ライフサイエンスコーパス: recombination event

1 ecule has been lost due to an intramolecular recombination event.

2 ot be explained by one simple end-joining or recombination event.

3 nd provide evidence for a 30-kb H1-H2 double recombination event.

4 man samples with virus originating from this recombination event.

5 rand invasion but are unable to complete the recombination event.

6 ype originated from a C. parvum x C. hominis recombination event.

7 ), which is silenced as a consequence of the recombination event.

8 rom three non-contiguous regions in a single recombination event.

9 bination to adaptively reverse almost lethal recombination events.

10 matic infections with viruses with secondary recombination events.

11 mutations, taking into account the effect of recombination events.

12 both constrains and is altered by crossover recombination events.

13 stances between gene segments and facilitate recombination events.

14 y believed to result from illegitimate V(D)J recombination events.

15 regions of homology to control the order of recombination events.

16 nce of inhibitory effects of other (nascent) recombination events.

17 tro model differs statistically from natural recombination events.

18 beans and detecting several hundred thousand recombination events.

19 rmally limit the frequency of these aberrant recombination events.

20 C3H were generated through relatively recent recombination events.

21 e used to recover relatively rare homologous recombination events.

22 her than has been observed for other Ty1-Ty1 recombination events.

23 is method requires two sequential homologous recombination events.

24 on pressures and the genomic distribution of recombination events.

25 matin and spatial environment for subsequent recombination events.

26 A replication involved in fusion and allelic recombination events.

27 morphisms and mobile genetic elements and by recombination events.

28 B2-associated protein that ensures regulated recombination events.

29 SB) repair or genes involved in other repeat recombination events.

30 reference line, capturing a total of 136,000 recombination events.

31 y by the incorporation of a refined model of recombination events.

32 chromosomes arise through BP3:BP3 or BP4:BP5 recombination events.

33 features that were predictive of homologous recombination events.

34 stranded ends that are generated during many recombination events.

35 f lesional tissue demonstrating Cre-mediated recombination events.

36 plastid DNA (ptDNA) introgression and micro-recombination events.

37 tial for DNA replication, transcription, and recombination events.

38 e genomic DNA through two joint illegitimate recombination events.

39 y evolve in the host by random mutations and recombination events.

40 peats) to build mapping panels with targeted recombination events.

41 -LTR form, thought to result from homologous recombination events.

42 us 1 might have arisen from multiple genetic recombination events.

43 stantial increase in usage of TRAV12 in Tcrd recombination events.

44 d do not elucidate the frequency or range of recombination events.

45 pected effects of global DSB levels on local recombination events.

46 cleotide and copy number variants as well as recombination events.

47 between these subtypes have been ascribed to recombination events.

48 y either compensatory mutations or secondary recombination events.

49 hrough relatively small numbers of secondary recombination events.

50 ere the Satellite chromosome arose by a rare recombination event about 500,000 years ago.

51 We found that recombination events across the 40kb stretch were relati

52 most likely arose from sequential ancestral recombination events across the region.

53 nic effects in deletion and intrachromosomal recombination events against ethyl methanesulfonate and

54 ia that stimulates certain site-specific DNA recombination events, alters DNA topology, and serves as

55 ustering of new genomes, (iii) detect recent recombination events among different evolutionary lineag

56 We show that recombination events among distantly related Athila retr

57 Interestingly, we also found evidence of recombination events among qnr alleles that may lack any

58 g HAdVs is needed to better predict possible recombination events among wild-type viruses and adenovi

59 is the difficulty of identifying homologous recombination events amongst non-specific events.

60 equisite length are created through uncommon recombination events, an alternative mode of apex bindin

61 in South America and Haiti, revealing recent recombination events and adaptation to a broad host and

62 odels that can be used to predict historical recombination events and can model background linkage di

63 ile sites." Using DNA microarrays, we mapped recombination events and chromosome rearrangements induc

64 rimental and bioinformatic identification of recombination events and genome-wide recombination hotsp

65 te and reliable identification of individual recombination events and global recombination rate param

66 neous SCEs are the end product of endogenous recombination events and implicates FANCD2 in the promot

67 d nonrandom coincidence of Cre-mediated loxP recombination events and meiotic recombination events wh

68 n complex viral ecosystems, through frequent recombination events and mutations.

69 ergence of viable recombinants by decreasing recombination events and reducing the ability of the rec

70 ocations that resulted from illegitimate RAG recombination events and resembled oncogenic translocati

71 roposed lineage suggested the possibility of recombination events and revealed differences in coding

72 The strong correlation between non-allelic recombination events and the effects of the alternative

73 Spatiotemporal characteristics of recombination events and the emergence of this previousl

74 on and inactivation of T cell receptor locus recombination events and the phenomenon of Tcrb allelic

75 for our understanding of the distribution of recombination events and the processes that govern them.

76 nts of Rad51 recombinase to prevent spurious recombination events and unwind trinucleotide sequences

77 significant associations between intragenic recombination events and variation in gene expression an

78 SIGLEC13 was deleted by an Alu-mediated recombination event, and a single base pair deletion dis

79 ory of this outbreak in detail, identified a recombination event, and investigated whether there was

80 There was evidence of point mutations, recombination events, and coinfection with epidemic and

81 Recombination Graph, sampling only relevant recombination events, and using augmented skip lists to

82 f divergence appears to be a hotspot for DNA recombination events, and we suggest that this region ha

83 inally, we show that the placement of female recombination events appears to become increasingly dere

84 We find that many recombination events are associated with repair of doubl

85 negative regulation will help to ensure that recombination events are dispersed evenly and arranged o

86 opose that initial V(beta)-to-D(beta)J(beta) recombination events are generally monoallelic in develo

87 mosomal abnormalities that likely arise from recombination events are more prevalent in multiple huma

88 Bacteriophage T4 homologous recombination events are promoted by presynaptic filamen

89 Recombination events are regulated by two developmental

90 host, viruses with between 1 and 3 secondary recombination events arose, which had greatly increased

91 ata demonstrated genetic flow and homologous recombination events around mutS.

92 ditionally determine insertion, deletion and recombination events as well as to detect complex sequen

93 However, recombination events at a subset of CO-designated sites

94 Os), we performed high-resolution mapping of recombination events at an intensely active mouse hot sp

95 cycles-to phase the personal genome and map recombination events at high resolution, which are nonun

96 Regulation of V(D)J recombination events at immunoglobulin (Ig) and T-cell r

97 t-after factor that suppresses inappropriate recombination events at mammalian replication forks.

98 Recombination events at multiple loci in individual cell

99 equential switching, and reduces intraswitch recombination events at native Smu.

100 sperm DNA has provided a means of monitoring recombination events at specific hotspots in male meiosi

101 meric RNA structure and causes a decrease in recombination events at the 5' end of the viral genome.

102 Using this technique, we analyzed recombination events at the Hlx1 hotspot located on mous

103 plotypes, the approach can directly identify recombination events (averaging 1.1 per chromosome) with

104 109 is likely the product of an interspecies recombination event between ancestral members of the HEV

105 a patient spanning exon 35 as a result of a recombination event between flanking intronic Alu sequen

106 ain class switch is mediated by a deletional recombination event between micro and gamma, alpha, or e

107 f SAFV and preliminary evidence of a distant recombination event between the ancestors of the Theiler

108 (S) regions, with CSR involving a deletional recombination event between the donor Smu region and a d

109 Allele KIR3DL1*009 resulted from a gene recombination event between the inhibitory receptor alle

110 This amplification arises from a recombination event between two flanking Ty1 elements to

111 s within individual molecules and homologous recombination events between different DNAs at their tel

112 is caused by meiotic non-allelic homologous recombination events between flanking low copy repeats t

113 Crossover recombination events between homologous chromosomes are

114 ersification, supported by finding ancestral recombination events between isolates from different lin

115 on mediated by meiotic nonallelic homologous recombination events between low-copy repeats, also know

116 ions can also be introduced by nonreciprocal recombination events between paralogous sequences, a phe

117 Most recombination events between such pairs of maize polymor

118 Pilin Av is the result of RecA-mediated recombination events between the gene encoding the major

119 and the JEV system, we detected two aberrant recombination events, both of which yielded unnatural ge

120 , the Srs2 helicase eliminates inappropriate recombination events, but the functional equivalent of S

121 lineages, (iv) manual inspection of detected recombination events by similarity plots and (v) annotat

122 n subnuclear positioning may influence locus recombination events by unknown mechanisms.

123 NA recombination, rare inter-molecular mtDNA recombination events can also occur.

124 In addition, rare recombination events can occur across shorter repeats, c

125 to full recovery, small numbers of secondary recombination events can still yield tremendous fitness

126 ways, the probability distribution of hidden recombination events cannot be inferred directly from th

127 t subtypes; these sites may be segregated by recombination events, causing the newly generated inters

128 at BRCA1 influences post-synaptic homologous recombination events, controlling the balance between sh

129 Further recombination events created different groupings in 5' a

130 2) that the first to enter meiosis have more recombination events (crossovers) than those that enter

131 In intra-molecular recombination events, deletion breakpoints were close to

132 Further experiments showed that a subset of recombination events destined to become crossover produc

133 This result explains why the frequency of recombination events does not increase with increasing d

134 types, one of which corresponds to crossover recombination events during or prior to SC formation.

135 -switching' lentiviral vector that harnesses recombination events during reverse-transcription.

136 gradually increasing selection pressure, and recombination events either at the end or dispersed thro

137 Data from recombination events, expression analysis, and sequence

138 ent from the wild-type situation, programmed recombination events failed to take place in the rDNA-R

139 tion, with punctuated, biologically relevant recombination events for the survival of viruses, both a

140 By combining data sets, we have collected recombination events from over 100,000 meioses and have

141 Visual selection was used to select recombination events from which fertile plants were rege

142 Recombination events generated during a single cycle of

143 This recombination event has created a new 1,125-bp-long open

144 Several recombination events have been detected in RHDV strains,

145 species contains multiple subtypes and that recombination events have occurred across the astrovirus

146 ions of parental genomes contributing to the recombination events highlighted a dynamic virome where

147 ss through the acquisition of ToV-PLP from a recombination event.IMPORTANCE Enteroviruses comprise a

148 cated potential horizontal gene transfer and recombination events important for the evolution of A1 s

149 us to hypothesize that type V emerged from a recombination event in a type IX background.

150 the cox2 polymorphism can be attributed to a recombination event in the mitochondrial DNA, the nad2 t

151 le nucleotide polymorphisms to precisely map recombination events in 12 artificial maize segregating

152 We identified 56 recombination events in 56 proviruses; the distribution

153 -based system was designed previously to map recombination events in a 459-bp region spanning the pri

154 pplications, including direct observation of recombination events in a family trio, deterministic pha

155 concentration affects the amount and type of recombination events in a growth-phase-dependent manner.

156 two tightly linked loci (Rf1 and Rf2) by <10 recombination events in a large (N = 6153) fine-mapping

157 at PARI inhibits DNA repair synthesis during recombination events in a PCNA interaction-dependent way

158 hromosome, ranging from a virtual absence of recombination events in a region estimated to be >30 Mb

159 We also reveal that most recombination events in both human and avian HBV tend to

160 n exons are assembled by RAG-initiated V(D)J recombination events in developing gammadelta thymocytes

161 g effects of micronutrient status on meiotic recombination events in human sperm.

162 to genome rearrangements through nonallelic recombination events in humans and other organisms.

163 d frameshift mutations as well as homologous recombination events in intraspecific Arabidopsis hybrid

164 ty, we found evidence for 14 QTLs in only 32 recombination events in less than 3000 mice, and with an

165 ly affects the frequency and distribution of recombination events in maize.

166 The data suggest that common recombination events in prevalent Vbeta genes may provid

167 Based on 109,273 phased SNPs, recombination events in RILs were identified, and a tota

168 Sequencing of the viral RNAs revealed recombination events in the 3' untranslated region of RN

169 levels of interaction when in cis to meiotic recombination events in the budding yeast Saccharomyces

170 To carry out homologous recombination events in the cell, recombination proteins

171 By mapping the distribution of recombination events in the genome of flock house virus,

172 Genetic recombination events in the pathogen can generate hybrid

173 In contrast, intrachromosomal recombination events in the progeny decrease with the ag

174 aplotypes IRiS first detects high confidence recombination events in their shared genealogy.

175 sfully detected multiple sub-populations and recombination events in these diverse mixtures.

176 t topology for some retroviruses, suggesting recombination events in which heterologous env sequences

177 age excision involves a second site-specific recombination event, in which the sites generated by int

178 rmined to frequently result from non-allelic recombination events, including non-reciprocal transloca

179 potential, tropism trait, coding potential, recombination event, integration age, and primer binding

180 An ancestral translocation or recombination event involving SRK/SCR and Lal2/SCRL like

181 PCR and sequence analyses revealed a recombination event involving three RepMP1-containing ge

182 l sequences in avian genomes for evidence of recombination events involving env.

183 c antirecombination function that suppresses recombination events involving more than two DNA duplexe

184 ts suggest 6C strains arose from independent recombination events involving only serotype 6A and 6C p

185 f magnitude higher than observed for mitotic recombination events involving single-copy genes.

186 and core X in stabilizing the genome against recombination events involving telomeric sequences.

187 evolution, cross-species transmissions, and recombination events involving the env gene.

188 In addition, two further interspecies recombination events involving the S gene were identifie

189 had at least one evolutionarily significant recombination event, involving IYSVBR and IYSVNL.

190 We described unreported large recombination events, involving the cps IV operon and re

191 This recombination event is upregulated during immune respons

192 on genetic data about whether one of the two recombination events is absent.

193 The spatial distribution of recombination events is strongly positively correlated b

194 This naturally occurring recombination event may have broad implications for othe

195 ar mating system was initiated by an ectopic recombination event mediated by similar repetitive centr

196 f the IE2 proteins occurs only following DNA recombination events mediated by Cre and FLP recombinase

197 n - acting to initiate a replication-coupled recombination event mediating a cell type change.

198 gether, these results suggest that potential recombination events might have happened frequently duri

199 This kept the overall number of intragenic recombination events nearly invariable in a given popula

200 However, intragenic recombination events not associated with flanking marker

201 variety of organisms the majority of meiotic recombination events occur at a relatively small fractio

202 These ectopic recombination events occur at nearly all Y-linked palind

203 tional TCR loci contain evidence that such a recombination event occurred, rather they demonstrate a

204 Intriguingly, recombination events occurred as a founding event of mos

205 A series of recombination events occurred over this period, which ha

206 Furthermore, within genogroups, sporadic recombination events occurred, such as the linkage of tw

207 o a valid lower bound for the true number of recombination events occurred.

208 sm, we have observed reproducible asymmetric recombination events occurring at specific locations in

209 ods that allow analysis of nearly all of the recombination events occurring in a single meiosis.

210 equencing has also been employed to identify recombination events occurring within the genomes of hig

211 Such recombination events often lead to loss of heterozygosit

212 nt study, we quantify the relative excess of recombination events on smaller chromosomes by a linear

213 The rearrangement involved two recombination events, one with a contaminant having a wi

214 es that were either directly involved in the recombination events or located in the intervening seque

215 s to have been caused by multiple homologous recombination events or possibly prophage replacement.

216 ter progeny; this evidence suggests that the recombination event partially alleviates clonal interfer

217 s accompanied by a decrease in the number of recombination events per gene.

218 he main mechanisms controlling the number of recombination events per meiosis is CO homeostasis, whic

219 Thus, NCO recombination events play a substantial role in mammalia

220 able to consider genetic histories including recombination events, precluding their use on most align

221 sequence variation correlated with estimated recombination events, predicted amino acid changes, and

222 T cell receptor alpha recombination in which recombination events progress in multiple small steps do

223 mplicates a role for BLM helicase in meiotic recombination events, prompting us to explore the meioti

224 n terms of minimal histories of mutation and recombination events, quantifying the scales and identif

225 t of samples contain frequent homoplasies or recombination events quasi-median networks will have a c

226 onses and viral evolution indicated that the recombination events quickly facilitated viral escape fr

227 s maximal at the centromeres, and homologous recombination events result in homozygosity toward the t

228 Mitotic recombination events resulting in extended loss of heter

229 lations is to estimate the minimum number of recombination events, Rmin, in the history of a DNA samp

230 meiotic program, the number and location of recombination events, sex chromosome segregation, and ch

231 tested the method by generating a panel with recombination events spaced along a yeast chromosome arm

232 s an important model system for studying DNA recombination events such as HIV-1 DNA integration and R

233 ting the cellular milieu toward illegitimate recombination events such as iHR and CN-LOH.

234 nine-based herbicides, control the timing of recombination events such as marker excision, influence

235 condition is prevalent for markers flanking recombination events, suggesting that recombination occu

236 Immunoglobulin (Ig) isotype switching is a recombination event that changes the constant domain of

237 alled "flesh-eating" bacterium) identified a recombination event that coincides with the global M1 pa

238 ionary relationship, with Rpg1b containing a recombination event that combined a NB domain closely re

239 med and spread, we estimated the date of the recombination event that generated the 2k/1b strain usin

240 R/cd, consistent with previous data that the recombination event that led to the generation of XMRV c

241 ghly choreographed, site-specific homologous recombination event that replaces one MAT allele with di

242 on into cells was assessed by a CRE-mediated recombination event that resulted in beta-galactosidase

243 t a new method to reconstruct the history of recombination events that affected a given sample of bac

244 The t-circles most likely arose from recombination events that also resulted in telomere trun

245 f the cell cycle, in contrast to spontaneous recombination events that are initiated by double-strand

246 erochromatin structures that prevent illicit recombination events that cause genomic instability.

247 leaps in protein function occur through gene recombination events that connect two or more protein do

248 Haplotype analysis revealed potential recombination events that could reduce the size of the c

249 r chromatid recombination in the CUP1 array; recombination events that delete the URA3 insertion from

250 Moreover, the recombination events that did take place at the nuclear

251 n chromosomes that show evidence of atypical recombination events that involve regions outside the co

252 re clustering is required for the homologous recombination events that maintain chromosome ends in ce

253 s or sequence fragments and detect candidate recombination events that may later be further analyzed

254 eneities in the average frequency of meiotic recombination events that occur along the physical exten

255 During meiosis, recombination events that occur between homologous chrom

256 S locus comprising several genes, with rare recombination events that result in self-fertile homosty

257 s that they were derived from one another by recombination events that scrambled the four major pepti

258 the position of LOH in multiple independent recombination events to a resolution of approximately 4

259 tool that provides high diversity and dense recombination events to allow routine quantitative trait

260 h was designed to allow the products of rare recombination events to be selected and amplified.

261 data would suggest that the "designation" of recombination events to become crossovers is separable f

262 e that HIM-6/BLM enforces biased outcomes of recombination events to ensure that both (a) CO-designat

263 uation to relate radiative and non-radiative recombination events to measured photoluminescence effic

264 n breakpoints) and the capacity of secondary recombination events to recoup these costs.

265 Targeting recombination events to regions of interest allows us to

266 iation, and then targeting a high density of recombination events to the region of interest.

267 These cagY recombination events typically lead to a reduction in T4

268 ertion/deletions in DNA and also affects the recombination events underlying pilin antigenic variatio

269 uced interhomolog recombination, we analyzed recombination events using a reporter in mouse embryonic

270 urther reports of such group exist, but this recombination event was also detected in an Iberian hare

271 callus stage, and one DD43 homology-directed recombination event was transmitted to T1 generation.

272 n increase in the number of genes containing recombination events was accompanied by a decrease in th

273 Recombination events were detected between these allelic

274 Eight recombination events were localized to different sites i

275 We found that the recombination events were nonrandomly associated with a

276 originated from the Emv30 provirus and that recombination events were not necessary for virus replic

277 The lines carrying the critical recombination events were tested for whole plant frost s

278 diated loxP recombination events and meiotic recombination events when the two occurred at linked pos

279 ecause rare centromeric (or pericentromeric) recombination events, when they do occur, can disrupt pr

280 esis, in addition to the virus evolution and recombination events which have, on occasion, resulted i

281 rint at the mating-type locus1 initiates the recombination event, which is required for cellular diff

282 ntly are associated with a second homologous recombination event, which may be related to the mitotic

283 the allelic variation that results from this recombination event, which replaces the chromosomal regi

284 stis jirovecii genome, we can infer multiple recombination events, which are consistent with meiotic

285 the 56 proviruses analyzed, we identified 96 recombination events, which are significantly more frequ

286 inase enzyme (RAG1/2) in a defined series of recombination events, which drive the progression of B a

287 to the target DNA substrate ensures that the recombination event will not damage the DNA.

288 variants although one showed evidence for a recombination event with a P.t.e.-derived HBV variant in

289 result of independent nonallelic homologous recombination events with a frequency of approximately 0

290 We detect hundreds of thousands of recombination events, with single-nucleotide resolution,

291 In addition, we identified an intersubclade recombination event within EV-D68, the first recombinant

292 HAdV-C6 contains a recombination event within the constant region of the he

293 We propose that strand exchange during recombination events within guanine-rich segments, could

294 Recombination events within or between Asian and Brazili

295 J-Western group is attributable to ancestral recombination events within the 5' region of cagA.

296 Seven lines with recombination events within the CBF cluster were used to

297 Recombination events within the rDNA appear to contribut

298 ithms for recombination detection identified recombination events within the S segment.

299 fter HIV superinfection coincides with rapid recombination events within two narrow regions of Gag an

300 almost lethal, and 91 consecutive secondary recombination events would be required to reconstitute e