ライフサイエンスコーパス: segregation

1 few affected in the families to confirm the segregation.

2 gnaling, resulting in error-prone chromosome segregation.

3 le, microtubule organization, and chromosome segregation.

4 tic interlinks, thus facilitating chromosome segregation.

5 a process critical for successful chromosome segregation.

6 r synthesis that ensures faithful chromosome segregation.

7 tial for accurate chromosome duplication and segregation.

8 axis of osteoblasts and yet maintain spatial segregation.

9 proposed to be a fingerprint of core-mantle segregation.

10 on, and ensuring accurate meiotic chromosome segregation.

11 ogous pairing, recombination, and chromosome segregation.

12 in and the mitotic spindle during chromosome segregation.

13 neurophysiological model of auditory stream segregation.

14 interpolar microtubules in driving acentric segregation.

15 dle microtubules is essential for chromosome segregation.

16 critical for normal chromosome movement and segregation.

17 1 kinase is critical for faithful chromosome segregation.

18 ater depth, contribute to behavioural sexual segregation.

19 glements, and complete failure in chromosome segregation.

20 essential mechanical role to ensure regular segregation.

21 its assembly with chromosome replication and segregation.

22 oint signaling to ensure accurate chromosome segregation.

23 plicated in spindle stability and chromosome segregation.

24 artitioning system in plasmid and chromosome segregation.

25 ty independently of their role in chromosome segregation.

26 and thus ensures the fidelity of chromosome segregation.

27 r attachments and ensure faithful chromosome segregation.

28 of SIRPalpha with CD47 abrogates nanocluster segregation.

29 tional hearing does not contribute to source segregation.

30 ed by evolution for high fidelity of plasmid segregation.

31 sister centromere orientation and chromosome segregation.

32 drives rapid, shear rate-dependent advective segregation.

33 rable to findings for blacks and black-white segregation.

34 ntly delayed sister chromatid separation and segregation.

35 effects of poverty, inequality, and economic segregation.

36 le, and in fact act as brakes for chromosome segregation.

37 ch as axial or spherically symmetric species segregation.

38 centromere function and faithful chromosomes segregation.

39 AP) family, regulates mitosis and chromosome segregation.

40 DNA and earmark the bacterial chromosome for segregation.

41 xcursive, the daughter foci undergo directed segregation.

42 roles for H2A phosphorylation in chromosome segregation.

43 in packaging and chromosome condensation and segregation.

44 own (NEBD) is required for proper chromosome segregation.

45 are well suited to support robust chromosome segregation.

46 s whether ParA polymerizes on DNA to mediate segregation.

47 ave roles in genome stability and chromosome segregation.

48 esolution is essential for proper chromosome segregation.

49 ments is essential for successful chromosome segregation.

50 orphogenesis to the completion of chromosome segregation.

51 eates genetic diversity and balances homolog segregation.

52 replication intermediates impair chromosome segregation.

53 heory, for studying the spatial structure of segregation.

54 encing, chromosome packaging, and chromosome segregation.

55 we bypassed the requirement of Nup2 for NPC segregation.

56 tivate the MutL homolog 1 (Mlh1)-postmeiotic segregation 1 (Pms1) endonuclease in the presence of a m

57 ubules and ensuring high-fidelity chromosome segregation [1-3].

58 d cells demonstrated that mitotic arrest and segregation abnormalities lead to cell death through mit

59 , dam1-3A cells show dramatic chromosome mis-segregation after treatment with nocodazole, presumably

60 In addition, solute segregation along cellular walls and low-angle grain bou

61 ome, but not all, permutants with low charge segregation, although there is considerable variation.

62 oft-confinement pattern-induced nanoparticle segregation) an attractive method for fabricating nanost

63 t generation sequencing, bioinformatics, and segregation analyses followed, to determine a loss of fu

64 Co-segregation analyses in F2 individuals segregating for d

65 Subsequently, Sanger sequencing and segregation analysis were performed in additional family

66 This leads to defective chromosome segregation and accumulation of CFS-associated DNA damag

67 Chromosome segregation and anaphase onset are initiated through the

68 Crossovers mediate homolog segregation and arise from self-inflicted double-strand

69 er flip-flop that opposes asymmetric lateral segregation and causes a mismatch.

70 ations were evaluated for genotype-phenotype segregation and classified according to the contemporary

71 How GABAergic interneurons regulate the segregation and communication among intermingled PC subs

72 equired for spindle organization, chromosome segregation and cytokinesis in meiotic cells.

73 topo II), an enzyme essential for chromosome segregation and DNA supercoiling homeostasis.

74 self-organization that is marked by spatial segregation and frequent self-interaction.

75 lterations in this process impair chromosome segregation and genome stability, which are also comprom

76 Segregation and integration are distinctive features of

77 Critically, both modular segregation and network efficiency are associated with e

78 zed chromatin domains that enable chromosome segregation and orchestrate faithful cell division.

79 e mechanism by which cells ensure chromosome segregation and preserve genome integrity.

80 ndles exhibit reduced fidelity of chromosome segregation and promote genetic instability.

81 e relationship between Hispanic metropolitan segregation and respondent-rated health for US-born and

82 l nonessential genes for roles in chromosome segregation and spore formation.

83 nd a maternal-effect on embryonic chromosome segregation and survival, which was completely dependent

84 We also report the hierarchy of network segregation and the level of clusters integration as a f

85 Based on the familial segregation and the reported functional studies, 6 of th

86 n with wide-ranging importance in chromosome segregation and, in multicellular organisms, transcripti

87 aled both context-free (greater default mode segregation) and context-specific (greater frontoparieta

88 itotic spindle abnormalities, chromosome mis-segregation, and aneuploidy, which then lead to apoptosi

89 itotic structures that facilitate chromosome segregation, and decondensed interphase structures that

90 tionship between DNA replication, chromosome segregation, and division site selection in the pneumoco

91 order kinetics, as expected for random virus segregation, and elimination within six cell doublings,

92 a surprising link between H2A.Z, chromosome segregation, and organ development.

93 ics, transcriptomics, proteomics, chromosome segregation, and replication analysis-to provide a thoro

94 compositional variations induced by surface segregation are accompanied by misfit strain and the for

95 Given that local excursion and directed segregation are the most commonly observed modes of plas

96 ng chromosomes and aligned along the axis of segregation, are essential.

97 Accurate segregation, as well as SAC proficiency, is rescued by r

98 during meiosis I ensures accurate chromosome segregation at the first meiotic division.

99 mes and is essential for accurate chromosome segregation at the first meiotic division.

100 At 51 wt %/83 mol % H2 O, this segregation becomes unfavorable, and the DES structure i

101 only the final round of DNA replication and segregation being synchronous and coordinated with daugh

102 viour associations are related to functional segregation between brain networks.

103 nd robust diagnosis of neurodegeneration and segregation between different dementias.

104 This study shows that increasing segregation between hydrophobic and cationic moieties in

105 g computational models, where these enable a segregation between metacognitive and perceptual decisio

106 ler females, resulting in a partial temporal segregation between sexes.

107 relationship depends on maintaining spatial segregation between these bacteria and the intestinal ep

108 sitioning is crucial for faithful chromosome segregation but also influences cell size, position, or

109 or cLmx1b in the chick) allows sensory organ segregation by antagonizing lateral induction and promot

110 lex and that this mechanism ensures accurate segregation by constraining chromosome motion following

111 totic checkpoint ensures faithful chromosome segregation by delaying anaphase onset even when a singl

112 genetic elements to violate Mendel's law of segregation by increasing the chance of segregating to t

113 of divergent associations between health and segregation by nativity points to the wide range of expe

114 Overall, these findings show that temporal segregation can be modified by sensory entrainment, prov

115 irst evidence that the frequency of temporal segregation can be modified by sensory entrainment, supp

116 meiosis I-specific modulators of reductional segregation can contribute to oncogenic chromosome dynam

117 romotes UPD by uniquely affecting chromosome segregation, causing a reductional segregation of one ho

118 and structural factors, such as residential segregation, come into play in determining Hispanic heal

119 /6 complex is essential for the formation of segregation-competent bivalents during meiosis I, and fi

120 l, morphological, functional, haplotype, and segregation data all indicate that LMNA p.(Arg331Gln) is

121 nalog (SM15) was shown to produce chromosome segregation defects in cancer cells by inhibiting the co

122 ms of PP2A by quantifying meiotic chromosome segregation defects in double or triple mutants.

123 nucleoid decompaction leading to chromosome segregation defects.

124 , spindle elongation defects, and chromosome segregation defects.

125 uce spindle asymmetry and that non-Mendelian segregation depended on this asymmetry.

126 DFT calculations indicate that the observed segregation depends on what is adjacent to the Pbx Sn1-x

127 Segregation distortion was detected for many markers, so

128 e. construction of linkage groups in case of segregation distortion; (iv) data imputation on VCF file

129 progression delay, and defective chromosome segregation during anaphase.

130 type II topoisomerases to permit chromosome segregation during cell division.

131 an important process for accurate chromosome segregation during cell division.

132 complex is required for accurate chromosome segregation during mitosis [1-6] and consists of two cop

133 e spindle microtubules to promote chromosome segregation during mitosis.

134 ivity for proper chromosome condensation and segregation during mitosis.

135 This occurs in the context of a matrigel-segregation effect where cancer cells are transiently is

136 cancer cells are differently subjected to a segregation effect, this needs to be considered when com

137 interfaces lead to significant compositional segregation effects.

138 e the reason the SAC is weak, and chromosome segregation error-prone, in mammalian oocytes.

139 ifically marked by a lacO repeat, chromosome segregation errors and the appearance of aneuploid cells

140 Segregation errors lead to an abnormal chromosome number

141 ate PLK1 activity contributing to chromosome segregation errors, formation of micronuclei, and subseq

142 ow the mitotic kinase PLK1 drives chromosome segregation errors, with a specific focus on Gravin, a P

143 g mitosis, which leads to ongoing chromosome segregation errors.

144 he tempo of ParF assembly cycles and plasmid segregation events by stimulating ParF adenosine triphos

145 leading to monopolar spindle and chromosome segregation failure.

146 le plays a vital role in accurate chromosome segregation fidelity and is a therapeutic target in canc

147 al and environmentally driven control system segregation for greater reward value) signatures of inhi

148 and context-specific (greater frontoparietal segregation for higher cognitive load; greater attention

149 While no segregation for single bilayers was observed, segregatio

150 several sensory patches arise by progressive segregation from a common prosensory domain in the embry

151 Increasing charge segregation from WT RAM sharply decreases transcriptiona

152 ck groups with the highest metropolitan area segregation had the highest estimated noise exposures, r

153 Results indicated that segregation has a consistent, detrimental effect on the

154 ncy dependent trapping and spatial frequency segregation has implications for energy concentrators an

155 underlying mechanisms that govern chromosome segregation have been thoroughly investigated.

156 The kinetic segregation hypothesis proposes that CD45 exclusion shif

157 tallization, He bubble or void formation, or segregation in all irradiated samples.

158 ositional guide proteins used for chromosome segregation in bacteria.

159 the kinetochore structure during chromosome segregation in living cells.

160 overs, which are critical for proper homolog segregation in Meiosis I.

161 Faithful chromosome segregation in meiosis requires crossover (CO) recombina

162 cyte, we studied the mechanism of chromosome segregation in meiosis.

163 ner centromere to ensure faithful chromosome segregation in metazoans.

164 The fidelity of chromosome segregation in mitosis is safeguarded by the precise reg

165 ore mature adulthood was typified by reduced segregation in the default network with increasing rewar

166 plate tectonic) rates of melt generation and segregation in the lower crust with new evidence for rap

167 ation density distribution, showed Pb and Sn segregation in the soap-affected areas.

168 loci were not linked, as indicated by random segregation in the T2 generation.

169 rms of temporal windows (TWs) of integration/segregation, in which the phase of ongoing neural oscill

170 ta spindle is fully competent for chromosome segregation independently of motor activity, except for

171 lycrystalline nickel, we found that ordered, segregation-induced grain boundary superstructures occur

172 irst years of life, emphasizing strengthened segregation/integration balance, a remarkable hierarchic

173 eption after the entrainment, we sampled the segregation/integration performance densely in time.

174 The segregation into two functional subgroups coincides with

175 Ethnoracial residential segregation is a complex, multiscalar phenomenon with im

176 Genome segregation is a fundamental step in the life cycle of e

177 Modeling the structure and dynamics of segregation is a pressing problem for sociology and urba

178 This segregation is a self-organizing process driven by feedb

179 Understanding causative variant segregation is extremely important, even for monogenic t

180 Biased, or non-Mendelian, segregation is frequently observed but not well understo

181 stingly, the role of Nup2 during mitotic NPC segregation is independent of its importin alpha- and Ra

182 Furthermore, Na and K segregation is not correlated to hampering donors, (In,

183 By contrast, compartmental segregation is preserved and even reinforced.

184 This segregation is thermodynamically favored to occur when P

185 global brain modularity-a measure of network segregation-is markedly reduced during episodic memory r

186 To ensure accurate chromosome segregation, it performs three major functions using dis

187 To facilitate chromosome movement and segregation, kinetochores must maintain associations wit

188 Under segregation lift, loci can exhibit conspicuous seasonal

189 This general mechanism, which we call "segregation lift," requires seasonal changes in dominanc

190 of Suc in the phloem, even in the absence of segregation, lowers the sugar content in the leaf requir

191 We show that directed segregation maximizes the fidelity of plasmid partition.

192 re than one system for eukaryotic chromosome segregation may exist.

193 t the requirement for polymers and suggest a segregation mechanism by which ParA-ATP dimers equilibra

194 ng partitioning bias for old cell poles by a segregation mechanism that is mediated by ternary AcrAB-

195 ynamics simulations reveal distinct physical segregation, membrane permeation, and amyloid aggregatio

196 Beyond the stage of lineage segregation, miR-337-3p controls the transcriptional net

197 ic chromosomal cross-links recapitulates the segregation, morphology and self-interaction of the nucl

198 Chromatid segregation must be coordinated with cytokinesis to pres

199 omatids are present at the midzone.Chromatid segregation must be coordinated with cytokinesis to pres

200 Thanks to this segregation, neurons in different layers of the network

201 Normally, acentric poleward segregation occurs at the periphery of the spindle in as

202 Initial segregation of a thin platinum, rather than cobalt oxide

203 Although poleward segregation of acentric chromosomes is well documented,

204 Segregation of AD from dementia with Lewy bodies (DLB; n

205 onds to polarity cues and promotes efficient segregation of aPKC toward the anterior but holds aPKC i

206 ems are ubiquitous in nature and mediate the segregation of bacterial and archaeal DNA.

207 ogically successful and showed transgressive segregation of bill morphology.

208 Here, we reconstitute segregation of CD45 from bound receptor-ligand pairs usi

209 a mineral franckeite and show that the phase segregation of chemical species into discrete layers at

210 aptic receptors clusters, but a pre-synaptic segregation of cholinergic and glutamatergic release sit

211 racterized by slow consolidation of TADs and segregation of chromatin compartments.

212 Faithful segregation of chromosomes during cell division relies o

213 specifically promotes proper compaction and segregation of chromosomes during mitosis remains poorly

214 Proper segregation of chromosomes in meiosis is essential to pr

215 n level of this is required for the faithful segregation of chromosomes, but the majority of DSBs are

216 structural unit responsible for the faithful segregation of chromosomes.

217 The mitotic spindle ensures the faithful segregation of chromosomes.

218 The segregation of dense core-forming melts by porous flow i

219 ortical responses may reflect the functional segregation of direction-selective, high spatial frequen

220 Here, we reveal the surface segregation of dopant cations and oxygen vacancies and o

221 pindle is an essential process for the equal segregation of duplicated DNA into two daughter cells du

222 e encoded, arguing against strict anatomical segregation of effectors.

223 vation, Src-family kinase signaling leads to segregation of FcgammaRI and SIRPalpha nanoclusters to b

224 Such a segregation of function would predict that when activity

225 e of ongoing oscillations in the integration/segregation of information over time.

226 h fluorocarbon coating, to achieve selective segregation of ionic and/or hydrophilic analytes from ba

227 pathway functions via a mechanism involving segregation of its protein components to opposite cells

228 s to drive the unique reductional chromosome segregation of meiosis I, which also results in chromoso

229 iple Component Analysis revealed significant segregation of microbiota compositions which was validat

230 Our findings indicate that random segregation of mitochondrial genomes under uniparental i

231 of GUCY2C to intestinal apical membranes and segregation of mucosal and systemic immunity.

232 In another eight families segregation of multiple pathogenic variants was observed

233 /Plxnc1 interactions are responsible for the segregation of nigrostriatal and mesolimbic dopaminergic

234 oncentration of Suc in the mesophyll and (2) segregation of oligomers and the inverted gradient of to

235 organization in the mammalian retina is the segregation of ON and OFF pathways in the inner plexifor

236 hromosome segregation, causing a reductional segregation of one homologue.

237 Increased segregation of oppositely charged residues leads to line

238 egregation for single bilayers was observed, segregation of Pb to the surface of three bilayer thick

239 This selective segregation of PGNPs is induced by the conformational en

240 h measures of behavioural impairment and the segregation of resting-state networks empirically measur

241 ute to MEI-S332's ability to ensure accurate segregation of sister chromatids, but, as in centromere

242 n posteromedial auditory cortex disrupts the segregation of speech from background noise, leading to

243 PV+ INs and contribute to the processing and segregation of tactile and nociceptive information.

244 e materials, thermal treatments in air cause segregation of the base metal oxide phase in close proxi

245 cell fate choice in mouse development is the segregation of the embryonic inner cell mass and the ext

246 lated kinase (ERK) signalling is involved in segregation of the EPI and PrE lineages; however, the me

247 zones of D. corymbosa contribute to spatial segregation of the fungal community and likely enhance f

248 nary mixtures, geometry dictates the spatial segregation of the more volatile component as it is depl

249 The segregation of the readily releasable pool of synaptic v

250 n response to pMHC binding is accompanied by segregation of the transmembrane phosphatase CD45 away f

251 olarization and cell-cell contact drives the segregation of these lineages, providing a framework for

252 The current study reveals the segregation of these pathways in their subsequent projec

253 Co-segregation of this expression phenotype with the LanFTc

254 ected N2a neuroblastoma cells, likely due to segregation of transmembrane PrP(C) and GPI-anchored PrP

255 r to be narrowly tuned, there is no apparent segregation of tuning responses within any discrete HsOr

256 Here we show that meiotic segregation of X chromosomes in the trioecious nematode

257 UniFrac distances also revealed considerable segregations of GM structure among healthy, asymptomatic

258 previous documentation of genotype-phenotype segregation, our findings suggest that many KCNE2 varian

259 During chromosome segregation, outer kinetochore components track depolyme

260 Human NIAM is involved in chromosome segregation, p53 regulation and cell proliferation in so

261 ions with Sanger sequencing, and analyses of segregation patterns in parents and siblings, to shed ne

262 a temporal dense sampling of the integration/segregation performance.

263 quences can drive in meiosis by cheating the segregation process [2], but the underlying mechanisms a

264 seldomly utilized as part of the microphase segregation process in ultralow-molecular-weight block c

265 The efficiency of this particle segregation process within patterned mesa-trench films c

266 red for the efficient splicing of chromosome segregation related genes, probably by stabilizing the U

267 inks DNA replication, repair, and chromosome segregation, represents a novel target for the synthetic

268 t centromeres to promote faithful chromosome segregation, revealing functions of R loops and ATR in s

269 ner, while preserving the fundamental ON-OFF segregation scheme for parallel visual processing and hi

270 w studies have investigated how metropolitan segregation shapes the health of the fastest-growing pop

271 us remains a viable model of auditory stream segregation.SIGNIFICANCE STATEMENT According to the popu

272 ion separation (PS) model of auditory stream segregation, sounds that activate the same or separate n

273 een shown to influence or trigger chromosome segregation, sporulation, aerotaxis, and social behavior

274 While other models of stream segregation, such as temporal coherence, are not exclude

275 onnections of L4B neurons preserve CO-stream segregation, suggesting that across-stream integration o

276 is similarly required for linear chromosome segregation, suggesting that linear chromosomes also rem

277 e close to the cell's center, but chromosome segregation takes place at the cell periphery where half

278 prestimulus period of a temporal integration/segregation task.

279 etween two ceramide effects; namely, lateral segregation that facilitates permeabilization, and at lo

280 ights in the structure and dynamics of urban segregation that would be otherwise easy to miss or diff

281 To ensure accurate chromosome segregation, the spindle assembly checkpoint (SAC) preve

282 f auditory scene analysis is auditory stream segregation-the organization of sound sequences into per

283 MPK genes were readily obtained via genetic segregation, thereby eliminating any positional effects

284 . nidulans cells ensure accurate mitotic NPC segregation to daughter nuclei by linking mitotic DNA an

285 sets of endolysosomal proteins undergo early segregation to distinct domains of the Golgi complex by

286 ic spindle that is required for their proper segregation to the two daughter cells.

287 the complex correlation among the elemental segregation, types of chemical compounds formed, and pos

288 ughter nuclei by linking mitotic DNA and NPC segregation via the mitotic specific chromatin associati

289 In contrast, segregation was salutary (though not always significant)

290 encies, bioinformatic criteria, and familial segregation, we identified 20 FLNC candidate variants (1

291 unction to bridge NPCs with chromatin during segregation, we provided an artificial link between NPCs

292 Temperate ectomycorrhizal (ECM) fungi show segregation whereby some species dominate in organic lay

293 variant, a synonymous LMNA VUS, demonstrated segregation with cardiomyopathy affection status and alt

294 ced cingulo-opercular and subcortical system segregation with increasing cognitive load.

295 enicity of these alleles was supported by co-segregation with the phenotype, low frequency in control

296 cent findings point to a possible anatomical segregation, with cortical and subcortical brain regions

297 This unexpected ON-OFF segregation within a small-field amacrine cell arose fro

298 Several of these variants showed disease co-segregation within families.

299 l feature led us to hypothesize a functional segregation within the VS in terms of the regulation of

300 The ocular phenotype-genotype segregation within XP patients suggests that XP is a het