ライフサイエンスコーパス: interphase

1 epigenetic landscape and gene expression in interphase.

2 leolar localization of NADs and Ki-67 during interphase.

3 localized with chromatin during prophase and interphase.

4 ypothesis that MTAs induce cell death during interphase.

5 ting, ionically conducting solid electrolyte interphase.

6 rophe and that cell death occurred also from interphase.

7 de material with a well-ordered hydroxylated interphase.

8 independent of ARHGEF17's RhoGEF activity in interphase.

9 allowed Cdc20 to increase APC/C activity in interphase.

10 sembly during the transition from M phase to interphase.

11 tromeres in metaphase but is not required in interphase.

12 nctions in regulating gene expression during interphase.

13 es and the centrosome, across the NE, during interphase.

14 an directly influence gene expression during interphase.

15 taphase II and declines again upon exit into interphase.

16 th the formation of an electrode-electrolyte interphase.

17 microtubule organizing centers (MTOCs) into interphase.

18 t together to extrude unknotted loops during interphase.

19 exes and is involved in cell motility during interphase.

20 hed at the cell surface in mitosis and 37 in interphase.

21 ity carrier trapping across a donor-acceptor interphase.

22 itosis, is sequestered in the nucleus during interphase.

23 cient to drive Celsr1 internalization during interphase.

24 tes topologically associating domains during interphase.

25 during mitosis and across many cell types in interphase.

26 that were tightly synchronized in mitosis or interphase.

27 which disrupts cellular architecture during interphase.

28 hibition during mitosis but sensitive during interphase.

29 [NADs]) and proteins to the nucleolus during interphase.

30 nodes around the equator of the cell during interphase.

31 ng with the formation of a solid-electrolyte interphase.

32 energy for ion transport at a sodium bromide interphase.

33 nction of the chemistry of solid-electrolyte interphase.

34 Here we present a view of the interphase 3D genome characterized by extensive physical

35 centrosome separation and positioning during interphase, a phenotype also detected in kinesin-1 mutan

36 sed unscheduled separation of centrosomes in interphase, a phenotype also observed upon overexpressio

37 factor GATA1 exerts site-specific changes in interphase accessibility that are most pronounced at dis

38 loci maintaining none, some, or all of their interphase accessibility.

39 bridges induced nuclear envelope rupture in interphase, accumulated the cytoplasmic 3' nuclease TREX

40 s a powerful regulator of MT dynamics during interphase and affects heterogeneous cell functions.

41 thium deposition, unstable solid electrolyte interphase and almost infinite relative dimension change

42 nal NLS, TgEB1 resides in the nucleoplasm in interphase and associates with the spindle MTs during mi

43 the plasma membrane at the cell tips during interphase and at the division site during cell division

44 i(SCA), which enable real-time monitoring of interphase and cell-cycle biology.

45 in vivo to ensure proper NPC distribution in interphase and centrosome separation in the mitotic prop

46 that mediates functional interactions during interphase and compacts chromosomes during mitosis.

47 atase counteracts Cdk phosphorylation during interphase and delays phosphorylation of late Cdk substr

48 h are in equilibrium with the nucleoplasm in interphase and disassemble during mitosis or upon treatm

49 mitotic interaction is more dynamic than in interphase and is facilitated by both DNA binding and nu

50 sult of the formation of a solid electrolyte interphase and Li trapping at the anodes, remains unreso

51 t proteins, are reported to function in both interphase and mitosis.

52 es to proper MT cytoskeletal organization in interphase and mitosis.

53 different 3D concentration distributions in interphase and mitosis.

54 Thus, interphase and mitotic cells share similar mechanisms fo

55 mmunolabelling protocols, FACS separation of interphase and mitotic cells, including mitotic subphase

56 g video recording of microtubule dynamics in interphase and mitotic cells.

57 ose proximity to SF3B1 in the nucleoplasm of interphase and mitotic cells.

58 Cnd2 kleisin subunit of condensin to mediate interphase and mitotic chromosomal organization in fissi

59 rning the topology and structure of both the interphase and mitotic chromosomes from effective energy

60 osomal condensin complex, a key component of interphase and mitotic chromosomes.

61 ein abundance and phosphorylation changes in interphase and mitotic fractions from asynchronously gro

62 on is shown to involve targeting Nup2 to its interphase and mitotic locations.

63 Crocin depolymerized both the interphase and mitotic microtubules of different cancer

64 These may influence interphase and mitotic MT mechanisms and indeed, centros

65 In this manner, p150N coordinates both interphase and mitotic nuclear structures via Ki67.

66 h negative signaling by the cell tips during interphase and positive signaling by the centrally place

67 showed variation in chromatin compaction in interphase and the formation of chromosome territories.

68 The interphase APC/C activator Fizzy-related (Fzr or Cdh1) i

69 el whereby centrosome-MT interactions during interphase are important for centrosome clustering and c

70 of condensins and their functional roles in interphase are poorly understood.

71 DSBs are continuously formed throughout interphase, are enriched on both sides of strong topolog

72 cheduled Plk1 activity, either in cycling or interphase-arrested cells, accelerated centriole maturat

73 analysis to uncover the dynamic formation of interphases at the solid electrolyte/electrode interface

74 es and traced the positions of TADs in human interphase autosomes and X chromosomes.

75 Interphase bacterial artificial chromosome fluorescence

76 z6) communicate the long axis orientation of interphase basal cells to neighbouring basal mitoses so

77 application of a plastic-crystal electrolyte interphase between a solid electrolyte and a solid catho

78 ntroduction of a plastic-crystal electrolyte interphase between a solid electrolyte and solid cathode

79 presents multipotent cells that arise at the interphase between ectoderm and prospective epidermis of

80 hat the sea ice environment is a significant interphase between the polar ocean and the atmosphere an

81 measurement of polypeptide structure on the interphase boundary.

82 (ER-alpha)-bound eRNA(+) active enhancers in interphase breast cancer cells, exhibiting non-canonical

83 he rate of S384 dephosphorylation is high in interphase but low in mitosis.

84 omplex embraces sister chromatids throughout interphase, but during mitosis most cohesin is stripped

85 ctions in nuclear anchorage and migration in interphase, but little is known about their involvement

86 t transient nuclear envelope ruptures during interphase, but the responsible biophysical processes re

87 show that a NaBr enriched solid-electrolyte interphase can lower the surface diffusion barrier for s

88 y issue is that the static solid electrolyte interphase cannot match the dynamic volume changes of th

89 ion and instability of the solid-electrolyte interphase caused by the large volume change ( approxima

90 d that divisions align better with the long, interphase cell axis than with the monolayer stress axis

91 arity and further suggest that disruption of interphase cell behavior by supernumerary centrosomes co

92 In epithelial tissues, the shape of the interphase cell is influenced by cell adhesion, mechanic

93 Structure of interphase cell nuclei remains dynamic and can undergo v

94 es occupy preferred spatial positions within interphase cell nuclei.

95 romal cells, affect microtubule dynamics and interphase cell polarity.

96 ion of a mitotic cell to a differentiated or interphase cell results in rapid reactivation of the cen

97 entation of mitotic spindles is sensitive to interphase cell shape and the direction of extrinsic mec

98 patial landmarks, encoding information about interphase cell shape anisotropy to orient division in t

99 s, and the effect of the aspect ratio of the interphase cell shape in defining the final alignment ax

100 The mechanisms underlying interphase cell shape sensing in tissues are therefore u

101 The DAB polymer does not affect interphase cell viability, but inhibits Golgi fragmentat

102 of cell division along the long axis of the interphase cell--the century-old Hertwig's rule--has pro

103 n essential tool for quantitative studies of interphase cell-cycle regulation.

104 Cs) and nuclear-envelope associated MTOCs in interphase cells (iMTOCs).

105 ion of SUV39H1 with chromatin in mitotic and interphase cells - effects that can be recapitulated by

106 required for both centrosome positioning in interphase cells and proper spindle orientation during m

107 This provides a mechanism whereby interphase cells can oppose autocatalytic cyclin E degra

108 etiolated seedlings consisting of primarily interphase cells in Arabidopsis thaliana, AUG8 is an int

109 Chromatin condensation in interphase cells is characterized by an unexpected mitos

110 specimens, tissue XY-karyotyping of the RPM interphase cells was consistent with the host sex karyot

111 addition, when mitotic cells are fused with interphase cells, "wait anaphase" signals are diluted, r

112 localization, having diffuse localization in interphase cells, and robust clustering during M phase.

113 s were generally similar between mitotic and interphase cells, and the majority of new mitotic protei

114 furrow formation can be initiated in rounded interphase cells, but not adherent cells.

115 1(T37/T46+) saturation levels than pH3(S10-) interphase cells.

116 rare chromosome breaks and translocations in interphase cells.

117 ary basal body in addition to the nucleus in interphase cells.

118 ly observed for the dynamics of chromatin in interphase cells.

119 s fundamentally different from that of other interphase cells.

120 omain protein Sad1 remains stable but severs interphase centromere-LINC contacts.

121 -A nucleosomes recruits the Mis18 complex to interphase centromeres to promote new CENP-A nucleosome

122 s of extended Cnn flares, to maintain robust interphase centrosome activity and promote the formation

123 omatid cohesion, and higher order folding of interphase chromatin are mediated by condensin and cohes

124 a simple biochemical procedure that enriches interphase chromatin in all its complexity.

125 The compaction of diffuse interphase chromatin into stable mitotic chromosomes ena

126 mechanisms required to sustain these complex interphase chromatin structures are unknown.

127 caRNAs) via its RGG domain to regulate human interphase chromatin structures in a transcription-depen

128 The topologically associating domains of the interphase chromosome exhibit multistability with varyin

129 omains have been proposed as the backbone of interphase chromosome structure.

130 Thus, interphase chromosome-LINC contacts constitute a cell-cy

131 Interphase chromosomes adopt a hierarchical structure, a

132 hromatin Model) that explains the folding of interphase chromosomes and generates chromosome conforma

133 t, simple and generic force able to organize interphase chromosomes at all scales.

134 interband regions drives the organization of interphase chromosomes by creating stable physical separ

135 Mammalian interphase chromosomes interact with the nuclear lamina

136 Fixed human metaphase and interphase chromosomes were labeled with the DNA minor g

137 Improved pulse-chase labeling of endogenous interphase chromosomes yields a model in which the globa

138 domains and loops as a pervasive feature of interphase chromosomes, but the biological implications

139 Biophysicists are modeling conformations of interphase chromosomes, often basing the strengths of in

140 estigating the structure and organization of interphase chromosomes.

141 observation thus reveals the architecture of interphase chromosomes.

142 embryos, we show that the elaboration of the interphase Cnn scaffold defines a major structural rearr

143 and covered with a uniform solid electrolyte interphase coating.

144 rtant, unanticipated transcriptional role of interphase condensins in modulating estrogen-regulated e

145 the formation of a robust solid electrolyte interphase consisting of Li2 CO3 -LiF, which enables fas

146 ducting passivation layer (solid-electrolyte interphase) containing Li3P and Li8ZrO6 that is wet by t

147 reatly reduced at the furrow compared to the interphase cortex, suggesting their stabilization during

148 The ability to use interphase cytoplasm in SCNT could aid efforts to genera

149 de a likely explanation for the inability of interphase cytoplasm to induce reprogramming.

150 localization of Fzr to the centriole during interphase depends on direct interaction with Spd2.

151 This work provides a paradigm for interphase design to address the dendrite challenge, pav

152 Here we identify a previously unrecognized interphase distribution of Mad1 at the Golgi apparatus.

153 de, reveals the dynamic behaviour of cathode interphases driven by conductive carbon additives (carbo

154 rylation, the mitotic checkpoint complex and interphase early mitotic inhibitor 1 (Emi1) ensures the

155 mitotic checkpoint genes can have unexpected interphase effects that influence tumor phenotypes.

156 nucleated away from the centrosome and that interphase egg cytoplasm supported spontaneous nucleatio

157 and solution, based on the constants of the interphase equilibria and the concentrations established

158 ime is determined by the corresponding local interphase equilibria.

159 s were highly expressed at the biofilm-solid interphase, exposing a critical gap in the knowledge of

160 Thus, the means by which the interphase expression pattern is transduced to daughter

161 ecome smaller in the presence of cytoplasmic interphase extract isolated from post-gastrula Xenopus e

162 ts on the formation and evolution of cathode interphases, facilitating development of in situ surface

163 In the interphase, FgCdc14-GFP localized to the nucleus and spi

164 e mitotic cohesin SMC1A, and used four-color-interphase-FISH coupled with BrdU incorporation and anal

165 atus and genetic abnormalities determined by interphase fluorescence in situ hybridization (FISH) in

166 Cytogenetic aberrations detected by interphase fluorescence in situ hybridization (iFISH) of

167 In this study, we used three-dimensional interphase fluorescence in situ hybridization to deciphe

168 Using a quantitative interphase-fluorescence in situ hybridization approach,

169 h chromosomal abnormalities (CA) detected by interphase fluorescent in situ hybridization after CD138

170 sult of the formation of a solid electrolyte interphase followed by gradual loss in subsequent cycles

171 ycling cohesin so that it can be reloaded in interphase for both non-mitotic and mitotic functions.

172 ess and composition of the solid electrolyte interphase formed over a silicon anode in situ as a func

173 n nanocomposites with dynamically asymmetric interphases formed by a high-glass transition temperatur

174 phosphorylation marks put by the kinases in interphase (G1, S, and G2), where Cdck7/Kin28 phosphoryl

175 Intriguingly, an interphase gap introduced between the recharging phases

176 teristics (three involving alteration of the interphase gap of the biphasic current pulse and one inv

177 apture had shown that cohesin's main role in interphase genome organization is in mediating interacti

178 Conversely, interphase H3S10ph domains expand in Ehmt1 (also known a

179 guingly, centrosome maturation occurs during interphase in an MLK-dependent manner, independent of th

180 of the most active housekeeping genes during interphase in human cells, but the SUMOylated targets on

181 e tracking of tagged chromosomal loci during interphase in live yeast cells together with polymer mod

182 tokinetic contractile ring accumulate during interphase in nodes-precursor structures around the equa

183 awal into quiescence or for the remainder of interphase including G2 phase, implying 3D structure is

184 rences in multiple cellular functions during interphase, including cell migration, focal adhesion dyn

185 pectrometry shows that a cathode-electrolyte interphase, initially formed on carbon black with no ele

186 As proliferating cells transit from interphase into M-phase, chromatin undergoes extensive r

187 ishment of polarity and adhesion during each interphase is associated with a process of whole-embryo

188 through nuclear pore complexes (NPCs) during interphase is facilitated by the nucleoporin Nup2 via it

189 ssociated with chromatin but its function in interphase is not known.

190 In eukaryotes, the basal transcription in interphase is orchestrated through the regulation by kin

191 s the amplitude of transcription observed in interphase is reestablished during mitotic exit.

192 Although the duration of interphase is similar in haploid and diploid cells, hapl

193 f the tracking problem-tracking cells during interphase-is straightforward and can be executed with s

194 This showed that the interphase landscape characterized by small chromatin do

195 fectively fabricate stable solid-electrolyte interphase layer for solving the issues associated with

196 that a stable and uniform solid electrolyte interphase layer is formed due to a synergetic effect of

197 elf-formed flexible hybrid solid-electrolyte interphase layer through co-deposition of organosulfides

198 ve as "plasticizer" in the solid-electrolyte interphase layer to improve its mechanical flexibility a

199 The as-formed robust solid-electrolyte interphase layers enable dendrite-free lithium depositio

200 ion of stable and flexible solid-electrolyte interphase layers which serve to address both issues.

201 l structure stabilized the solid electrolyte interphase leading to superior reversible capacity of ov

202 sites mutated to alanine, mto2[24A], retains interphase-like behaviour even in mitotic cells.

203 n of stretch induces a global realignment of interphase long axes along the direction of extension, t

204 racks and fractures of the solid electrolyte interphase, low Coulombic efficiency, and dendritic grow

205 rks regulatory regions of inducible genes in interphase mammalian cells, implicating mitosis-independ

206 ing the spreading of repressive chromatin in interphase mammalian cells.

207 mal cells, and all higher plant cells, build interphase microtubule arrays of specific architectures

208 Interphase microtubule organization is critical for cell

209 otubule sliding in anaphase B and sliding of interphase microtubules during neurite formation.

210 -63 phosphorylation are required to preserve interphase microtubules in response to hyperosmotic stre

211 toxicity in human tumors by interfering with interphase microtubules.

212 particularly susceptible to perturbation of interphase microtubules.

213 g with trafficking of DNA repair proteins on interphase microtubules.

214 ing protein EBP50/NHERF1 in the formation of interphase microvilli, E3KARP S303D cannot.

215 lo kinase activity shifts the system from an interphase mode into an enhanced mitotic mode.

216 (FUCCI), we found that 30% of the genome in interphase mouse embryonic stem cells (ESCs) is marked w

217 rosome activity and promote the formation of interphase MT asters required for normal nuclear spacing

218 ed a hyper-stabilization of both mitotic and interphase MTs.

219 10ph is also anti-correlated with H3K9me2 in interphase murine embryonic fibroblasts (MEFs) and is re

220 esulting in an uptake of Celsr1 protein from interphase neighbors.

221 that linking planar cell division plane with interphase neighbour long axis geometry reinforces axial

222 G2 phase of the cell cycle, seven different interphase node proteins maintain constant concentration

223 the structures and assembly of two types of interphase nodes-multiprotein complexes associated with

224 escent fusion proteins revealed two types of interphase nodes.

225 antitative structural analysis revealed that interphase NPC assembly proceeds by an asymmetric inside

226 of the nuclear pore complexes (NPCs) in the interphase nuclear envelope, whereas deletion of B-type

227 g DNA-PLM, we achieved nanoscopic imaging of interphase nuclei and mitotic chromosomes, allowing a qu

228 a model of chromatin architecture in intact interphase nuclei consistent with variable longitudinal

229 a pair of homologous chromosomal loci in the interphase nuclei of Caenorhabditis elegans embryos.

230 DAPI lifetime variations across interphase nuclei showed variation in chromatin compacti

231 romoting complex/cyclosome, is excluded from interphase nuclei, but enters nuclei at mitotic onset an

232 In higher eukaryotic interphase nuclei, the 100- to >1,000-fold linear compac

233 rved diffusely throughout the nucleoplasm in interphase nuclei, whereas, the nucleolus region exhibit

234 light on the organization of chromosomes in interphase nuclei.

235 with regions of little or no interaction, in interphase nuclei.

236 addresses mechanisms by which NR can form in interphase nuclei.

237 ization on mitotic metaphase chromosomes and interphase nuclei.

238 nization of the genome within the eukaryotic interphase nucleus directly influence how the genes are

239 of metazoan organisms are partitioned in the interphase nucleus into discrete topologically associati

240 n of the glucocorticoid receptor (GR) in the interphase nucleus of living cells.

241 on of protein kinase C family members in the interphase nucleus to disrupt the nuclear lamina, demons

242 In the interphase nucleus, chromatin is organized into three-di

243 The 4D organization of the interphase nucleus, or the 4D Nucleome (4DN), reflects a

244 nisms shape the topological landscape in the interphase nucleus.

245 During the short interphase of early embryonic cells, AL are rapidly deli

246 During interphase of syncytial embryos of Drosophila, cortical

247 of the NLRP3 inflammasome was restricted to interphase of the cell cycle by NEK7, a serine-threonine

248 Eukaryotic cells spend most of their life in interphase of the cell cycle.

249 nvoluted mechanisms of the solid-electrolyte interphase on Si electrodes.

250 to more effective formation of a protective interphase on the anode along with further suppression o

251 s capable of stabilizing a solid-electrolyte interphase on the Li anode.

252 The interplay between hydroxylated interphase on the surface and the unique bivalence struc

253 serious limitations of spontaneously formed interphases on high-capacity metal anodes.

254 al function in MT-dependent MT nucleation in interphase plant cells.

255 In particular, we find that a sodium bromide interphase presents an exceptionally low energy barrier

256 lds spindle assembly checkpoint signaling in interphase, providing a store of inhibitory signals that

257 During interphase, Rab11-GTPase-containing endosomes recycle en

258 Dynamics of the interphase region between matrix and bound polymers on n

259 nsition is in any way distinct from later in interphase remains unknown.

260 abolic and genomic regulation that occurs in interphase requires the demarcation of precise phase bou

261 reveals that the apicosome forms de novo in interphase, retains its structure during mitosis, is asy

262 ymeric components into the solid-electrolyte interphase (SEI) but also to accommodate Li deposition/d

263 Solid-electrolyte interphase (SEI) films with controllable properties are

264 for Li-ion batteries, the solid electrolyte interphase (SEI) formed during electrochemical cycling o

265 uring the formation of the solid electrolyte interphase (SEI) from reduced electrolytes in the first

266 An artificial solid electrolyte interphase (SEI) is demonstrated for the efficient and s

267 electrolyte forms a stable solid electrolyte interphase (SEI) layer with a metallic lithium anode.

268 to construct a passivating solid-electrolyte interphase (SEI) layer.

269 hance the stability of the solid electrolyte interphase (SEI) of a Si electrode over long-term cyclin

270 The solid electrolyte interphase (SEI) of the high capacity anode material Si

271 e a component of the anode solid electrolyte interphase (SEI), leading to a significant increase of t

272 e electrode surface, hence solid electrolyte interphase (SEI).

273 gh reactivity and unstable solid electrolyte interphase (SEI).

274 d their interface with the solid electrolyte interphase (SEI).

275 y to create durable hybrid solid-electrolyte interphases (SEIs) on metal anodes.

276 The nuclear sequestration of anillin during interphase serves to restrict anillin's function at the

277 d-liquid interface is non-isothermal and the interphase spacing varies in ways that are poorly unders

278 tate chromosome segregation, and decondensed interphase structures that accommodate transcription, ge

279 are incorporated into the solid electrolyte interphase surface layer at the graphite negative electr

280 in AurA(Thr-295) phosphorylation late during interphase that corresponded with delayed cyclin-depende

281 During interphase, the inactive X chromosome (Xi) is largely tr

282 of sodium deposition at sodium bromide-rich interphases.The chemistry at the interface between elect

283 By tuning the interphase thickness, we demonstrate its robustness in s

284 mitosis, followed by steady increase during interphase to double the initial number.

285 The abrupt and irreversible transition from interphase to M phase is essential to separate DNA repli

286 As cells transition from interphase to mitosis, the microtubule cytoskeleton is r

287 ESCRT-III also acts during interphase to repair the NE upon migration-induced ruptu

288 es with its binding partner Kinesin-1 during interphase to trigger centrosome separation.

289 Focusing on the mitotic-to-interphase transition in Drosophila melanogaster embryos

290 ression and protein abundance changes during interphase under minimally perturbed conditions.

291 le centromere associations formed in meiotic interphase undergo a progressive polarization (clusterin

292 se I sensitivity of chromatin in mitosis and interphase, using a murine erythroblast model.

293 Lamin-A,C phosphorylation is low in interphase versus dividing cells, and its levels rise wi

294 role of anillin targeting to the nucleus in interphase, we identified the nuclear targeting motif.

295 le1 to the NE during mitosis, but not during interphase when Gle1 is at NPCs.

296 odimerization and autophosphorylation during interphase, whereas the Asl C terminus stabilizes Plk4 d

297 a chemically stable and mechanically strong interphase, which minimizes the corrosion reaction with

298 While the formation of interphases widens the electrochemical window, their ele

299 Detailed thermodynamic analysis shows an interphase with low electronic conductivity, high ionic

300 in both intact and enucleated metaphase and interphase zygotes and two-cell embryos.