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1 inc metalloprotease whose closest homolog is angiotensin I-converting enzyme.
2 Susceptibility to infection correlated with angiotensin I converting enzyme 2 (ACE2) expression leve
3 encoded residues dominate recognition of the angiotensin I converting enzyme 2 (ACE2)-binding site.
5 valuate transgenic mice expressing the human angiotensin I-converting enzyme 2 (ACE2) receptor driven
6 gain insights into its interactions with the angiotensin I-converting enzyme 2 (ACE2)-solute carrier
9 he angiotensin II (Ang II)-breakdown enzyme, angiotensin I converting enzyme (ACE) 2, suggests the im
10 cal use of several therapeutic drugs, mostly angiotensin I converting enzyme (ACE) inhibitors and ang
11 identify peptides with dual antioxidant and angiotensin I converting enzyme (ACE) inhibitory activit
12 shed Amadori ketoses showed moderate to weak angiotensin I converting enzyme (ACE) inhibitory activit
14 he activity of the peptide inhibitors of the angiotensin I converting enzyme (ACE), and the antiradic
15 othelin 1 (EDN1); we assayed the activity of angiotensin I converting enzyme (ACE), which catalyses t
19 fraction of the heart and skeletal muscles, angiotensin I-converting enzyme (ACE) and neutral endope
20 g white, and (ii) evaluate the inhibition of angiotensin I-converting enzyme (ACE) by the obtained hy
21 n expended to determine whether the gene for angiotensin I-converting enzyme (ACE) confers susceptibi
25 dipeptidyl peptidase-IV (DPP-IV) (0.62) and angiotensin I-converting enzyme (ACE) inhibitor peptides
30 To investigate further the relationship of angiotensin I-converting enzyme (ACE) inhibitors to acti
31 es, majority of them were found identical to angiotensin I-converting enzyme (ACE) inhibitors, antiox
33 hiols content but at the same time increased angiotensin I-converting enzyme (ACE) inhibitory activit
35 In addition, the effects of digestion on the angiotensin I-converting enzyme (ACE) inhibitory activit
38 showed different amino acid compositions and angiotensin I-converting enzyme (ACE) inhibitory potenti
42 Although both LFHs <3 kDa showed in vitro angiotensin I-converting enzyme (ACE)-inhibitory activit
43 anti-obesity, immunomodulatory, antioxidant, angiotensin I-converting enzyme (ACE)-inhibitory, anti-m
51 and mechanism of action towards antioxidant, angiotensin-I converting enzyme (ACE) inhibition, and di
52 activity (DPPH), degree of hydrolysis (DH), angiotensin-I converting enzyme (ACE) inhibitory activit
55 egation analysis have shown that circulating angiotensin-I converting enzyme (ACE) levels are influen
59 -binding proteins were identified as porcine angiotensin-I-converting enzyme (ACE I) and aminopeptida
60 hey protein hydrolysates (WPHs) obtained had angiotensin-I-converting enzyme (ACE) and dipeptidyl pep
61 work in animals suggests that inhibitors of angiotensin-I-converting enzyme (ACE) protect against ca
62 l phenotype [C1Inh, C4, spontaneous amidase, angiotensin-I-converting enzyme (ACE), aminopeptidase P
63 eutral endopeptidase (NEP, EC 3.4.24.11) and angiotensin-I-converting enzyme (ACE, EC 2.4.15.1), have
65 he causes of hypertension is the activity of angiotensin-I converting enzyme (ACEI), making its inhib
67 as associated with a significant decrease in angiotensin I-converting enzyme activity and a small, bu
68 pairs, we identified 91 that had discordant angiotensin I-converting enzyme and glutathione S-transf
69 system gene regions (angiotensinogen, renin, angiotensin I-converting enzyme, and angiotensin II rece
70 nd an insertion/deletion polymorphism of the angiotensin I-converting enzyme gene (ACE) may be relate
72 These results confirm the association of the angiotensin I-converting enzyme indel with Alzheimer's d
73 or FT was assessed to release peptides with angiotensin-I converting enzyme inhibition (ACEi) and di
74 II type 1 receptor antagonist (AT1RA) and/or angiotensin I converting enzyme inhibitor (ACEI) were in
75 are also less responsive to monotherapy with angiotensin-I converting enzyme inhibitors or angiotensi
76 sk diverse population where monotherapy with angiotensin-I converting enzyme inhibitors or angiotensi
78 amino groups, GABA content, antioxidant and angiotensin I-converting enzyme inhibitory (ACEI) activi
79 ffect on proteolysis and negatively affected angiotensin I-converting enzyme inhibitory activity of f
80 acids), bioactivity (antioxidant effect and angiotensin I-converting enzyme inhibitory activity), rh
82 haracteristics, and in vitro antioxidant and Angiotensin-I converting enzyme-inhibitory activities we
84 eported previously a novel mode of action of angiotensin I-converting enzyme (kininase II; ACE) inhib
85 e N- and C-terminal domains of human somatic angiotensin I converting enzyme (sACE-1) demonstrate dis
88 nst alpha-glucosidase, pancreatic lipase and angiotensin I-converting enzyme, using in vitro models.
89 xidant activity persisted, and inhibition of angiotensin-I converting enzyme was improved after the d