ライフサイエンスコーパス: cohesion

1 in can contribute to genome organisation and cohesion.

2 nurses and midwives is fragmented and lacks cohesion.

3 1 that is specifically required for telomere cohesion.

4 empirical features, such as coalignment and cohesion.

5 ich abstractness contributes to cement group cohesion.

6 oups to reduce prejudice and increase social cohesion.

7 ognized species is constrained by a force of cohesion.

8 governments concerned with promoting social cohesion.

9 portant role in maintaining year-round group cohesion.

10 vation and establishment of sister chromatid cohesion.

11 ssociation with telomeres, and resolution of cohesion.

12 leavage efficiency, promoting dissolution of cohesion.

13 cted to occur in tissues of widely differing cohesion.

14 the ESCO1 gene has little effect on mitotic cohesion.

15 nization: network fragmentation and subgroup cohesion.

16 ely passive and serve solely in the membrane cohesion.

17 t the cohesin loader to establish centromere cohesion.

18 diated junctional remodeling and increase of cohesion.

19 ous recombination linked to sister-chromatid cohesion.

20 senders and receivers by facilitating social cohesion.

21 g prices, and erosion of neighborhood social cohesion.

22 for telomere cohesion and SA2 for centromere cohesion.

23 lizes with Pds5 and Eso1 resulting in stable cohesion.

24 s role in establishing and maintaining group cohesion.

25 occur before dissolution of sister chromatid cohesion.

26 quate tankyrase 1 to resolve sister telomere cohesion.

27 arental care, coalition signaling, and group cohesion.

28 S-K entrapment required for sister chromatid cohesion.

29 y immobile Holliday junctions and sticky end cohesion.

30 ces, such as feelings of gratitude or family cohesion.

31 ich is essential to its ability to establish cohesion.

32 ication but dispensable for sister chromatid cohesion.

33 n and in the nurse cells to maintain cluster cohesion.

34 tes with apical membranes and decreases cell cohesion.

35 le simultaneously promoting sister chromatid cohesion.

36 mbination of crossovers and sister chromatid cohesion.

37 in ALT cells results in diminished telomere cohesion.

38 ity, or hunting party size, composition, and cohesion.

39 y, coordinates border cell shape and cluster cohesion.

40 ediating DNA repair through sister chromatid cohesion.

41 he hallmarks of local interaction and global cohesion [3,4].

42 hed role in promoting affiliation and social cohesion [6-8].

43 e found no evidence of an increase in social cohesion after simulated conflicts, measured as grooming

44 Can intergroup contact build social cohesion after war?

45 Low cohesion allows molecules to escape from the original as

46 20)) activates separase and thereby destroys cohesion along chromosome arms.

47 re separation, as well as precocious loss of cohesion along the arms of achiasmate chromosomes.

48 evelopment, such as informal social control, cohesion among neighbors, and organizational participati

49 se with a crucial role in the dissolution of cohesion among sister chromatids during chromosome segre

50 may have been rooted in mechanisms of social cohesion among small groups that might have granted stre

51 maximizing counterion-mediated electrostatic cohesion among the ensemble of charged particles.

52 lts provide proof-of-concept that literature cohesion analysis is useful for evaluating the quality o

53 ir and that this role involves both telomere cohesion and a DAXX-dependent pathway.

54 y of the interplay of the protein structure, cohesion and adhesion effects, fiber processing, and mec

55 onal connectivity in terms of within-network cohesion and between-network integration, and by their d

56 ainst Ecad drastically reduced intercellular cohesion and blocked lipid production of HMGECs.

57 ra finches can simultaneously promote social cohesion and breeding boundaries.

58 ignificance: these activities increase group cohesion and cause participants to like each other and b

59 architecture with roles in sister chromatid cohesion and chromosome compaction.

60 leads to premature loss of sister chromatid cohesion and chromosome missegregation, whereas COs at a

61 Despite key roles in sister chromatid cohesion and chromosome organization, the mechanism by w

62 LRRK2-mediated centrosomal cohesion and ciliogenesis alterations are observed in pa

63 suggest that the LRRK2-mediated centrosomal cohesion and ciliogenesis defects are distinct cellular

64 r selection mechanisms to foster coalitions' cohesion and combativeness in intergroup conflict [corre

65 xytocinergic system, potentially engendering cohesion and cooperation when facing an out-group threat

66 These mutations improve sister chromosome cohesion and delay genome replication in Rec8-expressing

67 rily focus on the association between social cohesion and depression, as these associations were gene

68 ily focus on the associations between social cohesion and depression, as these associations were gene

69 ween perceived neighborhood disorder, social cohesion and depressive symptoms among 50-year-olds in 1

70 to prevent the untimely release of chromatid cohesion and disastrous chromosome distribution defects.

71 lular matrix that affords bacterial adhesion-cohesion and drug tolerance, making them difficult to tr

72 rtant for establishing both sister chromatid cohesion and enhancer-promoter communication.

73 how this adaptation contributes to cell-cell cohesion and eventually to tissue-scale dynamics and mec

74 ferent properties (triadic balance, internal cohesion and external division of subgroups, and overall

75 replication help establish sister chromatid cohesion and facilitate enhancer-promoter communication.

76 ound chromosomes to mediate sister chromatid cohesion and facilitate long-range control of gene trans

77 bound complex that mediates sister chromatid cohesion and facilitates long-range interactions through

78 e bacterial cell surface increases cell wall cohesion and favors the projection of elongated SasG pro

79 e progenitors differentiate, they migrate in cohesion and form bud-like islet precursors, or "peninsu

80 to guide policies aimed at increasing social cohesion and health.

81 otic cell cycle, modulating sister chromatid cohesion and higher-order chromatin structure.

82 Thus, how these tumors maintain chromosomal cohesion and how STAG2 loss contributes to tumorigenesis

83 o their epistemic truth value, such as group cohesion and identity.

84 y less within-group aggression, higher group cohesion and improved winter survival in both tit specie

85 Remarkably, impaired social cohesion and increased seizure susceptibility were found

86 s that hominoids vary with regards to social cohesion and intergroup tolerance due to their feeding e

87 tively appraised in terms of both functional cohesion and intra-subnetwork association strengths vers

88 ny were respectively associated with greater cohesion and lower integration.

89 h, but both are required to resolve telomere cohesion and maintain mitotic spindle integrity.

90 Sensory and motor RSNs showed greater cohesion and metastability, likely to respectively refle

91 se 1 (Pp1) activity controls collective cell cohesion and migration.

92 DNA interactions to mediate sister chromatid cohesion and other aspects of chromosome structure and f

93 epatotoxicity, the mechanism by which tissue cohesion and polarity are affected remains unclear.

94 status, disruption in epithelial integrity, cohesion and polarity, increased cell division and a dis

95 to promote establishment of sister chromatid cohesion and possibly other post-replicative processes.

96 PARP inhibitors, defective sister chromatid cohesion and reduced DNA replication fork speed.

97 n of DDX11 is essential for sister chromatid cohesion and resistance to G4 stabilizers.

98 subunit, where SA1 is required for telomere cohesion and SA2 for centromere cohesion.

99 y Shugoshin and BUBR1 to protect centromeric cohesion and stabilise kinetochore-microtubule attachmen

100 on, telomeres are no longer able to maintain cohesion and subtelomere copying ensues.

101 ithin the blastoderm margin, increasing cell cohesion and thereby counteracting the effect of mitotic

102 ight the possibility that either centrosomal cohesion and/or ciliogenesis alterations may serve as ce

103 e dimension (perceptions of community social cohesion) and a structural dimension (informal socializi

104 interactions both between (sister chromatid cohesion) and within chromosomes (DNA looping).

105 tion, DNA repair, DNA replication, chromatid cohesion, and chromosome segregation.

106 ic chromosome condensation, sister chromatid cohesion, and higher order folding of interphase chromat

107 odules, DNA replication and sister chromatid cohesion, and inactivated a third, the DNA damage checkp

108 ssed but neither required nor sufficient for cohesion, and its function remains unknown.

109 on, chromosome maintenance, sister chromatid cohesion, and mitotic chromosome compaction, it appears

110 romoting physical activity, fostering social cohesion, and reducing stress and exposure to air pollut

111 Pds5 is required for sister chromatid cohesion, and somewhat paradoxically, to remove cohesin

112 Current models of chromatin folding and cohesion are based on assumptions of how many cohesin an

113 hospho-RAB10, and the effects on centrosomal cohesion are dependent on RAB8, RAB10 and RILPL1.

114 r relative contributions to sister chromatid cohesion are unknown.

115 Cohesion arises at a common length scale (~5 mum), where

116 Because cohesion around centromeres is protected by shugoshin-2,

117 fluidity transition mediated by loss of cell cohesion as a critical regulator of embryo morphogenesis

118 Shoal cohesion, as assessed via mean neighbor distance, showed

119 taxa and insight into the levels of genetic cohesion associated with bacterial species.

120 t where cohesin binds, little is known about cohesion at individual chromosomal binding sites and how

121 his requires that sister chromatids maintain cohesion at the centromere as cohesion is released on th

122 ndard-deviation change in predisaster social cohesion at the community level reduced the risk of depr

123 ere region until release of sister-chromatid cohesion at the metaphase II/anaphase II transition.

124 :dT) tract in the gene promoter and mediated cohesion before induction.

125 the chromosomal cohesin complex establishes cohesion between newly replicated sister chromatids.

126 Phosphorylation increased cohesion between osteopontin polymers, and adhesion of o

127 acetylated (ac) during S phase to establish cohesion between replicated chromosomes.

128 lie the unique ability of ESCO2 to establish cohesion between sister chromatids precisely as they are

129 er cohort), which are insufficient to confer cohesion but can bind to individual chromatids, suggesti

130 SA2 mutation that supports sister chromatid cohesion but is unable to repress transcription at DSBs.

131 Linkages persist in the absence of cohesion, but inhibition of topoisomerase II prevents th

132 Cohesin mediates sister chromatid cohesion, but this is not always perturbed in cancer cel

133 RNA in the establishment of sister chromatid cohesion by modulating DDX11 enzymatic activity.

134 The Shugoshin proteins preserve centromere cohesion by protecting the cohesin complex from cleavage

135 This behavior supports social cohesion by providing a key mechanism for minimizing mut

136 racks dynamic changes in large-scale network cohesion by quantifying the level of within-network and

137 ding DNA loops and mediates sister chromatid cohesion by topologically entrapping DNA.

138 Group cohesion can be altered by an array of factors, includin

139 ins, microtubule crosslinking, and chromatid cohesion can modulate spindle size and shape, and yet mo

140 rotein complex required for sister chromatid cohesion, chromosome condensation, DNA damage repair, an

141 e cohesin complex regulates sister chromatid cohesion, chromosome organization, gene expression, and

142 Smc5/6 complex, involved in sister chromatid cohesion, chromosome segregation, and DNA repair.

143 ms in several qualitative aspects, including cohesion, coalignment, and collision suppression, none o

144 oding RNA polymerase subunits and chromosome cohesion complex suggests a surprising degree of functio

145 be composed of grains whose roughness lowers cohesion consistently with contact mechanics.

146 rs at risk of suicidal behaviour, and social cohesion contributing to the diffusion of ideas and atti

147 ow that Ctf18-RFC's role in sister chromatid cohesion correlates with PCNA loading but is separable f

148 tested whether literature derived functional cohesion could be used as an objective metric in lieu of

149 ing a genomic subcompartment, rather than by cohesion/CTCF-mediated extrusion.

150 dently of checkpoint signaling or chromosome cohesion, Ctf18-RFC functions in parallel to Chl1 and Mr

151 n interaction, thereby promoting centromeric cohesion de-protection and timely chromosome segregation

152 HyperD-ALL cells show chromatid cohesion defects and an impaired spindle assembly checkp

153 ion stress confers WAPL-dependent centromere cohesion defects that maintain spindle assembly checkpoi

154 izing compounds induce chromosome breaks and cohesion defects which are strongly aggravated by inacti

155 dent manner and causes chromosome breaks and cohesion defects, independent of the expressed pseudogen

156 n of phosphorylated RAB8A causes centrosomal cohesion deficits in dividing cells, including in periph

157 RAB8 and RAB10 contribute to the centrosomal cohesion deficits.

158 s hold the network together), making network cohesion dependent on key organizations.

159 and packing fraction are normalized by their cohesion-dependent quasistatic values, they are governed

160 arkably strong, hierarchical clusters, whose cohesion derives from grain size rather than mineralogy.

161 ation includes functions in sister chromatid cohesion, DNA repair, and transcriptional regulation.

162 upling with magnetic tweezers, and cell-cell cohesion during collective cell movements, further highl

163 ted in larger group sizes, increasing social cohesion during disturbance.

164 ated hormone levels were linked with greater cohesion during intergroup conflicts, rather than with t

165 tter explain the potential dilution of group cohesion during peacetime and inform novel, more effecti

166 Cohesins establish sister chromatid cohesion during S phase and are removed when cohesin Scc

167 es throughout the cell cycle, it only builds cohesion during S phase.

168 s5's role in maintenance of sister chromatid cohesion during the mitotic prophase-analogous stage of

169 Sister chromatid cohesion essential for mitotic chromosome segregation is

170 We conclude that cohesion established in fetal oocytes is maintained for

171 Several replication-fork-associated "cohesion establishment factors," including the multifunc

172 Here we show that cohesion establishment is critically dependent upon Esco

173 well studied, the underlying determinant of cohesion establishment on chromosomal arms remains enigm

174 c replisome proteins with different types of cohesion establishment opens the way to a mechanistic un

175 cation fork progression and sister chromatid cohesion establishment.

176 ction as mechanisms that can support species cohesion even when hybridization has been pervasive thro

177 hose of the strong reversible intermolecular cohesion exhibited by adhesion proteins of marine mussel

178 ze to the centriole proximal end through the cohesion factor C-Nap1 and that sDAP function redundantl

179 sis shows that the loading of Pds5 and other cohesion factors on replication forks is not affected by

180 netic regulators, transcription factors, and cohesion factors, suggesting diverse genetic/epigenetic

181 Mitotic arrest then drives cohesion fatigue and triggers mitotic death through a pr

182 icient mutant, exacerbates the occurrence of cohesion fatigue in MG132-arrested cells.

183 e under selective pressure to maintain group cohesion, favoring effective leadership rather than grou

184 entrosome/spindle pole body, centromere, and cohesion function.

185 c couplings) could have been crucial for the cohesion, functional integration, and intrinsic stabilit

186 otein complex essential for sister chromatid cohesion, gene expression and DNA damage repair.

187 tes 3D genome organization, sister chromatid cohesion, gene expression, and DNA repair.

188 In contrast to social cohesion, high levels of social participation at the com

189 romosome axis that mediates sister chromatid cohesion, homologous recombination and chromosome synaps

190 d support the model that accelerated loss of cohesion in aging human oocytes is caused, at least in p

191 This was accompanied by increased cell cohesion in cardiac myocyte cultures and murine heart sl

192 Removal of telomeric cohesion in combination with DAXX deficiency recapitulat

193 is insufficient for efficient dissolution of cohesion in early anaphase; subsequent Smc3 deacetylatio

194 Timely resolution of sister chromatid cohesion in G2/M is essential for genome integrity.

195 USP13 was dispensable for sister chromatid cohesion in HCT116 and HeLa cells, whereas it was requir

196 Therefore, we studied the regulation of cell cohesion in human meibomian gland epithelial cells (HMGE

197 omatids in STAG2 mutant tumor cells maintain cohesion in mitosis at chromosome arms and telomeres.

198 Social cohesion in multiethnic societies depends on whether pro

199 istinct cohesin complexes generate loops and cohesion in oocytes and propose that the same principle

200 Our findings suggest that low internal cohesion in protein systems could facilitate the conform

201 erated extrachromosomal DNA circles to study cohesion in response to transcriptional induction of a m

202 cally, STAG1 loss abrogates sister chromatid cohesion in STAG2 mutated but not in wild-type cells lea

203 omoting dynamic chromosomal organization and cohesion in the nucleus.

204 logical index of arousal, and within-network cohesion in the salience network, indicating that coordi

205 precise contributions of Esco1 and Esco2 to cohesion in vertebrate cells.

206 disrupts junctional integrity and epithelial cohesion in vitro however, the fate of free-floating cel

207 entrosomal Golgi localization and centrosome cohesion, independent of its localization to, and role i

208 when under stress and do not modulate shoal cohesion, indicative of abnormal social behaviour.

209 males are sterile [13], and sister chromatid cohesion is abolished on all chromosomes, leading to a f

210 Sister-chromatid cohesion is established by Eco1-mediated acetylation on

211 riptional enhancers, or how sister chromatid cohesion is established.

212 A key question is whether cohesion is generated by conversion of cohesin complexes

213 Sister chromatid cohesion is intact in FACT-depleted cells, although chro

214 Together, these data demonstrate that cell cohesion is maintained differently in meibomian gland ce

215 In mammalian oocytes, cohesion is mediated by Rec8-cohesin.

216 The unique ability of Esco2 to promote cohesion is mediated by sequences in the N terminus of t

217 complexes, supporting a model wherein sister cohesion is mediated locally by a single cohesin ring.

218 co1 substrate recognition and acetylation in cohesion is not fully understood.

219 mitosis and enter G1, ensuring that telomere cohesion is not resolved prematurely in S phase.

220 atids maintain cohesion at the centromere as cohesion is released on the chromatid arms when the homo

221 members is known to be important to maintain cohesion, it is not clear how many neighbors each indivi

222 itotic processes, including sister chromatid cohesion, kinetochore-microtubule attachment and the spi

223 little is known about how it stimulates the cohesion-loading activity.

224 RIM), is reported, to minimize intercellular cohesion loss for accurate antibacterial therapy.

225 irls, whereas centromeric and more extensive cohesion loss limit fertility as women age.

226 urin that ultimately causes sister chromatid cohesion loss.

227 ted link between stress and sister chromatid cohesion loss.

228 e Smc3p hinge and Pds5p cooperate to promote cohesion maintenance and condensation.

229 vealed an unexpected role for this domain in cohesion maintenance and condensation.

230 le multi-skyrmion clustering and large-scale cohesion mediated by out-of-equilibrium elastic interact

231 Sister chromatid cohesion mediated by the cohesin complex is essential fo

232 crystal structures, and experimental lattice cohesion metrics.

233 ions of the centrosome, and failed chromatid cohesion, mirroring findings from cancer biology.

234 mutant MT1-MMP expression results in altered cohesion of epithelial sheets and the formation of more

235 dherin) is responsible for the intercellular cohesion of epithelial tissues.

236 -pi interactions drive the self-assembly and cohesion of many biological molecules, including the adh

237 a multiprotein ring that is responsible for cohesion of sister chromatids and formation of DNA loops

238 RX affects telomeric DSB repair by promoting cohesion of sister telomeres and that loss of ATRX in AL

239 ry mediator, and it alters the integrity and cohesion of the blood-brain barrier in several pathophys

240 at silenced chromatin domains persisted but cohesion of the domains was abolished.

241 a critical role in maintaining intercellular cohesion of the epidermis during photothermal therapy.

242 warming is predicted to increase the spatial cohesion of the habitat network that diminishes effects

243 monotonically increases with arousal, while cohesion of this network with the executive control netw

244 ved neighborhood disorder and lack of social cohesion on depression was estimated using two-stage ind

245 y rescued by mutants that weaken pericentric cohesion or mutants that decrease constriction on the nu

246 (odds ratio (OR) = 1.25) and lack of social cohesion (OR = 1.76) were significantly associated with

247 er [Odds Ratio (OR)=1.25] and lack of social cohesion (OR=1.76) were significantly associated with de

248 hborhood disorder: OR = 1.35; lack of social cohesion: OR = 1.93).

249 ighborhood disorder: OR=1.35; lack of social cohesion: OR=1.93).

250 hin an intervention, building broader social cohesion outside of it is more challenging.

251 the previously developed literature-derived cohesion p-value (LPv) and benchmarked against 'gold sta

252 s than aprotic solvents with similar solvent cohesion parameters.

253 , salience-executive control between-network cohesion peaked at moderate arousal.

254 tivation occurred after DNA circularization, cohesion persisted.

255 uble-stranded breaks and concomitant loss of cohesion, possibly at DNA replication forks.

256 Cohesion produced by cohesin conversion requires Tof1/Cs

257 that at high population densities, less cell cohesion promotes string formation.

258 cient Sgo1 mutant fully supports centromeric cohesion protection but delays chromosome segregation, s

259 At anaphase onset, Sgo1 function of cohesion protection must be disabled to allow timely chr

260 Our findings suggest that the persistent cohesion protects short telomeres from inappropriate rec

261 Multiple meiosis-specific cohesion proteins act to facilitate homolog segregation

262 In vertebrates, sister chromatid cohesion requires the activity of the ESCO2 acetyltransf

263 ng on the illness to also longing for social cohesion, sense of community and wellbeing in diabetes h

264 e we show that, despite a loss in centromere cohesion, sister chromatids in STAG2 mutant tumor cells

265 es of community-level social capital: social cohesion, social participation, and reciprocity.

266 We predicted that social cohesion (specifically male-to-male and female-to-male g

267 mage markers in meiosis and to problems with cohesion stability at the centromere.

268 under negative pressure as explained by the cohesion-tension theory by coating hydrophobic surfaces

269 During the cell cycle, sister-chromatid cohesion tethers sister chromatids together from S phase

270 ATPase activity but remarkably confer robust cohesion that bypasses the need for the cohesin protecto

271 dual loss of TRF1 and concomitant persistent cohesion that occurs with telomere shortening ensures a

272 erlie properties, such as the maintenance of cohesion, the regulation of kinetochores and the assembl

273 It was shown recently that ESCO2 promotes cohesion through interaction with the MCM replicative he

274 in protein complex mediates sister chromatid cohesion to ensure accurate chromosome segregation, and

275 s lining the tissue periphery break up their cohesion to migrate within the tissue.

276 us, STAG1 and STAG2 support sister chromatid cohesion to redundantly ensure cell survival.

277 Increasing intermolecular cohesion using longer peptide sequences that form stable

278 during S phase and mediate sister-chromatid cohesion, usually occur as individual complexes, support

279 Importantly, overall group cohesion was disrupted when even one fish within a shoal

280 ved neighborhood disorder and lack of social cohesion was estimated using 2-stage individual-particip

281 Thermodynamic work of cohesion was highest in PCN and may have contributed to

282 ivation occurred before DNA circularization, cohesion was lost.

283 Using a mechanical model of tissue cohesion, we show that, instead, a combination of local

284 eterochromatin and no defects in centromeric cohesion were observed.

285 Rec8 establishes cohesion when activated during DNA replication in fetal

286 binding sites and how transcription affects cohesion when cohesin complexes redistribute.

287 es cerevisiae represent specialized sites of cohesion where cohesin binds silent chromatin in a Sir2-

288 s, HMGECs drastically enhanced intercellular cohesion, whereas lipid production did not change.

289 anagement system, including 1) strong social cohesion, whereby leaders played a critical role in know

290 ells, cohesin also mediates sister chromatid cohesion, which is essential for chromosome segregation.

291 rrations through causing defects in telomere cohesion, which reconciles the long-standing paradox bet

292 ID1A inactivation causes defects in telomere cohesion, which selectively eliminates gross chromosome

293 s which uses contact calls to maintain group cohesion while foraging.

294 A challenge of group-living is to maintain cohesion while navigating through heterogeneous landscap

295 nal mechanism couples resolution of telomere cohesion with completion of telomere replication to ensu

296 f perceived neighborhood disorder and social cohesion with depressive symptoms among persons aged 50

297 et al., religion's ability to foster social cohesion within religious groups has been a key factor i

298 UBY is a Gal oxidase that strengthens pectin cohesion within the middle lamella, and possibly the muc

299 cess via inter-tissue attachment, as well as cohesion within the neuroectoderm.

300 Results demonstrate that cohesion within the salience network monotonically incre