ライフサイエンスコーパス: segregation

1 epresented in leadership positions (vertical segregation).

2 -replication, leading to aberrant chromosome segregation.

3 to live may lead to the emergence of social segregation.

4 ortex, in which sound repetition facilitates segregation.

5 nds of genome replication without chromosome segregation.

6 of visual information, such as figure-ground segregation.

7 fects in kinetochore assembly and chromosome segregation.

8 nisms underlying its functions in chromosome segregation.

9 mitosis to ensure the fidelity of chromosome segregation.

10 s of R-loops at CEN chromatin and chromosome segregation.

11 to dictate widespread changes in compartment segregation.

12 tic chromosomes as they prepare for anaphase segregation.

13 mere DNA is required for faithful chromosome segregation.

14 the efficiency of cell growth and chromosome segregation.

15 scription, DNA damage repair, and chromosome segregation.

16 ery of Cas9-edited barcodes to query lineage segregation.

17 inetochores that ensures accurate chromosome segregation.

18 ructures that maximize the useful impacts of segregation.

19 ological advantage of hemispheric functional segregation.

20 as spreading, to enable efficient chromosome segregation.

21 d disrupts MI spindle function in chromosome segregation.

22 a structure that is competent for chromosome segregation.

23 ble centromeres after replication and before segregation.

24 odeling processes that facilitate homologous segregation.

25 logous chromosomes is essential for faithful segregation.

26 g mitosis, which ensures accurate chromosome segregation.

27 o barrels and thalamocortical afferent (TCA) segregation.

28 ls exiting mitosis without proper chromosome segregation.

29 entified the metabolites responsible for the segregation.

30 ated by kinetochores (KTs) during chromosome segregation.

31 in and Shugoshin is not required for meiotic segregation.

32 g network that guards fidelity of chromosome segregation.

33 more states, especially those with the most segregation.

34 ses crossovers and Uup prevents nucleoid mis-segregation.

35 along meiotic chromosomes for their accurate segregation.

36 ked to aberrant chromosomal condensation and segregation.

37 ntromere instability and abnormal chromosome segregation.

38 ubule-mediated forces for mitotic chromosome segregation.

39 metaphase I plate, and causes chromosome mis-segregation.

40 onsiveness for much more accurate chromosome segregation.

41 sandwich-type structures and vertical phase segregation.

42 nucleation, which is critical for chromosome segregation.

43 iffusion length and further suppressed phase segregation.

44 e chromosome alignment and proper chromosome segregation.

45 and along the spindle to control chromosome segregation.

46 ote Dam1c oligomerization to ensure accurate segregation.

47 stand the logic of the underlying functional segregation.

48 crossing over must occur for correct meiotic segregation(1,2).

49 ototypical pattern of functional hemispheric segregation (44%) or deviate from this pattern in only o

50 ome is restructured to facilitate chromosome segregation, accompanied by dramatic changes in gene exp

51 er-equality paradox" is the fact that gender segregation across occupations is more pronounced in mor

52 ons is tightly regulated, resulting in their segregation along different transport routes, which limi

53 f dynamic interaction (e.g., integration and segregation) among neuronal populations in cognitive fun

54 Furthermore, segregation analysis of F2 progeny of parental C57Bl/6N

55 el-based genomic DNA sequencing, followed by segregation analysis of large kindreds and transcription

56 Family segregation analysis showed familial disease in 46% of p

57 rarely by cellular functional validation and segregation analysis.

58 FLAgs), these structures show incomplete T/B segregation and a partially differentiated stromal archi

59 esin mutations in the fidelity of chromosome segregation and aneuploidy.

60 omeres are essential for accurate chromosome segregation and are marked by centromere protein A (CENP

61 tween chromosome (and specifically terminus) segregation and cell division may result in asymmetric d

62 Our model combines the effect of segregation and compaction on chromosomal organization w

63 Meiotic crossovers facilitate chromosome segregation and create new combinations of alleles in ga

64 ination, which facilitates proper chromosome segregation and enables the reciprocal exchange of DNA s

65 dress the self-organizing dynamics of social segregation and explore the space of possibilities that

66 ear domains strictly required for chromosome segregation and genome stability.

67 are required for achieving proper chromosome segregation and highlights how these are both conserved

68 followed by spontaneous alternations between segregation and integration, each being dominant for a f

69 rophase is important for accurate chromosome segregation and normal activation of gene expression in

70 prophase I, resulting in accurate chromosome segregation and providing a mechanism to prevent aneuplo

71 properly for sophisticated features of gene segregation and recombination in an autotetraploid meios

72 has essential roles in chromosome structure, segregation and repair.

73 pinning auditory scene analysis-sound source segregation and sound event grouping-in a cohort of 21 p

74 he competitive hierarchy is caused by active segregation and spatial exclusion within the patch: a sm

75 lution of angiosperms was accompanied by the segregation and specialisation of their xylem tissues.

76 first comprises genes involved in chromosome segregation and stability (CSM3, CTF4, YKE2, DCC1, and G

77 tradictory experimental results such as root segregation and the tragedy of the commons in plant root

78 cating sounds, which leads to impaired sound segregation and threat detection.

79 is essential for accurate meiotic chromosome segregation and timely anaphase onset.

80 of polyploidy, genome stability, chromosome segregation, and bioenergy.

81 oupling between changes in DNA condensation, segregation, and cell division.

82 rs, and motors involved in the condensation, segregation, and digestion of DNA.

83 ved in sister chromatid cohesion, chromosome segregation, and DNA repair.

84 leads to audience fragmentation, ideological segregation, and echo chambers with no cross-cutting exp

85 at kinetochores, the fidelity of chromosome segregation, and genome stability in larval neuroblasts

86 defect in ribosomal DNA (rDNA) and telomere segregation, and it ultimately delays cell division.

87 ers mitotic spindle orientation, chromosomal segregation, and nuclear migration.

88 e to DNA repair, gene expression, chromosome segregation, and potentially other biological processes.

89 chromosomes, errors of homologous chromosome segregation, and production of aneuploid oocytes.

90 ensure high-fidelity replication, chromosome segregation, and repair of germ cell genomes remain inco

91 urces among these avian predators is spatial segregation, and secondarily prey size and species.

92 a fraction of cells favor mixing, the others segregation, and that these cells are randomly distribut

93 stern harmony, acoustic constraints on sound segregation appear to induce perceptual structure on not

94 le assembly and chromosome biorientation and segregation are not fully understood, despite extensive

95 g that rapidly evolving genomic battles over segregation are rampant on young sex chromosomes and uti

96 , mutations in genes that control chromosome segregation are rare in human tumors as these mutations

97 g centrosome asymmetry and biased centrosome segregation are unclear.

98 eas) or no defined pathway (incomplete or no segregation, areas shared with patients with COVID-19).

99 re key to unlocking the full potential of GB segregation as an alloy design tool, and enable the desi

100 nd be fertilised, despite chaotic chromosome segregation at the first meiotic division.

101 specific predictions from this hypothesis on segregation behaviour in mouse and human mtDNA.

102 The first STS dimension reflected segregation between drought-tolerant and waterlogging-to

103 This 'segregation bias' is a long-standing biological mystery

104 mbination is critical for meiotic chromosome segregation, but how mammalian crossing over is accompli

105 elomere dysfunctions also perturb chromosome segregation by contributing to the formation of chromati

106 eckpoint (SAC) prevents premature chromosome segregation by inactivating the anaphase promoting compl

107 DeltaSUV(max) approach, for example, for the segregation by iPET response, where the event-free survi

108 g of the nuclear envelope enables chromosome segregation by the mitotic spindle(1).

109 We argue that hydrologic niche segregation can be a useful lens through which to interp

110 that are not directly involved in chromosome segregation can lead to aneuploidy induction.

111 were characterized using measures of network segregation (clustering and modularity), network integra

112 s, including functions related to chromosome segregation, cohesin removal, and kinetochore orientatio

113 This subcellular segregation coincides with DREPP-dependent MT fragmentat

114 The resulting machine learning models and segregation database are key to unlocking the full poten

115 , and that its depletion leads to chromosome segregation defects and increased levels of endogenous D

116 metaphase plate leading to robust chromosome-segregation defects and nonmodal karyotypes.

117 tubulin autoregulation and showed chromosome segregation defects during mitosis.

118 systematic quantitation of these chromosome segregation defects in cells undergoing mitosis.

119 Accurate chromosome segregation demands efficient capture of microtubules by

120 re transcriptionally distinct prior to their segregation, dendritic outgrowth, and synapse formation.

121 Chromosome segregation depends on a regulated connection between sp

122 Accurate chromosome segregation depends on the proper attachment of kinetoch

123 during IVF-these receptors act as 'suicidal' segregation distorters that impair their own transmissio

124 h assay (TeSLA), we show that chromosome mis-segregation due to imperfect DDR signaling in response t

125 ysfunctional mitochondria through asymmetric segregation during active division.

126 fication, RNAi components promote chromosome segregation during both mitosis and meiosis and regulate

127 Chromosome segregation during cell division is driven by mitotic sp

128 a dynamic structure orchestrating chromosome segregation during cell division.

129 complex ensures their accurate alignment and segregation during cell division.

130 ssential for mitotic chromosome assembly and segregation during cell divisions, however, little is kn

131 Chromosome segregation during male meiosis is tailored to rapidly g

132 erequisite for achieving accurate chromosome segregation during meiosis [1, 2].

133 Homologous chromosome segregation during meiosis I (MI) in mammalian oocytes i

134 ultimately defines the pattern of chromosome segregation during meiosis I.

135 Crossovers (COs) ensure accurate chromosome segregation during meiosis while creating novel allelic

136 kinetochore assembly and faithful chromosome segregation during meiosis.

137 ination is essential for accurate chromosome segregation during meiosis.

138 itotic spindle to ensure faithful chromosome segregation during mitosis, cell polarization and migrat

139 matin formation in interphase and chromosome segregation during mitosis, demonstrating that active re

140 opriate cell cycle progression and chromatid segregation during mitosis, possibly in a nontranscripti

141 on, which is essential for proper chromosome segregation during mitosis.

142 kinase is essential for faithful chromosome segregation during mitosis.

143 n, recombination, DNA repair, and chromosome segregation during mitosis.

144 etween sister chromatid compaction and their segregation during mitosis.

145 Chromosome segregation during the cell cycle is an evolutionarily c

146 Second, we find evidence of a segregation effect, since mobility contraction is strong

147 oy space, and build an extensive database of segregation energy spectra for more than 250 metal-based

148 t the segregation tendency-quantified by the segregation enthalpy spectrum-of solute atoms at GB site

149 in part, from DNA replication and chromosome segregation errors due to cell division during developme

150 erstanding of the contribution of chromosome segregation errors to the development of aneuploidy.

151 required for meiosis I to prevent chromosome segregation errors.

152 meiosis I, and others showed more meiosis II segregation failures.

153 y elements for the maintenance of chromosome segregation fidelity via a specialized chromatin marked

154 The segregation findings suggest a possible signature of alt

155 of Atg14 and observed homologous chromosome segregation followed by sister chromatid separation; cel

156 electrostatic energy determine the extent of segregation for a given overpotential and atmosphere rel

157 ss and then promoted DDB2 ubiquitination and segregation from chromatin, thereby facilitating downstr

158 ted protein complex essential for chromosome segregation, gene expression, and repair of DNA damage.

159 The Schelling model of segregation has been shown to have a simulation trace wh

160 s a major determinant of accurate chromosome segregation has not been previously directly analyzed in

161 l whole-exome sequencing of the patients and segregation in available family members identified loss-

162 of the kinetochore during meiotic chromosome segregation in C. elegans oocytes has been a matter of c

163 Genotype-phenotype segregation in CASQ2-CPVT families was assessed, and the

164 This sex segregation in elephant movement decisions highlights th

165 bserved a suppression of light-induced phase segregation in films even at 100-sun illumination intens

166 structure affect socio-economic residential segregation in global cities.

167 adhesive forces and lead to efficient strain segregation in heterogenous populations, indicating that

168 ion of a molecular cascade that initiates TE segregation in human, cow and mouse embryos.

169 Kinetochores direct chromosome segregation in mitosis and meiosis.

170 Accurate chromosome segregation in mitosis requires sister kinetochores to b

171 e mitotic spindle, enabling sister chromatid segregation in mitosis.

172 evident from the TiO(2)-assisted halide ion segregation in mixed halide perovskite (MHP) films under

173 ve been associated with light-induced halide segregation in mixed-halide perovskite compositions(7) a

174 We also verified if spatial segregation in nesting areas could be another mechanism

175 ommunity membership emphasized lower network segregation in OCD compared to healthy controls.

176 ra B pool that supported faithful chromosome segregation in otherwise unchallenged cells.

177 ion of ribosomal RNA synthesis and nucleolar segregation in response to rDNA breaks.

178 ers transcriptional inhibition and nucleolar segregation in response to rDNA breaks.

179 g movement patterns, which can result in sex segregation in responses to mitigation methods.

180 umbers and increase in retinogeniculate axon segregation in the lateral geniculate nucleus.

181 for the onset of polarization and cell fate segregation in the mouse.

182 -olds, racial/ethnic minorities, residential segregation, income inequality, uninsured, diabetics, or

183 Since segregation-induced banded microstructures commonly occu

184 on diffraction experiments, the influence of segregation-induced microstructure bands of austenite (g

185 ls, we reconstructed histories of chromosome segregation, inferring that 55 (74%) embryos possessed m

186 pancreatic progenitor cells (MPCs) and their segregation into bipotent progenitors (BPs) and unipoten

187 bly, ES7L-mutated ribosomes showed increased segregation into cytoplasmic foci containing soluble mis

188 ough the complex process of equal chromosome segregation into daughter cells.

189 This additive also retards compositional segregation into impurity phases and pinhole formation i

190 endogenous intermediate filament system and segregation into protein aggregates.

191 Finally, we demonstrate that lesion segregation is a unifying property of exogenous mutagens

192 focus on resolving quantitatively how dopant segregation is affected by oxygen chemical potential, wh

193 Delayed segregation is controlled by the MatP protein, which bin

194 Component segregation is due to unstable inhomogeneous membrane cu

195 Orderly chromosome segregation is enabled by crossovers between homologous

196 Proper chromosome segregation is essential for faithful cell division and

197 The resulting spatial segregation is lost for weak growth-migration trade-offs

198 of fidelity of mitochondrial morphology and segregation is one type of HSC divisional memory and dri

199 This segregation is only observed when deposited on an ETL su

200 onserved requirement in mediating chromosome segregation, kinetochores display remarkable plasticity

201 auses defects in chromosome organization and segregation leading to a block in cell division.

202 ystals, based solely on the undecorated (pre-segregation) local atomic environment of such sites.

203 ey steps of cell division such as chromosome segregation, mitotic duration and cytokinesis.

204 sions inspired on the rules of the Schelling Segregation model and rewards for interactions.

205 termine that cholesterol facilitated lateral segregation most with the SMs that had 16 carbon-long ac

206 a general approach for quantifying chemical segregations near voids within an APT dataset, in which

207 ernative possibility, in which early, active segregation occurs even for strongly spectrotemporally o

208 Here we demonstrate the segregation of a novel missense variant in CYLD (c.2155A

209 We also provide evidence for familial segregation of a rare nonsense KDR variant with these ph

210 hen influences the mechanisms underlying the segregation of aliovalent dopants.

211 s building principle in cells, which permits segregation of biological elements and reactions.

212 EDX analysis has revealed homogeneous segregation of chromium and iron along GBs.

213 ellular processes, including the capture and segregation of chromosomes during mitosis.

214 proper execution of mitosis and the accurate segregation of chromosomes to daughter cells.

215 gnaling systems is a prerequisite for proper segregation of ectodermal cell types.

216 ors by phosphorylation, preventing premature segregation of entangled chromosomes formed during HR re

217 ay a key role in the expression, repair, and segregation of eukaryotic genomes.

218 f extra centrioles, or by grossly asymmetric segregation of extra centrioles in mitosis.

219 The degree of segregation of fields of study declined dramatically in

220 Our current study further establishes the segregation of GPe neuron classes and illustrates the co

221 e tracking of hydrogen atoms reveal that the segregation of hydrogen atoms at the grain boundaries, r

222 Using this tool, we uncovered partial segregation of inhibitory spontaneous and evoked neurotr

223 The functional integration and functional segregation of LDAI and LVAI were further supported by t

224 The segregation of lipids into lateral membrane domains has

225 ACD can be manifested in the biased segregation of macromolecules, the differential partitio

226 mics the epidermal-dermal interface, spatial segregation of mean ERK activity and pulses was observed

227 Our data suggest a model in which spatial segregation of membrane protein complex assembly and qua

228 Autonomous replication and segregation of mitochondrial DNA (mtDNA) creates the pot

229 ucei depends on the faithful duplication and segregation of multiple flagellum-associated cytoskeleta

230 de proper pairing, recombination and correct segregation of multiple homologous chromosomes, which ca

231 eta T cell receptor activation by preventing segregation of N-glycosylated CD45 from the immune synap

232 hemispheres as well as sensory versus motor segregation of neural pathways along the brain-spinal co

233 tion and phospho-protein analyses reveal the segregation of oncogenic STAT5 and ERK activation to com

234 ely 1000 M(2) families were screened for the segregation of pale-green seedlings in the M(3) generati

235 e demographic expansions associated with the segregation of primitive and fat-tailed phenotypes.

236 While modularity suggests segregation of processing streams, here we show that loc

237 Spatial segregation of proteins to neuronal axons arises in part

238 model of post-traumatic stress disorder with segregation of rats as susceptible and resilient based o

239 coupling between a stochastic model for the segregation of signaling molecules and a simplified mech

240 alignment at metaphase facilitates the equal segregation of sister chromatids to each of the nascent

241 The segregation of solute atoms at grain boundaries (GBs) ca

242 terior-posterior polarization and initiating segregation of somatic and germline cell lineages.

243 ith PME were characterized by less change in segregation of structural networks over time.

244 espread motif across the brain involving the segregation of structures into discrete subregions based

245 herited and up to 85% of those may be due to segregation of susceptibility genes with low and moderat

246 The spatial segregation of TADs is further exacerbated during cell d

247 Segregation of the CC and LC is dependent on the GP and

248 known to promote the accurate and symmetric segregation of the genome.

249 monstrate its relationship to the functional segregation of the human brain.

250 ei, the spreading stage would be preceded by segregation of the nuclei into a large number of cluster

251 g a COVID-19-free surgical pathway (complete segregation of the operating theater, critical care, and

252 Segregation of the RNAi transgene produces non-genetic m

253 -cell heterogeneities that appear before the segregation of the trophectoderm and the inner cell mass

254 n latent viral DNA replication and efficient segregation of the viral genome to the daughter cells fo

255 The spatial segregation of these components of epithelial water tran

256 extended PWD population confirmed perfect co-segregation of this genetic variant with the disease.

257 r-proficient cell types exhibit an increased segregation of topologically associating domains (TADs).

258 idered as an alternative etiology to that of segregation of unbalanced gametes in infertile men harbo

259 ation are the result of convergence, and not segregation, of sensory input.

260 borhood socioeconomic deprivation and racial segregation on organ donor registration rates.

261 f an ecDNA-specific sequence may improve its segregation or expression.

262 The faithful segregation, or "partition," of many low-copy number bac

263 by more than one function from the standard segregation pattern showed poorer cognitive performance,

264 ured to accommodate a specialized chromosome segregation pattern.

265 ion from the carryover of mitotic chromosome segregation patterns into meiotic cells.

266 s required for accurate meiosis I chromosome segregation, predominantly releases Scc1-cohesin from ch

267 d speech, suggests an active cortical stream segregation process, which could explain a range of beha

268 three distinct approaches, we show that mis-segregation rates vary among different chromosomes under

269 ns at metaphase I, and in turn alter allelic segregation ratios through double reduction.

270 Accurate chromosome segregation requires assembly of the multiprotein kineto

271 inactivating CDK1 and permitting chromosome segregation, respectively.

272 Marker segregation revealed that ploidy reduction rarely involv

273 Despite the segregation reward, our experiments show that spatial in

274 tion of sister chromatids (PSSC) and reverse segregation (RS) in meiosis I.

275 rray variants explained the high-risk family segregation; sequencing of these regions will be needed

276 We tested these predictions in a texture-segregation task using un-natural, synthetic textures.

277 ted understanding of the variation of solute segregation tendencies across the full, multidimensional

278 ng framework that can accurately predict the segregation tendency-quantified by the segregation entha

279 the background provides evidence for stream segregation that emerges in A1 and is refined in PEG.SIG

280 (integration) or as two interleaved streams (segregation); the initial percept is typically integrati

281 te that Cdc23 is required for the chromosome segregation through regulating the spindle assembly chec

282 o neocentromeres, causing their preferential segregation to egg cells in a process known as meiotic d

283 different mechanisms of erroneous chromosome segregation to the production of aneuploid eggs.

284 link racist practices, including residential segregation, to the heterogeneous patterns of flora and

285 driving DNA damage and disrupted chromosomal segregation under certain conditions of replication stre

286 ation (HOLC) nationalized residential racial segregation via "redlining," whereby HOLC designated and

287 Sexual segregation was evident: delta(13)C values were signific

288 Segregation was highest in New York and lowest in Tokyo.

289 enic variant in a patient with DCM, familial segregation was performed.

290 boundaries through relaxation and molybdenum segregation was used to prevent this softening effect in

291 neural mechanisms that facilitate perceptual segregation, we can develop strategies for ameliorating

292 a HEK293 model of EphB2(+)/ephrinB1(+) cell segregation, we found that the scaffold adaptor protein

293 requires coordination of DNA replication and segregation with cell growth and division.

294 ome-wide evidence (p = 2.02E-07-1.30E-18) of segregation with completed suicide.

295 Yta7 causes defects in growth and chromosome segregation with mutations in components of the inner ki

296 Sanger sequencing demonstrated variant co-segregation with WMS, and absence in 150 population matc

297 ndividual professions or sectors (horizontal segregation), with women also under-represented in leade

298 07 genes, we investigated these for specific segregation within the high-risk families, and for assoc

299 facilitating chromosome capture and accurate segregation, without compromising division plane orienta

300 ust be broken to allow for proper chromosome segregation; yet how this occurs remains ill-understood.