ライフサイエンスコーパス: reassembly

1 collateral arteries, which we termed "artery reassembly".

2 onomer (a marker for ongoing PSII repair and reassembly).

3 do not require fork adjustment or replisome reassembly.

4 changes lead to community disaggregation and reassembly.

5 ery of its deubiquitinase activity and Golgi reassembly.

6 ic DNA and as a regulator of mitotic nuclear reassembly.

7 d the vacuolar lumen was not acidified after reassembly.

8 t undergoes partial mitotic NE breakdown and reassembly.

9 ce results in changes in bacterial community reassembly.

10 nt of multiple chromosomal breaks and random reassembly.

11 ane-bound and required for postmitotic Golgi reassembly.

12 d the time of focal adhesion disassembly and reassembly.

13 1p, caused a significant defect in chromatin reassembly.

14 4) components in DNA repair-linked chromatin reassembly.

15 disassemble actin filaments and limit their reassembly.

16 histone tetramer during cycles of nucleosome reassembly.

17 age of the target gene cluster, facilitating reassembly.

18 complex disassembly and regain motility upon reassembly.

19 1/Clr4 to Swi6/Chp2 to allow heterochromatin reassembly.

20 ures that readily undergo disintegration and reassembly.

21 ntromeres concomitantly with heterochromatin reassembly.

22 yanions is not important for in vitro capsid reassembly.

23 at switches positions during disassembly and reassembly.

24 ecruitment to intercellular junctions and TJ reassembly.

25 ns (inositol triphosphate) induced no capsid reassembly.

26 ide in the context of map-based WGS sequence reassembly.

27 A also displayed tonicity-driven disassembly/reassembly.

28 ation, and postmitotic nuclear envelope (NE) reassembly.

29 tanding mechanisms through decomposition and reassembly.

30 ents contribute to the efficiency of protein reassembly.

31 of TJ and was gradually increased during the reassembly.

32 g, between protein fragments is key to their reassembly.

33 ng I-TASSER by iterative structural fragment reassembly.

34 ing the steady-state or calcium-dependent AJ reassembly.

35 liation of crystalline KxMnO2 and subsequent reassembly.

36 shed during the late phase of post-IR genome reassembly.

37 bnucleosomal states and promoting nucleosome reassembly.

38 tazoans: kinetochore disassembly and nuclear reassembly.

39 R mutant in cells impairs post-mitotic Golgi reassembly.

40 analysis to test different models of tissue reassembly.

41 ers back to stacked regions for supercomplex reassembly.

42 To assay chromatin reassembly accompanying DNA double strand break repair,

43 The assembly-disassembly-organization-reassembly (ADOR) mechanism is a recent method for prepa

44 Assembly-Disassembly-Organization-Reassembly (ADOR) method overcoming this limitation was

45 ntional assembly, disassembly, organization, reassembly (ADOR) method represents one exciting new app

46 eps of the assembly-disassembly-organization-reassembly (ADOR) process for the synthesis of zeolites

47 The assembly-disassembly-organization-reassembly (ADOR) process has been used to disassemble a

48 tocol, the assembly-disassembly-organization-reassembly (ADOR) process, for a relatively new method o

49 i markers in interphase cells, delayed Golgi reassembly after brefeldin A treatment, delayed retrogra

50 state conditions and also during junctional reassembly after calcium switch.

51 ry signaling components and supported cilium reassembly after cell division.

52 eficit and restored the capacity for synapse reassembly after cooling.

53 In a current model for reassembly after mitosis, the nuclear envelope forms by

54 roperly aligned cisternae, and delayed Golgi reassembly after nocodazole washout.

55 ATPase activity at steady state and V-ATPase reassembly after readdition of glucose to glucose-depriv

56 that prevent K56 acetylation block chromatin reassembly after repair.

57 x suggests how Prp3 may be involved in U4/U6 reassembly after splicing.

58 ing logistic requirements for U4/U6 di-snRNP reassembly after splicing.

59 at does not involve replisome disassembly or reassembly, albeit with loss of one of the two chromosom

60 asses the requirement for Asf1 for chromatin reassembly and checkpoint recovery, whereas mutations th

61 may provide a template for postmitotic Golgi reassembly and cisternal remodeling.

62 s signaling pathways that affect microtubule reassembly and dynein-dependent motility.

63 We studied the mechanism of the reassembly and folding process of two fragments of a spl

64 Such SAC inactivation allows normal nuclear reassembly and mitotic exit without DNA segregation.

65 V-ATPase reassembly and reactivation requires intervention of the

66 at dimers, and not multimers, potentiate the reassembly and reorganization of Drp1 for mitochondrial

67 antibodies into HL half-molecules and allow reassembly and reoxidation to form highly pure bsAbs.

68 Glucose readdition triggers reassembly and resumes proton transport and organelle ac

69 ally secreted protein, is dependent on Golgi reassembly and stacking protein (GRASP) for its secretio

70 acidocalcisomes, with the Golgi marker Golgi reassembly and stacking protein, and with antibodies aga

71 pletion of IL-1beta secretion requires Golgi reassembly and stacking proteins (GRASPs) and multi-vesi

72 Homotypic membrane tethering by the Golgi reassembly and stacking proteins (GRASPs) is required fo

73 r to form their characteristic stacks: Golgi reassembly and stacking proteins 55 and 65 (GRASP55 and

74 its duration is coupled to nuclear envelope reassembly and the nuclear sequestration of the Rho-GEF

75 in recruitment to the membrane during cortex reassembly and to explore dependency relationships.

76 n of Pfk2p alters glucose-dependent V-ATPase reassembly and vacuolar acidification.

77 ion checkpoint" that delays nuclear envelope reassembly and, consequently, Pebble nuclear sequestrati

78 RAVE-assisted glucose-dependent reassembly and/or glucose signals were disturbed in pfk2

79 nction of epithelial monolayers, rapid AJ/TJ reassembly, and formation of three-dimensional cysts.

80 ve developed a defined Golgi disassembly and reassembly assay that reconstitutes this process using p

81 ble and then migrate in new directions after reassembly at a different location, which forms the new

82 ring transcription activation and nucleosome reassembly at coding regions during transcription elonga

83 y completed septa to prevent their immediate reassembly at new cell poles.

84 We observed that reassembly at pH 6.2, 7.2, and 8.2 yielded regular parti

85 dynamics during early mitosis and defective reassembly at telophase, increased formation of multiple

86 In summary, Cx43 is crucial for TJ reassembly at the BTB during its cyclic restructuring th

87 t16 in the absence of San1 impairs chromatin reassembly at the coding sequence, similarly to the resu

88 in vivo, which undergo cycles of disassembly/reassembly at the promoter for each round of transcripti

89 Reassembly begins by sorting two epithelial cell types,

90 that they can affect repair-linked chromatin reassembly but that their contributions are not equivale

91 Pea2p to promote efficient, polarized actin reassembly but that this requirement can be bypassed by

92 eutralization of ANG2 did not prevent vessel reassembly, but did impair subsequent angiogenic expansi

93 Interestingly, capsid reassembly can be induced by polyanions, including oligo

94 lation fluctuations, we found that community reassembly can be rapidly adjusted via foraging plastici

95 inding protein, which has roles including NE reassembly, cell cycle, and chromatin organization in ce

96 hromatids induce a delay in nuclear envelope reassembly concomitant with prolonged cortical myosin ac

97 Using immobilised CP monomers under reassembly conditions with "free" CP subunits, we have p

98 ditions for reversible vault disassembly and reassembly could enable application of these nanocapsule

99 CT or Spt6, the lack of efficient nucleosome reassembly coupled to pervasive incorporation of H2A.Z b

100 gene expression through promoting nucleosome reassembly coupled with H2B monoubiquitination.

101 e in the frequency of local nuclear envelope reassembly delays, resulting in an increase in the frequ

102 deletion of ankyrinG from RGCs to block AIS reassembly did not affect axon regeneration, indicating

103 Furthermore, microtubule reassembly did not arise from a central focus but instea

104 disentangled whether storm influences avian reassembly directly via functional traits (i.e. behavior

105 Chromatin reassembly during DSB repair was dependent on the HIRA h

106 filaments undergoing dynamic disassembly and reassembly during endocytosis.

107 ight junctions (TJs) undergo disassembly and reassembly during morphogenesis and pathological states.

108 on interdependently to facilitate nucleosome reassembly during transcription elongation, thereby demo

109 function of Nap1 is to facilitate nucleosome reassembly during transcription elongation.

110 ultiple stages of nucleosome disassembly and reassembly during transcription.

111 Conversely, promoter chromatin reassembly during transcriptional repression is accompan

112 s that mediate the fusion stage of ER and NE reassembly, emphasize an unexpected tolerance of nucleus

113 , such as membrane fusion, postmitotic Golgi reassembly, endoplasmic reticulum-associated degradation

114 Efficient chromatin reassembly enhances the fidelity of transcriptional elon

115 f Cx43 by RNAi also perturbed the TJ-barrier reassembly following BPA removal.

116 reports that clathrin is required for Golgi reassembly following disruption with pharmacological age

117 We show that chromatin reassembly following double-strand break (DSB) repair re

118 lled ADOR (assembly-disassembly-organisation-reassembly), for the synthesis of zeolites is reviewed h

119 tosis, there are also two processes in Golgi reassembly: formation of single cisternae by membrane fu

120 of apical intercellular junctions and their reassembly, impaired the development of TEER, and increa

121 ted FAK associated with AJ and stimulated AJ reassembly in a Fyn-dependent manner.

122 ithin 1 to 3 min) reversible disassembly and reassembly in intact cells exposed sequentially to hypot

123 mbly in the active zone periphery, and SNARE reassembly in newly docked vesicles.

124 oes extensive disassembly during mitosis and reassembly in post-mitotic daughter cells.

125 ulating the chromosomal fragments for random reassembly in the subsequent interphase.

126 tin proteasome system in promoting chromatin reassembly in the wake of elongating RNA polymerase II a

127 pment of epithelial barrier and inhibited TJ reassembly independently of other basolateral polarity p

128 g of blocked replication forks and replisome reassembly, indicating that colocalization of Rep and Dn

129 mmature CA capsid for its subsequent de novo reassembly into mature cores and establish the importanc

130 apid release of free P-TEFb, followed by its reassembly into the 7SK snRNP.

131 PSII repair and reassembly involve the breakage and formation of disulfi

132 known to be involved in histone disassembly/reassembly, is required for clock function and is recrui

133 er a calcium switch indicate that junctional reassembly kinetics are also impaired.

134 green fluorescent proteins (GFPs), fragment reassembly leads to a fluorescent readout, which has bee

135 We propose that during nuclear reassembly LEM2 condenses into a liquid-like phase and c

136 ol concentration, led to equivalent 60% V1Vo reassembly levels.

137 Only this system exhibits a different reassembly mechanism from that of the unsplit protein, i

138 ucleation mechanism) plays a key role in the reassembly mechanism of the split system.

139 hrough the assembly-disassembly-organization-reassembly mechanism.

140 scription, require chromatin disassembly and reassembly mediated by histone chaperones.

141 ennas in a single complex available for PSII reassembly, minimizing the risk of randomly diluting mul

142 not disassembled prior to incubation with a reassembly mixture containing nuclear extract also encap

143 ture HIV-1 core: the disassembly and de novo reassembly model and the non-diffusional displacive mode

144 of sister chromatids before nuclear envelope reassembly (NER).

145 However, cilia reassembly occurs rapidly in response to an in vivo mech

146 28-effector repertoire of a model strain and reassembly of a minimal functional repertoire reveals th

147 can involve the fragmentation and subsequent reassembly of a single chromatid from a micronucleus.

148 competitive binding assay dependent upon the reassembly of a split reporter protein, we have tested t

149 We tested the reassembly of a split-luciferase enzyme guided by argona

150 Serum, however, could not trigger the reassembly of actin filaments if the HepII domain was pr

151 l model coupling the dynamic disassembly and reassembly of actin stress fibers and associated focal a

152 tracted sheath, which resets the systems for reassembly of an extended sheath that is ready to fire a

153 aterials open the door to stimuli-responsive reassembly of BBs and BBCPs into new morphologies driven

154 il stoichiometry and spatial distance in the reassembly of below-ground fungal communities in a cold

155 encapsidation of a BMV RNA in plants and the reassembly of BMV virions in vitro.

156 hesized histone H4 results in defects in the reassembly of chromatin structure that accompanies the r

157 iquitous replication-related disassembly and reassembly of chromatin, H1 is deposited into chromatin

158 ckout plants revealed a significant delay in reassembly of complex I, suggesting an indirect role for

159 The community reassembly of cool and warm groups was essentially due t

160 The post-replicative reassembly of Dam, Lrp, and the local regulator PapI ont

161 microtubules in MCF-7 cells and delayed the reassembly of depolymerized microtubules.

162 oth biosynthesis of the enzyme and regulated reassembly of disassembled V(1) and V(0) sectors.

163 The reversal of this process results in reassembly of facultative heterochromatin.

164 The subsequent reassembly of fibers upregulates the rate of JNK activat

165 followed by diffusion of these species, and reassembly of filaments at the new location following re

166 of a rapid disassembly, transition, and slow reassembly of focal adhesions of the cells in response t

167 general design paradigms for the conditional reassembly of fragmented proteins in the presence of any

168 subunits, can be reconstituted by sequential reassembly of fusion proteins based on antibody fragment

169 oams have been synthesized by the controlled reassembly of graphene sheets; from their initial stacke

170 kdown of rck/p54 or LSm1 did not prevent the reassembly of GWB that were induced by and correlated wi

171 ee V1 and Vo functions to prevent unintended reassembly of holo V-ATPase when activity is not needed.

172 the Golgi complex, inhibits tubule-mediated reassembly of intact Golgi ribbons, and slows secretion

173 ) was dominated by interaction rewiring (the reassembly of interactions among species).

174 eceptor (SNARE) complexes and the subsequent reassembly of new SNARE complexes in trans.

175 lishment of RGC AIS, remyelination, and even reassembly of nodes in regions proximal, within, and dis

176 Post-mitotic reassembly of nuclear envelope (NE) and the endoplasmic

177 T16 and SSRP1) promotes both disassembly and reassembly of nucleosomes during gene transcription, DNA

178 H2B ubiquitylation is required for efficient reassembly of nucleosomes during RNA polymerase II (Pol

179 al an emerging commonality among such cases: reassembly of old genetic variation into new combination

180 hat disassembly, membrane translocation, and reassembly of podocalyxin complexes controls epithelial

181 Dynamic disruption and reassembly of promoter-proximal nucleosomes is a conserv

182 ty under high light by regulating repair and reassembly of PSII complexes.

183 Surprisingly, reassembly of rTbHK2 with an inactive rTbHK1 variant yie

184 The concept of stepwise antibody-based reassembly of split cytokines could be useful for the de

185 We previously demonstrated sequence-enabled reassembly of TEM-1 beta-lactamase (SEER-LAC), a system

186 Reassembly of the [4Fe-4S] cluster in NO-modified DinG r

187 ential to significantly alter the subsequent reassembly of the bacterial community as it recovers fro

188 This lack of laminin prevents reassembly of the BMZ and mature hemidesmosomes after ke

189 itch" to direct the cyclical disassembly and reassembly of the BTB during the epithelial cycle of spe

190 cular mechanism mediating both integrity and reassembly of the cell-cell adhesive interface formed th

191 The reassembly of the cortical array has often been consider

192 microscopic features that differentiate the reassembly of the different split systems studied.

193 er energetic cost than de novo synthesis and reassembly of the entire CI.

194 wing for zinc finger binding and concomitant reassembly of the fragmented luciferase.

195 y on new substrates based on enzyme-mediated reassembly of the gene encoding beta-lactamase that conf

196 ch showed that TUG is required for efficient reassembly of the Golgi complex after brefeldin A remova

197 embranes with interphase cytosol allowed the reassembly of the Golgi fragments into new Golgi stacks.

198 nthesized, suggesting that the defect was in reassembly of the hemidesmosomes.

199 current flow across the bilayer by allowing reassembly of the ion channels in the bilayer.

200 tion with protein phosphatase PP2A, leads to reassembly of the membranes into new Golgi stacks.

201 In the work reported here, we analyzed the reassembly of the most abundant HMW adiponectin species,

202 n shown to play an important role during the reassembly of the nuclear envelope at the end of mitosis

203 osomes induce highly localized delays in the reassembly of the nuclear envelope.

204 hus, the cell cycle-controlled breakdown and reassembly of the nuclear membrane and the restoration o

205 eins with such double duties help coordinate reassembly of the nucleus with chromosomal segregation.

206 SII requires degradation of key subunits and reassembly of the OEC as frequently as every 20 to 40 mi

207 ompositions, by an independent phenomenon of reassembly of the partially solubilized lipid bilayers.

208 The reassembly of the pyramids can still be attained via eng

209 final product, the T=3 viral capsid, during reassembly of the RNA bacteriophage MS2.

210 brid complex is established with concomitant reassembly of the split-luciferase enzyme.

211 shed conditions for in vitro disassembly and reassembly of the viral capsid.

212 Sequencing and reassembly of the well-studied tomato and Arabidopsis pa

213 biosynthetic assembly and glucose-stimulated reassembly of the yeast vacuolar H(+)-ATPase (V-ATPase).

214 disrupts these cis-SNARE complexes, allowing reassembly of their subunits into trans-SNARE complexes

215 The programmed-reassembly of thermal shifters inspired by LEGO enable t

216 tes Hxk2 binding to the Mig1 protein and the reassembly of theSUC2repressor complex.

217 interest translated in the cytosol, the self-reassembly of this Bi-Genomic-encoded Split-GFP is confi

218 PSII often lead to damage, degradation, and reassembly of this molecular machine.

219 ons to stabilize the Vo sector for efficient reassembly of V1Vo.

220 Postfire reassembly of vegetation--paramount to C storage and bio

221 the concentration of wild-type SS18 leads to reassembly of wild-type complexes retargeted away from t

222 Calcium-induced reassembly of Y398D/Y402D mutant occludin in Madin-Darby

223 f chromosomal proteins from parental DNA and reassembly on daughter strands in a specific order.

224 imity to the replication complex followed by reassembly on nascent DNA shortly after replication.

225 "taco" complex in the presence of KPF(6) and reassembly on subsequent addition of DB18C6 was initiall

226 Spt6 as the factor that mediates nucleosome reassembly onto the PHO5, PHO8, ADH2, ADY2, and SUC2 pro

227 dual binding activity of PPM1G blocks P-TEFb reassembly onto the snRNP to sustain NF-kappaB-mediated

228 y overall defects in mitotic NPC disassembly-reassembly or general nuclear import.

229 During early reassembly, parasite accumulation was biased towards a s

230 These observations support the disassembly-reassembly pathway for core formation.

231 of assembly processes that might drive such reassembly patterns: environmental filtering based on ho

232 The temperature at which lysis and reassembly prevailed was approximately 25 degrees C, thu

233 s, and the reversibility and kinetics of the reassembly process can be controlled by selecting approp

234 ergoes a ubiquitin-dependent disassembly and reassembly process during each cycle of cell division.

235 It must undergo a repair and reassembly process following photodamage, many facets of

236 ice model to analyze how the dynamics of the reassembly process for two model proteins was affected b

237 This disassembly and reassembly process is critical for Golgi biogenesis duri

238 Thus, this semisynthetic reassembly process offers a general route for studying t

239 sion occurs through a unique disassembly and reassembly process that is regulated by ubiquitination.

240 ll division is mediated by a disassembly and reassembly process, and this process is precisely contro

241 atid cohesion, had no effect on this spindle reassembly process, clearly separating the roles of cohe

242 Later in the reassembly process, we established that host traits, as

243 g the initial junctional formation of the AJ reassembly process.

244 lar intervention to the assembly-disassembly-reassembly process.

245 mbination of both displacive and disassembly/reassembly processes for HIV-1 maturation.

246 inery that control the Golgi disassembly and reassembly processes in the cell cycle.

247 t controls the mitotic Golgi disassembly and reassembly processes.

248 es to reconstitute the Golgi disassembly and reassembly processes.

249 determine the role in this pathway of Golgi reassembly protein (GRASP)55, a Golgi-localized target o

250 To dissect the mechanism of Golgi reassembly, rat NRK and GH3 cells were treated with 1-bu

251 We also show that the reassembly rate can be either increased or decreased by

252 seudogenome are resistant to the disassembly/reassembly reaction.

253 Localized delays of nuclear envelope reassembly require Aurora B kinase activity.

254 vesiculation at the onset of mitosis and its reassembly requires factors that are in part segregated

255 Chromosome shattering and reassembly resembling chromothripsis (a single genomic e

256 ar protein with functions in mitotic nuclear reassembly, retroviral preintegration complex stability,

257 cles undergo iterative rounds of disassembly/reassembly, seemingly sampling DNA until a suitably size

258 However, these data on reassembly show that a contractile tone of the PAMR is e

259 ome, at least one of the two mammalian Golgi reassembly stacking protein (GRASP) paralogues, GRASP55

260 The mammalian Golgi reassembly stacking protein (GRASP) proteins are Golgi-l

261 We have found that cells lacking Golgi reassembly stacking protein (GRASP), a protein attached

262 We find that Golgi reassembly stacking protein (GRASP), an unconventional s

263 ows a new fold and is required to bind Golgi reassembly stacking protein 55 with approximately 1 micr

264 In mammalian cells, the Golgi reassembly stacking protein 65 (GRASP65) has been implic

265 The Golgi matrix protein Tb Golgi reassembly stacking protein defines a region between the

266 acking protein of 65 kDa (GRASP65) and Golgi reassembly stacking protein of 55 kDa (GRASP55) were ori

267 Golgi reassembly stacking protein of 65 kDa (GRASP65) and Golg

268 In mammalian cells, the Golgi reassembly stacking protein of 65 kDa (GRASP65) has been

269 , we probe the disassembly, organization and reassembly steps of the ADOR process through a combinati

270 disassembly of yVLPs and subsequent in vitro reassembly, suggesting a role for cellular components in

271 , we established an in vitro disassembly and reassembly system using bacterially expressed HBV capsid

272 ylakoids, where key steps of PSII repair and reassembly take place.

273 a more prominent role for Hif1p in chromatin reassembly than either Hat1p or Hat2p, Hif1p exists in c

274 ginine, has a pronounced effect on chromatin reassembly that is similar to that observed in an asf1De

275 identified a novel step in postmitotic Golgi reassembly that requires the clathrin heavy chain (CHC).

276 ns significantly altered bacterial community reassembly that was evident at multiple taxonomic levels

277 Our work indicates that regulation of actin reassembly through ARP2/3 complex activity is crucial fo

278 ocations, insertions, deletions, and complex reassembly through chromothripsis coupled to classical n

279 even, and these patterns varied tightly with reassembly time.

280 II (PSII) requires constant disassembly and reassembly to accommodate replacement of the D1 protein.

281 We have examined VLP dissociation and reassembly to define the important features of the assem

282 on, resulting in the need for time-consuming reassembly to fix these issues.

283 nits that maintain fork licensing and direct reassembly to the appropriate location after processing

284 level rise on spatial and temporal community reassembly trajectories that are dynamically re-shaping

285 oteasome mediated protein degradation, Golgi reassembly, transcription activation, and cell cycle con

286 -square estimation method and found that the reassembly transition is best described by a combination

287 protect the mismatch region from nucleosome reassembly until repair occurs, and they could potential

288 gi fragments and promotes post-mitotic Golgi reassembly upon ubiquitin removal by VCIP135.

289 Glucose-dependent reassembly was 50% reduced in pfk2Delta, and the vacuola

290 d recovery was not affected by Galpha12, but reassembly was accelerated by Galpha12 depletion.

291 Gene reassembly was detectable over several orders of magnitu

292 Artery reassembly was nearly absent in adults but was induced b

293 Vessel reassembly was not limited by VEGFA neutralization, sugg

294 ucose-deprived cells, glucose-dependent V1Vo reassembly was proportional to the glycolysis flow.

295 Steady-state level of assembly (100% reassembly) was reached at 4% glucose when glycolysis re

296 3)C,(15)N)/74-108((15)N) labeled thioredoxin reassembly, we demonstrate that dipolar dephasing follow

297 ine 56, have been shown to promote chromatin reassembly when DNA double strand break repair is comple

298 ome remodeling is unknown, unlike nucleosome reassembly which is shown to be required for other DNA r

299 s to cytosolic V(1) subcomplexes and assists reassembly with integral membrane V(o) complexes.

300 ng of rTbHK1 and rTbHK2 monomers followed by reassembly yielded enzyme with an approximately 3-fold i