ライフサイエンスコーパス: gamma-glutamyl transpeptidase

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

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

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

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

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

6 r demonstrated higher activity of the enzyme gamma-glutamyl transpeptidase, a membrane-bound enzyme i

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

8 gamma-Glutamyl transpeptidase activity was deficient in

9 the influence of Tat on glutathione levels, gamma-glutamyl transpeptidase activity, and the expressi

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

11 a decreases glutathione levels and increases gamma-glutamyl transpeptidase activity.

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

13 ids transfer, alkaline phosphatase activity, gamma-glutamyl-transpeptidase activity and physiological

14 ficant increases in the urinary excretion of gamma-glutamyl transpeptidase, alkaline phosphatase, lac

15 Surface gamma-glutamyl transpeptidase, an indirect indicator of

16 2-fold increases in the urinary excretion of gamma-glutamyl transpeptidase and alkaline phosphatase,

17 ductular structures, which are positive for gamma-glutamyl transpeptidase and CK-14 and CK-19 and do

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

19 dex less than 30 kg/m(2), genotype 2, normal gamma-glutamyl transpeptidase and increased alanine amin

20 had lower concentrations of the liver enzyme gamma-glutamyl transpeptidase and lower scores on a meas

21 ine aminotransferases, alkaline phosphatase, gamma glutamyl transpeptidase, and homeostasis model ass

22 utilization, thermostable carboxypeptidase, gamma glutamyl-transpeptidase, and deblocking aminopepti

23 50 mg, significantly reduced levels of ALP, gamma-glutamyl transpeptidase, and alanine aminotransfer

24 concentrations of alanine aminotransferase, gamma-glutamyl transpeptidase, and alkaline phosphatase.

25 ed to the GSH usage (glutathione peroxidase, gamma-glutamyl transpeptidase, and glutathione S-transfe

26 d levels of catalase, glutathione reductase, gamma-glutamyl transpeptidase, and glutathione synthetas

27 pression of catalase, glutathione reductase, gamma-glutamyl transpeptidase, and glutathione synthetas

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

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

30 GGL and gamma-glutamyl transpeptidase constitute a small gene fa

31 nary concentrations of alkaline phosphatase, gamma-glutamyl transpeptidase, cystatin C, neutrophil ge

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

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

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

35 e aminotransferase (14 of 44, 32%), elevated gamma-glutamyl transpeptidase (eight of 44, 18%), hyperb

36 nositol-anchored proteins, and transmembrane gamma-glutamyl transpeptidase exhibited the expected api

37 after 5 days liver histology was normal, but gamma-glutamyl transpeptidase expression was observed, w

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

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

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

41 ic (sBP) and diastolic blood pressure (dBP), gamma-glutamyl transpeptidase (gamma-GTP), and serum cre

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

43 gamma-Glutamyl transpeptidase (gammaGTase) catalyzes the

44 gamma-Glutamyl transpeptidases (gammaGTases) are the onl

45 at two H. pylori virulence determinants, the gamma-glutamyl transpeptidase GGT and the vacuolating cy

46 Two H. pylori persistence determinants, the gamma-glutamyl-transpeptidase GGT and the vacuolating cy

47 holestasis with bile duct hypoplasia and low gamma glutamyl transpeptidase (gGT) activity.

48 surrogate markers of NAFLD, such as elevated gamma glutamyl transpeptidase (GGT) and alanine aminotra

49 The role of gamma-glutamyl transpeptidase (GGT) and cysteine-S-conju

50 cury-glutathione complex by the ectoproteins gamma-glutamyl transpeptidase (GGT) and dipeptidase.

51 Plasma levels of gamma-glutamyl transpeptidase (GGT) are associated with

52 phosphatase, alanine transaminase (ALT), and gamma-glutamyl transpeptidase (GGT) as well as histologi

53 The expression of the membrane antigen gamma-glutamyl transpeptidase (GGT) during the promotion

54 ly we identified an additional member of the gamma-glutamyl transpeptidase (GGT) family, gamma-glutam

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

56 The mouse gamma-glutamyl transpeptidase (GGT) gene encodes seven d

57 putative HGT in all MIL isolates within the gamma-glutamyl transpeptidase (ggt) gene, a key componen

58 in either CagA, VacA, lipopolysaccharide, or gamma-glutamyl transpeptidase (GGT) implicated the latte

59 rone are capable of altering the activity of gamma-glutamyl transpeptidase (GGT) in human prostate ca

60 Expression of gamma-glutamyl transpeptidase (GGT) in tumors contribute

61 gamma-Glutamyl transpeptidase (GGT) is a heterodimeric m

62 gamma-Glutamyl transpeptidase (GGT) is an ectoenzyme tha

63 gamma-Glutamyl transpeptidase (GGT) is an enzyme located

64 Expression of the ectoenzyme gamma-glutamyl transpeptidase (GGT) is regulated on T ly

65 gamma-Glutamyl transpeptidase (GGT) is the enzyme respon

66 gamma-Glutamyl transpeptidase (GGT) is the only enzyme k

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

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

69 We used mice deficient in gamma-glutamyl transpeptidase (GGT) to analyze the effec

70 The cell surface glycoprotein gamma-glutamyl transpeptidase (GGT) was isolated from he

71 Histochemical evaluation, via staining for gamma-glutamyl transpeptidase (GGT), a marker for dyspla

72 ion, normal serum ALP values (but not normal gamma-glutamyl transpeptidase (GGT), alanine aminotransf

73 (EHS) and H. pylori These include flagellin, gamma-glutamyl transpeptidase (ggt), collagenase, the se

74 they also expressed alpha-fetoprotein (AFP), gamma-glutamyl transpeptidase (GGT), cytokeratin 19 (CK-

75 SH is degraded by the sequential reaction of gamma-glutamyl transpeptidase (GGT), gamma-glutamyl cycl

76 Acivicin, which inhibits GSH breakdown by gamma-glutamyl transpeptidase (GGT), had no effect on th

77 Apical proteins, including gamma-glutamyl transpeptidase (GGT), Na(+)-glucose cotra

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

79 d the metabolism of leukotriene C4 (LTC4) in gamma-glutamyl transpeptidase (GGT)-deficient mice and h

80 m of the cisplatin-glutathione complex via a gamma-glutamyl transpeptidase (GGT)-dependent pathway in

81 llowing removal of a gamma-glutamyl group by gamma-glutamyl transpeptidase (GGT).

82 The ectoenzyme, gamma-glutamyl transpeptidase (GGT, EC ) cleaves glutath

83 Furthermore, serial sections stained for gamma-glutamyl-transpeptidase (GGT, a marker of fetal he

84 nsaminase [AST], lactate dehydrogenase [LDH] gamma-glutamyl transpeptidase [GGT]).

85 ase [ALT], aspartate aminotransferase [AST], gamma-glutamyl transpeptidase [GGT], alkaline phosphatas

86 mma-glutamyl compounds have been identified: gamma-glutamyl transpeptidase (GGT1) and gamma-glutamyl

87 Overexpression of gamma-glutamyl transpeptidase (GGT1) has been implicated

88 Blood levels of gamma glutamyl transpeptidase (GGTP), a liver enzyme ind

89 gamma-Glutamyl transpeptidases (GGTs) are essential for

90 e proximal tubule under the direction of the gamma-glutamyl transpeptidase-I promoter were developed.

91 otransferase, aspartate aminotransferase, or gamma-glutamyl transpeptidase in donors with HGV infecti

92 The function of gamma-glutamyl transpeptidase is to cleave glutathione a

93 ter surgery, urinary protein and creatinine, gamma-glutamyl transpeptidase, lactate dehydrogenase, hi

94 creened using a blood alcohol concentration, gamma glutamyl transpeptidase level, and short Michigan

95 linking induces greater phosphorylation, and gamma-glutamyl transpeptidase levels are reduced compare

96 ough RBC count, mean corpuscular volume, and gamma-glutamyl transpeptidase levels remained significan

97 the age group, but all of them had elevated gamma-glutamyl transpeptidase levels.

98 nder, higher body mass index, triglycerides, gamma-glutamyl transpeptidase, maximum alanine aminotran

99 Increased activity of gamma-glutamyl transpeptidase may be one mechanism under

100 of alkaline phosphatase of 75.6%; P<0.0001; gamma-glutamyl transpeptidase of 117.9%, P<0.0001; bilir

101 o the tumour interstitium, the overexpressed gamma-glutamyl transpeptidase on the cell membrane cleav

102 including gamma-glutamylcysteine synthetase, gamma-glutamyl transpeptidase, or multidrug resistance p

103 P = 1.69 x 10(-33), beta = -1.47) and higher gamma -glutamyl transpeptidase (P = 8.30 x 10(-8), beta

104 .002 for ferritin) and fibrosis (P<.0001 for gamma-glutamyl transpeptidase, P=.01 for alkaline phosph

105 ll be a useful animal model for the study of gamma-glutamyl transpeptidase physiology and glutathione

106 mine; 2) loss of TA1 response to arginine in gamma-glutamyl transpeptidase-positive transformed and t

107 ubunits Dug1, Dug2, and Dug3) but not by the gamma-glutamyl-transpeptidase, raising the question of t

108 d, we designed, synthesized, and evaluated a gamma-glutamyl transpeptidase-resistant glyoxalase subst

109 Here, we present a gamma-glutamyl transpeptidase-responsive camptothecin-po

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

111 the presence of excess CapD, a B. anthracis gamma-glutamyl transpeptidase, the protective capsule is

112 lso believed to function consecutively after gamma-glutamyl transpeptidase to cleave cystinyl-bis-gly

113 bypasses the need for GSNO bioactivation by gamma-glutamyl transpeptidase to increase CFTR maturatio

114 the albumin-bilirubin (ALBI) score, and the gamma-glutamyl transpeptidase to PLT ratio (GPR) with re

115 is showed that pretreatment body mass index, gamma-glutamyl transpeptidase, triglyceride, IL-28B TT g

116 3-4 adverse events were increased levels of gamma-glutamyl transpeptidase (two [4%]), a reduction in

117 Level of gamma-glutamyl transpeptidase was significantly higher i

118 ts; mean corpuscular volume, SGOT, SGPT, and gamma-glutamyl transpeptidase were significantly higher.

119 Recent studies of a related enzyme, gamma-glutamyl transpeptidase, which is subject to inhib

120 bile duct-like structures were positive for gamma-glutamyl transpeptidase, which suggests that they