ライフサイエンスコーパス: autocatalysis

1 te nanotubes to promote their own formation (autocatalysis).

2 a second-order (or higher) form of nonlinear autocatalysis.

3 nal residue and, therefore, does not require autocatalysis.

4 partic acid at the P1 position blocked Ced-3 autocatalysis.

5 igate the copper accounting for the observed autocatalysis.

6 n and mechanism of S(2)O(8)(2-)/C(2)O(4)(2-) autocatalysis.

7 h reproduction; and undergoes growth without autocatalysis.

8 mental understanding of asymmetry-amplifying autocatalysis.

9 ly insoluble forms of ASC promoted caspase-1 autocatalysis.

10 mework so far prevents a systematic study of autocatalysis.

11 tallic nanostructures to boost photochemical autocatalysis.

12 gether with their physical separation govern autocatalysis.

13 ein, a process which very likely proceeds by autocatalysis.

14 Mpl and pH and that Mpl maturation occurs by autocatalysis.

15 for SNAP25 cleavage, SNAPtide cleavage, and autocatalysis.

16 DA-aryllithium mixed dimers, and evidence of autocatalysis.

17 eland-Claisen rearrangement with evidence of autocatalysis.

18 te for maturation, suggesting a mechanism of autocatalysis.

19 rimary and secondary structures required for autocatalysis.

20 he relationship between intron stability and autocatalysis.

21 lf-splice or complete only the first step of autocatalysis.

22 H-induced conformational change suitable for autocatalysis.

23 ead ribozyme, both prevents and enhances RNA autocatalysis.

24 ed by protease A and the second results from autocatalysis.

25 Preliminary evidence indicates that autocatalysis also results in a chemical traveling react

26 an active form is referred to hereafter as "autocatalysis." Analyses of the autocatalytic activation

27 nt proportions (pH = pKa +/- 1.6): (i) self-/autocatalysis and (ii) sequential disproportionations of

28 Autocatalysis and chemical amplification are characteris

29 Autocatalysis and chemical amplification are properties

30 In many higher organisms, autocatalysis and decarboxylation are stimulated by putr

31 ine residue is absolutely required for Psd1p autocatalysis and function; 2) yeast Psd1p does not requ

32 literature since the first examples of lipid autocatalysis and highlight state-of-the-art synthetic s

33 in a single serine protease that can undergo autocatalysis and is secreted upon egg activation.

34 echanism involving micelle-mediated physical autocatalysis and led to the rational design of a second

35 formation of Turing patterns are short-range autocatalysis and long-range inhibition which usually on

36 enological laws on growth rate, and studying autocatalysis and network evolution.

37 We show here that both autocatalysis and organocatalysis can be engineered into

38 Autocatalysis and phase separation are particularly inte

39 of glycerol, the light chain did not display autocatalysis and retained 100% of the original activity

40 on with zinc was not a direct consequence of autocatalysis and that the environment of the active sit

41 on progress, detect kinetic features such as autocatalysis, and resolve complex behaviours including

42 require its substrate phosphatidylserine for autocatalysis; and 3) contrary to a prior report, yeast

43 The prevalence and implications of such autocatalysis are discussed.

44 demonstrations of S(2)O(8)(2-)/C(2)O(4)(2-) autocatalysis are presented.

45 on energy difference coupled with asymmetric autocatalysis as a rationalization for absolute asymmetr

46 Inhibition of autocatalysis at low pH by a competitive inhibitor of ca

47 yptase is sequentially processed in vitro by autocatalysis at R(-3) followed by cathepsin (CTS) C pro

48 S) L and CTSB, and sequentially processed by autocatalysis at R(-3), followed by CTSC proteolysis.

49 peroxide dismutase (SOD) enzymes and also by autocatalysis (autodismutation) reactions.

50 Autocatalysis by the resulting aryllithiums or catalysis

51 NomegaV is a unique model because autocatalysis can be precisely initiated in vitro and is

52 When coupled to other processes, autocatalysis can lead to complex systems-level behaviou

53 , without the help of any positive feedback (autocatalysis), can trigger spontaneous polarization of

54 thetic MMP inhibitors, which inhibit MT1-MMP autocatalysis, can act synergistically with TIMP-2 in th

55 profoundly impacted chemists' perspective of autocatalysis, chiral symmetry breaking, absolute asymme

56 chanistic studies reveal that this is due to autocatalysis comprising two factors: 1) complex 2, orig

57 hiometric relationships underpinning abiotic autocatalysis could broadly exist across a range of geoc

58 This 'autocatalysis' derives from the burial and positioning o

59 d 3) contrary to a prior report, yeast Psd1p autocatalysis does not require mitochondrial-specific ph

60 g our stoichiometric and kinetic analysis to autocatalysis emerging from coupled compartments.

61 anistic proposals for parallel catalysis and autocatalysis evaluated by kinetic simulation.

62 Autocatalysis has been extensively studied because it is

63 Autocatalysis has been proposed to play critical roles d

64 Beyond the sciences and science fiction, autocatalysis has found currency in economics and langua

65 the mitochondrial factor required for Psd1p autocatalysis has not been identified.

66 stoichiometric conditions for catalysis and autocatalysis in chemical reaction networks.

67 , by better characterizing the conditions of autocatalysis in complex reaction systems, this work bri

68 e the possibility that chemical feedback and autocatalysis in oscillating chemical reactions could am

69 cedented observation of asymmetry-amplifying autocatalysis in the alkylation of 5-(trimethylsilylethy

70 he isoform that binds to SSAT mRNA undergoes autocatalysis in the presence of polyamines, a result su

71 Studying autocatalysis - in which molecules catalyse their own fo

72 ed by systems exhibiting nonlinear kinetics: autocatalysis, in particular, is integral to the signal

73 ospondin type I motif was retained following autocatalysis, indicating that sites present in the C-te

74 Whereas autocatalysis is abolished in the cold, splicing is part

75 Autocatalysis is central to the propagation of life and

76 Autocatalysis is essential for the origin of life and ch

77 sing liposome-based assays, we observed that autocatalysis is essential for the potent membrane disru

78 activation process of CODH suggest that the autocatalysis is initiated by a small fraction of activa

79 Evidence is presented suggesting that autocatalysis is involved in subunit formation.

80 Autocatalysis is known to have a complex role in the dyn

81 Autocatalysis is observed, and the rate of oxidation inc

82 cause shifts in the rate-limiting steps, and autocatalysis is prevalent and can be acute.

83 Autocatalysis is seen as a potential key player in the o

84 Autocatalysis is the source of the large dendrimer effec

85 Muted autocatalysis is traced to a lithium enolate-mediated de

86 ic steps in the same reaction scheme--double autocatalysis--is the key to the sharp "turn-on" feature

87 They also support the notion that autocatalysis may be a prevalent mode for turning on the

88 nalyze their dependence on system volume and autocatalysis mechanism.

89 Mpl occurs exclusively by an intramolecular autocatalysis mechanism.

90 are well-described by a two-step nucleation-autocatalysis model but with a distribution of individua

91 -directed to the secretory pathway undergoes autocatalysis normally and is fully functional in vivo.

92 tonishing attribute of amplifying asymmetric autocatalysis-occupies a unique position in organic chem

93 the fragmentation reaction indicate that the autocatalysis occurs by both intramolecular and intermol

94 Moreover, autocatalysis of folding is inhibited by FK506, an inhib

95 st, FKBP folding may provide a prototype for autocatalysis of kinetically trapped macromolecular conf

96 uding the interplay of feedback control with autocatalysis of network products necessary to power and

97 xponential growth associated with fission or autocatalysis of protein aggregates.

98 ed ability of the amine to participate in an autocatalysis of the Michael reaction with enzyme cystei

99 domain that are believed to be important for autocatalysis of the protein.

100 ombin by vWbp, and may reveal a function for autocatalysis of the vWbp.prothrombin complexes during i

101 we aimed at determining whether pH regulates autocatalysis or secretion of the processed enzyme.

102 , originating from reactions of HCN, such as autocatalysis, oscillations, pattern formation, and phas

103 The unified approach to autocatalysis presented in this work lays a foundation t

104 hanistic investigations also reveal a unique autocatalysis process.

105 ems allows a disconnection of catalysis from autocatalysis, providing insights into the role played b

106 It was speculated that Psd1p autocatalysis requires a mitochondrial-specific factor a

107 on of a Psd1(ts) precursor unable to undergo autocatalysis requires the unprecedented cooperative and

108 Autocatalysis severs the protein into a large membrane-a

109 rsions, i.e., in the initiation stage before autocatalysis starts, are used to gauge the formation ra

110 Autocatalysis stems from ArLi-catalyzed deaggregation of

111 r experiments demonstrate that oligotriazole autocatalysis successfully leads to continual self-assem

112 Importantly, the model also shows that autocatalysis takes over long before significant amounts

113 ive in the absence of putrescine, with rapid autocatalysis that is not stimulated by putrescine.

114 pears to be differentially phosphorylated by autocatalysis, the levels of phosphorylation have minima

115 s in the absence of TIMP-2 MT1-MMP undergoes autocatalysis to a 44-kDa form, which displays a N termi

116 s a proprotein that undergoes intramolecular autocatalysis to release its catalytic domain.

117 The mature enzyme undergoes further autocatalysis to the two distinct intermediates (N termi

118 se three cases to classify systems involving autocatalysis, trimerization and genetic feedback loops.

119 tryptase to maturity, indicating no need for autocatalysis, unlike the CTSC pathway.

120 te is amplified by a factor of three through autocatalysis upon addition of ZnX(2) .

121 appear to be autocatalytic, whereas in Cwp13 autocatalysis was demonstrated as a Cys109Ala mutant did

122 The optimum pH 4.2-4.6 for autocatalysis was different than that (pH 7.3) for intri

123 d with their respective propeptide following autocatalysis, we aimed at determining whether pH regula

124 of defining molecular requirements for Psd1p autocatalysis, we demonstrate that: 1) despite the conse

125 pyridine substrates demonstrating amplifying autocatalysis were identified.

126 l amplification strategy based on photoredox autocatalysis, where eosin Y, a photocatalyst, amplifies

127 profile with quinuclidine showed significant autocatalysis, which suggested that the presence of prot

128 hieves chiral symmetry breaking by combining autocatalysis with asymmetric amplification.

129 only with a full reactor model that includes autocatalysis with olefins as cocatalysts is one able to

130 the mammalian membrane associated fission or autocatalysis with the membrane free fission of yeast an