ライフサイエンスコーパス: polymerisation

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

2 n to prevent this intermolecular linkage and polymerisation.

3 microM latrunculin B, an inhibitor of actin polymerisation.

4 lasin E, an inhibitor of actin microfilament polymerisation.

5 ion of flagellin subunit interactions during polymerisation.

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

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

8 apacity and that the capacity decreased with polymerisation.

9 ar) are rapidly prototyped via frontal photo polymerisation.

10 rties of the RBC membrane resulting from HbS polymerisation.

11 of the tested monomer antimutagenicity after polymerisation.

12 ve replicons compensates for inefficient DNA polymerisation.

13 following deoxygenation and hemoglobin (Hb) polymerisation.

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

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

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

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

18 Mixing IncC1 and IncC2 improved polymerisation and DNA binding.

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

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

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

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

23 0.5 wt% of DETC was required to promote both polymerisation and photoreduction of up to 20 wt% of gol

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 The progress in NCA polymerisation combined with advanced orthogonal functio

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

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

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

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

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

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

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

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

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

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

56 2D, and we recently showed that fibrin(ogen) polymerisation during blood clotting can be affected str

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 Actin polymerisation is thought to drive the movement of eukar

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

73 Haemoglobin polymerisation, leading to erythrocyte rigidity and vaso

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 DNA polymerisation was also inhibited by the presence of hyp

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

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

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