ライフサイエンスコーパス: liquid-liquid phase separation

1 II into membraneless domains, reminiscent of liquid-liquid phase separation.

2 These structures form through a process of liquid-liquid phase separation.

3 Clustering is also a prerequisite for liquid-liquid phase separation.

4 multicomponent condensates that assemble by liquid-liquid phase separation.

5 protein-protein interactions analogous to a liquid-liquid phase separation.

6 ding formation of biological condensates via liquid-liquid phase separation.

7 mation of a dense liquid precursor phase via liquid-liquid phase separation.

8 emonstrated that galectin-3 can also undergo liquid-liquid phase separation.

9 s such as RNA granules that assemble through liquid-liquid phase separation.

10 sts that these compartments assemble through liquid-liquid phase separation.

11 nequilibrium activity might impact classical liquid-liquid phase separation.

12 nge of phase transitions, possibly including liquid-liquid phase separation.

13 model lipid/cholesterol membranes exhibiting liquid-liquid phase separation.

14 al rearrangement of the PSD that may involve liquid-liquid phase separation.

15 gates of the TDP-43 CTD while GRN-5 mediated liquid-liquid phase separation.

16 biomolecular condensates that form due to to liquid-liquid phase separation.

17 Ps exhibit large-scale organization, such as liquid-liquid phase separation.

18 concentrate molecules and often form through liquid-liquid phase separation.

19 us structures that are mainly formed through liquid-liquid phase separation.

20 cleic acids, a process often associated with liquid-liquid phase separation.

21 nitor conformational changes associated with liquid-liquid phase separation.

22 as membraneless organelles that assemble by liquid-liquid phase separation.

23 -membrane-bound compartments, which form via liquid-liquid phase separation.

24 formation of heterochromatin condensates via liquid-liquid phase separation.

25 n for novel biosensing technologies based on liquid-liquid phase separation.

26 omatin and from nascent 40S subunits through liquid-liquid phase separation.

27 ating they showed properties consistent with liquid-liquid phase separation.

28 ts amino terminus, which binds RNA to induce liquid-liquid phase separation.

29 assemblies, which in some cases form through liquid-liquid phase separation.

30 e nucleosome remodeler Brg1 and FUS-assisted liquid-liquid phase separation.

31 four newcomers covering proteins involved in liquid-liquid phase separation.

32 ing to an RNA-binding protein in the case of liquid-liquid phase separation.

33 e found that filaggrin assembles KGs through liquid-liquid phase separation.

34 oposed to drive heterochromatin formation by liquid-liquid phase separation.

35 he question of how many proteins can undergo liquid-liquid phase separation.

36 ss organelles that assemble by intracellular liquid-liquid phase separation.

37 sates are formed from processes that include liquid-liquid phase separation.

38 tion during YAP reprogramming is mediated by liquid-liquid phase separation.

39 eveal that atmospheric particles can undergo liquid-liquid phase separations.

40 in droplet-like structures is a hallmark of liquid-liquid phase separation(1,2), but the mechanisms

41 eless organelles or condensates form through liquid-liquid phase separation(1-4), which is thought to

42 Here we implicate liquid-liquid phase separation(3) as the underlying mech

43 as microtubule coiling or hook formation, or liquid-liquid phase separation along the microtubule lat

44 gation inhibitor methylene blue promotes tau liquid-liquid phase separation and accelerates the liqui

45 The link between liquid-liquid phase separation and actin nucleation in t

46 cytoplasmic mRNP granules that assemble via liquid-liquid phase separation and are implicated in the

47 rtwined, here we show oligomers arising from liquid-liquid phase separation and beta-barrel formation

48 ers share properties of systems that undergo liquid-liquid phase separation and could be investigated

49 Moreover, we analyzed TDP-43 liquid-liquid phase separation and detected similar dete

50 red to encapsulate I3C and DIM by a combined liquid-liquid phase separation and ionic gelation method

51 d RBPs form liquid droplets in vitro through liquid-liquid phase separation and liquid-like non-membr

52 ng it less soluble in cells and affected its liquid-liquid phase separation and phase transition patt

53 raneless biomolecular condensates formed via liquid-liquid phase separation and related phase transit

54 Protein crystallization, aggregation, liquid-liquid phase separation, and self-assembly are im

55 intrinsically disordered proteins to achieve liquid-liquid phase separation, and we demonstrated that

56 There is a striking difference in the liquid-liquid phase separation behavior of E107A-alpha-c

57 rdered regions and a-helical regions promote liquid-liquid phase separation behaviour of Cavin1 in vi

58 iverse membraneless organelles originate via liquid-liquid phase separation, but how their distinct s

59 Many membraneless organelles form through liquid-liquid phase separation, but how their size is co

60 Reentrant liquid-liquid phase separation can occur when the conden

61 the Atlanta urban environment and found that liquid-liquid phase separation can result in increased c

62 teins, such as 53BP1, into foci that exhibit liquid-liquid phase-separation condensate properties.

63 on of clay particles with droplets formed by liquid-liquid phase separation could provide a physical

64 ed that AARS1 lactylation of p53 hinders its liquid-liquid phase separation, DNA binding, and transcr

65 Liquid-liquid phase separation, driven by collective int

66 Here, we present an up-to-date view of how liquid-liquid phase separation drives the formation of s

67 Biomolecular condensates formed via liquid-liquid phase separation enable spatial and tempor

68 ather via a two-step process involving first liquid-liquid phase separation followed by polymer micro

69 Biological liquid-liquid phase separation has gained considerable a

70 ity of proteins and nucleic acids to undergo liquid-liquid phase separation has recently emerged as a

71 The multivalent interactions necessary for liquid-liquid phase separation have been extensively stu

72 Coacervate microdroplets produced by liquid-liquid phase separation have been used as synthet

73 ensates, membrane-less entities arising from liquid-liquid phase separation, hold dichotomous roles i

74 in foci are dynamic and HP1alpha can promote liquid-liquid phase separation, HP1alpha-mediated phase

75 We report the observation of liquid-liquid phase separation in a solution of human mo

76 We have studied liquid-liquid phase separation in aqueous ternary soluti

77 of components that has produced large-scale, liquid-liquid phase separation in bilayers has stubbornl

78 With a few notable exceptions, liquid-liquid phase separation in bulk proceeds through

79 addition, theory has been developed to model liquid-liquid phase separation in bulk systems.

80 Liquid-liquid phase separation in giant unilamellar vesi

81 Here we show that liquid-liquid phase separation in monolayer membranes co

82 covering recent results on the inhibition of liquid-liquid phase separation in nanoscale particles an

83 excitement and progress toward understanding liquid-liquid phase separation in natural and artificial

84 Results are compared to previous studies of liquid-liquid phase separation in supermicrometer partic

85 Appreciation for the role of liquid-liquid phase separation in the functional organiz

86 show that the mammalian proteasome undergoes liquid-liquid phase separation in the nucleus upon amino

87 lipid, phase diagrams in which there can be liquid-liquid phase separation in the ternary system but

88 TIAR-2 undergoes liquid-liquid phase separation in vitro and forms granul

89 g proteins-YTHDF1, YTHDF2 and YTHDF3-undergo liquid-liquid phase separation in vitro and in cells.

90 ially modulate TDP-43 CTD aggregation and/or liquid-liquid phase separation in vitro GRN-3 promoted i

91 mbraneless compartments that assemble due to liquid-liquid phase separation, including biomolecular c

92 that the evolution of PCs proceeds first via liquid-liquid phase separation into polymer-rich droplet

93 Here, we show that liquid-liquid phase separation into solute-rich and solu

94 Liquid-liquid phase separation is emerging as the univer

95 y of aged atmospheric aerosols with internal liquid-liquid phase separation is inferred.

96 llow growth to detectable dimensions so that liquid-liquid phase separation is not observed within a

97 Formation of membrane-less organelles via liquid-liquid phase separation is one way cells meet the

98 lmark of biomolecular condensates formed via liquid-liquid phase separation is that they dynamically

99 Intracellular liquid-liquid phase separation is thought to drive the f

100 Liquid-liquid phase separation is ubiquitous in suspensi

101 We suggest that consideration of liquid-liquid phase separation, leading to complete or p

102 Recently, tau has been shown to undergo liquid liquid phase separation (LLPS) both in vivo and i

103 second phase transition can be described as liquid-liquid phase separation (LLPS) accompanied by gel

104 Although CPSF6 displays liquid-liquid phase separation (LLPS) activity in vitro,

105 interplay of transition pathways leading to liquid-liquid phase separation (LLPS) and amyloid fibril

106 rotein critical for NMJ formation, undergoes liquid-liquid phase separation (LLPS) and condensates in

107 hromatin protein 1alpha (HP1alpha) undergoes liquid-liquid phase separation (LLPS) and forms liquid d

108 Here, we asked whether PrP undergoes liquid-liquid phase separation (LLPS) and if this proces

109 reading activities, the CPC also can undergo liquid-liquid phase separation (LLPS) and proposed that

110 reveal that PcG condensates assemble through liquid-liquid phase separation (LLPS) and suggest that p

111 avirus 2 (SARS-CoV-2) condenses with RNA via liquid-liquid phase separation (LLPS) and that N protein

112 Biomolecular condensates formed by liquid-liquid phase separation (LLPS) are considered one

113 Here, we show that SGs assemble through liquid-liquid phase separation (LLPS) arising from inter

114 ent protein kinase (PKA), RIalpha, undergoes liquid-liquid phase separation (LLPS) as a function of c

115 Here, we identify liquid-liquid phase separation (LLPS) as a mechanism for

116 Marine organisms, for instance, use liquid-liquid phase separation (LLPS) as the precursor p

117 us bovine gammaS solutions, we have observed liquid-liquid phase separation (LLPS) at -8 degrees C an

118 show that chromogranin (CG) proteins undergo liquid-liquid phase separation (LLPS) at a mildly acidic

119 Here, we uncover a common liquid-liquid phase separation (LLPS) behavior shared by

120 a (diverging) wetting layer when approaching liquid-liquid phase separation (LLPS) by changing protei

121 Liquid-liquid phase separation (LLPS) compartmentalizes

122 d in the PEG400/Na(2)SO(4)/Water system near Liquid-Liquid Phase Separation (LLPS) conditions by both

123 Here, we demonstrate that Cep57 undergoes liquid-liquid phase separation (LLPS) driven by three cr

124 NONO, suggesting that AGGF1 is an important liquid-liquid phase separation (LLPS) driver for other t

125 12-hour ultradian rhythm of nuclear speckle liquid-liquid phase separation (LLPS) dynamics, separate

126 biomolecular condensate, whose formation by liquid-liquid phase separation (LLPS) facilitates the in

127 ormation of biomolecular condensates through liquid-liquid phase separation (LLPS) has been described

128 Liquid-liquid phase separation (LLPS) has been recognize

129 s can form membraneless compartments through liquid-liquid phase separation (LLPS) has challenged lon

130 Compartmentalization by liquid-liquid phase separation (LLPS) has emerged as a u

131 necessary biophysical properties to undergo liquid-liquid phase separation (LLPS) in cells.

132 Prion-like domains (PLDs) can drive liquid-liquid phase separation (LLPS) in cells.

133 uted chromatin undergoes histone tail-driven liquid-liquid phase separation (LLPS) in physiologic sal

134 disordered region (IDR) that facilitates its liquid-liquid phase separation (LLPS) in the nucleolus.

135 Here, we show that YBX1 undergoes liquid-liquid phase separation (LLPS) in vitro and in ce

136 erse microtubule-binding proteins to undergo liquid-liquid phase separation (LLPS) in vitro.

137 Moreover, increase of NEAT1 promotes TDP-43 liquid-liquid phase separation (LLPS) in vitro.

138 atenin and Axin interacting sites, undergoes liquid-liquid phase separation (LLPS) in vitro.

139 fluorescence have been widely used to detect liquid-liquid phase separation (LLPS) in vivo.

140 at the disease-related RBP hnRNPA1 undergoes liquid-liquid phase separation (LLPS) into protein-rich

141 ng the roles and therapeutic applications of liquid-liquid phase separation (LLPS) is increasingly of

142 Liquid-liquid phase separation (LLPS) is involved in the

143 Liquid-liquid phase separation (LLPS) is one proposed me

144 Liquid-liquid phase separation (LLPS) is thought to cont

145 The idea that liquid-liquid phase separation (LLPS) may be a general m

146 Liquid-liquid phase separation (LLPS) mediates formation

147 ning area of research involves mimicking the liquid-liquid phase separation (LLPS) observed in protei

148 Liquid-liquid phase separation (LLPS) occurs following a

149 Proteinaceous liquid-liquid phase separation (LLPS) occurs when a poly

150 e effect of polyethylene glycol (PEG) on the liquid-liquid phase separation (LLPS) of aqueous solutio

151 ars, there has been a jarring awakening that liquid-liquid phase separation (LLPS) of key protein and

152 hiral assemblies spontaneously occur through liquid-liquid phase separation (LLPS) of lyotropic mesop

153 Biomolecular condensates are formed by liquid-liquid phase separation (LLPS) of multivalent mol

154 les, corresponding to the droplet phase upon liquid-liquid phase separation (LLPS) of protein or prot

155 Liquid-liquid phase separation (LLPS) of proteins and nu

156 underpinning of biomolecular condensates is liquid-liquid phase separation (LLPS) of proteins and nu

157 cesses arising from spontaneous or transient liquid-liquid phase separation (LLPS) of proteins and ot

158 Engineering liquid-liquid phase separation (LLPS) of proteins and pe

159 Liquid-liquid phase separation (LLPS) of proteins into c

160 Liquid-liquid phase separation (LLPS) of proteins that l

161 Liquid-liquid phase separation (LLPS) of proteins underl

162 el for biomolecular condensates underlain by liquid-liquid phase separation (LLPS) of proteins, we co

163 Liquid-liquid phase separation (LLPS) of RNA-binding pro

164 Liquid-liquid phase separation (LLPS) of RNA-protein com

165 Cluster formation is induced by liquid-liquid phase separation (LLPS) of the SNARE domai

166 The mechanism that leads to liquid-liquid phase separation (LLPS) of the tau protein

167 tems, with membraneless organelles formed by liquid-liquid phase separation (LLPS) offering dynamic e

168 Biomolecular condensates formed via liquid-liquid phase separation (LLPS) play a crucial rol

169 lecular condensates formed by the process of liquid-liquid phase separation (LLPS) play diverse roles

170 Cellular liquid-liquid phase separation (LLPS) plays a key role i

171 Recent evidence suggests that a liquid-liquid phase separation (LLPS) process may drive

172 kaemias(1,2), are essential for establishing liquid-liquid phase separation (LLPS) puncta of chimera

173 FUS also undergoes liquid-liquid phase separation (LLPS) to accumulate in s

174 hat EB1 formed molecular condensates through liquid-liquid phase separation (LLPS) to constitute the

175 A variety of cellular processes use liquid-liquid phase separation (LLPS) to create function

176 me FOs can promote oncogenesis by undergoing liquid-liquid phase separation (LLPS) to form aberrant b

177 y expressed in late spermatids and undergoes liquid-liquid phase separation (LLPS) to merge messenger

178 Full-length FRQ undergoes liquid-liquid phase separation (LLPS) to sequester FRH a

179 In a recent study, Yasuda et al. show how liquid-liquid phase separation (LLPS) under hyperosmotic

180 It's widely appreciated that liquid-liquid phase separation (LLPS) underlies the form

181 Evidence is now mounting that liquid-liquid phase separation (LLPS) underlies the form

182 ry of D. melanogaster unexpectedly undergoes liquid-liquid phase separation (LLPS) upon binding DNA i

183 Here, we show that NLRP6 undergoes liquid-liquid phase separation (LLPS) upon interaction w

184 sols can undergo phase transitions including liquid-liquid phase separation (LLPS) while responding t

185 Here we show that Pex13 undergoes liquid-liquid phase separation (LLPS) with Pex5-cargo.

186 53BP1 at heterochromatin, where it undergoes liquid-liquid phase separation (LLPS) with the heterochr

187 2 nucleocapsid protein (N-protein) undergoes liquid-liquid phase separation (LLPS) with viral RNA.

188 hat TDP-43 at its endogenous level undergoes liquid-liquid phase separation (LLPS) within nuclei in m

189 ss organelles, or condensates, that form via liquid-liquid phase separation (LLPS)(1,2).

190 ) formation is the macroscopic completion of liquid-liquid phase separation (LLPS), a process by whic

191 th MeV triggers inclusion body formation via liquid-liquid phase separation (LLPS), a process underly

192 ar compartments that are proposed to form by liquid-liquid phase separation (LLPS), a thermodynamic p

193 he RNA-binding protein FUS (FUS LC) mediates liquid-liquid phase separation (LLPS), but the interacti

194 Biomolecules can undergo liquid-liquid phase separation (LLPS), forming dense dro

195 presence of crowding agents, tau can undergo liquid-liquid phase separation (LLPS), forming highly dy

196 on recent reports that tau readily undergoes liquid-liquid phase separation (LLPS), here we explored

197 EcSSB also undergoes liquid-liquid phase separation (LLPS), inhibited by ssDN

198 merous membraneless organelles assembled via liquid-liquid phase separation (LLPS), known as condensa

199 ecular condensates, formed in the process of liquid-liquid phase separation (LLPS), play key roles in

200 membraneless cellular compartments formed by liquid-liquid phase separation (LLPS), represent an impo

201 ated that although they are likely formed by liquid-liquid phase separation (LLPS), they have a diffe

202 RNA granules form through liquid-liquid phase separation (LLPS), whereby weak prom

203 rate that human IAPP undergoes AWI-catalyzed liquid-liquid phase separation (LLPS), which initiates h

204 which also has a high propensity to undergo liquid-liquid phase separation (LLPS).

205 ative disorders, has a propensity to undergo liquid-liquid phase separation (LLPS).

206 ration and tendency of the system to undergo liquid-liquid phase separation (LLPS).

207 Wet, coated particles were formed via liquid-liquid phase separation (LLPS).

208 solution of biomolecular condensates through liquid-liquid phase separation (LLPS).

209 ropensity to condensate via the mechanism of liquid-liquid phase separation (LLPS).

210 ructures that have been proposed to form via liquid-liquid phase separation (LLPS).

211 so modulates tensin3's propensity to undergo liquid-liquid phase separation (LLPS).

212 ding biomolecular condensates formed through liquid-liquid phase separation (LLPS).

213 in the host cell cytosol via the process of liquid-liquid phase separation (LLPS).

214 ty in homo-oligomerization, RNA association, liquid-liquid phase separation (LLPS).

215 ys are activated by different stresses or by liquid-liquid phase separation (LLPS).

216 d RNA-binding proteins (RBPs), which undergo liquid-liquid phase separation (LLPS).

217 and RNA-binding proteins and are formed via liquid-liquid phase separation (LLPS).

218 nent organic/inorganic system that undergoes liquid-liquid phase separation (LLPS).

219 ion of cellular material in a process termed liquid-liquid phase separation (LLPS).

220 through multivalent interactions that drive liquid-liquid phase separation (LLPS).

221 Emerging evidence reveals the role of liquid-liquid phase separation (LLPS)/biomolecular conde

222 Tau protein in vitro can undergo liquid-liquid phase separation (LLPS); however, observat

223 Perturbations that alter liquid-liquid phase separations (LLPS) driven by intrins

224 compartments resulting from crowding-induced liquid/liquid phase separation (LLPS) on the dynamic spa

225 and other tauopathies, was found to undergo liquid-liquid phase separation making it one of several

226 exokinase 2 expression subsequently promotes liquid-liquid phase separation, manifesting as stress gr

227 While liquid-liquid phase separation may drive RNP granule ass

228 Combining the polyethylene glycol-induced liquid-liquid phase separation measurements and the phen

229 ofluidic strategy for fundamental studies of liquid-liquid phase separation mediated by CO2 as well a

230 Formed from proteins and RNAs through liquid-liquid phase separation, membraneless organelles

231 etermined by the polyethylene glycol-induced liquid-liquid phase separation method.

232 entration, and protein composition, at which liquid-liquid phase separation occurs in a ternary solut

233 Gelation of protein condensates formed by liquid-liquid phase separation occurs in a wide range of

234 al pH, ionic strength, and Hb concentration, liquid-liquid phase separation occurs reversibly and rep

235 If liquid-liquid phase separation occurs, the gas-particle

236 lyzwitterionic complex, "pZC", formed by the liquid-liquid phase separation of a polyzwitterion and a

237 Specifically, we analyze the liquid-liquid phase separation of an in vitro model of c

238 Biomolecular condensates, formed by liquid-liquid phase separation of biomacromolecules, pla

239 Complex fibrillar networks mediate liquid-liquid phase separation of biomolecular condensat

240 l bodies and stress granules, which form via liquid-liquid phase separation of biomolecules, particul

241 Membrane-less organelles resulting from liquid-liquid phase separation of biopolymers into intra

242 lar membraneless compartments are formed via liquid-liquid phase separation of charged proteins and n

243 ic gel and provides a scaffold that supports liquid-liquid phase separation of chromatin binding prot

244 RNA-stimulated ATPase activities, as well as liquid-liquid phase separation of DDX3X in vitro.

245 s prevalent in eukaryotes, its impact on the liquid-liquid phase separation of disordered proteins is

246 Liquid-liquid phase separation of intrinsically disorder

247 Biomolecular condensation via liquid-liquid phase separation of intrinsically disorder

248 pernatant phase, a process implicated in the liquid-liquid phase separation of intrinsically disorder

249 Liquid-liquid phase separation of intrinsically disorder

250 is a membrane-less organelle formed through liquid-liquid phase separation of its components from th

251 are condensed liquid-like droplets formed by liquid-liquid phase separation of molecules through mult

252 ted into engineered condensates generated by liquid-liquid phase separation of multidomain scaffoldin

253 Liquid-liquid phase separation of multivalent intrinsica

254 Biomolecular condensates formed by liquid-liquid phase separation of proteins and nucleic a

255 in biology and in biomaterials development, liquid-liquid phase separation of proteins remains poorl

256 ion of these enzymes is in the regulation of liquid-liquid phase separation of RNP condensates.

257 by concentration-dependent condensation and liquid-liquid phase separation of soluble proteins.

258 Liquid-liquid phase separation of tau protein has been i

259 ntrinsically disordered region essential for liquid-liquid phase separation of the chromosome passeng

260 95, SynGAP, and NMDA receptors, and promotes liquid-liquid phase separation of those proteins in cult

261 mentalization might result from a process of liquid-liquid phase separation orchestrated by the epige

262 -rich regions in subcellular partitioning by liquid-liquid phase separation, our findings raise the p

263 Liquid-liquid phase separation plays an important role i

264 Liquid-liquid phase separation plays an important role i

265 ties of m(6)A-modified mRNAs are governed by liquid-liquid phase separation principles.

266 st dynein motor affect the efficiency of the liquid-liquid phase separation process.

267 Here, unexpectedly, we find that liquid-liquid phase separation, rather than nuclear loca

268 formation of hnRNPA1 that synchronizes with liquid-liquid phase separation, regulates the fluidity a

269 osol can undergo a phase transition in which liquid-liquid phase separation results in the formation

270 The liquid-liquid phase separation revealed the complex rela

271 well below the saturation concentration for liquid-liquid phase separation, so they can compete subu

272 Here we show that liquid-liquid phase separation strongly couples to the s

273 roteins (RNPs) form mesoscale condensates by liquid-liquid phase separation that play essential roles

274 es are membrane-less bodies, often formed by liquid-liquid phase separation, that compartmentalize pr

275 Although it is known that RNA undergoes liquid-liquid phase separation, the interplay between th

276 Here we identify an in vivo regulator of liquid-liquid phase separation through a genetic screen

277 e that TAZ forms nuclear condensates through liquid-liquid phase separation to compartmentalize its D

278 X(n)-Gly motifs that is predicted to mediate liquid-liquid phase separation to form biomolecular cond

279 compartment domains, and that can engage in liquid-liquid phase separation to form subnuclear bodies

280 ne kinetic theory of protein aggregation and liquid-liquid phase separation to study the spatial cont

281 active zone proteins RIM and RIM-BP undergo liquid-liquid phase separation to tether Ca(2+) channels

282 Mediator, and pol II itself, are capable of liquid-liquid phase separation, to form condensates that

283 esults indicate that the physical process of liquid-liquid phase separation, together with surface ef

284 des are hydrophobic, disordered, and undergo liquid-liquid phase separation upon self-assembly.

285 dal ketoprofen (KTP)-rich phase generated by liquid-liquid phase separation was evaluated.

286 Liquid-liquid phase separation was observed at pH 5.1 at

287 Liquid-liquid phase separation was studied for a monoclo

288 Liquid-liquid phase separations were discovered in monol

289 ymerase amplification (RPA) is controlled by liquid-liquid phase separation, where the condensate for

290 Complex coacervation is a form of liquid-liquid phase separation, whereby two types of mac

291 of biomolecular condensates can be driven by liquid-liquid phase separation, which arises from weak,

292 s show that coiled-coil proteins can promote liquid-liquid phase separation, which expands our unders

293 Accumulated glycogen undergoes liquid-liquid phase separation, which results in the ass

294 adhesion kinase phosphorylation by forming a liquid-liquid phase separation with integrin alpha5beta1

295 SynGAP-alpha1, which undergoes liquid-liquid phase separation with PSD-95, is highly en

296 ARS2-NP) is required for SARS2-NP to undergo liquid-liquid phase separation with RNA, which inhibits

297 , we elucidate the dynamics and mechanics of liquid-liquid phase separation within fibrillar networks

298 The actual occurrence of liquid-liquid phase separation within individual atmosph

299 via intrinsic disorder regions and promotes liquid-liquid phase separation within the NL.

300 , it was estimated that at room temperature, liquid-liquid phase separation would start when the tril