ライフサイエンスコーパス: genetic diversity

1 acteria drives high within-host pneumococcal genetic diversity.

2 nerating both multiallelic and combinatorial genetic diversity.

3 rulence and transmissibility induced by high genetic diversity.

4 gradients but with higher within-population genetic diversity.

5 on in maintaining the inbred load and linked genetic diversity.

6 and plant genomes and contribute to shaping genetic diversity.

7 on of both organisms, leading to their great genetic diversity.

8 representing a broad range of antigenic and genetic diversity.

9 e ancestral Asian clade with high amounts of genetic diversity.

10 iguration was associated with regional scale genetic diversity.

11 D, with the HWD showing significantly higher genetic diversity.

12 ual and it does not adequately reflect human genetic diversity.

13 pies a wider ecological niche and has higher genetic diversity.

14 neity also could have influenced the grass's genetic diversity.

15 e human genome, providing significantly more genetic diversity.

16 ive reference representation of global human genetic diversity.

17 enabling balanced segregation and generating genetic diversity.

18 le for hydrographic gradients in maintaining genetic diversity.

19 tinct genotypes, representing high levels of genetic diversity.

20 duces crossovers and noncrossovers to create genetic diversity.

21 ral genetic structure and the maintenance of genetic diversity.

22 th North American strains displaying highest genetic diversity.

23 bility may be compromised further by loss of genetic diversity.

24 hogen Helicobacter pylori displays extensive genetic diversity.

25 ticularly useful because of their restricted genetic diversity.

26 enotypic change, even in the face of reduced genetic diversity.

27 limatic fluctuations have shaped patterns in genetic diversity.

28 ient numbers to retain a large proportion of genetic diversity.

29 ble for studies of infra- and inter-specific genetic diversity.

30 call for increased efforts to monitor global genetic diversity.

31 consistent seasonal fluctuations in relative genetic diversity.

32 t RNA polymerase allows FMDV to exhibit high genetic diversity.

33 in compromised by lead poisoning and limited genetic diversity.

34 of heterogeneity, and including within-host genetic diversity.

35 which makes it very attractive for studying genetic diversity.

36 Analysis of shared genetic diversity across 15 sequence-validated transmiss

37 Here we compare genome-wide genetic diversity across 38 species of European butterfl

38 e and examined patterns of its intraspecific genetic diversity across Cuba.

39 Understanding the origin and distribution of genetic diversity across landscapes is critical for pred

40 In this issue, Reiter et al. assess genetic diversity across metastatic lesions and identify

41 Middle East, no evidence for reduced global genetic diversity across the breed, and unique genetic a

42 al features have differentially affected the genetic diversity across the regional frog assemblage.

43 etermined the changes in mosquito population genetic diversity after 20 years of intensive malaria co

44 tivated variety "Big Star*" and assessed the genetic diversity among 97 sweet cherry accessions repre

45 other continent, yet only a fraction of the genetic diversity among African individuals has been sur

46 Given that type O FMDV exhibits the highest genetic diversity among all seven serotypes of FMDV, we

47 lonies from culture, we examined within-host genetic diversity among C. difficile isolates collected

48 genizing effect prompted by increased shared genetic diversity among geographically distant regions a

49 Genetic diversity among metastases is poorly understood

50 vidence indicates an additional role for the genetic diversity among MTBC clinical strains.

51 his hypothesis, we also note lower levels of genetic diversity among northern mastodons than in endem

52 ture with an extraordinary disequilibrium of genetic diversity among regions, and signals of isolatio

53 rains, in which there is no (or very little) genetic diversity among subjects, it is difficult to ide

54 Genetic diversity analysis of Poncirus accessions and Po

55 The genetic diversity analysis revealed significant genome-w

56 total of 87 lily accessions was subjected to genetic diversity analysis using polymorphic SSRs and fo

57 f disease, the impact of pathogen and vector genetic diversity and a broad array of immune and inflam

58 Heirloom tomatoes retain extensive genetic diversity and a considerable range of fruit qual

59 t case scenario' for the maintenance of high genetic diversity and adaptive potential under climate-c

60 s, both human parasites have greatly reduced genetic diversity and an excess of nonsynonymous mutatio

61 uctural variants contribute substantially to genetic diversity and are important evolutionarily and m

62 varietal diversification with high levels of genetic diversity and asymmetric evolution between the n

63 ately, very little information exists on its genetic diversity and brix content.

64 persal, this is especially pertinent because genetic diversity and connectivity are key aspects of th

65 Here, the genetic diversity and connectivity of the brooding scler

66 igate how landscape heterogeneity influences genetic diversity and differentiation in the forest-asso

67 d the expected negative relationship between genetic diversity and distance from Africa in the global

68 bal dataset, but no relationship between HLA genetic diversity and distance from Africa when Native A

69 anagement and requires interpretation of the genetic diversity and ecological function of the taxon b

70 Global HIV-1 genetic diversity and evolution form a major challenge t

71 ful means to preserve, or even increase, the genetic diversity and evolutionary potential of endanger

72 strains, our results offer insights into the genetic diversity and gene functions in benthic diatoms.

73 We observe a remarkable correlation among genetic diversity and geographic distance, with the hunt

74 genomics analysis of T. sinense reveals its genetic diversity and geographic structure with implicat

75 e to its large and polyploid genome, limited genetic diversity and in-field phenotyping constraints.

76 ild isolates to understand the prevalence of genetic diversity and instability-generating mechanisms,

77 Cross-pollination increases genetic diversity and is favored by selection in the maj

78 We identified a relatively high genetic diversity and limited genomic clustering within

79 on for mapping quantitative trait loci, high genetic diversity and minimal population structure.

80 sess how interspecies interactions can shape genetic diversity and mobile gene elements.

81 Mutations are the source of both genetic diversity and mutational load.

82 The surviving individuals, with decreased genetic diversity and often fragmented ecology, are then

83 ease presentation are regulated by both host genetic diversity and pathogen immune evasion.

84 outpaced understanding of the links between genetic diversity and phenotypic variation.

85 es facilitate gene-flow and increase overall genetic diversity and population admixture of dispersal

86 ng systems can strongly affect the extent of genetic diversity and population structure among species

87 Our data on large scale SSR based genetic diversity and population structure analysis may

88 using online genetic resources for analyzing genetic diversity and population structure of Lilium spe

89 ding of A. digitata, including cytogenetics, genetic diversity and reproductive biology. The objectiv

90 , but also the influx of recruits to promote genetic diversity and retain cover following adult morta

91 tuitous combination of genetic architecture, genetic diversity and selection.

92 nd genetic drift, and their consequences for genetic diversity and structure at landscape and local s

93 onset of the last glacial maximum shaped the genetic diversity and structure detected in this study.

94 eading to habitat fragmentation and a higher genetic diversity and structure in ground-level populati

95 Comparing genetic diversity and structure in refugia versus recent

96 entify and understand the mechanisms driving genetic diversity and structure in their native range.

97 Atlantic hurricane season in 50 years on the genetic diversity and structure of a dispersal-limited i

98 we also demonstrate a quantitative effect of genetic diversity and temperature on the strength of the

99 However, because of genetic diversity and the diploid nature of the human ge

100 , and (iv) the accounting for within-species genetic diversity and the historical aspect of conservat

101 y habitat fragmentation, are known to affect genetic diversity and the long-term persistence of popul

102 satellite analysis showed that nests had low genetic diversity and the majority of queens had mated w

103 antic salmon by exploiting the high level of genetic diversity and trait expression among domesticate

104 multiscale, replicated landscapes with both genetic diversity, and differentiation to gain a more co

105 ation regarding their clinical epidemiology, genetic diversity, and mechanisms of carbapenem resistan

106 Alternative splicing of pre-mRNA increases genetic diversity, and recent studies estimate that most

107 ealed four distinct genetic clades, abundant genetic diversity, and widely distributed haplotypes.

108 les (SRWs, Eubalaena australis), patterns of genetic diversity are likely influenced by the glacial c

109 Human impacts on genetic diversity are poorly understood yet critical to

110 ct 'volcano' pattern with peaks of increased genetic diversity around the selected target, characteri

111 Gujjars exhibited lesser genetic diversity as compared to Ladakhi population.

112 America may have been an important source of genetic diversity as maize was becoming a staple grain i

113 The human genome contains vast genetic diversity as naturally occurring coding variants

114 ationship between pathogen diversity and HLA genetic diversity (as measured by polymorphism informati

115 ntly rely on our incomplete knowledge of the genetic diversity at HLA and BCR/TCR loci.

116 rsity, we evaluated the relationship between genetic diversity at HLA-A, HLA-B and HLA-DRB1 and patho

117 ersal would dilute demographic influences on genetic diversity at local scales.

118 panel (SDP1) was developed that captured the genetic diversity based on the combination of maximum le

119 on requires knowledge of temporal changes to genetic diversity before and after the advent of managem

120 s about mechanisms that can be influenced by genetic diversity between individuals.

121 tions from resource limitation, boosting the genetic diversity, body size, and reproductive output of

122 By reducing genetic diversity, bottlenecks may alter individual or p

123 ndem repeats (STRs) are important sources of genetic diversity but are not routinely analyzed in gene

124 across the Mediterranean contain comparable genetic diversity but display high genetic differentiati

125 associated with the loss of populations and genetic diversity, but also affects how animals behave.

126 nerates adaptive potential through increased genetic diversity, but examples demonstrating its exploi

127 y to buffer pathogen pressure with increased genetic diversity by varying the initial number of repro

128 Extant Canis lupus genetic diversity can be grouped into three phylogenetic

129 However, high densities and low genetic diversity could make their populations susceptib

130 on and gene flow were sufficient to preserve genetic diversity despite recent forest contraction and

131 The genetic diversity detected among the studied accessions

132 Topics include the reduction of genetic diversity during domestication and counteracting

133 ons to overcome environmental constraints on genetic diversity, even without strong demographic chang

134 ifications were probably driven by increased genetic diversity following polyploidizations and by tra

135 h-eastern Italy showed the highest values of genetic diversity for both markers, highlighting that th

136 hat pollen dispersal contributes to increase genetic diversity for these locally differentiated trait

137 Vs have been relatively stable in population genetic diversity for years.

138 We quantified genetic diversity from 17 sites across regional scales,

139 some species of social insects the increased genetic diversity from having multiple breeders in a col

140 the consequence of habitat fragmentation on genetic diversity, gene flow and genetic structure has r

141 lear and mitochondrial DNA markers to assess genetic diversity, gene flow and the genetic structure i

142 h-resolution estimates of genetic structure, genetic diversity, gene flow, and evolutionary history.

143 ns is species specific, suggesting that such genetic diversity has arisen through the evolutionarily

144 are affected not only by disease but also by genetic diversity (i.e. SNPs).

145 idespread implications for understanding how genetic diversity impacts disease susceptibility, and ra

146 This study assessed genetic diversity in a panel of 173 D. rotundata accessi

147 During metastasis, only a fraction of genetic diversity in a primary tumor is passed on to met

148 them is the inability to include measures of genetic diversity in addition to differentiation.

149 Greater genetic diversity in African populations improves predic

150 design and statistical models for estimating genetic diversity in all three host traits.

151 We found a significant reduction in genetic diversity in An. gambiae, but not in An. arabien

152 Exploring the large genetic diversity in classical animal models, such as mi

153 We found a significant decrease in genetic diversity in contemporary (compared to historica

154 and to perform a genome-wide analysis of the genetic diversity in cultivated coffee germplasm and in

155 es that underlie the current distribution of genetic diversity in endangered species is a goal of mod

156 This research has provided knowledge about genetic diversity in fire blight S genes in diverse appl

157 Using a new approach to model genetic diversity in human disease, referred to as varia

158 Although much more of the genetic diversity in human populations around the world

159 ies, drive biogeochemical cycles and enhance genetic diversity in nature(1,2).

160 Genetic diversity in offspring is induced by meiotic rec

161 diterranean is nonetheless comparable to the genetic diversity in populations from the Iberian Penins

162 As the virus genetic diversity in primary CMV infection and the chang

163 d, this study likely underestimated the true genetic diversity in primary CMV infection.

164 may improve immunity through an increase of genetic diversity in R. flavipes.

165 Reassortment is an important source of genetic diversity in segmented viruses and is the main s

166 ss gradients of parasite occurrence maintain genetic diversity in sorghum landrace resistance.

167 us agents that allow for rapid generation of genetic diversity in specific genomic loci as opposed to

168 the northwest Atlantic, with high levels of genetic diversity in the east Canadian Arctic.

169 ated with viral evolution and high levels of genetic diversity in the HIV envelope (Env) glycoprotein

170 tasis is seeded by multiple cells, then some genetic diversity in the primary tumor can be transmitte

171 sented here will enrich our understanding of genetic diversity in the region and introduce a PowerPle

172 f 736 C. arabica accessions, we analyzed the genetic diversity in the species and its relationship wi

173 Populations often exhibit genetic diversity in traits involved in responses to abi

174 site coevolution can maintain high levels of genetic diversity in traits involved in species interact

175 ics-based tools to characterize and identify genetic diversity in Vanilla and provide a significant t

176 Our study suggests that genetic diversity in Vpu may play an important role in t

177 ated for a comprehensive characterization of genetic diversity in white Guinea yam from West Africa a

178 ver, directly following the 2017 hurricanes, genetic diversity increased at five of the six sampled l

179 chanisms and fitness effects, early adaptive genetic diversity increases predictably, driven by the e

180 quency of recent H5 LPAIV isolates with high genetic diversity indicates the importance of continued

181 of pelagiphages regarding their morphology, genetic diversity, infection strategies, and distributio

182 The importance of drivers of genetic diversity is amplified in island populations tha

183 This suggests that genetic diversity is determined both by differences in l

184 with European ancestry despite the fact that genetic diversity is expected to be highest in Africa wh

185 Under the neutral theory, genetic diversity is expected to increase with populatio

186 Understanding the evolutionary dynamics of genetic diversity is fundamental for species conservatio

187 ith high resource diversity, whereas neutral genetic diversity is greatest in the largest lakes.

188 This study provides evidence that FMDV genetic diversity is important for viral virulence and t

189 Genetic diversity is key to crop improvement.

190 been extensively studied, its within-species genetic diversity is less well understood.

191 on information can be inferred when pathogen genetic diversity is low and metadata limited, we propos

192 Instead, neutral genetic diversity is negatively correlated with body siz

193 nt biological properties, characterizing the genetic diversity is thus important to vaccine and drug

194 nal lack of viral evolution and 8-fold lower genetic diversity (<0.01 s/n) in env gene than other EC.

195 the development of modern breeding impacted genetic diversity more dramatically than the previous mi

196 RSVs are undergoing a decrease in population genetic diversity, NADC34-like PRRSVs have been relative

197 conditions, have the heritable variation and genetic diversity necessary to evolve in response to cli

198 So far, neither genetic diversity, nor spatial distribution of circulati

199 The low genetic diversity observed in the vaquita carried signat

200 Genetic diversity of 1,485 clones within WCSRG and Louis

201 d use and human density on the intraspecific genetic diversity of 17 082 species of birds, fishes, in

202 family, further demonstrating the remarkable genetic diversity of archaeal viruses.

203 genome-wide SNP identification and to assess genetic diversity of both Chilean and Spanish germplasm

204 export to others, little is known about the genetic diversity of circulating strains.

205 n mycobacteria, and may allow correlation of genetic diversity of clinical Mtb isolates with clinical

206 We aimed to investigate the dynamics and genetic diversity of colistin-resistant commensal Escher

207 field collections suggest that among-colony genetic diversity of cultivars in small-scale farms may

208 We also quantified the genetic diversity of each serotype.

209 Previously, we showed that the genetic diversity of FMDV plays an important role in vir

210 Furthermore, the ubiquity and genetic diversity of gut bacterial azoreductases coupled

211 Two recent studies explored the genetic diversity of gut microbes and unraveled extensiv

212 tation, genetic drift, and fitness shape the genetic diversity of healthy blood (clonal hematopoiesis

213 During sexual transmission, the high genetic diversity of HIV-1 within an individual is frequ

214 equire prior knowledge of the composition or genetic diversity of HLA and BCR/TCR loci.

215 We assessed the genetic diversity of HLA class I and class II in this po

216 along short ecological gradients would boost genetic diversity of individual tree populations, and en

217 Overall, this work leverages the genetic diversity of multiple human cell lines to highli

218 first detailed insight into the within-host genetic diversity of Mycobacterium tuberculosis (M.TB),

219 Genetic diversity of Mycobacterium tuberculosis affects

220 On a background of high genetic diversity of NK cell receptor genes, this KLRA a

221 ls (CTC) that are more likely to reflect the genetic diversity of patient's disease than a single-sit

222 Quantifying the genetic diversity of riparian trees is essential to unde

223 cover an even broader host range and greater genetic diversity of S. aureus than is already known, an

224 Despite the high genetic diversity of S. enterica, all ancient bacterial

225 to understand the molecular epidemiology and genetic diversity of SARS-CoV-2 in China, we generated 5

226 Although the genetic diversity of several eukaryotic phytoplankton vi

227 d population genomics reveals high levels of genetic diversity of T. sinense and identifies four refu

228 population of 1,485 clones and captured the genetic diversity of the entire collection with an avera

229 The genetic diversity of the FMD viruses collected from the

230 ns, which in turn contribute to the enhanced genetic diversity of the population as a whole.

231 outcomes that are conditional on the overall genetic diversity of the population.

232 abitat suitability, or environment drive the genetic diversity of the regional frog assemblage.

233 The large number and high genetic diversity of the viral clusters seems to mirror

234 Although several studies have described the genetic diversity of the virus, the evolutionary process

235 eveal the evolutionary forces that shape the genetic diversity of the virus, which has implications f

236 nosis of LASV infection is challenged by the genetic diversity of the virus, which is greatest in Nig

237 l and molecular techniques, and characterize genetic diversity of the virus.

238 Two hypotheses were tested for the genetic diversity of these populations: (1) populations

239 is of tracheary element development, and the genetic diversity of this relict species.

240 the apparent contradiction between the high genetic diversity of this species and its extreme exploi

241 This study provides evidence that higher genetic diversity of type O FMDV could increase both vir

242 combination and exhibit spatially structured genetic diversity on a regional scale in China.

243 necessary to separate effects of species and genetic diversity on tree growth and community productiv

244 Our results revealed no change to genetic diversity or structure for the years prior to th

245 ious methods that take advantage of existing genetic diversity or that increase genetic variance in m

246 nt giant panda populations retain reasonable genetic diversity, our results suggest that this represe

247 d A. zeteki populations, describe changes in genetic diversity over time, assess the relationship bet

248 rge-scale comparative genomics to assess the genetic diversity, phylogeography and potential origins

249 e number of foreign antigens and thus, their genetic diversity plays a critical role in their functio

250 Our study shows that pre-existing genetic diversity plays a key role in shaping resistance

251 Digitaria accessions, enabling insights into genetic diversity, population structure, and domesticati

252 ns to understand three key aspects of ticks: genetic diversity, population structure, and pathogen di

253 Genetic diversity provides a rich repository for underst

254 was caused not just by increasing individual genetic diversity, rather new genomic variation from imm

255 However, PCA revealed a cline of genetic diversity reflecting a west-to-east geographical

256 The sampling used reveals wide genetic diversity regarding tannin contents.

257 pression [5, 6] and a reduction in available genetic diversity render the success of such approaches

258 To investigate the genetic diversity, spatiotemporal dynamics, and transmis

259 affect reproduction is key for understanding genetic diversity, speciation, and trait evolution in th

260 molecular markers to understand patterns of genetic diversity, structure, and gene flow of W. saluta

261 As demonstrated in other Plasmodia, such genetic diversity studies can provide insights into the

262 Here, we present the genetic diversity studies of Gujjars from Jammu region o

263 RSVs are undergoing a decrease in population genetic diversity, suggesting that a dominant population

264 inally, we uncover relatively high levels of genetic diversity, suggesting that Homotherium may have

265 indicate any increased inbreeding or reduced genetic diversity, suggesting that the population size r

266 species maintains a relatively high level of genetic diversity supporting the existence of random mat

267 a B virus populations have lower within-host genetic diversity than influenza A virus and experience

268 phic ranges would have greater intraspecific genetic diversity than more restricted species.

269 luenza B, we find that IBV accumulates lower genetic diversity than previously observed for influenza

270 This study reveals greater genetic diversity than suggested by geographically-focus

271 ncing alerted us to the existence of greater genetic diversity than was initially assumed, splitting

272 stock) that better models the behavioral and genetic diversity that is found in humans.

273 In addition to genetic diversity, the cell-to-cell variation that fuels

274 uggest that this represents only part of the genetic diversity this species harbored prior to its rec

275 overing native breeds and safeguarding their genetic diversity through specific conservation programs

276 They also retained higher individual genetic diversity through the bleaching event than did l

277 al of viral lineages and on viral population genetic diversity through time.

278 in temperature as a main predictor of viral genetic diversity through time.

279 ng approach for introducing novel traits and genetic diversity to breeding populations.

280 These results suggest that high levels of genetic diversity together with the positive pleiotropic

281 224 maize accessions which represent a wide genetic diversity under three water regimes; 73,573 eQTL

282 e of demography and dispersal on patterns of genetic diversity underlying adaptation, we used data fr

283 57C) to study the relationship between viral genetic diversity, virulence, and transmissibility in na

284 Strikingly, cell-to-cell genetic diversity was almost twice as high in aggressive

285 Substantial genetic diversity was detected within the receptor bindi

286 CMV genetic diversity was determined by genotyping of 5 gene

287 to mcr-5 genes by a multiplex PCR, and their genetic diversity was measured by repetitive extragenic

288 Genetic diversity was similar across sites, but there wa

289 High levels of viral genetic diversity were maintained in both plants and thr

290 SSRs revealed that TKS has low- to- moderate genetic diversity with most of it partitioned to the ind

291 l correlate of previously described species' genetic diversity, with wild accessions well differentia

292 he colonisation patterns and distribution of genetic diversity within a major ocean basin (the Atlant

293 Genetic diversity within and among 42 native populations

294 drift, and selection) that shape microbiome genetic diversity within and between hosts, as well as e

295 generate the first genome-wide estimates of genetic diversity within dwarf lemurs.

296 ncing have enabled detailed studies of viral genetic diversity within hosts.

297 Average genetic diversity within populations from the eastern Me

298 At local spatial scales, loss of genetic diversity within species can lead to species los

299 -wasp tripartite interaction depend upon the genetic diversity within the attacking wasp population,

300 Here we report on genetic diversity within the pelagic copepod Pleuromamma