a
267 enA mtrR penB gonococcal strain (PR100) as a spontaneous mutation that increased resistance to penici
268 (Wa-1) mice inherit an autosomal recessive, spontaneous mutation that results in a postnatal reducti
269 pinal tract defects in mice homozygous for a spontaneous mutation that truncates the Dcc transcript.
270 r-naked hairless (Hr(N)) is a semi-dominant, spontaneous mutation that was suggested by allelism test
272 used a frameshift reversion assay to examine spontaneous mutations that accumulate in yeast strains d
273 g resistance (MDR) transporters, we isolated spontaneous mutations that altered the substrate specifi
274 ents were identified in a genetic screen for spontaneous mutations that caused colonies of strain D39
276 Pif1-deficient cells, which was relieved by spontaneous mutations that eliminated their ability to f
277 on was initiated with the following premise: spontaneous mutations that increase virus release will b
278 n Oxytricha and a template that can transmit spontaneous mutations that may arise during somatic grow
283 with each other and mismatch repair to limit spontaneous mutation to less than 1 per genome per cell
284 for a frequency as high as 2.8 x 10(-6) for spontaneous mutation to resistance to optochin and was 1
285 n frequency was accompanied by high rates of spontaneous mutation to rifampicin and nalidixic acid re
286 hpC mutants differed in their frequencies of spontaneous mutation to rifampin resistance and in their
287 correlated with DNA damage, the frequency of spontaneous mutation to rifampin resistance was studied.
288 To estimate these quantities, we allowed spontaneous mutations to accumulate for 10 generations i
290 to measure the genome-wide mutation rate for spontaneous mutations, using measurements of traits in i
291 t the DNA lesions responsible for changes in spontaneous mutation, viability, and alkylation sensitiv
294 n, we found that the rate of accumulation of spontaneous mutations was similar in fetuses produced by
299 in the low-risk families is mainly caused by spontaneous mutation with high penetrance in males and r
300 nce exchange between strains as well as from spontaneous mutation, with interstrain recombination bei
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