ライフサイエンスコーパス: reassembly

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

2 ng I-TASSER by iterative structural fragment reassembly.

3 ce results in changes in bacterial community reassembly.

4 nt of multiple chromosomal breaks and random reassembly.

5 ane-bound and required for postmitotic Golgi reassembly.

6 d the time of focal adhesion disassembly and reassembly.

7 1p, caused a significant defect in chromatin reassembly.

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

9 disassemble actin filaments and limit their reassembly.

10 histone tetramer during cycles of nucleosome reassembly.

11 complex disassembly and regain motility upon reassembly.

12 1/Clr4 to Swi6/Chp2 to allow heterochromatin reassembly.

13 ures that readily undergo disintegration and reassembly.

14 liation of crystalline KxMnO2 and subsequent reassembly.

15 ntromeres concomitantly with heterochromatin reassembly.

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

17 yanions is not important for in vitro capsid reassembly.

18 at switches positions during disassembly and reassembly.

19 ecruitment to intercellular junctions and TJ reassembly.

20 ns (inositol triphosphate) induced no capsid reassembly.

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

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

23 tanding mechanisms through decomposition and reassembly.

24 ents contribute to the efficiency of protein reassembly.

25 of TJ and was gradually increased during the reassembly.

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

27 gene activation in the absence of nucleosome reassembly.

28 iption in the absence of competing chromatin reassembly.

29 re slowly occurred de novo concurrently with reassembly.

30 logy were used to follow the kinetics of the reassembly.

31 active site does not form properly following reassembly.

32 tazoans: kinetochore disassembly and nuclear reassembly.

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

34 analysis to test different models of tissue reassembly.

35 ers back to stacked regions for supercomplex reassembly.

36 do not require fork adjustment or replisome reassembly.

37 changes lead to community disaggregation and reassembly.

38 ery of its deubiquitinase activity and Golgi reassembly.

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

40 d the vacuolar lumen was not acidified after reassembly.

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

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

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

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

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

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

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

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

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

50 that prevent K56 acetylation block chromatin reassembly after repair.

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

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

53 start factor and hence must not require fork reassembly after the template-switch reaction.

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

55 shable from the original material, but their reassembly also correlated with the rheological analyses

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

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

58 sence of both DNA sites is necessary for the reassembly and concomitant fluorescence of the reassembl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 of oligomer breakdown, substrate binding and reassembly as the chaperone mechanism.

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

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

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

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

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

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

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

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

85 kdown and sequential reactivation upon Golgi reassembly at the end of mitosis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

102 filaments undergoing dynamic disassembly and reassembly during endocytosis.

103 ribed insights into Golgi disassociation and reassembly during mitosis and offer a powerful approach

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

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

106 ultiple stages of nucleosome disassembly and reassembly during transcription.

107 Conversely, promoter chromatin reassembly during transcriptional repression is accompan

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

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

110 Efficient chromatin reassembly enhances the fidelity of transcriptional elon

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 ble sliding diffusion model to interpret the reassembly involving complementary nanofiber cohesive en

128 Furthermore, promoter nucleosome reassembly is essential for transcriptional repression.

129 These methods reveal that Golgi reassembly is preceded by the formation of four colinear

130 dkins and Tyler demonstrates that nucleosome reassembly is required for gene repression and, striking

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

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

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

134 t a methodology termed mCpG-SEquence Enabled Reassembly (mCpG-SEER) of proteins utilizing a split gre

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

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

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

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

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

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

141 tive-site formation is fully reversible when reassembly occurs in the presence of the prodomain, and

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

143 alF-MalG complex was competent for efficient reassembly of a functional MalFGK(2) maltose transporter

144 28-effector repertoire of a model strain and reassembly of a minimal functional repertoire reveals th

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

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

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

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

149 Reassembly of actin filaments required the addition of s

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

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

152 We report here the reassembly of an ionic self-complementary peptide RADARA

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

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

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

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

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

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

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

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

161 ecting protein-protein interactions based on reassembly of dissected fragments of green fluorescent p

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

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

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

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

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

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

168 iculum-associated protein degradation or the reassembly of Golgi, ER and the nuclear envelope after m

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 ur data argue for a dynamic process in which reassembly of Htz1 is regulated by its acetylation at pr

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

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

175 nzyme turnover and transient assembly and/or reassembly of large signaling complexes.

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

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

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

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

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

181 ating a rapid and continuous disassembly and reassembly of protofilaments at steady state.

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

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

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

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

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

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

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

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

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

202 Reassembly of the nuclear envelope following mitosis is

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

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

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

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

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

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

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

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

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

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

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

217 Ypt7p regulates the reassembly of unpaired SNAREs with each other and with H

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

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

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

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

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

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

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

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

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

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

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

229 artitioning soluble TTR monomers between the reassembly pathway and the aggregation pathway should th

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

231 Therefore, the rate of every step in the reassembly pathway is dependent on the concentration of

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

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

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

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

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

237 This reassembly process is important for fabrication of new s

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 lar intervention to the assembly-disassembly-reassembly process.

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

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

246 The disassembly and reassembly processes were repeated four times and, each

247 t controls the mitotic Golgi disassembly and reassembly processes.

248 es to reconstitute the Golgi disassembly and reassembly processes.

249 Nucleosomal reassembly, prompted by temperature downshift, is also r

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

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

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

253 were repeated four times and, each time, the reassembly reached the original length.

254 seudogenome are resistant to the disassembly/reassembly reaction.

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

256 tic interphase lace-like morphology and that reassembly requires clathrin.

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

258 eplicative helicase and subsequent replisome reassembly requires the structure-specific recognition f

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

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

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

262 This system, designated sequence-enabled reassembly (SEER), was demonstrated in vitro to produce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

281 In the absence of Spt6-mediated nucleosome reassembly, the activators Pho4 and Pho2 are displaced f

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

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

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

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

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

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

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

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

290 ed for its full deposition during nucleosome reassembly upon repression of PHO5.

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

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

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

294 Gene reassembly was detectable over several orders of magnitu

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

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

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

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

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

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