ライフサイエンスコーパス: reassemble

1 sociated pentamers, leaving only hexamers to reassemble.

2 osphorylated as the Golgi fragments start to reassemble.

3 At the same time, kinetochores reassemble.

4 into which a new iron-sulfur cluster will be reassembled.

5 h a single chromosome is fragmented and then reassembled.

6 indle is dismantled and the nuclear envelope reassembles.

7 of 120 kb were obtained which contained the reassembled 3' J-C region in authentic configuration.

8 model in which recF and recR are required to reassemble a replication holoenzyme at the site of a DNA

9 ailed to enter meiosis II (MII) because they reassembled a nuclear structure containing decondensed c

10 an unattached population capable of rapidly reassembling a new monolayer, composed of temporarily at

11 is, the [2Fe-2S](2+) cluster in BioB must be reassembled, a process that could be conducted in vivo b

12 their marginal bundle of actin filaments and reassemble actin filaments into a geometric organization

13 ic and must disassemble prior to mitosis and reassemble after the event.

14 hron form during kidney development and must reassemble after tubular injury.

15 f the bacterium Deinococcus radiodurans gets reassembled after being shattered by high-dose radiation

16 Tether-less V(1)V(0) disassembled and reassembled after brief glucose depletion and readdition

17 fter a sequence of poorly understood events, reassembles after cytokinesis.

18 amics of O2 binding and cooperativity of the reassembled alphaV1M-betaV1M hemoglobin closely approxim

19 nc finger DNA-binding proteins, were able to reassemble an active reporter complex in the presence of

20 Golgi complexes, acentrosomal cells fail to reassemble an integral complex upon nocodazole washout.

21 domain attaches to the sex muscles, and then reassembles an anterior-posteriorly oriented sarcomere.

22 state was reached, nucleosomes were able to reassemble and to repeat the disassembly process.

23 Native, reassembled and succinylated milk proteins were used for

24 strate that the active form of ACCase can be reassembled and that it could form a high-molecular-mass

25 the self-organization mechanism continuously reassembles and remodels the constricting ring.

26 Chicago for improving existing assemblies by reassembling and scaffolding the genome of the American

27 s are dynamic, and field lines may misalign, reassemble, and release energy by means of magnetic reco

28 udy, being conveniently isolated, dissected, reassembled, and introduced into various hosts.

29 rly in their cell cycle, an acentriolar MTOC reassembled, and, prior to NEB, a functional amphiastral

30 We found that nuclear lamins begin to reassemble around chromosomes at the end of mitosis at t

31 hase, by which time the nuclear envelope has reassembled around the chromosomes, and they are thus un

32 transient; actin quickly disassembles, then reassembles around a distinct subpopulation, efficiently

33 These complexes do not reassemble as larger oligomers when dissociating deterge

34 ges may no longer remain intact and dis- and reassemble at current or new geographic locations.

35 These nucleosomes reassemble at later stages of gene expression.

36 is disassembled at the onset of mitosis and reassembled at the end of mitosis.

37 pe IV pili were disassembled at one pole and reassembled at the other pole.

38 ar envelope (NE) breaks down at prophase and reassembles at telophase.

39 ssembles prior to chromosome segregation and reassembles at the end of mitosis.

40 rs formed by urea dissociation, which can be reassembled back to the tetradecamer, the pressure-disso

41 We demonstrate herein that TTR homotetramers reassemble by an unusual monomer-dimer-trimer-tetramer (

42 genome, which is repeatedly taken apart and reassembled by recombination, nor on individual alleles

43 y reactivated, and elongation factors can be reassembled by subsequent addition of nonmitogenic agent

44 binding site are apparently disassembled and reassembled by the process of domain swapping.

45 reveal that the protein folds reversibly and reassembles by itself into the knotted dimeric conformat

46 Reassembled capsids comigrated with undigested parental

47 centers, we have explored the possibility of reassembling catalytically-active fatty acid synthase he

48 unwind DNA, synthesize new DNA strands, and reassemble chromatin.

49 constructing discriminating substructures by reassembling common medicinal chemistry building blocks.

50 We first asked whether reassembled communities differ from undisturbed communit

51 Our experiment demonstrates how warming reassembles communities within the constraints of energy

52 The in vitro reassembled complex has entirely normal properties, resp

53 A reassembled complex of ARMS/Kidins220 and CrkL, an upstr

54 t the secondary structure is retained in the reassembled complex prepared as a poly(ethylene glycol)

55 show that the PHO5 promoter nucleosomes are reassembled concomitant with transcriptional repression

56 umber of genomic elements that superficially reassemble CRISPRs but don't contain diverse spacers and

57 regulating the distribution of components to reassembling daughter cell nucleoli.

58 s coding for 2 hybrid proteins consisting of reassembled Der p 1 and Der p 2 fragments with (recombin

59 ological machines can locally break and then reassemble during function.

60 eoli disassemble at the onset of M-phase and reassemble during telophase.

61 The fragments are reassembled during cycles of denaturation, annealing and

62 Chromatin is disassembled and reassembled during DNA repair.

63 m the active rDNA genes during log phase and reassembled during the diauxic shift, largely accounting

64 the nuclear envelope (NE) disassembling and reassembling during mitosis and the peripheral ER underg

65 Moreover, these seasonal communities reassembled each year in all six rivers, suggesting a lo

66 With this protein, we have reassembled empty capsids and RNA-filled capsids.

67 However, this complex did not reassemble following a shift back to pH 8.0.

68 ytoskeleton is rearranged during mitosis and reassembled following completion of cytokinesis.

69 ly using a cross-section of communities that reassembled for different periods of time since last exp

70 results suggest that clathrin is required to reassemble fragmented Golgi elements.

71 PEI-PAA bilayers using strong acid and then reassembling fresh PEI-PAA bilayers on the membrane supp

72 The full molecule is reassembled from calculations carried out on the kernels

73 Also examined were actin filaments reassembled from cross-linked and purified ANP cross-lin

74 polyculture were more productive than those reassembled from isolates that had evolved in monocultur

75 f these experimental ecosystems: communities reassembled from isolates that had evolved in polycultur

76 ution structure of bacteriophage MS2 capsids reassembled from recombinant protein in the presence of

77 Green fluorescent protein (GFP) has been reassembled from two pieces, a large fragment 214 amino

78 show that GroES is capable of refolding and reassembling from a urea denatured state.

79 yketides in E. coli by using a dissected and reassembled fungal polyketide synthase (PKS).

80 n a full-length functional SNF1 sequence was reassembled, further supporting this hypothesis and indi

81 Out of these, 12 and 9 reassembled genes with the same orientation, capable of

82 assembly and concomitant fluorescence of the reassembled GFP.

83 The reassembled HBL's were characterized by scanning transmi

84 The oxygen binding affinity of reassembled HBLs was similar to that of the native Hb, b

85 all microemulsions of POPC and triolein, and reassembled HDL (apolipoprotein A-I plus phospholipid).

86 Reassembled HDL (rHDL) consisting of 1-palmitoyl-2-oleoy

87 Reassembled HDL increased the second-order rate constant

88 s as an elongation factor to disassemble and reassemble histones during Pol II elongation.

89 rally different phycobiliproteins refold and reassemble in a cooperative manner from their unfolded p

90 o analyzed the mutant E219K, whose capsomers reassemble in vitro into procapsids with vacant vertices

91 x breaks down at mitosis and is subsequently reassembled in a process that involves cisternae formati

92 When these polymers were disassembled and reassembled in H2O/8% DMSO, the products were microtubul

93 tric measurements of these apoheteropolymers reassembled in vitro showed that they were redox-active

94 tion in E. coli were purified separately and reassembled in vitro with GDPNP, producing a stable init

95 an Golgi vesiculates and, upon partitioning, reassembles in each daughter cell; however, it is not cl

96 recombinant congenic strains to separate and reassemble interacting QTL for future study.

97 into soluble intermediates that were able to reassemble into 23- and 38-nm VLPs upon dialysis, sugges

98 chromosome to 'shatter into many pieces' and reassemble into a functioning chromosome.

99 disassemble and the liberated CA proteins to reassemble into a morphologically distinct mature capsid

100 Invadosomes can reassemble into circular rosette-like superstructures, b

101 eric VacA proteins disassemble at low pH and reassemble into membrane-spanning hexamers.

102 These sonicated fragments not only quickly reassemble into nanofibers that were indistinguishable f

103 ysis, and then they exchange GDP for GTP and reassemble into new protofilaments, all on a time scale

104 ully oxidized adiponectin hexamers failed to reassemble into octadecamers at a rate comparable to tha

105 are colocalized in a confined space and can reassemble into the native Spinach conformation, yieldin

106 plexes (NPCs) disassemble during mitosis and reassemble into the newly forming nuclei.

107 o inactive fragments and these fragments can reassemble into the original properly folded and functio

108 ed reversibly under acidic conditions, which reassemble into the original rod-like aggregates upon re

109 S-layer proteins show the ability to reassemble into two-dimensional arrays on solid surfaces

110 27- and the 40-kDa fragments of DHFR-TS had reassembled into a 140-kDa hybrid complex.

111 The rat liver proteins can be refolded and reassembled into active dimers after unfolding at low pH

112 ceptual alternations, and the patchworks are reassembled into coherent forms by most observers.

113 is field, isolated atomic planes can also be reassembled into designer heterostructures made layer by

114 in which structural fragments are repeatedly reassembled into different complete conformations in mol

115 s reduced by glutathione (GSH) and H2 O2 and reassembled into nanoDVD, which can be monitored by acti

116 uted into the daughter cells, where they are reassembled into new Golgi stacks.

117 enly distributed into the daughter cells and reassembled into new Golgi stacks.

118 ety-five attenuated mutants were identified, reassembled into new pools, and rescreened using the sam

119 s were initially disassembled in slices, but reassembled into normal axial arrays after 5 minutes.

120 reduced trimers partially and spontaneously reassembled into octadecamers upon oxidative formation o

121 d ahead of the replication fork and are then reassembled into their original epigenetic states behind

122 ial for infectivity, the capsid protein (CA) reassembles into a conical core.

123 CA reassembles into cores housing the viral RNA and replica

124 GC dimers into monomers just preceding their reassembling into amyloid aggregates, as revealed by the

125 ffuse across the entire lamellipodium before reassembling into the network.

126 remodel and reshape the ECM by degrading and reassembling it, playing an active role in sculpting the

127 erstretched original filaments with the new (reassembled), less stretched filaments.

128 generating CNS axons can be remyelinated and reassemble new AIS and nodes of Ranvier.

129 Here, we reassemble NFs in vitro from varying weight ratios of th

130 shows that the Golgi apparatus disperses and reassembles normally after treatment with brefeldin A an

131 ations and histone chaperones collaborate to reassemble nucleosomes on replicated DNA is explored by

132 It is a histone chaperone capable of reassembling nucleosomes, a central component of transcr

133 ted to monomers, which did not significantly reassemble on depressurization.

134 ins with a unit cell dimension of 20 nm were reassembled on silicon substrate to form 2D arrays with

135 response to osmotic insult and is induced to reassemble only after osmotic balance with the environme

136 is known about how protective structures are reassembled or whether this process is controlled by the

137 ACv1 Triticum aestivum genome assemblies and reassembling or mapping of IWGSC CSS chromosome sorted r

138 Finally, we show that nucleosomes are reassembled over the PHO5 promoter during repression.

139 On average, reassembled parasite communities had lower abundance, bu

140 Consequently, the best strategy for managing reassembling parasite communities may also need to shift

141 er investigated by examining dissociation of reassembled particles.

142 Up to 80% yields of reassembled pentamer can be obtained in vitro from mater

143 g in the supply of chlorophyll to nascent or reassembling photosynthetic complexes, and regulate the

144 s both origin usage and the time required to reassemble prereplication complexes at replication origi

145 sequences containing multiple copies of the reassembled product.

146 We show that the reassembled protein can be taken apart and the peptide r

147 We demonstrate that the reassembled protein has identical absorption and excited

148 er, the pressure-dissociated monomers do not reassemble readily.

149 ough time while helping to inform efforts to reassemble robust communities.

150 Finally, pyrophosphate inhibits active reassembled rTbHK2 oligomers but not oligomeric rTbHK1,

151 bility that a given nucleotide position in a reassembled sequence is the site of a crossover event ar

152 The fraction of reassembled sequences containing zero, one, two, or more

153 gorithm to infer crossover allocation in the reassembled sequences.

154 ve as two argonaute domains provided minimal reassembled split-luciferase.

155 Tetramic forms of mtSSB reassemble spontaneously after thermal denaturation and

156 n of the BMV T=1 particles was made with the reassembled T=1 particles produced from the coat protein

157 ns have the capacity to both remyelinate and reassemble the axon initial segments and nodes of Ranvie

158 oteins beneath the migrating spermatocyte to reassemble the BTB.

159 Together, these libraries allow us to reassemble the entire genome without the need of a refer

160 mmature lattice by proteolyzing Gag and then reassemble the key proteolytic product, the structural p

161 rom dense carbon nanotube arrays are used to reassemble the nanotubes into two-dimensional contiguous

162 zeolite with the UOV structure type and then reassemble the resulting layers into a novel structure,

163 in or protein-nucleic acid interactions that reassemble the split polypeptides.

164 g, U2/U6 is unwound and U6 annealed to U4 to reassemble the tri-snRNP.

165 address these questions, we resequenced and reassembled the genome of H. dujardini, a limnoterrestri

166 data analysis showed that the produced model reassembled the geometric features of the original CT da

167 s to allow polymerases to access DNA, and it reassembles the nucleosomes afterward.

168 n MDS separately on each partition, and then reassembles the partitions using low-resolution MDS.

169 However, reassembling the DRR restores the complete range of expr

170 hydrolytically unstable frameworks and then reassembling the resulting products to form materials wi

171 The gene delivery vehicle was created by reassembling the VP1 pentamers in the presence of the de

172 f the non-covalent beta-sheet cross-links to reassemble, the hydrogels can self-heal after being stra

173 When disassembled and reassembled, the resulting particles have improved stabi

174 kable specificity by which surviving neurons reassemble their connectivity upon regeneration of their

175 Animal cells disassemble and reassemble their nuclear envelopes (NEs) upon each divis

176 in B, myocytes with decreased nebulin levels reassembled them to unrestricted lengths, demonstrating

177 monstrated that XP-D/CS cells were unable to reassemble these gene promoters and thus to restart tran

178 Reassembling these constituent parts into a functioning

179 Reassembling these fragments into a working model of an

180 By reassembling thin isolated atomic planes of hexagonal bo

181 enriched 1-73(U-(13)C,(15)N)/74-108(U-(15)N) reassembled thioredoxin on multiple time scales using a

182 ta(sigma), reveal the backbone mobilities in reassembled thioredoxin, as reflected in the average <S>

183 The actin network disassembles and reassembles throughout the lamellipodium within seconds,

184 eric aggregate that must dissociate and then reassemble to form a 2:1 catalyst-substrate complex in t

185 shows that a limited number of proteins can reassemble to form unique, spatially restricted signalin

186 s show that, although the caspase-3 subunits reassemble to the heterotetramer, the activity return is

187 genome yet must be dynamically displaced and reassembled to allow access to the underlying DNA for tr

188 ss in which features in the core library are reassembled to provide larger features that strongly dif

189 sidues of the catalytic triad and need to be reassembled to reconstitute enzymatic activity.

190 elongation factor and histone chaperone that reassembles transcribed chromatin.

191 constituting depleted splicing extracts with reassembled U5 snRNP particles, molecular neighbors were

192 Prohead-I can be disassembled and reassembled under mild conditions and it cannot mature f

193 e excised from the top-scoring templates and reassembled under the guide of an optimized force field,

194 semble upon the addition of a surfactant and reassemble upon its removal over an indefinite number of

195 r mixtures of wild type and mutant chains to reassemble using as criteria: the formation (or not) of

196 ved Drosophila melanogaster genome sequences reassembled using a standardized pipeline provides a uni

197 mRNA transcript and can be disassembled and reassembled using different buffer conditions.

198 fter the peptides are detected, proteins are reassembled via a reference database of protein or gene

199 The ability to disassemble and reassemble VLPs in vitro and in bulk allows basic featur

200 by disulfide reduction of purified VLPs and reassembled VLPs formed from capsomeres upon removal of

201 nst either purified VLP starting material or reassembled VLPs similarly neutralized infectious HPV-11

202 ging selected exogenous compounds within the reassembled VLPs.

203 lament network that must be disassembled and reassembled when cells divide.

204 The arrays melted at 50 degrees C and reassembled when introduced to fresh colloid suspension,

205 inant proteins, rSFDalpha and rSFDbeta, when reassembled with SFD-depleted holoenzyme, are functional

206 ng) when injected through a syringe and then reassemble within seconds (self-healing) when shear forc