ライフサイエンスコーパス: glutamyl transpeptidase

1 ught about by the action of the enzyme gamma-glutamyl transpeptidase.

2 plasmic fibers; it contains urease and gamma-glutamyl transpeptidase.

3 gamma-Glutamyl transpeptidase 1 (GGT1) is a cell surface, N-te

4 gamma-Glutamyl transpeptidase (28%) and alanine transaminase (

5 39.9 +/- 28.6U/L vs 23.8 +/- 14.1U/L), gamma-glutamyl transpeptidase (34.3 +/- 16.6 vs 24.5 +/- 16.8U

6 nstrated higher activity of the enzyme gamma-glutamyl transpeptidase, a membrane-bound enzyme involve

7 1.87; 95% CI, 1.10; 3.18; P = 0.021); gamma-glutamyl transpeptidase above the upper limit of normal

8 gamma-Glutamyl transpeptidase activity was deficient in kidney

9 nfluence of Tat on glutathione levels, gamma-glutamyl transpeptidase activity, and the expression and

10 erum bile acid (BA) levels, and normal gamma-glutamyl transpeptidase activity.

11 eases glutathione levels and increases gamma-glutamyl transpeptidase activity.

12 glutathione levels and an increase in gamma-glutamyl transpeptidase activity.

13 ansfer, alkaline phosphatase activity, gamma-glutamyl-transpeptidase activity and physiological respo

14 increases in the urinary excretion of gamma-glutamyl transpeptidase, alkaline phosphatase, lactate d

15 Surface gamma-glutamyl transpeptidase, an indirect indicator of redox

16 increases in the urinary excretion of gamma-glutamyl transpeptidase and alkaline phosphatase, and pi

17 lar structures, which are positive for gamma-glutamyl transpeptidase and CK-14 and CK-19 and do not e

18 n of two cholangiocyte-specific genes (gamma-glutamyl transpeptidase and cytokeratin 19) was similar

19 ss than 30 kg/m(2), genotype 2, normal gamma-glutamyl transpeptidase and increased alanine aminotrans

20 wer concentrations of the liver enzyme gamma-glutamyl transpeptidase and lower scores on a measure of

21 , significantly reduced levels of ALP, gamma-glutamyl transpeptidase, and alanine aminotransferase, c

22 ntrations of alanine aminotransferase, gamma-glutamyl transpeptidase, and alkaline phosphatase.

23 the GSH usage (glutathione peroxidase, gamma-glutamyl transpeptidase, and glutathione S-transferase).

24 on of catalase, glutathione reductase, gamma-glutamyl transpeptidase, and glutathione synthetase in t

25 ls of catalase, glutathione reductase, gamma-glutamyl transpeptidase, and glutathione synthetase.

26 inotransferases, alkaline phosphatase, gamma glutamyl transpeptidase, and homeostasis model assessmen

27 zation, thermostable carboxypeptidase, gamma glutamyl-transpeptidase, and deblocking aminopeptidases

28 Glyoxalase-I and gamma-glutamyl transpeptidase, both involved in GSH salvage, w

29 ne S-transferase pi 7, and for luminal gamma-glutamyl transpeptidase, but they did not express immuno

30 GGL and gamma-glutamyl transpeptidase constitute a small gene family.

31 oncentrations of alkaline phosphatase, gamma-glutamyl transpeptidase, cystatin C, neutrophil gelatina

32 Among secondary end points, levels of gamma-glutamyl transpeptidase decreased 48%-63%, on average, a

33 (BSEP) disease, and 4 others with low gamma-glutamyl transpeptidase disease (levels <100 U/L), were

34 Dug2p/Dug3p complex, and the vacuolar gamma-glutamyl transpeptidase, Ecm38p.

35 otransferase (14 of 44, 32%), elevated gamma-glutamyl transpeptidase (eight of 44, 18%), hyperbilirub

36 l-anchored proteins, and transmembrane gamma-glutamyl transpeptidase exhibited the expected apical lo

37 5 days liver histology was normal, but gamma-glutamyl transpeptidase expression was observed, with al

38 athione (GSNO), and GSNO activation by gamma-glutamyl transpeptidase (gamma-GT) is required.

39 tamyl adducts that could be cleaved by gamma-glutamyl transpeptidase (gamma-GT), found predominantly

40 c cholestasis (PFIC) with raised serum gamma-glutamyl transpeptidase (gamma-GT).

41 P) and diastolic blood pressure (dBP), gamma-glutamyl transpeptidase (gamma-GTP), and serum creatinin

42 We found that inhibition of gamma-glutamyl-transpeptidase (gamma-GT) protects human acute

43 gamma-Glutamyl transpeptidase (gammaGTase) catalyzes the trans

44 gamma-Glutamyl transpeptidases (gammaGTases) are the only enzy

45 H. pylori virulence determinants, the gamma-glutamyl transpeptidase GGT and the vacuolating cytotoxi

46 . pylori persistence determinants, the gamma-glutamyl-transpeptidase GGT and the vacuolating cytotoxi

47 The contribution of glutamyl transpeptidase (GGT) (gamma-glutamyltransferase

48 e substituted CyBam was applied to imaging y-glutamyl transpeptidase (GGT) activity in a metastatic m

49 asis with bile duct hypoplasia and low gamma glutamyl transpeptidase (gGT) activity.

50 ate markers of NAFLD, such as elevated gamma glutamyl transpeptidase (GGT) and alanine aminotransfera

51 The role of gamma-glutamyl transpeptidase (GGT) and cysteine-S-conjugate b

52 lutathione complex by the ectoproteins gamma-glutamyl transpeptidase (GGT) and dipeptidase.

53 Plasma levels of gamma-glutamyl transpeptidase (GGT) are associated with risk f

54 atase, alanine transaminase (ALT), and gamma-glutamyl transpeptidase (GGT) as well as histological gr

55 The expression of the membrane antigen gamma-glutamyl transpeptidase (GGT) during the promotion and p

56 identified an additional member of the gamma-glutamyl transpeptidase (GGT) family, gamma-glutamyl leu

57 GGL), a newly identified member of the gamma-glutamyl transpeptidase (GGT) family, we generated null

58 The mouse gamma-glutamyl transpeptidase (GGT) gene encodes seven distinc

59 ive HGT in all MIL isolates within the gamma-glutamyl transpeptidase (ggt) gene, a key component in t

60 her CagA, VacA, lipopolysaccharide, or gamma-glutamyl transpeptidase (GGT) implicated the latter in H

61 re capable of altering the activity of gamma-glutamyl transpeptidase (GGT) in human prostate carcinom

62 Expression of gamma-glutamyl transpeptidase (GGT) in tumors contributes to r

63 gamma-Glutamyl transpeptidase (GGT) is a heterodimeric membran

64 gamma-Glutamyl transpeptidase (GGT) is an ectoenzyme that cata

65 gamma-Glutamyl transpeptidase (GGT) is an enzyme located on th

66 Expression of the ectoenzyme gamma-glutamyl transpeptidase (GGT) is regulated on T lymphocy

67 gamma-Glutamyl transpeptidase (GGT) is the enzyme responsible

68 gamma-Glutamyl transpeptidase (GGT) is the only enzyme known t

69 ALT, aspartate transaminase (AST), and gamma-glutamyl transpeptidase (GGT) levels (P <.01).

70 Both the presence of gamma-glutamyl transpeptidase (GGT) on the apical brush-border

71 We used mice deficient in gamma-glutamyl transpeptidase (GGT) to analyze the effects of

72 The cell surface glycoprotein gamma-glutamyl transpeptidase (GGT) was isolated from healthy

73 ochemical evaluation, via staining for gamma-glutamyl transpeptidase (GGT), a marker for dysplastic c

74 ormal serum ALP values (but not normal gamma-glutamyl transpeptidase (GGT), alanine aminotransferase

75 and H. pylori These include flagellin, gamma-glutamyl transpeptidase (ggt), collagenase, the secreted

76 lso expressed alpha-fetoprotein (AFP), gamma-glutamyl transpeptidase (GGT), cytokeratin 19 (CK-19), O

77 degraded by the sequential reaction of gamma-glutamyl transpeptidase (GGT), gamma-glutamyl cyclotrans

78 vicin, which inhibits GSH breakdown by gamma-glutamyl transpeptidase (GGT), had no effect on the enha

79 Apical proteins, including gamma-glutamyl transpeptidase (GGT), Na(+)-glucose cotransport

80 ase (ALT), alkaline phosphatase (ALP), gamma-glutamyl transpeptidase (GGT), or total bilirubin.

81 metabolism of leukotriene C4 (LTC4) in gamma-glutamyl transpeptidase (GGT)-deficient mice and have fo

82 he cisplatin-glutathione complex via a gamma-glutamyl transpeptidase (GGT)-dependent pathway in the p

83 g removal of a gamma-glutamyl group by gamma-glutamyl transpeptidase (GGT).

84 The ectoenzyme, gamma-glutamyl transpeptidase (GGT, EC ) cleaves glutathione (

85 rthermore, serial sections stained for gamma-glutamyl-transpeptidase (GGT, a marker of fetal hepatobl

86 ase [AST], lactate dehydrogenase [LDH] gamma-glutamyl transpeptidase [GGT]).

87 LT], aspartate aminotransferase [AST], gamma-glutamyl transpeptidase [GGT], alkaline phosphatase [ALP

88 utamyl compounds have been identified: gamma-glutamyl transpeptidase (GGT1) and gamma-glutamyl leukot

89 Overexpression of gamma-glutamyl transpeptidase (GGT1) has been implicated in an

90 Overexpression of y-glutamyl transpeptidase (GGT1) has been implicated in an

91 Blood levels of gamma glutamyl transpeptidase (GGTP), a liver enzyme indicator

92 gamma-Glutamyl transpeptidases (GGTs) are essential for hydrol

93 imal tubule under the direction of the gamma-glutamyl transpeptidase-I promoter were developed.

94 ferase, aspartate aminotransferase, or gamma-glutamyl transpeptidase in donors with HGV infection alo

95 The function of gamma-glutamyl transpeptidase is to cleave glutathione and S-n

96 rgery, urinary protein and creatinine, gamma-glutamyl transpeptidase, lactate dehydrogenase, histolog

97 d using a blood alcohol concentration, gamma glutamyl transpeptidase level, and short Michigan Alcoho

98 g induces greater phosphorylation, and gamma-glutamyl transpeptidase levels are reduced compared with

99 BC count, mean corpuscular volume, and gamma-glutamyl transpeptidase levels remained significantly di

100 ge group, but all of them had elevated gamma-glutamyl transpeptidase levels.

101 higher body mass index, triglycerides, gamma-glutamyl transpeptidase, maximum alanine aminotransferas

102 Increased activity of gamma-glutamyl transpeptidase may be one mechanism underlying

103 kaline phosphatase of 75.6%; P<0.0001; gamma-glutamyl transpeptidase of 117.9%, P<0.0001; bilirubin o

104 tumour interstitium, the overexpressed gamma-glutamyl transpeptidase on the cell membrane cleaves the

105 ing gamma-glutamylcysteine synthetase, gamma-glutamyl transpeptidase, or multidrug resistance protein

106 9 x 10(-33), beta = -1.47) and higher gamma -glutamyl transpeptidase (P = 8.30 x 10(-8), beta = 0.84)

107 or ferritin) and fibrosis (P<.0001 for gamma-glutamyl transpeptidase, P=.01 for alkaline phosphatase,

108 a useful animal model for the study of gamma-glutamyl transpeptidase physiology and glutathione metab

109 2) loss of TA1 response to arginine in gamma-glutamyl transpeptidase-positive transformed and tumorig

110 s Dug1, Dug2, and Dug3) but not by the gamma-glutamyl-transpeptidase, raising the question of the rol

111 designed, synthesized, and evaluated a gamma-glutamyl transpeptidase-resistant glyoxalase substrate,

112 Here, we present a gamma-glutamyl transpeptidase-responsive camptothecin-polymer

113 gamma-Glutamyl transpeptidase, the first enzyme of the gamma-g

114 resence of excess CapD, a B. anthracis gamma-glutamyl transpeptidase, the protective capsule is degra

115 lieved to function consecutively after gamma-glutamyl transpeptidase to cleave cystinyl-bis-glycine (

116 ses the need for GSNO bioactivation by gamma-glutamyl transpeptidase to increase CFTR maturation; 4)

117 lbumin-bilirubin (ALBI) score, and the gamma-glutamyl transpeptidase to PLT ratio (GPR) with respect

118 wed that pretreatment body mass index, gamma-glutamyl transpeptidase, triglyceride, IL-28B TT genotyp

119 dverse events were increased levels of gamma-glutamyl transpeptidase (two [4%]), a reduction in the n

120 Level of gamma-glutamyl transpeptidase was significantly higher in the

121 an corpuscular volume, SGOT, SGPT, and gamma-glutamyl transpeptidase were significantly higher.

122 Recent studies of a related enzyme, gamma-glutamyl transpeptidase, which is subject to inhibition

123 duct-like structures were positive for gamma-glutamyl transpeptidase, which suggests that they posses