ライフサイエンスコーパス: polymerization

1 ke extract via oxidative disruption of actin polymerization.

2 toxin substrate 1 GTPase activity and actin polymerization.

3 of total actin levels and preserves F-actin polymerization.

4 nd that a polarized array drives microtubule polymerization.

5 nd PI(3)P in a curved vesicle triggers actin polymerization.

6 naway domain swap mechanism for antithrombin polymerization.

7 tly bound to graphene oxide via free-radical polymerization.

8 osin-II activity and not to elevated F-actin polymerization.

9 epared through a scalable chemical oxidative polymerization.

10 ction and the Arrhenius activation energy of polymerization.

11 ractivation of cofilin and inefficient actin polymerization.

12 nitiated CVD (iCVD) and oxidative CVD (oCVD) polymerization.

13 cular properties obtained through RAFT/MADIX polymerization.

14 and the adjacent domain, which drive further polymerization.

15 human IMPDH2 that either prevent or promote polymerization.

16 d similarities to foundational principles of polymerization.

17 next droplet in the sequence, akin to living polymerization.

18 response mechanism acts as the catalyst for polymerization.

19 eroxidases activating monolignols for lignin polymerization.

20 ole using synthesized MIPs via precipitation polymerization.

21 r(VI)/SiO2 Phillips catalyst during ethylene polymerization.

22 size fidelity by eliminating swelling after polymerization.

23 ion sites by the living anionic ring opening polymerization.

24 an RNA polymerase domain that catalyzes RNA polymerization.

25 gh cell surface-initiated controlled radical polymerization.

26 res as an off-target effect with microtubule polymerization.

27 common backbone to control for the degree of polymerization.

28 ers that show a large change in density upon polymerization.

29 yrene was synthesized via nitroxide-mediated polymerization.

30 ized with MipZ, a negative regulator of FtsZ polymerization.

31 ross multiple contexts, and depends on actin polymerization.

32 has been proposed for this pressure-induced polymerization.

33 the ability to realize a controlled radical polymerization.

34 PA of different MW profiles (mean degree of polymerization 8.3 and 19.5) to investigate how PA polym

35 uced during transfer/handling by interfacial polymerization, a facile oxygen-plasma etch is used to c

36 ment of pharmaceuticals against antithrombin polymerization, an improved understanding of the polymer

37 e properties such as high activity in olefin polymerization and alkane dehydrogenation (M = Cr) or ef

38 ector protein that plays roles in both actin polymerization and caspase-3 activation in intestinal ep

39 Polymerization and crystallization of 3a affords diamagn

40 them to dynamic microtubule ends during both polymerization and depolymerization of tubulin.

41 tein kinase 2 (MK2) pathway to promote actin polymerization and endothelial cell migration.

42 Polymerization and enzyme activity are regulated in part

43 -321/Ser-324 that coordinately regulates tau polymerization and function.

44 signaling to N-WASP-cortactin-mediated actin polymerization and GLUT4 vesicle translocation.

45 reactive oxygen species-regulated effects on polymerization and glutathionylation on the one hand and

46 ytrap model that merges the concepts of ParA polymerization and gradient formation and speculate that

47 -20 that manifested as modification of actin polymerization and inhibition of a broad range of actin-

48 Trio is a RhoGEF protein that promotes actin polymerization and is implicated in the regulation of gl

49 organization by studying the effect of actin polymerization and nuclear rigidity on the diffusive beh

50 er flippase candidate MurJ, impairs lipid II polymerization and peptide cross-linking activities of P

51 combines the advantages of both ring-opening polymerization and radical polymerization, that is the p

52 l hollow SiNPs@C composites are produced via polymerization and subsequent carbonization.

53 ing a delicate balance between the extent of polymerization and the SWCNT diameter.

54 LP) chemistry, were synthesized via Yamamoto polymerization and their interactions with the strong Le

55 e important role of Pfn1 in regulating actin polymerization and various fundamental actin-based cellu

56 ent of chemical precursors before initiating polymerization, and identifying a suitable mechanism has

57 on tumor cell growth, inhibition of tubulin polymerization, and induction of cell cycle arrest.

58 ogous late-transition-metal-catalyzed olefin polymerizations, and a number of carbonylative methods f

59 table nanoscale compartments via an emulsion polymerization approach in which a vinyl-terminated macr

60 ents such as monolignol oxidation and lignin polymerization are difficult to study in intact trees.

61 We found that the sites involved in ethylene polymerization are mainly divalent Cr ions in a 6-fold c

62 bes by 3D printing followed by post-printing polymerization are reported.

63 Polymerizations are first-order in ethylene pressure and

64 ced as thin films on electrodes by oxidative polymerizations, are pi-conjugated organic semiconductor

65 omophore quench-labeling applied to 1-octene polymerization as catalyzed by hafnium-pyridyl amido pre

66 VI) species are also present during ethylene polymerization as well as reduced Cr species (either Cr(

67 Polymerization assays using Lmod2 mutants of helix h1 an

68 c capping protein (CAPZ), which blocks actin polymerization at barbed ends.

69 ontribution of myosin contraction, and actin polymerization at bundles' terminals when the product of

70 tic simulations of force generation by actin polymerization at obstacles coated with actin "nucleatio

71 tingly, XGh and XGo undergo spontaneous TAAC polymerization at room temperature; the latter shows fas

72 hicine site of tubulin and inhibited tubulin polymerization at submicromolar concentrations.

73 -ray diffraction, we find that the degree of polymerization at the crossing points is crucial in the

74 et al. demonstrate that INF2 mediates actin polymerization at the endoplasmic reticulum (ER), result

75 y employing low processing temperatures, CVD polymerization avoids damaging substrates and underlying

76 ferent-sized substrates that contain or lack polymerization barriers and endonuclease assays performe

77 Here we report a new dynamic polymerization based on Michael addition-elimination rea

78 is the first case of a scsc two-dimensional polymerization based on this cycloaddition and the third

79 er tremendous advantages for stereoselective polymerization because their activity and selectivity ca

80 ers and oligomers, with an average degree of polymerization between 4.7 and 10.7 and caffeoylquinic a

81 xerogels for thermally induced topochemical polymerization but also the first report on a spontaneou

82 Fetal hemoglobin (HbF) interferes with this polymerization, but HbF is epigenetically silenced from

83 ng established that RHAMM stabilized F-actin polymerization by controlling ROCK signaling.

84 exchange factor (RhoGEF) Trio promotes actin polymerization by directly activating the small GTPase R

85 Mechanistically, Lpd promotes actin polymerization by interacting with F-actin and the actin

86 Cells can control actin polymerization by nucleating new filaments or elongating

87 ll inform the rational development of 2D COF polymerizations by controlling the rate of nucleation, t

88 The type of polymerization can be regulated and switched between rin

89 Oxidative polymerization can be tuned in a sequence-dependent mann

90 Additionally, applied force from actin polymerization can bypass the instability by inducing a

91 esemble the ancillary ligands in homogeneous polymerization catalysis.

92 niques represent a means to study commercial polymerization catalysts that operate with high efficien

93 The photocatalytic polymerization clearly depends on the concentration of t

94 pot cross metathesis-ring-opening metathesis polymerization (CM-ROMP) strategy that affords functiona

95 support polymerase activity by (i) bringing polymerization-competent actin monomers in proximity to

96 the structural dynamics of each subunit in a polymerization-competent antithrombin dimer.

97 al subunit-specific deuterium uptake of this polymerization-competent dimer strongly supports a beta4

98 the JCI, McKee and colleagues use a laminin polymerization-competent, designer chimeric BM protein i

99 We propose that the polymerization-condensation dynamics creates mechanistic

100 Our calculations show that polymerization confers upon a transcription factor the u

101 h a model in which PMS-dependent microtubule polymerization contributes to their maintenance in axons

102 We have developed a method of polymerization control in which the differential diffusi

103 BM protein in vivo to restore function of a polymerization-defective laminin, leading to normalized

104 on increased myotube surface accumulation of polymerization-deficient recombinant laminins, with rete

105 ineered expression of alphaLNNd can overcome polymerization deficits to increase laminin, stabilize B

106 The exclusion range is from 1 to 49 of polymerization degree (180-7966Da).

107 Additionally, it could be hypothesized that polymerization-depolymerization dynamics may be an addit

108 gated polymers from direct (hetero)arylation polymerization (DHAP) has been achieved for the first ti

109 er vesicles are prepared via RAFT dispersion polymerization directly in mineral oil.

110 from Ln(3+) coordination alterations, borate polymerization diversity and soft ligand coordination se

111 gen chimeric protein that provides a missing polymerization domain.

112 rom the S. rebaudiana stems with a degree of polymerization (DP) of 12, and FOS with a DP<6.

113 exponential growth strategy with a degree of polymerization (DP) of 2(n) -1.

114 gosaccharide mixtures with various degree of polymerization (dp) ranging from dp4 to dp8, two dp4 iso

115 lyses to determine parameters like degree of polymerization (DP), fraction of acetylation (FA), or pa

116 xidant capacity in relation to the degree of polymerization (DP).

117 not interact with fibrinogen, affect fibrin polymerization during clot formation, or abrogate plasma

118 increased coat rigidity and force from actin polymerization enables robust vesiculation even at high

119 xyl, thus serving as primers to initiate the polymerization extension and nicking endonuclease cleava

120 ng a palladium catalyzed cyclopentannulation polymerization followed by a cyclodehydrogenation reacti

121 deling through its availability and stepwise polymerization for fibrillogenesis.

122 ators so as to trigger the surface-initiated polymerization for the in situ growth of electroactive p

123 Altering the dynamics of actin or MT polymerization, for example, is a common strategy employ

124 d chain extended using atom transfer radical polymerization from the model protein bovine serum album

125 ymerase responsible for the bulk of galactan polymerization, GlfT2, was produced, and its catalytic a

126 While switching of controlled radical polymerization has been achieve using light, applied vol

127 Supramolecular polymerization has been traditionally focused on the the

128 Z; therefore, how these proteins affect FtsZ polymerization has been unclear.

129 prepared by chemical vapor deposition (CVD) polymerization have found broad acceptance in research a

130 rchers investigating photoinitiated cationic polymerizations have delivered tremendous success in bot

131 the integrated processes of HbS nucleation, polymerization, HbS fiber interaction, and subsequent di

132 s because a reducing agent is present during polymerization, however the molecular weight distributio

133 Whether talin ABDs regulate actin polymerization in a constitutive or regulated manner has

134 first used as a catalyst for living radical polymerization in a nonpolar solvent to produce a polyme

135 plate format that is based on laser-induced polymerization in sickle trait cells and robust, automat

136 MagLev also made it possible to monitor polymerization in the presence of solids (aramid fibers,

137 that colloidal self-assembly is analogous to polymerization in three aspects: ensemble growth statist

138 trast to crystals, the xerogels undergo TAAC polymerization in two distinct stages as shown by DSC an

139 hat can mitigate the effect of Pfn1 on actin polymerization in vitro As a further proof-of-concept te

140 s proteins form fibrils by prion-like seeded polymerization in vitro, only some are transmissible and

141 a concise historical perspective on cationic polymerization induced by light and discusses the latest

142 pproach-starting from monomers-that combines polymerization-induced and crystallization-driven self-a

143 copolymer vesicles were prepared via aqueous polymerization-induced self-assembly in either the prese

144 the development of novel and potent tubulin polymerization inhibitors.

145 lock copolymers using an isoselective alkene polymerization initiator.

146 that the synthesis of nucleotides and their polymerization into RNA occurred in just one to a few we

147 Overall, our data show that ring-like polymerization is an intrinsic property of Syt1 with rea

148 atios between the various CHx radicals whose polymerization is at the origin of the IOM.

149 ailored medium undergoing controlled radical polymerization is capable of forming giant polymer vesic

150 laining the lack of side reactions until the polymerization is complete.

151 ss, that partial inhibition of branching and polymerization lead to different characteristic response

152 The initiator diffuses outward and induces polymerization, leading to a shell of polymer 1.

153 hotoredox catalysis of atom transfer radical polymerization lies in their ability to minimize fluores

154 chanistic insight into two critical steps in polymerization: ligand association upon cleavage of the

155 hesis, tetrameric subunit assembly, tetramer polymerization, localization at disk rims, interaction w

156 trate availability and purine balance, while polymerization may allow cooperative transitions between

157 ssociation with non-specific DNA afforded by polymerization may enable regulatory behaviors that are

158 ntum chemical studies are used to reveal the polymerization mechanism and origin of stereoselectivity

159 le, the reactions proceeded via a "dead-end" polymerization mechanism, and only low to moderate monom

160 The ability to combine two polymerization mechanisms in a one-pot setup and switch

161 gomerization mechanisms play distinct roles: polymerization mediates the activation of the receptor b

162 ition-fragmentation chain transfer (SCARAFT) polymerization method was developed to coat capillaries

163 hanging the functional vinyl monomers in the polymerization mixture.

164 Post-polymerization modification via copper-catalyzed azide-a

165 Here we design and construct dynamic polymerization networks that exploit metastable prion cr

166 Next, the primers released from above "polymerization-nicking" cycles were separated out to tri

167 mods, acting as powerful nucleators of actin polymerization, not capping proteins.

168 es formed due to arrested coalescence during polymerization, occurring as a result of internal elasti

169 QDs) can be used as catalysts to promote the polymerization of 2,2',5',2''-ter-3,4-ethylenedioxythiop

170 The method is based on polymerization of 3,3'-diaminobenzidine by endocytosed h

171 graphite electrode (PGE) by means of electro-polymerization of 3-Thienyl boronic acid and Thiophen.

172 ars that the cause of sickle cell disease is polymerization of a hemoglobin mutant, hydroxyurea is th

173 hows how a self-rolling process initiated by polymerization of a micropatterned layer of fibronectin

174 tresses within the gel are due to continuous polymerization of actin filaments against the membrane s

175 e protein INF2 is an important player in the polymerization of actin filaments.

176 ctive repair process, driven by a stimulated polymerization of actin, results in asymmetrical membran

177 composite was synthesized by electrochemical polymerization of aniline and 3-aminobenzoic acid, in th

178 ses within the cell, which often require the polymerization of DLPs.

179 e carbonate, was synthesized by ring-opening polymerization of ethylene carbonate.

180 tion of CO and oligomer formation during the polymerization of ethylene due to the presence of a N-do

181 a-hydrogen elimination allows for the direct polymerization of ethylene in water to nanocrystal dispe

182 electron-withdrawing substituents allow for polymerization of ethylene to higher molecular weights w

183 agents, form highly active catalysts for the polymerization of ethylene.

184 We found stimulated polymerization of F-actin is not required for Syk recrui

185 This leads to deposition and polymerization of fibronectin and recruitment of paxilli

186 Additionally, MALDI-ToF-MS indicates the polymerization of glyoxal/glyoxylic acid and EPR shows t

187 nd long-chain cellodextrins with a degree of polymerization of greater than two as a glucose acceptor

188 opic model to capture the dynamic process of polymerization of HbS fibers, while maintaining the mech

189 the root cause of sickle cell disease is the polymerization of hemoglobin S (HbS) to form fibers that

190 chieving effective, persistent inhibition of polymerization of hemoglobin S.

191 mutation in the beta-globin gene that causes polymerization of hemoglobin S.

192 Furthermore, we report nucleotide-dependent polymerization of hGBP1F, which competes with membrane b

193 ercially by the metal-catalyzed ring-opening polymerization of lactide.

194 domain, a domain required for extracellular polymerization of laminin trimers and basement membrane

195 t ST8Sia-II autopolysialylation promotes the polymerization of longer polySia chains on SynCAM 1, sug

196 of the colour-producing multilayers are the polymerization of melanin during the ecdysis and the cha

197 MagLev characterized both the thermal polymerization of methacrylate-based monomers and the ph

198 pairing enables their application toward the polymerization of methyl methacrylate for the synthesis

199 intensity, carbonyl formation, and extensive polymerization of myosin.

200 ve catalytic sites achieve template-directed polymerization of new polymers.

201 also were able to preferentially promote the polymerization of one of the isomers (l or d) with respe

202 yze the influence of natural antioxidants on polymerization of partially hydrogenated rapeseed oil he

203 The carbon chains are fabricated by polymerization of prochiral 1,3,5-tris(3-bromophenyl)ben

204 st and selective for the living ring-opening polymerization of several common monomers, including lac

205 The mechanical barrier formed by the polymerization of Si beneath the cuticle and in the cell

206 Understanding of intracellular polymerization of sickle hemoglobin (HbS) and subsequent

207 surfaces but, instead, recruits and induces polymerization of soluble plasma Fn (pFn), an abundant p

208 c cascades of ROAMP followed by ring-opening polymerization of strained epsilon-caprolactone.

209 redict that (1) relative to passive loading, polymerization of Suc in the phloem, even in the absence

210 The tert-butylacetyl chloride initiated polymerization of the alt-lactam proceeds smoothly to af

211 ility strongly depends on both the degree of polymerization of the core-forming block and the fibre l

212 a reactive cation-this species initiates the polymerization of the vinyl ether monomer-and a dithioca

213 ons is demonstrated by the near quantitative polymerization of these monomer families to yield well-d

214 Here, we describe the supramolecular polymerization of triarylamine molecules and their light

215 to characterize the kinetics of free-radical polymerization of water-insoluble, low-molecular-weight

216 observed in enzymatic processes and protein polymerizations often relies on the use of supramolecula

217 coat, membrane tension, and force from actin polymerization on bud formation.

218 Supramolecular polymerization or assembly of proteins or large macromol

219 dase fail to induce either actin and tubulin polymerization or NET formation on activation.

220 each family's ability to promote microtubule polymerization or pause.

221 equences associated with FN availability and polymerization, our findings provide new insights into t

222 fin chemistry, through pericyclic reactions, polymerizations, oxidations, or reductions, has an essen

223 Before polymerization, particles are discrete and nonconducting

224 ignaling pathway, leading to defective actin polymerization, platelet activation, and shape change.

225 zoline chain is grafted through ring opening polymerization, possess homogeneous spherical nanopartic

226 Inhibition of actin filament polymerization prevented the transport of CRF2betaR to t

227 Subsequently, an electrochemical polymerization procedure was carried out in an aqueous s

228 MIPs were synthesized under different polymerization process and their recognition efficiency

229 and cell wall composites during or after the polymerization process controlled by CesA proteins.

230 tions of oDMSi-BTA sergeants (<10 mol%), the polymerization process is cooperative and the supramolec

231 of the polymerizable diyne group; thus, the polymerization process, typically used to stabilize the

232 he disordered microtubule associated Tubulin Polymerization Promoting Protein (TPPP/p25) and the NAD(

233 n filament regulation processes - inhibiting polymerization-promoting signaling through sequestration

234 3 (actin-related protein 3, a branched actin polymerization protein) and palladin (an actin bundling

235 fficient photomediated atom transfer radical polymerization protocol is reported for semi-fluorinated

236 oth proteins are involved in explosive actin polymerization, pseudopod formation, and cell migration.

237 udies showed a first-order dependence of the polymerization rate on the epoxide, a zero-order depende

238 he model: substrate adhesion strength, actin polymerization rate, myosin contractility, and the integ

239 istic responses, and that a limited range of polymerization-rate values provide effective invaginatio

240 Overall polymerization rates and comonomer incorporations depend

241 ncentration required to support the observed polymerization rates, implying that the majority of mono

242 With the appropriate urea anions, the polymerizations reached high conversions ( approximately

243 electron acceptors during the photocatalytic polymerization reaction.

244 Template-directed polymerization reactions enable the accurate storage and

245 demonstrate switching of controlled radical polymerization reactions using temperature "LOW"/"HIGH",

246 benzene derivatives through dehydration and polymerization reactions, and may possess several possib

247 talyst to achieve logic gating of controlled polymerization reactions.

248 ng integrin activation and controlling actin polymerization) remain largely unknown.

249 ther, we find that this force-promoted actin polymerization requires torsionally unconstrained actin

250 unctionalized ring-opening alkyne metathesis polymerization (ROAMP) initiators [R-C6H4C identical wit

251 The rate of living ring-opening metathesis polymerization (ROMP) of N-hexyl-exo-norbornene-5,6-dica

252 via grafting-through ring-opening metathesis polymerization (ROMP).

253 polymers via living ring-opening metathesis polymerization (ROMP).

254 Ring-opening polymerization (ROP) of an allyl-substituted caprolacton

255 regulated and switched between ring-opening polymerization (ROP) of BBL and CHO/CO2 copolymerization

256 Radical ring-opening polymerization (rROP) combines the advantages of both ri

257 Here, it is shown that polymerization shrinkage in DLW can be utilized to creat

258 ) by surface initiated atom transfer radical polymerization (SI-ATRP) and hexamethylene diamine (as a

259 shes by surface-initiated controlled radical polymerization (SI-CRP) techniques has become a powerful

260 trochemically mediated atom transfer radical polymerization (SI-eATRP).

261 solvation, whereas the rate constant for the polymerization step is influenced by the physical nature

262 However, the rate constant for the polymerization step is regulated by hydrogen-bonding int

263 esign of 2D chemical interfaces in which the polymerization step reconfigures the monolayer to promot

264 Here, we show that INF2-mediated actin polymerization stimulates a second mitochondrial respons

265 The success of our polymerization strategy can provide a new way to develop

266 ix-membered cyclic phosphoester ring-opening polymerization strategy is demonstrated, herein, by an i

267 n the organic matrix side, concerns over the polymerization stress and the potential damage to the bo

268 ys, live-cell imaging of motility, and actin polymerization studies to confirm a role for CD13 in imp

269 rsible addition-fragmentation chain-transfer polymerization), synthetic polymers with narrow polydisp

270 noparticles were synthesized by miniemulsion polymerization technique.

271 rt discusses the mechanisms of the major CVD polymerization techniques and the recent progress of the

272 sion has been limited because of the lack of polymerization techniques for conventional polymer synth

273 In this regard, the progress in controlled polymerization techniques opens new possibilities to con

274 anic polymer (POP) using simple free radical polymerization techniques to prepare a cost-effective ma

275 e synthesized using thermo- and UV-initiated polymerization techniques.

276 both ring-opening polymerization and radical polymerization, that is the preparation of polymers bear

277 es are discrete and nonconducting, but after polymerization the carbon materials become entangled to

278 nstream Rho GTPase effectors mediating actin polymerization through Arp2/3 nucleation, Wiskott-Aldric

279 We previously showed that actin polymerization through ER-bound inverted formin 2 (INF2)

280 pochemical azide-alkyne cycloaddition (TAAC) polymerization to 1,4-triazole-linked oligopeptides.

281 ',5'-cyclic monomer can promote ring-opening polymerization to afford the resulting poly(3',5'-cyclic

282 ia a regio- and stereoselective ring opening polymerization to generate multiple glycosidic bonds in

283 MIPs were synthesized by bulk polymerization using methacrylic acid or methyl methacry

284 A with rGO, and VS-PANI through free radical polymerization using methylene bis-acrylamide, and ammon

285 more slowly and continuously throughout the polymerization (using the combination of iodosylbenzene

286 zation by considerable down-regulation of MT polymerization via changes in the spatiotemporal express

287 r CO2 capture were synthesized by suspension polymerization via oil-in-oil emulsion.

288 In ck2beta(-/-) platelets, tubulin polymerization was disrupted, resulting in an impaired t

289 ATP promotes octamer polymerization, whereas GTP promotes a compact, inactive

290 achieved "AND" gating of controlled radical polymerization wherein various combinations of three sti

291 We show that oxygen plays a role in hydrogel polymerization which is mechanistically similar to the r

292 indicated that this mutation impairs laminin polymerization, which we hypothesized to be the cause of

293 rotubule organization as inhibition of actin polymerization with a low dose of latrunculin A disrupts

294 ng concentration polarization-enhanced graft-polymerization with a surfactant added to the reactive s

295 Logic-controlled polymerization with Gel-PTH offers a straightforward app

296 The inhibition of actin polymerization with latrunculin in Rictor KO B cells res

297 statistics following models for step-growth polymerization, with nanoparticles as linkable "monomers

298 novel, G-actin-dependent regulation of actin polymerization within spine heads.

299 d as an efficient catalyst in living radical polymerization, yielding a well-defined polymer-iodide.

300 ROAMP followed by RAFT polymerization yields hybrid poly-(o-phenylene ethynylen