ライフサイエンスコーパス: cellular enzyme

1 nisms modulate the activity of this critical cellular enzyme.

2 e and convenient model for understanding the cellular enzyme.

3 role in host-pathogen interactions for this cellular enzyme.

4 due to low-level genome circularization by a cellular enzyme.

5 it is itself an RNase or somehow activates a cellular enzyme.

6 active protein or enzymatic activity of this cellular enzyme.

7 the processing of protein-DNA cross-links by cellular enzymes.

8 and its intensity was used for assessment of cellular enzymes.

9 time scales, for example, substrates of many cellular enzymes.

10 sed by antibody aldolases but not by natural cellular enzymes.

11 yQ repeat fragments for degradation by other cellular enzymes.

12 les and controlling the activity of multiple cellular enzymes.

13 RNA polymerases are key multisubunit cellular enzymes.

14 move potentially toxic secondary products of cellular enzymes.

15 a required cofactor for a number of critical cellular enzymes.

16 ore completion of the integration process by cellular enzymes.

17 ressed by using small molecule inhibitors of cellular enzymes.

18 e the functional links between the viral and cellular enzymes.

19 at is hypothesized to prevent debranching by cellular enzymes.

20 d cannot be efficiently substituted by other cellular enzymes.

21 s are derived largely through the actions of cellular enzymes.

22 only slightly but increased the affinity for cellular enzymes.

23 tic co-factors in a wide variety of critical cellular enzymes.

24 tudies and reveals reversible modulations of cellular enzyme activities under different metabolic con

25 tion rate [fV ]), metabolic rate (M O2), and cellular enzyme activity were measured.

26 cross cells, which rendered intra- and trans-cellular enzyme activity.

27 , due to reduced expression of JAR1 mRNA and cellular enzyme activity.

28 se and temporally regulated interaction of a cellular enzyme and a noncoding RNA provides a new parad

29 ocesses, groups that include the majority of cellular enzymes and components of amino acid, carbohydr

30 oteins, which can activate a wide variety of cellular enzymes and ion channels.

31 the peroxynitrite avoids the inactivation of cellular enzymes and modification of the cytoskeleton.

32 otin and used as markers in the detection of cellular enzymes and receptors.

33 Copper is a cofactor for many cellular enzymes and transporters.

34 ction and time-varying concentrations of the cellular enzymes are used as decision variables.

35 ith and inhibiting adenosine kinase (ADK), a cellular enzyme associated with the methyl cycle that ge

36 In vitro mutagenesis of normal cellular enzymes can be exploited to identify mutations

37 atalytic function of IkappaB kinase (IKK), a cellular enzyme complex that phosphorylates and inactiva

38 M2 bound to TopoII and resulted in decreased cellular enzyme content.

39 with mAspAT mRNA (r = .90), reaching 808% of cellular enzyme content/24 hours at 80 mmol/L.

40 There are some P. aeruginosa cellular enzymes controlled by quorum sensing, and we sh

41 ver, this TNTase was later purported to be a cellular enzyme copurifying with the HCV RdRp.

42 ke structure is subsequently resolved by the cellular enzyme DBR1, leaving a 5' phosphate.

43 poptosis-related genes, zinc finger protein, cellular enzymes, expressed sequence tag clones, and CpG

44 polyglutamylated, as mediated in vivo by the cellular enzyme folyl polyglutamate synthetase.

45 s that inhibit vitamin B9 (folic acid)-using cellular enzymes, have been used over several decades fo

46 Therefore, modulation of the cellular enzyme HO-1 may represent a novel therapeutic s

47 ith and inactivate adenosine kinase (ADK), a cellular enzyme important for adenosine salvage and meth

48 Cyclooxygenase-2 (COX-2) is a cellular enzyme in the eicosanoid synthetic pathway that

49 lins revealed little, if any, role for these cellular enzymes in the modulation of furin cleavage.

50 Cellular enzymes interact in a post-translationally regu

51 ldehyde 3-phosphate dehydrogenase (GAPDH), a cellular enzyme involved in glycolysis, binds specifical

52 HeLa extracts, we identified several of the cellular enzymes involved in AAV DNA replication.

53 In this study, potential cellular enzymes involved in encephalomyocarditis virus

54 ellular leukotriene production by activating cellular enzymes involved in leukotriene formation.

55 est itself when the adducts are processed by cellular enzymes involved in replication, repair, and tr

56 ons are corrected in a reaction catalyzed by cellular enzymes involved in various DNA repair processe

57 thermore, there is no evidence that the same cellular enzyme is involved in the synthesis of both RNA

58 mic phosphorylation involving both viral and cellular enzymes is likely a key regulator of multiple B

59 n involving the vaccinia virus B1 kinase and cellular enzymes is likely a key regulator of multiple B

60 ite is thought to be catalyzed by one of the cellular enzymes known as adenosine deaminases that act

61 hought to be catalyzed by one or more of the cellular enzymes known as adenosine deaminases that act

62 IgM- and IgG-AECA were determined by cellular enzyme-linked immunosorbent assay using fixed c

63 Immunofluorescence microscopy and a cellular enzyme-linked immunosorbent assay using purifie

64 Thymidine phosphorylase, a cellular enzyme markedly induced by ORFK13/vFLIP, can me

65 While cellular enzymes may take part in mediating this recombi

66 e that phosphoregulation of BAF by viral and cellular enzymes modulates this protein at multiple mole

67 Therefore, targeting cellular enzymes necessary for HIV-1 transcription, whic

68 of Epstein-Barr virus (EBV) is replicated by cellular enzymes only once per cell cycle in human cells

69 igens using a mechanism that did not involve cellular enzymes or lipid cleavage, but was regulated by

70 the endogenous baculovirus gene product or a cellular enzyme, point mutations were introduced into a

71 The drug targets in this assay are viral and cellular enzymes required for HCV replication, which are

72 nine adenosyltransferase (MAT), an essential cellular enzyme responsible for S-adenosylmethionine bio

73 GLO1 is a ubiquitous cellular enzyme responsible for the detoxification of th

74 polymerase, the identity of the (presumably cellular) enzyme responsible for this reaction remains u

75 These results support the hypothesis that cellular enzyme(s) may catalyze the late steps of retrov

76 ng that these modifications can be made by a cellular enzyme(s).

77 This report demonstrates that a cellular enzyme, SIRT1, is part of the HPV16 DNA replica

78 Cellular enzymes synthesize atRA from Vitamin A, which i

79 Telomere shortening is counteracted by the cellular enzyme telomerase.

80 by viral 2A protease (2A(pro)) or a putative cellular enzyme (termed eIF4Gase) which is activated by

81 Endonuclease G appears to be the only cellular enzyme that can specifically cleave the a seque

82 O-GlcNAc transferase (OGT) is an important cellular enzyme that catalyzes the posttranslational add

83 levels of Ty1 transposition require Dbr1p, a cellular enzyme that cleaves 2'-5' RNA bonds.

84 SAMHD1 is a cellular enzyme that depletes intracellular deoxynucleos

85 Here we show that TET2, a cellular enzyme that initiates DNA demethylation by conv

86 have examined whether expression of TET2, a cellular enzyme that initiates DNA demethylation by conv

87 n likely is the inhibition of cathepsin L, a cellular enzyme that is essential for the processing of

88 APOBEC3G is a human cellular enzyme that is incorporated into retroviral par

89 belson (Abl) tyrosine kinase is an important cellular enzyme that is rendered constitutively active i

90 (O-GlcNAc) transferase (OGT) is an essential cellular enzyme that posttranslationally modifies nuclea

91 Tyrosyl-DNA phosphodiesterase I (Tdp1) is a cellular enzyme that repairs the irreversible topoisomer

92 One such factor, telomerase, is the cellular enzyme that synthesizes DNA repeats at the ends

93 Telomerase is a cellular enzyme that synthesizes nucleotide repeats at t

94 Fatty acid synthase (FAS), the cellular enzyme that synthesizes palmitate, is expressed

95 te extracts, we demonstrate the existence of cellular enzymes that can efficiently utilize O-acetyl-A

96 be universally adaptable to other viral and cellular enzymes that have deISGylating activities.

97 etic DNA analogs resistant to degradation by cellular enzymes that hybridize to single-stranded DNA (

98 Topoisomerases are essential cellular enzymes that maintain the appropriate topologic

99 infection with FeLV-B due to the activity of cellular enzymes that mutate the viral genome.

100 l-prolyl isomerases (PPIases) are ubiquitous cellular enzymes that play roles in cellular signaling a

101 However, the cellular enzymes that regulate the addition and removal

102 lear antigen (PCNA), and polymerase delta as cellular enzymes that were essential for AAV DNA replica

103 and trans-phosphorylations (by PKC and other cellular enzymes) that contribute to the spatiotemporal

104 ingers differ from the zinc finger motifs of cellular enzymes, the requirement for efficient hydrogen

105 dized NFI-C can be catalyzed in vitro by the cellular enzyme thioltransferase (glutaredoxin) coupled

106 ngle stranded RNA viruses, which hijack this cellular enzyme to remodel intracellular membranes of in

107 iolabile groups, which need to be cleaved by cellular enzymes to release the parent molecules.

108 that, as opposed to what is observed for the cellular enzyme, two different mRNAs are encoded by the

109 In contrast, three IFN-induced cellular enzymes, viperin, ISG20, and double-stranded-RN

110 ze that these cdks regulate the functions of cellular enzymes which modify ICP0, and are, consequentl

111 Poly(ADP-ribose) polymerase 1 (PARP-1) is a cellular enzyme with a fundamental role in DNA repair an