ライフサイエンスコーパス: interphase

1 of inherited perinuclear ER and duration of interphase.

2 n about how Aurora B levels are regulated in interphase.

3 on, and the formation of a solid-electrolyte interphase.

4 Mto1 on DNA repair and recombination during interphase.

5 for subsequent CENP-A nucleosome assembly in interphase.

6 brids with uniquely stable solid electrolyte interphase.

7 concentration around centrosomes during late interphase.

8 urora B also executes important functions in interphase.

9 role of MTs in chromosomal functions during interphase.

10 ally associating domains (TADs) and loops in interphase.

11 Chromosomes are not very mobile during interphase.

12 le dependent and weakens considerably during interphase.

13 and activation of the NLRP3 inflammasome in interphase.

14 he formation of a stable cathode-electrolyte interphase.

15 d ANAPC1 protein levels, and prolongation of interphase.

16 nodes around the equator of the cell during interphase.

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

18 rophe and that cell death occurred also from interphase.

19 nctions in regulating gene expression during interphase.

20 microtubule organizing centers (MTOCs) into interphase.

21 tes topologically associating domains during interphase.

22 checkpoint--induced cell-cycle arrest during interphase.

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

24 tribute to shaping chromatin organization in interphase.

25 ear architecture across human cell nuclei in interphase.

26 stinct mother and daughter centrioles before interphase.

27 on at the mitotic exit, and nuclear shape in interphase.

28 /Tpr at nuclear pore complexes (NPCs) during interphase.

29 between the metal and the solid-electrolyte interphase.

30 a3, which loads onto the procentriole during interphase, ahead of Rcd4 and before mitosis.

31 uced defects in heterochromatin formation in interphase and chromosome segregation during mitosis, de

32 d restructuring of eukaryotic chromosomes in interphase and during mitosis.

33 med Li(+) compounds in the solid electrolyte interphase and electrically isolated unreacted metallic

34 ogy and composition of the solid electrolyte interphase and extend the cycle life of the Li metal ano

35 omatin tethering to the INM is controlled in interphase and how this process contributes to subsequen

36 olyaniline yields a stable solid-electrolyte interphase and inhibits the continuous growth of poorly

37 ometimes fail to complete replication during interphase and instead enter mitosis with regions of inc

38 This ensures that both NPCs in interphase and kinetochores in mitosis can generate anap

39 guish between Li(+) in the solid electrolyte interphase and metallic Li(0), but their detection range

40 fact that naked linker regions of DNA in the interphase and metaphase of eukaryotic cells are unprote

41 The NE undergoes extensive remodeling in interphase and mitosis, so mechanisms that seal NE holes

42 nd eIF4G bind eIF4E at similar levels during interphase and mitosis.

43 raction of eIF4E with 4E-BP1 or eIF4G during interphase and mitosis.

44 vealed different in situ interactions during interphase and mitosis.

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

46 nously tagged CK1delta and CK1epsilon during interphase and mitosis.

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

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

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

50 this complex in nuclear organization during interphase and mitotic chromosome folding.

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

52 es cohesin and condensin are thought to fold interphase and mitotic chromosomes, respectively, into l

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

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

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

56 rt that NuMA is associated with chromatin in interphase and prophase but released upon nuclear envelo

57 racterized the F-actin interactome in spread interphase and round mitotic cells.

58 nd telomeres, remain under-replicated during interphase and subsequently complete locus duplication i

59 rises concurrently with Cdk1 activity during interphase and suppresses substrate phosphorylation.

60 x string-shape alongside the plastids during interphase and these string-shaped nuclei then condense

61 Li(+) in components of the solid electrolyte interphase and unreacted metallic Li(0) has not been pos

62 pates in the formation of hybrid passivation interphases and contributes to dendrite-free Li depositi

63 the properties of the electrode/electrolyte interphases and thus the battery performances.

64 leolar association status of all NORs during interphase, and found that nucleolar association of acro

65 At first interphase, apposed pronuclei align obliquely to the ani

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

67 l and the formation of a large oil - ethanol interphase area during the ethanolysis.

68 ed to the filler surface to use this created interphase as a potential source of compliance to minimi

69 ically formed Li(+) in the solid electrolyte interphase, as the dominant source of inactive lithium a

70 We conclude that NPC interphase assembly is a major challenge for aging mitot

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

72 olid electrode and a liquid electrolyte, the interphase between a liquid metal and a liquid electroly

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

74 Different from the conventional interphase between a typical solid electrode and a liqui

75 suggested that sevoflurane would bind to the interphase between Fas death domain (DD) and Fas-associa

76 ron-insulating LPO-derived solid-electrolyte interphase between the Li metal and the GSE.

77 ) is still impeded by the instability of the interphase between the lithium metal and the electrolyte

78 gabases in length that became trapped within interphase bridges and then shattered, thereby producing

79 During interphase, BUB3 is protected from CRL4-mediated degrada

80 nctate foci along the microtubule lattice in interphase but exhibited reduced association with spindl

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

82 e cells maintained constant SNACS throughout interphase but showed dynamic changes during mitosis.

83 that Ras(V12)-expressing cells are softer in interphase but stiffen more upon entry into mitosis.

84 ggless gradually accumulates on chromatin in interphase but then dissociates in mitosis, and its accu

85 TADs and CTCF loops are readily detected in interphase, but absent during prometaphase.

86 em2-Nur1 complex at the INM are remodeled in interphase by the ESCRT-III/Vps4 machinery.

87 eate an artificial lithium metal/electrolyte interphase by treating the lithium anode with a tin-cont

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

89 arbon matrix and sealed by solid electrolyte interphase, can operate under lean electrolyte condition

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

91 Capitalizing on dielectrophoresis and interphase capacitance sensing, we have developed an imm

92 to orient their mitotic spindles along their interphase cell axis, setting up the axis of cell divisi

93 However, interphase cell shapes demonstrate the opposite bias.

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

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

96 rescence to quantify microtubule bundling in interphase cells and aberrant mitoses.

97 r, mechanisms regulating Pavarotti itself in interphase cells and specifically in neurite outgrowth a

98 d in parallel during mitosis, recent work in interphase cells has implicated the centrosome in both m

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

100 ndicate that taxanes target both mitotic and interphase cells in vivo and that resistance is through

101 Movement of chromosome sites within interphase cells is critical for numerous pathways inclu

102 hich are positioned at the nuclear lamina in interphase cells prior to mitosis, re-associate with the

103 entrosomes throughout the cell cycle, and in interphase cells to the nucleus, and in both a diffuse a

104 OPBP1 recruitment to DSBs in mitotic but not interphase cells, accompanied by mitotic radiosensitivit

105 dElys localized to the nuclear rim in interphase cells, but during mitosis it was absent from

106 In interphase cells, EBV promoters drive the expression of

107 hrough nuclear pore complexes and can infect interphase cells, including those actively replicating c

108 r post-abscission MBs can be internalized by interphase cells, where they reside in the cytoplasm as

109 s fundamentally different from that of other interphase cells.

110 nown about where EBV episomes are located in interphase cells.

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

112 Here we show that the interphase centrosome protein AKNA has a key role in thi

113 t Nup188 is vicinal to the inner core of the interphase centrosome.

114 ad Nek2A, prematurely displaced DAs from the interphase centrosomes of immortalized retina pigment ep

115 Here, we investigate the interphase chromatin dynamics in human cells in response

116 cking shows that condensin markedly confines interphase chromatin movements.

117 t condensin to determine its contribution to interphase chromatin organization.

118 orm a dynamic nuclear mesh that can regulate interphase chromatin structure.

119 tions (PTMs) of histones alter compaction of interphase chromatin, but it remains poorly understood h

120 partially condensed, extended structures in interphase chromatin.

121 he kinetics and order of events by which the interphase chromosome state is formed and identify telop

122 The marked reorganization of interphase chromosomes in the inverted nuclei of rods in

123 ption and reveal a remarkable flexibility of interphase chromosomes.

124 romatin density in the nucleus by stretching interphase chromosomes.

125 Our data suggest that a distinct form of interphase cohesin regulation ensures mitotic fidelity a

126 This interphase cohesin regulation relies on cohesin release

127 pillar cells ensure mitotic fidelity through interphase cohesin regulation.

128 As a result, an artificial solid electrolyte interphase composed of lithium fluoride, tin, and the ti

129 We also report that cathode electrolyte interphases composed of preformed anionic polymers and s

130 mine which components are required to render interphase cytoplasm spindle-assembly competent in the a

131 In vitro, immunodepletion of DjA1 from interphase cytosol reduced its activity to enhance GRASP

132 ionic contacts, eliminate solid-electrolyte interphase debris, and allow the reversible deposition/s

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

134 g the notion that recombination can occur in interphase diploids.

135 es can compact mitotic chromosomes, organize interphase domains, and juxtapose bacterial chromosomal

136 Experimental manipulation of interphase duration shows that cell cycle speed regulate

137 including extended cell cycle arrest, longer interphase durations, and death, which overall results i

138 ant with decreasing density almost until the interphase edge.

139 laevis egg extracts to show that homogenized interphase egg cytoplasm self-organizes over the course

140 itotic CDK (Cyclin B1-CDK1) is used to drive interphase egg extracts into a mitotic state, the replic

141 Our results indicate that, during interphase, entanglements between chromosomes and chromo

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

143 uence of canonical histone PTMs that dictate interphase euchromatin (acetylation) and heterochromatin

144 In interphase eukaryotic cells, almost all heterochromatin

145 In this module, ATR interphases exclusively with the cell cycle to implement

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

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

148 , serving as an artificial solid-electrolyte interphase filter in minimizing parasitic reactions at t

149 We confirmed this model by interphase fluorescent in situ hybridization (FISH) and

150 ations will be helpful in engineering better interphases for future batteries.

151 r-concentration, leading to lithium fluoride interphase formation, while precipitation of the lithium

152 ndrite growth and unstable solid electrolyte interphase formation.

153 y detailed analyses of the solid-electrolyte interphase formed on copper and lithium, where the dispa

154 Highly stable passivation interphases formed on both electrodes in the novel IL el

155 Intriguingly, an interphase gap introduced between the recharging phases

156 nuclear envelope (NE) aids in organizing the interphase genome by tethering chromatin to the nuclear

157 Application of the model to the interphase genome indicates that active loop extrusion c

158 rophase are commensurate with or higher than interphase growth rates.

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

160 rangement of chromosome territories (CTs) in interphase has been posited to influence the outcome and

161 died extensively in S phase, the response in interphase has not, and the question of whether homologo

162 mosomal kinase JIL-1 is responsible for most interphase histone H3S10 phosphorylation and has been pr

163 overs the critical role of solid-electrolyte interphase in regulating the migration of Na ions and th

164 ion after the formation of solid electrolyte interphase in the first deep lithiation, completely avoi

165 tructure-function relationships of electrode interphases in Li ion batteries.

166 also facilitates nuclear membrane repair in interphase, in part through recruitment of the nuclear m

167 n represses transcription at DSBs throughout interphase, indicating that this is distinct from its kn

168 Longer interphase intervals evoked Ca(2+) responses that were g

169 with ultrashort pulses can be modulated with interphase intervals of tens of nanoseconds, a predictio

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

171 sin contributes to chromatin organization in interphase is less well understood.

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

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

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

175 r that imposes similar features in mammalian interphase, is absent in S. cerevisiae, suggesting alter

176 ormation and chromosome movement, and during interphase, Kif11 mediates diverse trafficking processes

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

178 binding energy of atoms evaporated from the interphase layer between bulk phase and vapor is much sm

179 sity up to 0.6 mA cm(-2) A solid electrolyte interphase layer formed in situ between the metallic lit

180 temperature and density profiles within the interphase layer indicate that the averaged kinetic ener

181 motivating studies of the solid-electrolyte interphase layer that forms on the lithium, which is key

182 A protective interphase layer will be formed outside templates when t

183 ector, or the breakdown of solid electrolyte interphase layer.

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

185 Abnormal modulation of Aurora B in interphase leads to cell cycle defects often linked to a

186 With such an artificial solid electrolyte interphase, lithium symmetrical cells show outstanding p

187 microtubules align bipolar spindles with the interphase long cell axis, without requiring a fixed cue

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

189 quired for post-mitotic re-establishment and interphase maintenance of chromatin accessibility, and t

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

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

192 The interphase mass transfer coefficient (K(L)a) was determi

193 the hormone auxin and through regulation of interphase microtubule (MT) orientation.

194 the core of centrosomes, which organize the interphase microtubule cytoskeleton of most animal cells

195 of closed mitosis in fission yeast, wherein interphase microtubules assemble to form the spindle wit

196 or NEK7 reduced the association of EML4 with interphase microtubules.

197 own eukaryotic cells, Naegleria amoebae lack interphase microtubules; this suggests that actin alone

198 centriole asymmetry in mitosis primes biased interphase MTOC activity, necessary for correct spindle

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

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

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

202 ical during cytokinesis, over-accumulates in interphase nodes following cell division in a manner dep

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

204 termediate filament protein critical for the interphase nuclear architecture, was reduced.

205 1, a transmembrane nucleoporin essential for interphase nuclear pore biogenesis.

206 Nup358, a late marker for interphase nuclear pore complex (NPC) biogenesis, is und

207 plex and this activity is also important for interphase nuclear pore complex insertion into growing g

208 3D chromatin organization characteristic of interphase nuclei is attenuated in meiotic prophase.

209 onal organization of the genome in mammalian interphase nuclei is intrinsically linked to the regulat

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

211 ic chromosomes and to a lesser extent within interphase nuclei, implying nuclear disassembly.

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

213 s, in the pachytene stage of meiosis, and in interphase nuclei.

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

215 ization on mitotic metaphase chromosomes and interphase nuclei.

216 The interphase nucleus and mitotic spindle scale with cell s

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

218 upon NuMA loss, its precise function in the interphase nucleus remains elusive.

219 In interphase, NuMA is localized to the nucleus and hypothe

220 Nuclear membrane rupture during interphase occurs in a variety of cell contexts, both he

221 of monomolecular Langmuir films (LFs) at the interphase of aqueous barium acetate solution, supplemen

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

223 During interphase of the eukaryotic cell cycle, the microtubule

224 ormation and functions of the interfaces and interphases of the active materials in these devices is

225 formation of a hydrophobic solid-electrolyte interphase on a metallic-lithium anode that allows for h

226 in situ formed, stable electrode/electrolyte interphases on both the Li anode and the LCO cathode, wi

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

228 mising approaches for creating purpose-built interphases on Li, as well as for fabricating advanced L

229 t and then replenished during the subsequent interphase, only a few are required to induce a cell-cyc

230 on patterns emerge, reminiscent of mammalian interphase organisation, but with distinct regulation.

231 te additive used to form a solid-electrolyte interphase passivation layer on the anode that is unstab

232 We previously demonstrated that there is an interphase pool of KIF11 present in glioblastoma cancer

233 e found that WDR5 and TBP, which bind active interphase promoters(6,7), recruit the anaphase-promotin

234 building of fluoridized cathode-electrolyte interphases, protecting both the electrolyte and aluminu

235 at nuclei undergo substantial growth in each interphase, reaching a maximal size prior to mitosis tha

236 erties of the resultant new material phases (interphases) regulate all interfacial processes at a Li

237 other critical envelope functions, including interphase repair(8-13) and chromatin organization(14-17

238 hripsis accumulates, beginning with aberrant interphase replication of bridge DNA.

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

240 defective nuclear localization of M18BP1 in interphase, resulting in defective CENP-A nucleosome ass

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

242 his new type of liquid electrode/electrolyte interphase reveal its important role in regulating charg

243 These results demonstrate an unexpected interphase role for Mad1 in tumor promotion via p53 dest

244 However, interphase roles of Mad1 that do not impact mitotic chec

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

246 aconformal and stretchable solid-electrolyte interphase (SEI) composed of parallelly stacked few-laye

247 The solid-electrolyte interphase (SEI) dictates the performance of most batter

248 ees ), producing a uniform solid electrolyte interphase (SEI) during the initial galvanostatic format

249 the formation of unstable solid electrolyte interphase (SEI) during the Li plating/stripping process

250 the solvation rule for the solid-electrolyte interphase (SEI) enabler in an electrolyte system.

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

252 The importance of the solid-electrolyte interphase (SEI) for reversible operation of Li-ion batt

253 d and applied to study the solid electrolyte interphase (SEI) formation on copper current collectors

254 volution, redox mechanism, solid-electrolyte interphase (SEI) formation, side reactions, and Li-ion t

255 hanism associated with the solid-electrolyte interphase (SEI) formation, which we name the Li-SEI mod

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

257 physical properties of the solid electrolyte interphase (SEI) formed on an Li anode as a point of dep

258 tes, the organic-inorganic solid electrolyte interphase (SEI) formed on the Li-metal anode surface is

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

260 The solid-electrolyte interphase (SEI) is probably the least understood compon

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

262 ZnSO(3), and ZnS enriched-solid electrolyte interphase (SEI) preventing Zn dendrite and further supp

263 ZnF(2) -Zn(3) (PO(4) )(2) solid electrolyte interphase (SEI) preventing Zn dendrite and water decomp

264 um fluoride (LiF)-enriched solid electrolyte interphase (SEI) through the lithiation of surface-fluor

265 orm stable versus unstable solid electrolyte interphase (SEI), covering the current understanding of

266 studying the nature of the solid-electrolyte interphase (SEI), little attention has been paid to unde

267 its heterogeneous "native" solid electrolyte interphase (SEI).

268 tive ionic pathways in the solid electrolyte interphase (SEI).

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

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

271 mitotic rounding is sufficient to translate interphase shape into a cortical pattern that can be rea

272 equiring a fixed cue or a physical memory of interphase shape.

273 H and (19)F NMR spectra of solid-electrolyte interphase species selectively, revealing their chemical

274 chromosome conformation transforms into the interphase state.

275 e and phased nucleosomal arrays, not only in interphase steady-state but also immediately after repli

276 A novel filler-resin matrix interphase structure was developed and evaluated for den

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

278 The lateral contraction of alpha' imposed an interphase tensile microstress in the transverse directi

279 condensin-mediated chromatin interactions in interphase that are qualitatively similar to those obser

280 In interphase, the cohesin complex generates loops and topo

281 rge-transfer through the lithium-electrolyte interphase, the corrosion observed here is found to be g

282 During interphase, the eukaryotic genome is organized into chro

283 In interphase, the human genome sequence folds in three dim

284 When cells encounter DSBs in interphase, they are able to arrest the cell cycle until

285 29) and breast cancer (MCF-7) cells from the interphase through mitosis and then to the cytokinesis s

286 netic contractile ring are reemployed during interphase to create compartments used for cellular remo

287 with a limited nanogel content filler-resin interphase to lower volumetric shrinkage and dramaticall

288 y, we find that condensin is required during interphase to prevent ongoing transcription from eliciti

289 In interphase, TRAIP helps replisomes overcome DNA interstr

290 idine RNA translation was active and, unlike interphase translation, resistant to mTOR inhibition.

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

292 chromosomes in an oscillatory manner during interphase via linkages through the nuclear envelope (NE

293 trength associated with the nanogel-modified interphase was observed.

294 g chromosomal region in human T-cells during interphase, we discover that at these larger scales inte

295 the electrolyte and in the solid-electrolyte interphase, which allows uniform Li-ion distribution as

296 curs at >1.5 V and forms an initial LiF-rich interphase while electrolyte solvent reduction at <0.8 V

297 rminus binds DNA in vitro and chromosomes in interphase, while its coiled-coil acts as a central regu

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

299 e coatings that can form a solid electrolyte interphase with a high interfacial energy and self-heali

300 on mechanisms: An unstable solid electrolyte interphase with most organic electrolytes, "mossy" and "