ライフサイエンスコーパス: polymerisation

1 ormation, dependent on ARP2/3 branched actin polymerisation.

2 of the tested monomer antimutagenicity after polymerisation.

3 ve replicons compensates for inefficient DNA polymerisation.

4 following deoxygenation and hemoglobin (Hb) polymerisation.

5 ci for the initiation of beta-sheet mediated polymerisation.

6 n to prevent this intermolecular linkage and polymerisation.

7 microM latrunculin B, an inhibitor of actin polymerisation.

8 lasin E, an inhibitor of actin microfilament polymerisation.

9 ion of flagellin subunit interactions during polymerisation.

10 lates in the oocyte, where it inhibits actin polymerisation.

11 the formation of the inverted phase during a polymerisation.

12 molar mass polymer TPA5 through free radical polymerisation.

13 ossibly because of greater disulphide-bonded polymerisation.

14 s and the elevated temperatures required for polymerisation.

15 equent amyloid fibril formation by nucleated polymerisation.

16 la1 at the membrane up to the burst of actin polymerisation.

17 of N-WASP and Arp2/3 complex-mediated actin polymerisation.

18 opolymer nanoparticles by aqueous dispersion polymerisation.

19 e manufacture by way of layer-by-layer resin polymerisation.

20 bres, independently of actin and microtubule polymerisation.

21 ing ends, which has a fundamental role in MT polymerisation.

22 oxidation, dehydrogenation, dehydration and polymerisation.

23 ttling, formin- and redox-dependent filament polymerisation.

24 apacity and that the capacity decreased with polymerisation.

25 ar) are rapidly prototyped via frontal photo polymerisation.

26 itope mapping and synthesized by solid phase polymerisation.

27 rties of the RBC membrane resulting from HbS polymerisation.

28 nt in the flour (3.5 g/100 g, mean degree of polymerisation 3).

29 parable to the rate of fingers-opening after polymerisation (3.4 s(-1)); this indicates that the fing

30 sicles and IQGAP1 silencing influenced actin polymerisation after vesicle fusion.

31 unstable and disappeared as a consequence of polymerisation and browning reactions.

32 In response to signal-induced actin polymerisation and concomitant G-actin depletion, MRTFs

33 Mixing IncC1 and IncC2 improved polymerisation and DNA binding.

34 ble defects in an LC device using two-photon polymerisation and explore the dynamic behaviour of defe

35 novel biosensor design utilizing two-photon polymerisation and graphene to fabricate an enhanced bio

36 printed polymers (MIPs) by the precipitation polymerisation and highlights the effect of porogen on p

37 that this interaction provokes dramatic FtsZ polymerisation and inter-filament association as well as

38 in knockout mice show abnormalities of actin polymerisation and mislocalisation of rhodopsin in photo

39 l-time measurements of the average degree of polymerisation and molar mass of milk saccharides throug

40 ng pathway that consequently increases actin polymerisation and myosin light chains phosphorylation,

41 posite structures by simultaneous two-photon polymerisation and photoreduction is demonstrated.

42 0.5 wt% of DETC was required to promote both polymerisation and photoreduction of up to 20 wt% of gol

43 min receptor (Tir) by intimin leads to actin polymerisation and pyroptotic cell death in macrophages.

44 conductance activated by deoxygenation, HbS polymerisation and RBC sickling.

45 rmolecular loop insertion is known as serpin polymerisation and results in a variety of diseases, mos

46 lyesters and polycarbonates via ring-opening polymerisation and ring-opening copolymerisation.

47 replicase activities including DNA priming, polymerisation and strand-displacement.

48 Microparticles accelerate fibrin polymerisation and support formation of more compact clo

49 are consistent with haemolysis requiring HbS polymerisation and support the hypothesis that this may

50 Tailoring the degree of polymerisation and the ratio of the components we have b

51 en shown to interact with FtsZ, to drive its polymerisation and to promote FtsZ filament bundling the

52 The regulation of polymerisation and translocation of biomolecules is fund

53 Nonanucleotides were optimum for polymerisation and up to 15 monomers were ligated.

54 ASP recruitment, Arp2/3 complex driven actin polymerisation and viral spread.

55 Basic research into the mechanism of protein polymerisation and virus assembly suggest that inhibitio

56 ormation, and found potential defects in the polymerisation and/or maintenance of the synaptonemal co

57 chemical ligation, Staudinger ligation, NCA polymerisation, and genetic engineering, that have been

58 dopts the fingers-closed conformation during polymerisation, and that the post-chemistry rate-limitin

59 tannins of varying degrees of phloroglucinol polymerisation are present in LMW fractions of the three

60 Activators of Arp2/3-mediated actin polymerisation are required for spine enlargement; howev

61 iable because they have different degrees of polymerisation, are composed by distinct types of subuni

62 edicts lateral forces corresponding to actin polymerisation around the nucleus, providing evidence fo

63 Inhibition of actin polymerisation at the base of the streak completely inhi

64 cess advantages and the position of emulsion polymerisation at the forefront of industrial latex synt

65 We use a polymerisation-based algorithm to generate an atomistic

66 ubation with the rate-limiting step in their polymerisation being the formation of the initial dimer.

67 [assessed by their ability to trigger actin polymerisation beneath adherent bacteria (fluorescent ac

68 anillin implies that activation requires HbS polymerisation but since the conductance was observed in

69 structures that resembles a living covalent polymerisation, but on a longer length scale of 10 nm-10

70 se that serpin dimers initiate and propagate polymerisation by having one exposed loop with an optima

71 ents dp6-dp36 (where dp stands for degree of polymerisation) can be determined by a combination of an

72 This tutorial review highlights efficient polymerisation catalysts based on Group 1, Group 2, Zn a

73 Correction for 'Main group metal polymerisation catalysts' by Eszter Fazekas et al., Chem

74 ) ) produced by catalytic chain transfer (co)polymerisation (CCTP) of methyl methacrylate (MMA) and m

75 hesion molecules, proteins involved in actin polymerisation, cell wall and outer membrane proteins, a

76 tochastic rule-based model of the underlying polymerisation chemistry.

77 tial effects for the aC-subregions in fibrin polymerisation, clot mechanical strength, and fibrinolyt

78 The advent of controlled/living radical polymerisation (CLRP) has greatly simplified block copol

79 The progress in NCA polymerisation combined with advanced orthogonal functio

80 from RGPR-mutated iPSCs had increased actin polymerisation compared with controls (mean confocal pix

81 mponent systems and careful selection of the polymerisation conditions, all of which can be used to f

82 btained towards the maltooligosaccharides of polymerisation degrees 3 and 4.

83 structures with previous work, we propose a polymerisation-depolymerisation cycle for the Pseudomona

84 e the polymerisation interface, facilitating polymerisation/depolymerisation and DNA binding, to prom

85 We present crystal structures of the primase/polymerisation domain (PolDom) of Mycobacterium tubercul

86 port the identification of a mutation in the polymerisation domain of LAMA5 in a patient with a compl

87 Combining exonuclease deficiency with a polymerisation domain substitution raised the organelle

88 mational activation of a Zona Pellucida (ZP) polymerisation domain.

89 The average degree of polymerisation (DP) of tannins is usually determined usi

90 inclusion of carbohydrates of 3-9 degrees of polymerisation (DP), decision which may be made individu

91 acetylglucosamine defined by their degree of polymerisation (DP), fraction of acetylation (F(A)), and

92 essing conditions (temperature and degree of polymerisation, DP) on the stability of short-chain fruc

93 F-actin de-polymerisation drugs abolish normal embryonic pattern fo

94 2D, and we recently showed that fibrin(ogen) polymerisation during blood clotting can be affected str

95 he specific functional importance of laminin polymerisation during development and tissue homeostasis

96 , while Augmin alone does not affect Tubulin polymerisation dynamics, it stimulates gamma-TuRC-depend

97 One of the major polymerisation effects was stalling, but each of the ind

98 terisation of cell-free extracts and the DNA polymerisation enzymes, PolB, PolD, and the p41/p46 comp

99 ants with increased myosin activity or actin polymerisation exhibited precocious cell contraction thr

100 polypyrrole (PPy) film during galvanostatic polymerisation film formation.

101 en shown that pCA groups arise during lignin polymerisation from the participation of monolignol conj

102 alised DNA were developed, along with a post-polymerisation functionalisation strategy for the produc

103 polymer hydroxyl groups are amenable to post-polymerisation functionalization.

104 Wzc regulates polymerisation functions through cycling the formation a

105 nctional degradable polymers by ring-opening polymerisation has driven wider interest in this area.

106 entation chain transfer (RAFT) grafting from polymerisation in a backbone-selective solvent.

107 Conditions designed to elicit HbS polymerisation in cells from sickle trait patients (deox

108 cal polymerisation in water and UV-initiated polymerisation in organic solvent.

109 The ligase directs polymerisation in the 3' to 5' direction which we propos

110 lsolin, without which abnormalities in actin polymerisation in the photoreceptor connecting cilia cau

111 a role for RDR6-catalysed RNA-dependent RNA polymerisation in these processes seems clear, the funct

112 l drug design for mimetics that will prevent polymerisation in vivo and so ameliorate the associated

113 ymers prepared using two protocols: chemical polymerisation in water and UV-initiated polymerisation

114 free, inertial centralisation, and ultrafast polymerisation, in a scalable flow reactor.

115 optosis in IECs in a Tir-dependent but actin polymerisation-independent manner, which was enhanced by

116 Polymerisation-induced self-assembly (PISA) has been eff

117 We report the polymerisation-induced self-assembly of poly(lauryl meth

118 0 mg), an oral once-daily sickle haemoglobin polymerisation inhibitor, was approved in the USA for th

119 ng effects of anticancer drugs (e.g. tubulin polymerisation inhibitors).

120 not the binding pockets of established actin polymerisation inhibitors.

121 Thus, the NTD may modulate the polymerisation interface, facilitating polymerisation/de

122 The rate limiting step for actin filament polymerisation is nucleation, and two types of nucleator

123 the Pol-DNA binary complex in the absence of polymerisation is slow (~5.3 s(-1)), and comparable to t

124 Actin polymerisation is thought to drive the movement of eukar

125 ent advances in the various fields of olefin polymerisation, it still remains a challenge to synthesi

126 Haemoglobin polymerisation, leading to erythrocyte rigidity and vaso

127 ich promotes centrosome-mediated microtubule polymerisation, leading to the incorporation of microtub

128 f-assembly within dispersed particles during polymerisation leads to novel nanostructured materials t

129 Under gastric conditions, the mean degree of polymerisation (mDP) of seed extracts, raw (mDP approxim

130 min (EA) fining decreased the mean degree of polymerisation (mDP) of tannin significantly by 26.4% an

131 by Folin-Ciocalteu reagent), mean degree of polymerisation (mDP), galloylation percentage (%G) and s

132 annin measurements, and the degree of tannin polymerisation (mDP).

133 of prodelphinidins with high mean degree of polymerisation (mDP).

134 from melamine by ultrasonic-assisted thermal polymerisation method and, along with the membrane, was

135 Two scalable polymerisation methods are used in combination for the s

136 We prepared pre-polymerisation mixtures containing different ratios of n

137 Finally, the post-polymerisation modification methods that have been appli

138 antly diminished the rapid increase in actin polymerisation observed in CLL cells following CXCL12 st

139 refore propose that heparan sulfate backbone polymerisation occurs by a simple dissociative mechanism

140 a pathway that proposes how controlled actin polymerisation occurs, and raises implications for furth

141 process of 3D cell culturing, starting from polymerisation of a bare 3D gelatin scaffold, to human m

142 tetrapeptide that preferentially blocks the polymerisation of a pathologically unstable serpin commo

143 that the change results in a failure of the polymerisation of alpha/beta/gamma laminin trimers.

144 To overcome some of these challenges, polymerisation of alternative functionalised monomers is

145 ge is the first reported example of a direct polymerisation of an agricultural waste extract.

146 irst proof-of-concept investigation into the polymerisation of both crude and purified Sauvignon blan

147 filament of the bacterial flagellum requires polymerisation of ca 20,000 flagellin (FliC) monomeric s

148 The roasting process is responsible for the polymerisation of early formed lower molecular weight co

149 ups (i.e. Nano-PEDOT-COOH) via controlled co-polymerisation of EDOT and EDOT-COOH monomers, using tet

150 id (MAA) are used as reagents in the radical polymerisation of ethylene (E) in dimethyl carbonate sol

151 this view, FliS was able to prevent in vitro polymerisation of FliC into filaments.

152 this review, the synthesis and ring-opening polymerisation of functional cyclic carbonates that have

153 channel, which modulates cell hydration and polymerisation of haemoglobin S.

154 The method can be applied in the polymerisation of hybrid systems consisting of more than

155 other diseases involving the aggregation or polymerisation of misfolded host proteins.

156 The importance of water in the polymerisation of monomers, however, has largely been ov

157 tion has recently been proposed in which the polymerisation of new actin filaments regulates apicompl

158 The assay comprised the polymerisation of oligo-nucleotides initiated from a 17

159 We report the adsorption and photo-polymerisation of P(4) molecules encapsulated in an indi

160 al for the formation of pili, catalysing the polymerisation of pilus subunits and enabling the secret

161 ions show very small changes, mean degree of polymerisation of proanthocyanidins decline slightly as

162 Seeded polymerisation of proteins forming amyloid fibres and th

163 re associated with the numbers and degree of polymerisation of reactive hydroxyl groups present in th

164 ctive loop peptides can block or reverse the polymerisation of serpins associated with cirrhosis and

165 Polymerisation of sickle hemoglobin results in erythrocy

166 nced by the polydispersity and the degree of polymerisation of tannins.

167 The R1 plasmid employs ATP-driven polymerisation of the actin-like protein ParM to move ne

168 and CS, but has no effect on the subsequent polymerisation of the backbone.

169 d emulsion droplets, followed by interfacial polymerisation of the interior.

170 between water-sensitivity and the degree of polymerisation of the oil medium; independent of other k

171 ng process is often used to ensure optimised polymerisation of the printed structures.

172 pectively, responsible for translocation and polymerisation of the repeat unit of the spore coat poly

173 preserve inhibitory activity but reduce the polymerisation of wild-type native alpha(1)-antitrypsin

174 n fork, for the presence of uracil and halts polymerisation on detecting this base.

175 Here we show that preventing actin polymerisation on either mitochondria or the ER disrupts

176 actin coat formation and the extent of actin polymerisation on fused vesicles.

177 onstrate the likely interactions that enable polymerisation on the cell membrane and the molecular pa

178 rmation of linear trimers, followed by rapid polymerisation once an additional actin monomer is posit

179 via doping, the formation of composites, co-polymerisation or blending in order to improve their bio

180 ipitation increased with increased degree of polymerisation (or size) from trimers to octamers (monom

181 yet provided a cumulative enhancement to the polymerisation performance of p41/p46.

182 the crosslinkers are incorporated during the polymerisation process, and its distinct properties, inc

183 A 17mer primer was used to start a polymerisation process.

184 d tyrosine, utilising a one-step interfacial polymerisation process.

185 Pronounced demyelination and tubulin polymerisation, promoting protein-positive oligodendrocy

186 with recruited host proteins to induce actin polymerisation, propelling the bacterium through the hos

187 tals have been exploited in a broad range of polymerisations, ranging from classical alkene polymeris

188 in which we show that annexin 2 reduces the polymerisation rate of actin monomers in a dose-dependen

189 rimental data, we demonstrate that the RAD51 polymerisation rate positively correlates with the flexi

190 By measuring actin polymerisation rates in the presence of barbed-end and p

191 on-catalysed reversible deactivation radical polymerisation (RDRP), with a range of metal-chelating a

192 conformational changes across the entire DNA polymerisation reaction in real-time, gaining direct acc

193 The polymerisation reaction is catalysed by a complex of an

194 ce matrix, sometimes making condensation and polymerisation reactions occur more favourably.

195 e of proto-enzymatic function from recursive polymerisation reactions using amino acids and glycolic

196 analysis of actin patterns identified actin polymerisation regulators, depletion of which suppresses

197 h sustainability at the forefront of current polymerisation research, the typically earth-abundant, i

198 hich are often prepared via ring-opening (co)polymerisation (RO(CO)P) using an organometallic catalys

199 prepared in the early 1990s by ring-opening polymerisation (ROP) of silicon-bridged [1]ferrocenophan

200 In eds1 mutants, inhibition of actin polymerisation severely compromised NHR in Arabidopsis a

201 ic composition (HPLC-DAD-MS), copigmentation/polymerisation (spectrophotometry), and colour (Tristimu

202 Polymerisation stabilises CBS and reduces thermal denatu

203 mmes in a manner dependent on its levels and polymerisation state.

204 ystal structures of different nucleotide and polymerisation states of Caulobacter MreB reveal conserv

205 nal change that may be critical both for the polymerisation step and discrimination between different

206 ucts for PDMS curing, using a combination of polymerisation steps, washes, and surface treatments.

207 main sections covering computational design, polymerisation strategies, material combinations, recent

208 (NO(3))(2) as the template ion, through bulk polymerisation technique.

209 ell as the integration with other controlled polymerisation techniques significantly widened the scop

210 nds, forming compounds with higher degree of polymerisation that became insoluble in wine along stora

211 ilm include 0.4M PPy, 6.2U/mL XOD, 40 mM Fc, polymerisation time of 200 s and applied current density

212 nert component, across a range of degrees of polymerisation to evaluate the effect that multivalency

213 ids to their melting point and initiation of polymerisation to produce polymeric chains.

214 lymerisations, ranging from classical alkene polymerisation to the synthesis of new bio-derived and d

215 Inhibition of actin polymerisation via local application of the inhibitor la

216 For CTs, the mean degree of polymerisation was 10.6, and the ratio of procyanidin to

217 DNA polymerisation was also inhibited by the presence of hyp

218 Oil deterioration by oxidation and polymerisation was also reduced by the use of vacuum dra

219 parent difference in the aDP (mean degree of polymerisation) was observed for the GBW (1.9) and the G

220 The main mechanisms of action involved are polymerisations, which result in changes in the molecule

221 bitor alpha(1)-antitrypsin to misfolding and polymerisation within hepatocytes, causing liver disease

222 t industry, was valorised into low degree of polymerisation xylooligosaccharides using alkaline pretr