ライフサイエンスコーパス: recombination event

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

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

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

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

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

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

7 man samples with virus originating from this recombination event.

8 ealing evidence of extensive duplication and recombination events.

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

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

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

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

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

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

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

16 between these subtypes have been ascribed to recombination events.

17 y either compensatory mutations or secondary recombination events.

18 hrough relatively small numbers of secondary recombination events.

19 bination to adaptively reverse almost lethal recombination events.

20 matic infections with viruses with secondary recombination events.

21 wheat lines with DT696 allele and additional recombination events.

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

23 both constrains and is altered by crossover recombination events.

24 stances between gene segments and facilitate recombination events.

25 everal known and novel nonallelic homologous recombination events.

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

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

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

29 tro model differs statistically from natural recombination events.

30 beans and detecting several hundred thousand recombination events.

31 rmally limit the frequency of these aberrant recombination events.

32 C3H were generated through relatively recent recombination events.

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

34 ies trees under horizontal gene transfer and recombination events.

35 is method requires two sequential homologous recombination events.

36 on pressures and the genomic distribution of recombination events.

37 A replication involved in fusion and allelic recombination events.

38 morphisms and mobile genetic elements and by recombination events.

39 B2-associated protein that ensures regulated recombination events.

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

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

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

43 A virus of yeast, are involved in interviral recombination events.

44 of these genes through multiple independent recombination events.

45 hods to visualize crossovers and to pinpoint recombination events.

46 tion loops that undergo complex dynamics and recombination events.

47 e used to recover relatively rare homologous recombination events.

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

49 matin and spatial environment for subsequent recombination events.

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

51 e genomic DNA through two joint illegitimate recombination events.

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

53 Recombination events across host orders, evolutionary re

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

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

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

57 netic diversity, numbers and distribution of recombination events along chromosomes vary among specie

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

59 positions indicative of cross-species virus recombination events among other betacoronaviruses of th

60 RNA recombination events among similar RNA viruses are frequ

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

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

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

64 ription is fixed in the products of an A1d1a recombination event and occurs somatically on other CTVT

65 ntal mtDNAs interacted through 28 homologous recombination events and a single case of illegitimate r

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

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

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

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

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

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

72 encing, we mapped the breakpoints of mitotic recombination events and other chromosome rearrangements

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

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

75 s involved in both intra- and intermolecular recombination events and that hosts like pepper could fo

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

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

78 the LRP reporter gene sequence leads to DNA recombination events and the expression of a range of tr

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

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

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

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

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

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

85 re fairly efficient as they rely on only one recombination event, and the probability of correct inse

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

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

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

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

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

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

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

93 The analysis provides evidence that recombination events are present in the Peninsular Malay

94 Bacteriophage T4 homologous recombination events are promoted by presynaptic filamen

95 Later-occurring recombination events are protected from Mph1-mediated di

96 Recombination events are regulated by two developmental

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

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

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

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

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

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

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

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

105 Recombination events at multiple loci in individual cell

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

107 be essential to prevent deleterious meiotic recombination events at repetitive centromeric sequences

108 th potential for regulation of site-specific recombination events at the protein level in vivo.

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

110 109 is likely the product of an interspecies recombination event between ancestral members of the HEV

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

112 een lost during domestication through a rare recombination event between male and female haplotypes.

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

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

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

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

117 Thus, naturally occurring homologous recombination events between 2 strains can involve numer

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

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

120 Crossover recombination events between homologous chromosomes are

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

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

123 represents T. pallidum strains that arose by recombination events between members of different T. pal

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

125 r to be the result of previously undescribed recombination events between ssDNA and ssRNA viruses.

126 Most recombination events between such pairs of maize polymor

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

128 Subsequent recombination events between these allele lineages have

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

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

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

132 than an order of magnitude, with half of the recombination events bypassing charge traps.

133 f a sweep coalesce during the sweep before a recombination event can occur, reducing their expected c

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

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

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

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

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

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

140 Further recombination events created different groupings in 5' a

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

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

143 oalescence, although the effects of multiple recombination events during a sweep are only treated heu

144 ene in recombinant-dependent AAV designs and recombination events during bacterial AAV plasmid produc

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

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

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

148 recombination analyses provided evidence for recombination events encompassing the 3'-end of the Rep

149 Data from recombination events, expression analysis, and sequence

150 me camel species, may have undergone similar recombination events facilitating its emergence or may d

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

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

153 ese genomes also display several presumptive recombination events for which gene truncation and ident

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

155 enoviruses that contain cross-species genome recombination events from three hosts: human, chimpanzee

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

157 morphisms affect the frequency of intragenic recombination events (gene conversions).

158 The recombination events generate conflicting phylogenetic s

159 Recombination events generated during a single cycle of

160 4 small, ancient HSV-1 x HSV-2 interspecies recombination events have affected the HSV-2 genome, wit

161 Several recombination events have been detected in RHDV strains,

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

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

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

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

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

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

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

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

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

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

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

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

174 However, the recombination events in African swine fever virus (ASFV)

175 ciency because it relies on two simultaneous recombination events in cis, an outcome that is dwarfed

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

177 an be primarily attributed to many identical recombination events in different cells, while abundant

178 that the sizes and locations of interspecies recombination events in HSV-2 are significantly more var

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

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

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

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

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

184 The recombination events in pepper were 1.8-fold higher than

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

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

187 Indeed, we have observed multiple recombination events in single recipients in real-time.

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

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

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

191 Genetic recombination events in the pathogen can generate hybrid

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

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

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

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

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

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

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

199 ppened as part of 11 simultaneous homologous recombination events involving 2 phylogenetically distan

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

201 individual latent proviruses but rather from recombination events involving multiple proviruses.

202 tions to intermolecular recombination and to recombination events involving relatively short (<200 bp

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

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

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

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

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

208 This recombination event is upregulated during immune respons

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

210 However, the interpretation of historical recombination events is hampered by the fact that driver

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

212 at metaphase and increased sister chromatid recombination events leading to rampant chromosome insta

213 ion of the genome can result in a cascade of recombination events leading to the generation of multip

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

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

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

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

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

219 However, intragenic recombination events not associated with flanking marker

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

221 train identified in this study, suggesting a recombination event occurred between the ''variant'' TGE

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

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

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

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

226 Such recombination events often lead to loss of heterozygosit

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

228 We describe 2 large (>5 kb) recombination events, one of which arose in its current

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

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

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

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

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

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

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

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

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

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

239 Mitotic recombination events resulting in extended loss of heter

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

241 ne in several ant species suggests that rare recombination events shape supergene evolution in surpri

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

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

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

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

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

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

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

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

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

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

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

253 , they play critical roles in the homologous recombination events that can restore broken ends of the

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

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

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

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

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

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

260 During meiosis, recombination events that occur between homologous chrom

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

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

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

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

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

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

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

268 Targeting recombination events to regions of interest allows us to

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

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

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

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

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

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

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

276 Recombination events were detected between these allelic

277 The recombination events were essentially associated with th

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

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

280 Mutational and recombination events were observed across clone progeny,

281 to each other across the homologs the fewer recombination events were observed.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

296 Recombination events within or between Asian and Brazili

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

298 and can be used by others to predict future recombination events within the enterovirus species A gr

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

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