ライフサイエンスコーパス: migratory

1 age, HeLa cells change from proliferating to migratory.

2 o osteogenesis/chondrogenesis, and increased migratory ability in KFs.

3 so resulted in cell stiffening and decreased migratory ability in KFs.

4 Moreover, GE eliminated the migratory ability of HEY cells by reducing the expressio

5 and VHR deficiency resulted in a higher cell migratory ability.

6 In vitro neutrophil migratory accuracy in the elderly deteriorated as the se

7 The migratory accuracy of blood neutrophils from young (aged

8 To assess neutrophil migratory accuracy with age during respiratory infection

9 dose (80-mg) simvastatin improved neutrophil migratory accuracy without impeding other neutrophil fun

10 tumor suppressor PTEN show strongly impaired migratory activity and adhere strongly to their substrat

11 These cells displayed enhanced migratory activity but similar suppressive function, whi

12 ver, CD177(pos) neutrophils exhibit no clear migratory advantage in vivo, despite interruption of in

13 ell-substrate adhesion is downstream of many migratory and chemotaxis signaling events.

14 entified marine provinces that described the migratory and foraging habitats of these seals.

15 sistance to TKIs and induced EMT, increasing migratory and invasive behaviors.

16 Here we report that NatD promotes the migratory and invasive capabilities of lung cancer cells

17 hich bestows stem cell properties as well as migratory and invasive capabilities upon differentiated

18 rganizing the cellular architecture toward a migratory and invasive phenotype.

19 se their epithelial properties and acquire a migratory and invasive phenotype.

20 tes S10 or T198, but not T157, abolished the migratory and invasive phenotypes.

21 ations, we observed that FVIIa increased the migratory and invasive potential of these cells.

22 rphologic changes concomitant with increased migratory and invasive potential.

23 ining a mesenchymal phenotype with increased migratory and invasive properties.

24 The Mena(INV) isoform is upregulated in migratory and invasive sub-populations of breast carcino

25 -of-LKB1 rendered breast cancer cells highly migratory and invasive, attaining cancer stem cell-like

26 way inhibition is required for the increased migratory and invasiveness ability of breast cancer cell

27 ate N-cadherin (CDH2) and CD133 along with a migratory and mesenchymal-like phenotype.

28 ing sarcoma cells profoundly inhibited their migratory and metastatic potential.

29 fibroblasts, which was associated with a pro-migratory and pro-invasive phenotype.

30 tions in cell mechanics, leading to enhanced migratory and proliferative potential of ECs during the

31 Understanding changes in the migratory and reproductive phenology of fish stocks in r

32 Neural crest cells are both highly migratory and significant to vertebrate organogenesis.

33 essed during EMT, in addition to suppressing migratory and stem-like properties of tumor cells, also

34 :1, suggesting that both sexes are partially migratory and that migration was not sex-biased across s

35 Cancer cells require both migratory and tumorigenic property to establish metastat

36 iPSC-EVs enhanced angiogenic, migratory, and antiapoptotic properties of murine cardia

37 y was undertaken to elucidate the molecular, migratory, and functional phenotypes of patrolling monoc

38 Migratory animals are threatened by human-induced global

39 Long-lived migratory animals must balance the cost of current repro

40 Specifically, many migratory animals that rely on wetlands are increasingly

41 evelop effective conservation strategies for migratory animals.

42 ent pivaloyl (Piv) ester, stability, minimal migratory aptitude, minimal orthoester formation, while

43 logical interval between spring green-up and migratory arrival for 48 breeding passerine species acro

44 antified seasonal shifts in the densities of migratory baleen whales.

45 nterstitial cell migration in the context of migratory barriers using a novel tissue Boyden chamber a

46 After vaccination, both migratory basic leucine zipper ATF-like transcription fa

47 ide-in signaling that promotes CD8(+) T-cell migratory behavior and effector functions.

48 In general, endothelial cells change their migratory behavior in response to shear stress patterns,

49 he ratio between S1PR1 and S1PR2 governs the migratory behavior of T cell subsets.

50 Tconv and provide a framework via which the migratory behavior of Treg versus Tconv might be regulat

51 hat urban sources of ALAN can broadly effect migratory behavior, emphasizing the need to better under

52 ongly adherent metastatic cells exhibit less migratory behavior, similar to nonmetastatic cell lines

53 merization, matrix degradation, and invasive migratory behavior.

54 cells display a more heterogeneous range of migratory behaviors at later stages of development, with

55 e mechanisms that coordinate individual cell migratory behaviors for collective movement are largely

56 er these data demonstrate previously unknown migratory behaviors of innate lymphocytes undergoing lin

57 on is crucial for tuning emergent collective migratory behaviors, such as vortical motions observed i

58 cal stress within the HFR and changes in HPC migratory behaviors.

59 ll biology of collective and individual cell migratory behaviors.

60 a, we analysed phenotypic differentiation of migratory behaviour among populations of the European ro

61 Our results show migratory behaviour in ungulates is an individually vari

62 ies examine the extent to which variation in migratory behaviour influences individual fitness across

63 arch on large mammals has often assumed that migratory behaviour is a fixed behavioural trait.

64 ndicated that intrapopulation variability in migratory behaviour is a general feature of the spatial

65 This migratory behaviour relaxes the boundaries between the f

66 ontrol that phytoplankton can exert on their migratory behaviour.

67 ll lines showed differences linked to unique migratory behaviours and cytoskeletal re-arrangements.

68 We also predicted that wide-ranging and migratory behaviours could increase infection risks with

69 ration timing of 13 species of long-distance migratory bird changed across a period of substantial cl

70 plications of these changes for transoceanic migratory bird populations have not been addressed.

71 Outside of the two migration periods, migratory bird populations presented stronger than expec

72 Migratory bird populations presented stronger than expec

73 tter understand the implications of ALAN for migratory bird populations.

74 across the annual cycle for 10 transatlantic migratory bird species.

75 rant males, females and pairs in a partially migratory bird.

76 responsible for magnetic compass sensing in migratory birds and a variety of magnetic behavioural re

77 requiring open vegetation structure (such as migratory birds and foraging bats) as well as the recrea

78 recent population declines of long-distance migratory birds in particular.

79 ion system under clear skies for experienced migratory birds in some areas of the globe.

80 Consequently, migratory birds must solve the longitude problem in a di

81 Migratory birds often make substantial detours from the

82 When conducting oceanic crossings, migratory birds tend to associate with mild or supportiv

83 susceptibility of highly mobile taxa such as migratory birds to global change requires information on

84 rapid declines of many populations of Arctic migratory birds, our results emphasize the urgency of mi

85 s the basis of the magnetic compass sense of migratory birds.

86 ns of three deer species as migratory or non-migratory, by means of three methods: seasonal home rang

87 Identifying the characteristic features of migratory cancer stem cells with tumorigenic property is

88 Partial silencing of S100A4 suppressed migratory capabilities of TMD cells, while Paclitaxel de

89 onic diseases exhibit poor proliferative and migratory capabilities, which impair overall reparative

90 be a useful tool for the quantitation of the migratory capability and anti-metastatic drug screening.

91 In accordance with a higher migratory capacity across the blood-brain barrier, CD56(

92 receptors on human macrophages enhanced the migratory capacity and prolonged the survival of neutrop

93 2S production and enhanced cell survival and migratory capacity in high glucose (HG)-treated BMCs.

94 useful assay to quantify alterations in cell migratory capacity in response to experimental manipulat

95 lity, which was accompanied with an enhanced migratory capacity in transwell assays and clonogenicity

96 n Rpl22-deficient tumor cells restores their migratory capacity in vitro The regulation of KLF2 and S

97 Although no MS-related changes in the migratory capacity of NK cells were observed, NK cells d

98 traced the defect in the Rpl22(-/-) lymphoma migratory capacity to downregulation of the KLF2 transcr

99 Tollip deficient neutrophils had compromised migratory capacity toward bacterial product fMLF due to

100 s from gut flora-depleted mice had decreased migratory capacity toward CX3CL1 and CCL2 ligands.

101 -10DCs, CD83(high) IL-10DCs exerted a strong migratory capacity toward the secondary lymphoid organ c

102 RCPS iNCCs have decreased migratory capacity, a distinct phenotype relative to oth

103 tion to mesenteric lymph nodes of intestinal migratory CD103(+) DCs carrying oral DNFB, especially th

104 the activation of CD8alpha(+) DCs, while the migratory CD103(+) DCs may play a role in sustaining the

105 s and antibodies by ELISA; the percentage of migratory CD1a(+) dermal DCs was significantly decreased

106 to wound sites and for the establishment of migratory cell morphology.

107 Adult-young dogs contained migratory cells capable to expand and differentiate in v

108 Clusters of migratory cells in these systems are capable of respondi

109 the mechanisms regulating the morphology of migratory cells on rigid substrates in cell culture are

110 ucleus is positioned toward the rear of most migratory cells.

111 anized in layers as in humans, but including migratory chains as in rodents.

112 live in-hive bees, stored pollen, and wax in migratory colonies over time and compared exposure to co

113 where species are able to breed, disrupting migratory connections globally.

114 Determining patterns of migratory connectivity for highly-mobile, wide-ranging s

115 out and mix during the non-breeding season (migratory connectivity) is essential for understanding a

116 We evaluate the Mantel test as a metric of migratory connectivity, and explore the extent to which

117 Here, we develop a full annual migratory cycle model from metabolic and foraging theory

118 tween traits and the migratory phases of the migratory cycle, we find that effects of body size on th

119 tifying fitness impacts over the full annual migratory cycle.

120 ography and movement patterns throughout the migratory cycle.

121 undergo decarboxylative pyrimidine/pyridine migratory cyclization (rather than deprotection of pyrim

122 lity also undergoes decarboxylative pyridine migratory cyclization using MeOTf/NaOMe in toluene provi

123 Nevertheless, CD302KO migratory DC exhibited reduced in vivo migration into LN

124 seI in D23580 reduced the number of infected migratory DCs and bacteria in the MLN.

125 ice, we herein provide in vivo evidence that migratory DCs execute targeted cell-to-cell interactions

126 antigens is mediated only by BatF3-dependent migratory DCs potentially acquiring apoptotic LECs.

127 on, LEC-archived antigens are exchanged with migratory DCs, both directly and through LEC apoptosis,

128 We reveal that MHCII(high) migratory DCs, neutrophils, and monocytes can acquire Ag

129 metabolism and this sensitivity could drive migratory decisions (forage hypothesis).

130 Cell migratory defects have been identified in animal models

131 ntigens between LECs and APCs is mediated by migratory dendritic cells (DC).

132 mesenteric lymph nodes (MLNs), via CD11b(+) migratory dendritic cells (DCs).

133 urther substantiate a critical role for skin migratory dendritic cells and in particular Langerhans c

134 echanical stress, including stress fibers in migratory distal tip cells and the proximal gonad sheath

135 owed that CLOCK knockdown increased neuronal migratory distance.

136 emonstrates that metastasized cells are less migratory due in part to the post-metastatic downregulat

137 ibronectin in Xenopus neural crest, a highly migratory embryonic cell population.

138 cated compared with sedentary endoparasites, migratory endoparasites are exquisitely suited to their

139 As migratory endoparasites, their presence in roots is less

140 nspicuous signs are skin lesions (necrolytic migratory erythema), while in subjects with inactivating

141 least partly responsible for the necrolytic migratory erythema, which resolves after amino acid admi

142 in situ differentiation or alternatively as migratory events and possible admixture with surrounding

143 on factor and its targets, including the key migratory factor sphingosine 1-phosphate receptor 1 (S1P

144 we present a novel modelling framework, the Migratory Flow Network (MFN), in which the seasonally va

145 e anti-migratory microRNA miR-198 or the pro-migratory follistatin-like 1 (FSTL1) protein from a sing

146 here a method for the catalytic, asymmetric, migratory geminal difluorination of beta-substituted sty

147 emarkable diversity in patterns of change in migratory habits [15-21], and these Argentine-breeding s

148 le in rivers throughout the world when large migratory herds were more common features of the landsca

149 Addressing population declines of migratory insects requires linking populations across di

150 vage of the unstrained C-C bond, followed by migratory insertion and reductive elimination.

151 om acetylide formation to the azide ligation/migratory insertion event allowing chemoselectivity inde

152 ional Wacker-type products, enantioselective migratory insertion is followed by beta-hydride eliminat

153 Au(III) complexes that participate in rapid migratory insertion of carbenes derived from silyl- or c

154 would offer new synthetic opportunities for migratory insertion of carbon-based species into gold-ca

155 Migratory insertion of carbon-based species into transit

156 tudies support a concerted mechanism for the migratory insertion of the alkene into the carbon-boron

157 proceeds by a succession of C-H activation, migratory insertion of the ylide into the carbon-metal b

158 Preliminary mechanistic study favors an Ir-C migratory insertion pathway.

159 kynes, in contrast to the generally accepted migratory insertion pathway.

160 ld-catalyzed processes incorporating carbene migratory insertion steps.

161 of one C horizontal lineO bond, followed by migratory insertion to generate the tungsten-oxo alkylid

162 e=NAd (R = (neo)Pe (3a), 1-nor (3b)) undergo migratory insertion to iron(II) amides (Me2IPr)RFe{NR(Ad

163 chanism proceeding via fluoride abstraction, migratory insertion, and C-F reductive elimination to ac

164 Epithelial cells acquire migratory/invasive and stemness traits upon conversion t

165 rough the integration of programs leading to migratory/invasive phenotypes, survival and resistance t

166 f the cytochrome P450 gene LmCYP4G102 in the migratory locust Locusta migratoria.

167 Typical of many migratory marine species, ontogenetic changes in habitat

168 potential for differential habitat use among migratory marine vertebrates, we measured the naturally

169 d a decrease in the frequency and numbers of migratory mDC within CD302KO LN compared with wild-type

170 However, the migratory mechanisms that bring juvenile eels to Europe

171 bluminal vascular surfaces, or extravascular migratory metastasis (EVMM).

172 witch involves production of either the anti-migratory microRNA miR-198 or the pro-migratory follista

173 mRNA expression of pro-proliferative and pro-migratory MKL1/2 target genes in VSMCs but not in ECs.

174 e greatest benefit to eastern North American migratory monarchs, but the population will likely remai

175 e mechanisms by which collectives maintain a migratory morphology while resisting physical constraint

176 s paper, we introduce a mechanistic model of migratory movement patterns in birds, inspired by ideas

177 a bottom up explanation of population-level migratory movement patterns.

178 source availability are important drivers of migratory movements, with birds from larger colonies or

179 In a population of migratory mule deer (Odocoileus hemionus), 31% surfed pl

180 Here, we identify in mouse a population of migratory myofibroblasts at the leading edge of the clos

181 Pax3-positive migratory myogenic progenitors, marked by expression of

182 g of the carapacial pigmentation as both the migratory neural crest cells and pigment localized only

183 ues and control dynamic interactions between migratory neuroblasts and surrounding astrocytes are of

184 neurogenic stem cell niche generates highly migratory neuroblasts that transit the anterior forebrai

185 strong and weak site fidelity strategies in migratory northern elephant seals performed similarly ov

186 om five populations of three deer species as migratory or non-migratory, by means of three methods: s

187 vels) could lead to the establishment of new migratory or resident populations within the Arctic Circ

188 Long-distance migratory organisms are under strong selection to migrat

189 paired mucosal site, reflecting their tissue-migratory origin.

190 ghost fibers impacted myogenic progenitors' migratory paths and division planes, causing disorganiza

191 oderm, and then it becomes absent along cell migratory pathways.

192 Differential migratory patterns illustrate the potential of our setup

193 c demographic dynamics, sexual behavior, and migratory patterns.

194 we find that effects of body size on the non-migratory phases are far more important determinants of

195 has focused on links between traits and the migratory phases of the migratory cycle, we find that ef

196 ature, suggesting that some of the shifts in migratory phenological response to climate are predictab

197 short-distance migrants have advanced spring migratory phenology by more than long-distance migrants.

198 This migratory phenomenon that we call Molecular Rheotaxis in

199 aracrine macrophage activation regulates the migratory phenotype associated with breast cancer initia

200 gulation is responsible for the MSX1-induced migratory phenotype in melanoma cells.

201 henotypic conversion from a contractile to a migratory phenotype is proposed to underlie cardiovascul

202 mography (PET/CT) of the arterial wall and a migratory phenotype of monocytes.

203 to the actin cytoskeleton, acquisition of a migratory phenotype, and upregulation of EWS/ETS-repress

204 tractile SMCs reprogramme into a 'synthetic' migratory phenotype, so-called phenotypic modulation, wh

205 information about the cell's morphology and migratory phenotype.

206 ticity with reversion to a neural crest cell migratory phenotype.

207 ted a polarized morphology consistent with a migratory phenotype.

208 -6 and IL-8 and rescued the tumor growth and migratory phenotypes of ovarian cancer cells expressing

209 nd blockade of terminal Le(x) regulated post-migratory PMN functions, increasing PMN phagocytosis and

210 EDD9/DLC1-RHOA regulatory axis to govern NCC migratory polarization.

211 benefits of migration, we studied a partial migratory population of European blackbirds (Turdus meru

212 emales and breeding pairs within a partially migratory population.

213 ded fully integrated demographic analyses of migratory populations in response to changing climatic c

214 anges in stopover habitat can severely limit migratory populations.

215 CORM-401-dependent suppression of neutrophil migratory potential associated with modulation of PAK1/2

216 Therefore, our data suggest that the migratory potential is elevated when GBM tumor cells are

217 ssay demonstrated a two-fold increase in the migratory potential of HA-treated MSC compared to untrea

218 P5 in these cells rescued their invasive and migratory potential.

219 DCs exhibited enhanced T cell activation and migratory potential.

220 le epithelial traits and acquire mesenchymal migratory potential.

221 g responses to climate forcing by a poleward migratory predator through varying sea ice property and

222 Chelonia mydas, which are long-lived, highly migratory, primarily herbivorous mega-consumers that may

223 head and face are derived from a multipotent migratory progenitor cell population called the neural c

224 uroblasts, in an IPC subdomain they generate migratory progenitors by epithelial-mesenchymal transiti

225 e-patterning occurring in their post-mitotic migratory progeny.

226 Kindlin-2 deficiency inhibited invasive and migratory properties in vitro without affecting prolifer

227 oducing pDCs exhibit enhanced CCR7-dependent migratory properties in vitro.

228 Cells acquire the invasive and migratory properties necessary for the invasion-metastas

229 Due to the migratory properties of DCs, EBOV infection of these cel

230 ible monocyte dysfunction in MS and analyzed migratory properties of monocyte subsets using human bra

231 phenotype CD8 T cells and influencing their migratory properties, accumulation, and functions.

232 T-related transcription factors and enhanced migratory properties.

233 ant implications for the conservation of the migratory red-crowned crane population that winters in t

234 receptor agonist JWH-133 induced a moderate migratory response in eosinophils.

235 antial intra- and interspecific variation in migratory response remains to be explained.

236 CL3 while abrogating the multiple myeloma PC migratory response to CXCL12.

237 from 12/15-LOX(-/-) mice exhibit diminished migratory response to monocyte chemotactic protein 1 (MC

238 troduce an in vitro system allowing to track migratory responses of DCs to precisely controlled immob

239 in why Pyk2 is important for chemotactic and migratory responses.

240 AR stimulation increased CCR2 expression and migratory responsiveness to CCL2 in BM.

241 droquinolines, and their homologues) undergo migratory ring expansion through deprotonation of their

242 alaria-induced splenic MO-DCs take a reverse migratory route.

243 asuring puffins' among-colony differences in migratory routes and day-to-day behavior (estimated with

244 Our results indicate that migratory routes are more than a link between seasonal r

245 x2 and Ephb2 to maintain distinct tangential migratory routes in the dorsal telencephalon.

246 ion of forage resources that propagate along migratory routes shape animal movement and presumably, e

247 d other methods to establish goliath catfish migratory routes, their seasonal timing and possible ret

248 e order, rate and duration of green-up along migratory routes, was the primary factor influencing sur

249 isrupted the separation of the VZ/SVZ and IZ migratory routes.

250 alcium channel-interneurons display abnormal migratory saltations.

251 movement across short (diel) and long-term (migratory) scales.

252 nd Western Europe, NW cluster) to completely migratory (Scandinavia and north-eastern Europe, NE clus

253 ment with Gc reduced the activity of the pro-migratory small GTPase regulator Rac1.

254 SMCs is difficult as no specific markers of migratory SMCs exist.

255 t in rhythmicity might be more common across migratory songbird species, but may not have been observ

256 cluding wood thrush, Hylocichla mustelina, a migratory songbird that has been declining for several d

257 birds with a 26-year demographic study of a migratory songbird to evaluate the relative effects of d

258 Although long-distance migratory songbirds are widely believed to be at risk fr

259 Nevertheless, experienced night-migratory songbirds can correct for east-west displaceme

260 Migratory species are likely to be particularly sensitiv

261 The geographic distribution of migratory species can span thousands of kilometers.

262 Conservation of migratory species faces the challenge of understanding t

263 tal changes for the long-term persistence of migratory species populations.

264 carry-over effects and can help predict how migratory species should respond to future climate-induc

265 ogenetic shifts in the habitat use of highly migratory species, along with possible intrapopulation v

266 multi-year habitat-use patterns of a remote migratory species, linked to estimated ages and body siz

267 This is particularly applicable to migratory species, such as salmon, where distinct tempor

268 igration, affects the population dynamics of migratory species.

269 es will be essential to effectively conserve migratory species.

270 population dynamics and the conservation of migratory species.

271 s of unknown migrants is applicable to other migratory species.

272 for their migration and was initiated by pro-migratory stimuli via a PI3K-mTORC2-mediated pathway cul

273 oss large geographical scales, how different migratory strategies emerge between populations, and how

274 reproductive performance associated with the migratory strategies of males, females and breeding pair

275 These modes thus represent distinctive migratory strategies.

276 isms, but imply that individual variation in migratory strategy and variation in pairing among reside

277 Disruption of this migratory strategy by turbulence is considered to be an

278 inoflagellates, can actively diversify their migratory strategy in response to hydrodynamic cues char

279 during migration; however, understanding how migratory strategy influences population dynamics is hin

280 ding success also varied with a pair's joint migratory strategy such that resident-resident pairs hat

281 dence of assortative pairing with respect to migratory strategy: observed frequencies of migrant-migr

282 The rostral migratory stream (RMS) is viewed as a glia-enriched cond

283 ate neuroblasts that migrate via the rostral migratory stream (RMS) to the olfactory bulb, where they

284 e astroglial meshwork of the SVZ and rostral migratory stream (RMS), yet are permissive to large-scal

285 neurons impacts on NPC-traits in the rostral migratory stream (RMS).

286 glial cells are dispersed along the rostral migratory stream in postnatal and adult brains.

287 factor (VEGF) is known to influence rostral migratory stream in rodents.

288 n up to length scales similar to that of the migratory stream observed in the adult brain.

289 sity and dynamics within a neural crest cell migratory stream that underlie complex directed and coll

290 ith an increase of SVZ neuroblast in rostral migratory stream, whereas VEGF ligand inhibition prevent

291 sion in cells within other subregions of the migratory stream.

292 discuss how MFNs could be applied to diverse migratory taxa and highlight the potential of MFNs as a

293 mechanisms mediating the transition from the migratory to bactericidal phenotype remain elusive.

294 4 satellite tagged adult Montagu's harriers; migratory tracks more closely approached straight-line r

295 idney rats with hydrocephalus, alteration of migratory trajectory is detected.

296 d TNS3 expressions are mutually exclusive in migratory tumor lesions, and GBM patients with MSI1(high

297 Salmon sharks Lamna ditropis are highly migratory, upper trophic level predators in North Pacifi

298 ovide fascinating new insights into the role migratory variability can play in shaping population dyn

299 influx channels (SOCs) in proliferative and migratory vascular smooth muscle cells (VSMCs) are quite

300 4(+) T cells within the meninges were highly migratory, whereas Tregs moved more slowly and were foun