ライフサイエンスコーパス: gene pool

1 are significant contributors to the oceanic 'gene pool'.

2 bility of genetic variability in the primary gene pool.

3 al structure was observed in the C. baccatum gene pool.

4 survival of the APOE epsilon4 allele in the gene pool.

5 the chromosomal background and the flexible gene pool.

6 e detrimental to the integrity of the native gene pool.

7 p between Basmati varieties and the Japonica gene pool.

8 quency in the West African than the European gene pool.

9 aladaptive alleles into the modern sunflower gene pool.

10 counts for 50.6% of the Tibetan Y-chromosome gene pool.

11 injection of a biased set of genes into the gene pool.

12 ion for salt tolerance within the cultivated gene pool.

13 rise a significant fraction of Earth's phage gene pool.

14 roteins that could be produced from a finite gene pool.

15 leles remain within the cultivated sunflower gene pool.

16 cies I to identify the conserved chromosomal gene pool.

17 urrently characterized avian influenza virus gene pool.

18 ed breeds, each of which represents a closed gene pool.

19 in the remaining 352 members of the variable gene pool.

20 ad a considerable influence on the Icelandic gene pool.

21 Neanderthals) have contributed to the modern gene pool.

22 gnized allelic isoforms present in the human gene pool.

23 VSG) genes and are thought to expand the VSG gene pool.

24 ent an ancestral mutation within the Italian gene pool.

25 f sustaining diversity of the global poultry gene pool.

26 largely replacing the Magdalenian-associated gene pool.

27 ssion of alleles from a pre-adapted northern gene pool.

28 wer1 and Autoflower2, exist in the C. sativa gene pool.

29 he region and the makings of the South Asian gene pool.

30 have significantly impacted the present-day gene pool.

31 most of which belonging to the Mesoamerican gene pool.

32 ns and contributed to the contemporary human gene pool.

33 yes access to a diverse and exploitable wild gene pool.

34 antly related wild relatives in the tertiary gene pool.

35 that reshuffled the ancestral Tibeto-Burman gene pool.

36 on of novel genes or alleles from the exotic gene pool.

37 r a genetic continuity model in the maternal gene pool.

38 vourable functional variation in the primary gene pool.

39 laining the formation of the modern Armenian gene pool.

40 c resources already available for the Andean gene pool.

41 populations through the sharing of a common gene pool.

42 among the founders of the domestic dromedary gene pool.

43 wer LGD load than typical genes in the human gene pool.

44 ahmaputra valley as the source of the indica gene pool.

45 ts small size and low frequency in the wheat gene pool.

46 icial rare genetic variation from the future gene pool.

47 ld best be practised within each common bean gene pool.

48 selectively eliminate the mutation from the gene pool.

49 contributed to the formation of the Na-Dene gene pool.

50 NA screening program in a breed with a small gene pool.

51 ng Middle American gene pool from the Andean gene pool.

52 manner consistent with a dynamic horizontal gene pool.

53 for all micronutrients than the world's Musa gene-pool.

54 domestication alleles between divergent rice gene pools.

55 ically reduce genetic diversity within elite gene pools.

56 ut varied considerably among deeply diverged gene pools.

57 vely, and 3432 SNPs could differentiate both gene pools.

58 and 11,805 SNPs could differentiate the two gene pools.

59 e development of two geographically distinct gene pools.

60 t of the Mesoamerican and Andean P. vulgaris gene pools.

61 important for the enrichment of African tea gene pools.

62 ate the split of the Mesoamerican and Andean gene pools.

63 lf was too rapid to be manifested in the moa gene pools.

64 of designated resistance genes in the wheat gene pool(1).

65 The post-Africanization gene pool (1998-2001) was composed of a diverse array of

66 ly facilitate characterization of the global gene pool accessible to individual bacterial species.

67 mpacts may be reduced through the sharing of gene pools amongst wheat breeding programs.

68 Narrow gene pools, an overemphasis on the sodium exclusion mech

69 ge" between the cultivated or primary potato gene pool and distantly related wild relatives in the te

70 n with clonal groups emphasize the extensive gene pool and frequent horizontal DNA transfer events th

71 This suggests a common gene pool and gene swapping of cyanophage-specific genes

72 ica, in the preservation of the patrilineage gene pool and in the affirmation of identity between gro

73 similarities to the early European Neolithic gene pool and modern-day Sardinians, as well as a geneti

74 omly selected from 184 soybean seed specific gene pool and their expressions were quantified using qu

75 y-wide access to the plasmid-borne accessory gene pool and thus potentiating future evolvability.

76 y mouse are derived from a limited ancestral gene pool and thus QTL detected in multiple crosses are

77 This suggests that Nc have the potential AMR gene pool and transfer sequences that can result in resi

78 MSP demethylation pathway dominated the DMSP gene pool and was harboured mostly by members of the alp

79 ing groups/clades of organisms with distinct gene pools and genomic properties, which may confer dist

80 ility to invade and proliferate in microbial gene pools and like symbionts when they coevolve with th

81 ons while in relative isolation from surface gene pools and their common ancestral populations of ori

82 the wide genetic background of the UK wheat gene pool, and facilitates tracing the origin of benefic

83 omo lineages contributed to the modern human gene pool, and more importantly, whether such contributi

84 Yangtze valley as the source of the japonica gene pool, and populations in Indochina and the Brahmapu

85 n-reducing alleles should be purged from the gene pool, and yet decades of genome-wide association an

86 equence clusters have recombined with shared gene pools, and show that these pools have distinct stru

87 this range, the species is divided into two gene pools (Andean and Middle American) along a latitudi

88 have also shown that a common "proto-Ugric" gene pool appeared in the Bronze Age from the admixture

89 etic improvement requirements that extensive gene pools are able to accommodate.

90 The concept and content of a crop's gene pools are being changed by advancements in plant sc

91 ority of the Lingayat and Vokkaliga paternal gene pools are composed of four Y-chromosomal haplogroup

92 mainly developed from the cultivated soybean gene pool, are losing resistance due to SCN race shifts.

93 individuals emerged from the same ancestral gene pool as early farmers in other parts of Europe, sug

94 thic central Anatolians belonged to the same gene pool as the first Neolithic migrants spreading into

95 manner, accompanied by gradual separation of gene pools as evidenced by increased habitat specificity

96 ervation and exploitation of the primary WEW gene pool, as a valuable resource for discovery of resis

97 By regrouping the gene pool-as in speciation-aneuploidy inevitably will al

98 Nevali Cori and Ba'ja demonstrate a diverse gene pool at Nevali Cori that supports connectedness wit

99 of the age (1.2-1.4 million yr) of the maize gene pool based on te1 is roughly consistent with previo

100 Further the separation according to the gene pool, bayesian analysis of the population structure

101 o leave extensive traces in the modern human gene pool because of genetic drift.

102 genetic variation in the recipient species' gene pool, but empirical examples of species-wide restor

103 nd Denisovan DNA persist in the modern human gene pool, but have been systematically purged by natura

104 , and subsequent dilution in the surrounding gene pool by admixture occurred only to a limited extent

105 estication and intense selection within each gene pool by breeders; association mapping would best be

106 e relative contributions to the Mestizo FRDA gene pool by Native American and European genes were 76-

107 iphtheriae clinical isolates for their pilin gene pool by PCR and for the expression of the respectiv

108 We find that the pandemic period shaped the gene pool by reducing long distance immigration, in part

109 greater contribution of African women to the gene pool compared to African men varies across the Amer

110 opulations that tend to have more delineated gene pools compared to continental populations.

111 parity between responding genes in different gene pools confirms recent evidence that surprisingly la

112 ed by haploblocks, genome segments where the gene pool consists of two highly divergent haplotypes, w

113 s via improved genetic representation in the gene pool contribute but a minor fraction.

114 two early diversified Arctic-alpine diploid gene pools contributed differently to the evolution of t

115 nd drug cultivars diverged from an ancestral gene pool currently represented by feral plants and land

116 ese findings support the idea that H. pylori gene pools differ regionally and emphasize the potential

117 estimate the degree and patterns of spatial gene pool differentiation, and their possible causes.

118 It is estimated that the two current wild gene pools diverged from a common ancestor approximately

119 rements of bacterial recombination rates and gene pool diversity of earlier eras.

120 l and South America, evidence for a putative gene pool division.

121 ntains the FV Leiden mutation in the general gene pool due to a survival advantage of VL+/- in severe

122 range expansions that dramatically alter the gene pool even in large microbial populations.

123 ral agreement on the origins of the European gene pool, even though Europe has been more thoroughly i

124 mes, the majority of the paternal Polynesian gene pool exhibits ties to East Asia.

125 utation that rose to prominence in the human gene pool faster than expected under neutral evolution.

126 i accounting for 52.2 % of the captive panda gene pool, followed by Minshan with 21.5 %, Qinling with

127 as hurricanes likely help to homogenize the gene pool for all Caribbean marine species susceptible t

128 egilops species represent the most important gene pool for breeding bread wheat (Triticum aestivum).

129 and China as well, providing a heterogeneous gene pool for viral reassortment.

130 ies, and inferred the distribution of shared gene pools for global Helicobacter pylori isolates.

131 xtensive wild introgression into the cassava gene pool from at least five wild species, including Man

132 e show that two haplotypes entered the maize gene pool from its wild progenitor, teosinte, and that o

133 number of migrants entering Middle American gene pool from the Andean gene pool.

134 This finding implies that both of the gene pools from South America originated through differe

135 l divergence, subsequent bottlenecks in each gene pool, gene pool-specific domestication and intense

136 ns found at high frequency in the cultivated gene pool had larger effects than low-frequency introgre

137 Thus, our findings show that a pan-domain gene pool has facilitated environmental adaptation in th

138 or sustaining, diversifying, and sharing the gene pool have shaped manioc diversity.

139 Crop gene pools have adapted to and sustained the demands of

140 Endemic gene pools have been severely endangered by human-mediat

141 recombination between distinct sweet potato gene pools, have reshuffled the crop's initial genetic b

142 or permafrost as a depository for an ancient gene pool, i.e., preexisting life, which hypothetically

143 ic variation due to introgression from other gene pools, (ii) quantitative genetic variation is lower

144 are crucial to the ongoing quest to Vanilla gene pool improvement.

145 turies, replacing more than 80% of the local gene pool in Eastern Germany, Poland and Croatia.

146 c and functional variability of the HSV-1 TK gene pool in paired trigeminal ganglia (TG) of 5 immunoc

147 We find that the Fe(III)-reducing gene pool in soil is dominated by acidophilic Acidobacte

148 ibet-where it forms approximately 84% of the gene pool in some groups-and to the Central Plain, where

149 by ~2,400 to 2,000 y ago, the P. dactylifera gene pool in the Eastern Mediterranean already contained

150 y play a critical role in shaping the mobile gene pool in these organisms, yet complex mobile element

151 uses, but little is known about the viruses' gene pool in wild birds.

152 approaches background levels of the parental gene pools in advanced generation backcrosses.

153 of both the mitochondrial and Y chromosomal gene pools in late Neanderthals.

154 he idea of using wild or currently unadapted gene pools in rice to enhance breeding efforts to secure

155 d that African and European contributions to gene pools in the Americas were much more sex biased tha

156 representative portion of the global chicken gene pool including 39 different breeds was examined in

157 ural variation into the cultivated sunflower gene pool, including >3,000 new genes.

158 further ancestry components into the English gene pool, including substantial southwestern European a

159 found marked substructuring of the maternal gene pool into four phylogeographic groups.

160 for an Indian contribution to the Australian gene pool is contradictory; most studies of autosomal ma

161 mechanism of persistence for the pan-immune gene pool is fundamentally similar to the "island migrat

162 of cultivated soybean (Glycine max) and it's gene pool is indisputably more diverse than G. max.

163 frican, and Near Eastern ancestry, the local gene pool is largely maintained across the first millenn

164 l species, suggesting that the mycobacterial gene pool is larger than previously suspected.

165 mmon genetic pool but in which access to the gene pool is not uniform for all phage.

166 stance, much of a given organism's essential gene pool is specific to that organism.

167 r component detected in the Grecia Salentina gene pool is the result of past immigration.

168 sequilibrium (LD) in samples of the parental gene pools is moderate and should respond to sampling sc

169 r odd features of the island's Y-chromosomal gene pool, is best explained as the genetic impact of a

170 ructure analysis allowed to discriminate the gene pools (K = 2, FST = 0.733).

171 mechanistic insights, a meta-data "knowledge gene pool" (KGP) is first constructed from multiple data

172 ted that 1-4% of the non-Sub-Saharan African gene pool may be Neanderthal derived, while 6-8% of the

173 erthal derived, while 6-8% of the Melanesian gene pool may be the product of admixture between the De

174 As a result, crop gene pools may be supplemented through more rapid and di

175 The plant science community and crop gene pools may be united and enriched as never before.

176 an-American and Caucasian-American H. pylori gene pools may bear on our understanding of H. pylori tr

177 sequences may have entered the H.influenzae gene pool more recently via horizontal transfer.

178 Here we present the matrilineal gene pool of 299 Cambodian refugees from three different

179 sources that likely shaped the mitochondrial gene pool of ancient Umbri over time, since early Neolit

180 Our results indicate that the paternal gene pool of both groups is shaped by several strata, th

181 Its absence from the founder gene pool of indigenous Australians may also partly expl

182 Wild birds harbor a large gene pool of influenza A viruses that have the potential

183 Our results are consistent with a gene pool of low haplotypic diversity, containing few no

184 is thought to have caused revolutions in the gene pool of many species, most evidently in microbial c

185 legacy remains as sedimentary layers in the gene pool of modern Europeans, and our understanding of

186 significant contribution to the contemporary gene pool of NEAS, and the Sino-Tibetan expansion has le

187 ja Sieb. and Zucc., which represents a large gene pool of potentially agronomically valuable traits.

188 Holocene thermal optimum did not affect the gene pool of the collared lemming in West Beringia but r

189 onservation efforts aimed at maintaining the gene pool of the current population or establishing new

190 ncestral populations that contributed to the gene pool of the current populations inhabiting Arabia a

191 n by associating with adaptive traits in the gene pool of the so-called mobilome.

192 ountain sickness and to be introduced in the gene pool of their ancestors by admixture with Denisovan

193 e needed to better use and conserve the vast gene pool of wheat biodiversity on which our food securi

194 n selecting the appropriate alleles from the gene pool of wild relatives to incorporate into modern w

195 hals made a small (1-4%) contribution to the gene pools of all non-African populations.

196 entified PvMYB26 mutations in all three main gene pools of common bean, including an 8 kb deletion in

197 We identify two gene pools of cultivated mango, representing Indian and

198 s for present and future efforts to conserve gene pools of endangered species.

199 lts support the hypothesis that the paternal gene pools of Jewish communities from Europe, North Afri

200 equencing of two diploids from the ancestral gene pools of quinoa, which enables the identification o

201 jeopardize the resilience of locally adapted gene pools of the native H. taimen populations.

202 ssumed that this high mortality affected the gene pools of these populations.

203 tinuous distribution, leaving five surviving gene pools of unknown genetic affinity.

204 ng local hunter-gatherer contribution to the gene-pool of farmers following the initial rapid Neolith

205 The presumably shallow elite gene pools often continue to yield genetic gains while t

206 e rapidly altering microbial composition and gene pools on plastics and adds new knowledge surroundin

207 Icelanders and the consequent impact on the gene pool over time.

208 iods, which allowed us to examine changes in gene pools over time and to test these migration hypothe

209 gy (GO) terms for enrichment among candidate gene pools, performs multiple hypothesis testing adjustm

210 n gene pool was more diverse than the Andean gene pool (pi(sil)=0.0089 vs 0.0068).

211 ivated olives clustered into three different gene pools (Q1, Q2 and Q3), corresponding loosely to the

212 fter the introduction of PCV7, the accessory gene pool re-expanded mainly by genes already circulatin

213 We conclude that the C. sativa gene pool remains only partially characterized, the exis

214 e broader genetic diversity within the Avena gene pool remains underexplored and underexploited.

215 he Andes of southern Peru, possess a diverse gene pool representing more than 100 tuber-bearing relat

216 icant portion of the temperate bacteriophage gene pool resides in prophages.

217 6 were exclusive to the Atlantic and Pacific gene pools, respectively, and 3432 SNPs could differenti

218 nce of spatial patterns of nuclear and mtDNA gene pools results from a phylogeographic background and

219 ions, and convergent evolution through local gene pool sampling.

220 By reducing the size of the gene pool, selfing should limit adaptive potential.

221 The Kulubnarti gene pool - shaped over a millennium - harbors dispropor

222 nd the structure of clonal relationships and gene pools shaping its origins.

223 evels and patterns of variation in different gene pools, shed light on relationships of allelic diver

224 omprehensive analyses of the global Bacillus gene pool showed that only an asymmetric region around t

225 that secondary symbionts form a "horizontal gene pool" shuttling adaptive genes among host lineages

226 ome 145 thousand years ago, owing to the 1/4 gene pool size of our matrilineally inherited haploid ge

227 e, subsequent bottlenecks in each gene pool, gene pool-specific domestication and intense selection w

228 uantitative evidence linking urbanization to gene pool spread and zoonoses.

229 rphisms (SNPs) between domesticated and wild gene pools, suggesting that domesticated gene pools were

230 portionately less to the modern Scandinavian gene pool than indicated by the ancestry of genomes from

231 an cultivars from the Andean or Mesoamerican gene pool that contain the dominant allele share the sam

232 ean mutant FRDA genes in the Native American gene pool that existed prior to contact with Europeans.

233 ion rates and diversity levels of the shared gene pool that has contributed to a given sample.

234 ondary symbiont community forms a horizontal gene pool that influences the adaptation and distributio

235 cal gene-exchange networks by tapping into a gene pool that is adaptive towards local, continuously c

236 both on determinants acquired from a mobile gene pool that is likely available to clinical and agric

237 of gene frequency, i.e. the 'success' in the gene pool that is supposed to be attributable to the 'se

238 resenting a highly diverse influenza A virus gene pool that merits continued monitoring.

239 ottleneck during the formation of the Andean gene pool that predates the domestication, which was sug

240 Our results reveal a persisting local gene pool that, during the Middle-Late BA, absorbed addi

241 lecting introgression between the respective gene pools that may have occurred hundreds of years ago.

242 Also, the genomes and gene pools, the products of evolution and crop domestica

243 frica has played in shaping the modern human gene pool through at least two--not one--major expansion

244 ansgenes) and perhaps by other native exotic gene pools through comparative analyses of plants' biolo

245 Third, mass mortality might alter the local gene pools through its impact on subsequent migration pa

246 The mitochondrial gene pool thus may contain signals of local population h

247 est that single mTECs shift through distinct gene pools, thus scanning a sizeable fraction of the ove

248 of Native American ancestors from the Asian gene pool to 23 kya or later [5, 6] and mtDNA analyses t

249 nformation for using the secondary Gossypium gene pool to breed for improved salt tolerance.

250 s of four different segments of the landrace gene pool to each inbred group's gene pool were estimate

251 n the egg surface,and serves to restrict the gene pool to individuals of the same species.

252 The resulting dependence of the Fe-cycling gene pool to pH determines the high iron-reducing potent

253 native microbial community with a beneficial gene pool to withstand extreme conditions.

254 of a mutant allele that enter a population's gene pool together due to replication from a premeiotic

255 e pools will soon be complemented by another gene pool (transgenes) and perhaps by other native exoti

256 Subsequently, each gene pool underwent a bottleneck immediately after diver

257 have persisted in the contemporary H5Nx HPAI gene pool until 2020.

258 ype specificity, to a high percentage of the gene pool used to construct the network.

259 cs, characterize their genetic potential (or gene pool) using metagenomics, and describe their ongoin

260 hreatened with extinction due to the lack of gene pool variability, susceptibility to climate change

261 ts suggest that the composition of H. pylori gene pools varies geographically and that other as-yet-u

262 y had more recently entered the H.influenzae gene pool via horizontal gene transfer from other specie

263 A 100-gene pool was identified that induced recognition of 293

264 Over all loci, the Middle American gene pool was more diverse than the Andean gene pool (pi

265 ge, more than half of the Northern Levantine gene pool was replaced, while in the rest of Anatolia an

266 The main factor structuring the gene pool was the mode of subsistence: settled agricultu

267 th internal genes from the chicken H9N2/H7N9 gene pool, was responsible for at least five human H5N6

268 cally differentiated Mesoamerican and Andean gene pools, we confirmed 2 independent domestications fr

269 he landrace gene pool to each inbred group's gene pool were estimated using a novel likelihood-based

270 ild gene pools, suggesting that domesticated gene pools were derived from multiple wild ancestors.

271 re generated in a plasmid vector, and mutant gene pools were transformed into N. gonorrhoeae to selec

272 lavobacteriales also dominated the rhodopsin gene pool when the highest rhodopsin levels were recorde

273 d with roughly 65.4% of the average European gene pool, which clinally diminishes with distance from

274 ure LD caused by occurrence of more than one gene pool, which would downwardly bias Ne and (2) reduct

275 Because the two sexes share a common gene pool while performing many different biological fun

276 barriers of sexual reproduction, the native gene pools will soon be complemented by another gene poo

277 a crucial resource that enriched the sorghum gene pool with novel diversity and a highly valuable too

278 etric gene flow was detected between the two gene pools with a larger number of migrants entering Mid

279 nd European apricots form two differentiated gene pools with high genetic diversity, resulting from i

280 of both sampled sequences and the unsampled gene pools with which they recombine.

281 and nonserpentine soils and sequenced each 'gene pool' with the Illumina Genome Analyzer.

282 eric genetic landscape among distinct barley gene pools, with different evolutionary processes drivin

283 Bottlenecks reduce the size of the gene pool within populations of all life forms with impl

284 nd japonica) arose from genetically distinct gene pools within a common wild ancestor, Oryza rufipogo