ライフサイエンスコーパス: migratory

1 erived from male mice are intrinsically more migratory.

2 Reported herein is a Ni-catalyzed migratory 3,3-difluoroallylation of unactivated alkyl br

3 f all migratory birds, ca. 51% are partially migratory [5]), speciation via switches in migratory beh

4 of DAPK1 activity significantly reduced the migratory ability of CD8(+) into the tumors.

5 ctrical properties of cancer cells and their migratory ability under an EF.

6 rkable developmental potential and extensive migratory ability.

7 demonstrate a link to calcium responses and migratory activation.

8 however regional variations, with increasing migratory activity in the Americas, which is not mirrore

9 the orientation of cellular protrusions and migratory activity within the tissue plane.

10 Here we consider how changing migratory and adhesive phenotypes contribute to human na

11 mediastinal draining lymph nodes and bearing migratory and immunoregulatory markers, including increa

12 and JPH203 suppressed cell proliferative and migratory and invasive abilities in bladder cancer cells

13 nnosidase I resulted in significantly higher migratory and invasive capabilities while masking cell s

14 PHIP silencing significantly suppressed the migratory and invasive capacity of glioblastoma cells, p

15 phenotypic plasticity processes that confer migratory and invasive properties to epithelial cells du

16 mesenchymal states associated with increased migratory and invasive properties.

17 hesion and apico-basal polarity, and acquire migratory and invasive traits.

18 oncogene ets1 is highly expressed in the pre-migratory and migratory neural crest (NC), and has been

19 Partial migration-wherein migratory and non-migratory individuals exist within the

20 quent than its gain, and speciation rates of migratory and partially migratory lineages (i.e., specie

21 s (ECs) must be activated and acquire highly migratory and proliferative phenotypes.

22 dergo reversible phenotype switching between migratory and proliferative states, with cells in the mi

23 unds and are also capital breeders that meet migratory and reproductive costs through seasonal energy

24 Similar changes in both migratory and resident DCs were also detected on day 14

25 cological factors that increase contact with migratory and resident waterfowl.

26 igratory lineages (i.e., species having both migratory and sedentary populations) exceeded those of s

27 al migration is an intermediate step between migratory and sedentary states in this family.

28 Because migratory and sedentary strategies involve alternative p

29 mpairment of differentiation and function of migratory and tissue-resident DCs, promoting disruption

30 highlights the importance of the Azores as a migratory and wintering habitat for three species of bal

31 that partial migration is widespread across migratory animals (e.g., of all migratory birds, ca. 51%

32 se to a warming planet with earlier springs, migratory animals are adjusting the timing of essential

33 In migratory animals for whom post-natal care is limited, i

34 Migratory animals have been dubbed "superspreaders" of i

35 Migratory animals move up to thousands of kilometers eve

36 Understanding how migratory animals respond to spatial and temporal variat

37 ortant areas during the annual life cycle of migratory animals, such as baleen whales, is vital for t

38 ic understanding of the parasite dynamics of migratory animals.

39 ce schedules of survival and reproduction in migratory animals.

40 tated surfing and explained the existence of migratory behavior across 61 populations of four ungulat

41 t, and the developmental shift in microglial migratory behavior along vessels corresponded to when as

42 mising model to uncover the genetic basis of migratory behavior and associated traits.

43 ent discoveries regarding the TBI-responsive migratory behavior and differentiation potential of neur

44 These findings suggest that migratory behavior does not require widespread modificat

45 aces and how recent investigation into their migratory behavior has provided unique insight into the

46 Research on migratory behavior is constrained by observational scale

47 However, whether a similar migratory behavior is performed by human Tfh cells is un

48 essed and integrated into the brain to drive migratory behavior is unknown.

49 y migratory [5]), speciation via switches in migratory behavior might be an important yet overlooked

50 tions and that this modification affects the migratory behavior of cells on such modified matrices, s

51 Numbers, activation state, and migratory behavior of eosinophils in bone marrow (BM), b

52 The migratory behavior of liposome-loaded neutrophils is con

53 y that predicts surfing and the existence of migratory behavior will be favored in environments where

54 se from shifting migratory patterns, loss of migratory behavior, or climate effects on parasite devel

55 unction is expected to accompany switches in migratory behavior, potentially accelerating speciation.

56 context of trafficking, analysis of specific migratory behaviors of lymphocytes within the tissue mic

57 erstand the environmental cues that regulate migratory behaviour across dietary guilds, consumer leve

58 basis for assessing the local prevalence of migratory behaviour across large landscapes.

59 ed for among-year variation in mortality and migratory behaviour and fit the model to a unique 50-yea

60 de a global analysis of associations between migratory behaviour and vertebrate life histories.

61 hat in long-lived species, the refinement of migratory behaviour and year-round spatial distribution

62 f a natural cross-breeding incident to study migratory behaviour in naturally occurring hybrids as we

63 also controls morphogenesis, we analysed the migratory behaviour of early olfactory neural progenitor

64 reased exposure to predators via maladaptive migratory behaviour reduces hybrid survival and can ther

65 roosting sites, allowing us to directly link migratory behaviour to predation risk in the wild.

66 rectly examine the contribution of divergent migratory behaviour to reproductive barriers.

67 ficult to test the relative contributions of migratory behaviour vs. other divergent traits to reprod

68 iversification and speciation, the causes of migratory behaviour, and how animal populations will lik

69 y is more likely to promote the evolution of migratory behaviour, rather than escape from infected co

70 nts is predictive of the local prevalence of migratory behaviour.

71 here was evidence of seasonal (intra-annual) migratory behaviours in a deep-sea fish assemblage on th

72 migrants to progressively acquire adult-like migratory behaviours, or which aspects take longer to re

73 Here we study both processes in the migratory Bewick's swan (Cygnus columbianus bewickii) us

74 to preferentially circulate within the same migratory bird flyway, suggesting a substantial role for

75 vegetation greenness for 230 North American migratory bird species in seven dietary guilds across th

76 Our results highlight the potential for many migratory bird species to encounter phenological mismatc

77 Across migratory bird species, variation in annual survival lar

78 s of 70 716 individuals of 52 North American migratory bird species, we demonstrate that increasing a

79 aset in which individuals of a long-distance migratory bird, the alpine swift Tachymarptis melba, wer

80 ement in response to changing phenology from migratory birds and ungulates to an apex predator, furth

81 By reconstructing how migratory birds are pushed towards the Canary Islands by

82 Over the past half century, migratory birds in North America have shown divergent po

83 synchronization with vegetation greenness by migratory birds in other dietary guilds, across the full

84 lyway, suggesting a substantial role for non-migratory birds or mosquito dispersal along the longitud

85 Each spring, migratory birds travel tens to tens of thousands of kilo

86 Migratory birds travel vast distances and the timing of

87 ing adults using GPS, monitored departure of migratory birds using weather radar and simulated their

88 lands (recording 137 species of resident and migratory birds), we focus on the landbirds from four is

89 pread across migratory animals (e.g., of all migratory birds, ca. 51% are partially migratory [5]), s

90 most prominent corridor for North America's migratory birds.

91 breeding areas of the massive population of migratory Black-eared kites wintering around the megacit

92 supported by Pdgfra+ fibroblasts, generating migratory but non-proliferative progeny.

93 ly scalable methods to sort millions of live migratory cancer and immune cells based on their spontan

94 Constraints in migratory capabilities, such as the disruption of gene f

95 he dermis despite their actomyosin-dependent migratory capabilities.

96 ted that these mutations conferred increased migratory capability, suggesting pathogenicity.

97 Macrophages from male mice maintained migratory capacity when cultured with FFA, whereas femal

98 ar ruler-based signaling pathway involved in migratory cell behaviors.

99 Active non-muscle myosin II (NMII) enables migratory cell polarization and controls dynamic cellula

100 Cardiac neural crest cells (cNCCs) are a migratory cell population that stem from the cranial por

101 lly distinct ProSG cell subsets, including a migratory cell population with a transcriptome distinct

102 rphological characteristics observed in many migratory cell populations.

103 Applied to both migratory cells and stationary cells, CFN revealed ultra

104 Migratory cells are known to adapt to environments that

105 Migratory cells exhibit a variety of morphologically dis

106 scopy-based metabolic analysis revealed that migratory cells selectively utilize oxidative metabolism

107 enesis, and the overall protein synthesis in migratory cells.

108 rent migratory species have evolved distinct migratory characteristics that improve fitness in their

109 of large populations of cells based on their migratory characteristics, cannot be easily performed.

110 tment alone, but the anti-proliferative/anti-migratory combination generally showed improvement over

111 ital role of stopover habitats in sustaining migratory communities.

112 thrush whole blood, provides favourable pre-migratory conditions allowing birds to delay departure f

113 We analysed the migratory connectivity between breeding and main non-bre

114 d additional data on life history timing and migratory connectivity from previous studies, eBird and

115 lightly different goals, and thereby promote migratory connectivity.

116 time- and size-selective mortality along the migratory corridor.

117 tory recovery due to parasite mortality, and migratory culling of infected individuals.

118 y our method to reveal that sorting the most migratory cytotoxic T lymphocytes yields a pool of cells

119 specific program between pathogen-presenting migratory DCs and T cells.

120 infected mice reduced the CD11b(-) subset of migratory DCs in RLN of TNFRp55(-/-) mice and significan

121 omic analysis of Langerin(+) and Langerin(-) migratory DCs revealed that Langerin(+) DCs became activ

122 ndings reveal underappreciated complexity in migratory decisions by long-distance migrants that contr

123 Migratory dendritic cells (DCs) in tumors transport anti

124 are taken up by a population of IRF4+ dermal migratory dendritic cells (migDC2) that similarly upregu

125 n the range of species that show fidelity to migratory destinations, as philopatry is hypothesized to

126 Rather, the dynamic conditions select for migratory diatoms that perform DNRA and can outcompete s

127 subspecies pair exhibited no evidence for a migratory divide and hybridised extensively.

128 rong reproductive isolation coincided with a migratory divide spanning 20 degrees of latitude.

129 he remarkable geographic coincidence between migratory divides and genetic breaks supports a long-sta

130 Migratory divides are proposed to be catalysts for speci

131 Comparing hybrid zones with and without migratory divides offers a rare opportunity to directly

132 e present evidence of speciation driven by a migratory drop-off in the fork-tailed flycatcher (Tyrann

133 Losses of migration (i.e., migratory drop-offs) occur when individuals of a migrato

134 mmed phase evolved to accommodate fluid-like migratory dynamics during episodes of tissue wound heali

135 of Maine and apparent changes in right whale migratory dynamics.

136 In contrast, the ability of migratory ectoparasitic nematodes to modify host plants

137 Kihnu native sheep originate from the first migratory episode.

138 are crucial events in human history, but the migratory episodes during the history of livestock remai

139 Previous research has revealed two migratory episodes of domesticated sheep from the Middle

140 parasite burdens within host populations via migratory escape from contaminated habitats and transmis

141 ) with changing social conditions (linked to migratory escape) in terms of infection-driven migration

142 an escape from infected conspecifics (social migratory escape).

143 mes coexisted within populations with social migratory escape, but never with migratory recovery.

144 volve for each migratory recovery and social migratory escape.

145 d under migratory recovery than under social migratory escape.

146 ature dermal adipocytes dedifferentiate into migratory extracellularmatrix-producing myofibroblasts.

147 nts (e.g. fresh and sea water in the case of migratory fish).

148 irds travel vast distances and the timing of migratory flights can affect survival and the ability to

149 layer is shown to become progressively more migratory, fluid-like, and unjammed.

150 sent recent introductions from Africa due to migratory fluxes.

151 rfowl throughout the Central and Mississippi Migratory Flyways in the United States and Canada.

152 d aquatic birds sampled along North American migratory flyways, we discovered an annual trend of incr

153 We demonstrate that guidance of inherent migratory forces is sufficient to disperse cell clusters

154 is accomplished by stabilizing and orienting migratory forces.

155 bundles, e.g., focal adhesion elongation or migratory front-back polarization.

156 precursor (CRP) that displays stem cell and migratory gene signatures, and contributes to homeostati

157 down- and upregulation of proliferative and migratory genes, respectively.

158 ation after small intestinal perturbation by migratory helminths and move to distant tissues to influ

159 For migratory herbivores, climate change poses a new and gro

160 Here, we show that a single migratory host-macroparasite model can give rise to thes

161 collective dataset provides an atlas of the migratory immune system and defines the nature of tissue

162 Partial migration-wherein migratory and non-migratory individuals exist within the same population-r

163 ical challenges for individuals, and data on migratory individuals would provide crucial context for

164 In migratory insects, increasing evidence has demonstrated

165 ave at last been demonstrated for gold, like migratory insertion and beta-H elimination reactions.

166 ally slow rate of chain transfer relative to migratory insertion in the nickel catalyst, and thus hig

167 The barrier to migratory insertion in these complexes is ca. 19.2 kcal/

168 study suggest that, despite fast double bond migratory insertion into Ir-H, the reaction proceeds thr

169 Highly stereoselective migratory insertion is facilitated by in situ formation

170 nsertion of allylbenzene, is unlikely as the migratory insertion needs to overcome a prohibitively hi

171 tive addition of pyridine-AlMe(3) before the migratory insertion of allylbenzene, is unlikely as the

172 eteroarylation, hydrosilylation reaction and migratory insertion of carbenes.

173 -membered cobaltacycle by C-H activation and migratory insertion of the diene is followed by beta-hyd

174 re, isomer equilibration is much faster than migratory insertion so that the barriers for insertion o

175 ures of 2-pyridone ligands in asymmetric 1,2 migratory insertion, and norbornene as a transient chira

176 cluding addition, substitution, elimination, migratory insertion, oxidative addition, and reductive e

177 ansition state (TS) for the regiocontrolling migratory insertion, triggered by the Rh-hydride additio

178 undergo fluoride abstraction followed by 1,1-migratory insertion.

179 lencing HNF1alpha reduced the proliferative, migratory, invasive and colony forming capabilities of p

180 eminated MCF7 cells (MCF7b), which were more migratory, invasive, and adhesive in vitro compared with

181 IRF4-dependent genomic programming of human migratory LCs appears to enable LC maturation while atte

182 criptional profiling demonstrates that human migratory LCs are robustly programmed for MHC-I and MHC-

183 nd that PI4P-containing vesicles move to the migratory leading edge during migration and that some of

184 r the targeted enrichment of the most potent migratory leukocytes in immunotherapies.

185 ental change acting widely across annual and migratory life cycles.

186 that can be attributed to their spectacular migratory lifestyle.

187 speciation rates of migratory and partially migratory lineages (i.e., species having both migratory

188 evealed a loss of AP-1B expression in highly migratory metastatic cancer cells suggesting that AP-1B'

189 et), we found that under TNFRp55 deficiency, migratory (MHC(high)CD11c(+)) DCs increased significantl

190 tive cell types that have markedly different migratory modes and physiological purposes: slowly migra

191 he downslope and reciprocal upslope seasonal migratory movements that characterize altitudinal migrat

192 istical challenges, however, have led to non-migratory movements that fall outside of the territory/h

193 Neural crest cells (NCCs) are migratory, multipotent embryonic cells that are unique t

194 multiple conservation challenges due to its migratory nature and philopatric behaviour.

195 is highly expressed in the pre-migratory and migratory neural crest (NC), and has been implicated in

196 und that stationary cells spontaneously turn migratory on substrates where integrin ligands are subje

197 t, cells elongate and align into cooperative migratory packs, and mesenchymal markers of EMT remain u

198 t response, immune cell infiltration and the migratory path of infiltrating H3K27M DMG cells into oth

199 er stores raises concerns over deteriorating migratory pathways, yet few studies have considered thes

200 these areas are likely important aspects of migratory pathways.

201 cination plays a major role in dictating the migratory pattern of lymphocytes, and thus vaccine effic

202 due to their limited prey selection, strict migratory patterns and high site fidelity.

203 persons of known HIV status to characterize migratory patterns and their relationship to HIV among 3

204 Understanding the migratory patterns of CP-infiltrating myeloid cells with

205 , we put forth the need to classify distinct migratory patterns that reflect the surveillance capacit

206 nts are known or believed to repeat the same migratory patterns throughout their lives, little is kno

207 rs enabled studying small bird species whose migratory patterns were widely unknown.

208 ratory wildlife that may arise from shifting migratory patterns, loss of migratory behavior, or clima

209 t of ageing was remarkably evident on spring migratory performance and phenology.

210 ariation in the probability of surviving the migratory period.

211 tural integrity of PGCCs and enhancing their migratory persistence.

212 roperties of PGCCs, as well as their unusual migratory persistence.

213 he cumulative nature of health risks at each migratory phase.

214 We documented the migratory phenotype of juncos (partial altitudinal migra

215 Our finding that a complex migratory phenotype results from a single gene region wi

216 ing hither to unexplained heterogeneities in migratory phenotypes within a cell population, and for t

217 f the complex evolutionary history of highly migratory philopatric species.

218 d receptor (GPCR), Tre1, to guide front-back migratory polarity radially from the cluster toward the

219 Stabilizing the declining eastern migratory population of monarch butterflies (Danaus plex

220 ical understanding and precise management of migratory populations in expansive, inaccessible marine

221 the length and complexity of many long-range migratory processes, including inflammation and germ cel

222 y increases matrix disassembly and increases migratory propensity in renal cancer cells.

223 recent studies on the developmental origins, migratory properties, and morphology of ChCs.

224 ermine when migration should evolve for each migratory recovery and social migratory escape.

225 aminated habitats and transmission hotspots, migratory recovery due to parasite mortality, and migrat

226 Our results suggest that migratory recovery is more likely to promote the evoluti

227 er fraction of the population migrated under migratory recovery than under social migratory escape.

228 ce of changing abiotic conditions (linked to migratory recovery) with changing social conditions (lin

229 with social migratory escape, but never with migratory recovery.

230 leton via alpha-actinin (DeltaABD) abrogated migratory responses to TGFbeta.

231 Migratory responsiveness, Ca(2+) -flux and apoptosis of

232 To predict thermal impacts on migratory riverine populations, we first expanded a spat

233 Despite phenological changes along the migratory route, mule deer closely followed drought-alte

234 drought and plant phenology across 99 unique migratory routes of mule deer (Odocoileus hemionus) in w

235 er crossings in prevailing winds can disrupt migratory routes towards slightly different goals, and t

236 d resulted in less sequential green-up along migratory routes.

237 ground (other cause) mortality of landlocked migratory salmonids over half a century.

238 the frequency of individuals with different migratory schedules has changed over time (a generationa

239 Migratory sea lamprey follow a larval cue into spawning

240 reversible state effects in a long-distance migratory shorebird, the Hudsonian Godwit Limosa haemast

241 These findings suggest that migratory signals result in expression changes of post-t

242 phingosine-1-phosphate and chemokine-induced migratory signals with the activation of Cdc42 and Pak s

243 creased Ag uptake by lymph node-resident and migratory skin dendritic cell subpopulations, including

244 helial layer that is unwounded, which is non-migratory, solid-like and jammed, the leading edge of th

245 cerns about the effects of climate change on migratory species and the critical role of plant phenolo

246 Smaller-bodied and migratory species are also more negatively associated wi

247 ndscape scales to equilibrium abundance of a migratory species at the continental scale.

248 Migratory species display a range of migration patterns

249 Migratory species form an important component of biodive

250 Different migratory species have evolved distinct migratory charac

251 atory drop-offs) occur when individuals of a migratory species stop migrating and establish founder s

252 eding season in constraining the response of migratory species to temperature changes at both the tra

253 n identifying the routes and connectivity of migratory species, which are still unknown for hundreds

254 des valuable insights into the demography of migratory species, which will help understand the extent

255 harvest management of economically important migratory species.

256 life history trajectories in a facultatively migratory species.

257 flammation resolution with slower neutrophil migratory speeds and retention of neutrophils within the

258 gration, which can lead to "parasite-induced migratory stalling" due to a positive feedback between i

259 and proliferative states, with cells in the migratory state being more motile than cells in the prol

260 , which evolved to maintain a solid-like non-migratory state that is more energetically economical.

261 lusters from a proliferative to a collective migratory state.

262 To test these hypotheses, we quantified migratory status- (resident/migrant) and season-specific

263 Here we report that the neural crest, a migratory stem cell population in vertebrate embryos, un

264 used chick neural crest (NC) cells, a highly migratory stem cell population likened to invasive cance

265 We also found that two distinct migratory strategies (e.g. some individuals always migra

266 re, we studied the ontogeny of long-distance migratory strategies and related patterns of spatial dis

267 However, how migratory strategies are shaped by winter habitat choice

268 The processes that drive the ontogeny of migratory strategies in long-lived animals with slow mat

269 ts that for some avian taxa, the ontogeny of migratory strategy is a prolonged, complex and dynamic p

270 An ontogenetic perspective on migratory strategy of a long-lived pelagic seabird: Timi

271 es of species with combinations of different migratory strategy or number of broods.

272 ADP levels in migrating cells in the rostral migratory stream of mouse revealed that decreases in ATP

273 cortical interneurons to rapidly depart from migratory streams and prematurely enter the cortical pla

274 duce multicellular clones as they move along migratory streams toward target brain areas.

275 results highlight the impact of spatial and migratory structure on genetic variation during processe

276 ant implications for risk assessment and the migratory success of monarchs in North America.

277 es that may serve as major regulators of the migratory syndrome.

278 When migratory T cells encounter antigen-presenting cells (AP

279 at may influence the fitness benefits of the migratory tactic at sea.

280 measured life history responses in terms of migratory tactics and freshwater maturation rates.

281 long that gradient and quantify variation in migratory tendency along that gradient.

282 titudinal migrants) and show that individual migratory tendency is higher among females than males an

283 phological and behavioural traits, including migratory tendency, of yellow-eyed juncos along a contin

284 how that individuals are consistent in their migratory timing in winter, indicating that the frequenc

285 We revealed that migratory timings and destinations of young shearwaters

286 In vitro, LPS-stimulated migratory TNFRp55(-/-) DCs of MLN increased IL-12/23p40

287 r parental species and explore links between migratory traits and predation risk.

288 However, when such species hybridize, migratory traits from parental species can combine malad

289 at all tumors continued to grow with an anti-migratory treatment alone, but the anti-proliferative/an

290 ual migration patterns (timing and number of migratory trips) in two common freshwater fish species,

291 For example, some migratory ungulates (i.e., hooved mammals) closely track

292 rasian dotterel (Charadrius morinellus) is a migratory wader, which has been the subject of uniquely

293 continental flyway increased their value to migratory waterbirds.

294 The study offers important insights into migratory waterfowl ecology and AI disease dynamics that

295 The habitat use of 344 wild migratory waterfowl over four migration cycles was estim

296 cted in 8,427 (10.8%) of 77,969 samples from migratory waterfowl throughout the Central and Mississip

297 spatial and temporal characteristics of wild migratory waterfowl's wintering habitat in the Republic

298 blue whales sing primarily at night, whereas migratory whales sing primarily during the day.

299 dition to domestic anseriforms in Asia, both migratory wild birds and domestic anseriforms in Europe

300 d mitigate future changes of disease risk in migratory wildlife that may arise from shifting migrator

301 ions leading to different health outcomes in migratory wildlife.