ライフサイエンスコーパス: autocatalysis

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

2 tallic nanostructures to boost photochemical autocatalysis.

3 gether with their physical separation govern autocatalysis.

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

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

6 for SNAP25 cleavage, SNAPtide cleavage, and autocatalysis.

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

8 eland-Claisen rearrangement with evidence of autocatalysis.

9 te for maturation, suggesting a mechanism of autocatalysis.

10 rimary and secondary structures required for autocatalysis.

11 he relationship between intron stability and autocatalysis.

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

13 H-induced conformational change suitable for autocatalysis.

14 ead ribozyme, both prevents and enhances RNA autocatalysis.

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

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

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

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

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

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

21 Autocatalysis and chemical amplification are characteris

22 Autocatalysis and chemical amplification are properties

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

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

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

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

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

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

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

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

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

32 The prevalence and implications of such autocatalysis are discussed.

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

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

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

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

37 Autocatalysis by the resulting aryllithiums or catalysis

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

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

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

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

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

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

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

45 Autocatalysis has been extensively studied because it is

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

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

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

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

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

51 Autocatalysis is central to the propagation of life and

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

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

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

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

56 Autocatalysis is observed, and the rate of oxidation inc

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

58 Autocatalysis is the source of the large dendrimer effec

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

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

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

62 nalyze their dependence on system volume and autocatalysis mechanism.

63 Mpl occurs exclusively by an intramolecular autocatalysis mechanism.

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

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

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

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

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

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

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

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

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

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

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

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

76 Autocatalysis severs the protein into a large membrane-a

77 Autocatalysis stems from ArLi-catalyzed deaggregation of

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

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

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

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

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

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

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

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

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

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

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

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

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

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