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1 ADPase retinal flatmounts were prepared, and morphometri
2 Pase activity, converting the enzyme into an ADPase with relative ADP:ATP hydrolysis rates of 6:1 or
6 propose that CD39 uses different ATPase and ADPase mechanisms in different quaternary structure cont
7 creased both the tendency to form dimers and ADPase activity, while double mutation of D228T/K224N la
8 in angiography, funduscopic examination, and ADPase preparations showed dilated and tortuous retinal
12 er biochemical characteristics, e.g., ATPase/ADPase ratios, inhibition by azide, and affinity for ATP
13 The D219E/W459A double mutant had an ATPase:ADPase ratio of 11:1 and a UTPase:UDPase ratio of 148:1.
17 ated postmortem for adenosine diphosphatase (ADPase) activity (labels viable retinal blood vessels) a
23 t lamp examination, adenosine diphosphatase (ADPase), and acid phosphatase staining as well as immuno
24 ours in flatmounted adenosine diphosphatase (ADPase)-stained rat retinas is analogous to clinically s
31 cells with human CD39 resulted in both ecto-ADPase activity as well as surface expression of CD39.
35 ethod of counting clock hours in flatmounted ADPase-stained retinas is valid for quantifying NV in ra
37 , and retinas were excised and incubated for ADPase activity, permitting the determination of the num
38 lium of the diabetic animals was stained for ADPase activity in flatmounts, and transverse sections w
44 man umbilical vein endothelial cells (HUVEC) ADPase was biochemically classified as an E-type ATP-dip
45 ld-type, S57A exhibited a 2-fold increase in ADPase activity without change in ATPase activity, while
47 ve no effect on ATPase activity and increase ADPase activity approximately 2-fold, resulting in equal
49 A demonstrated the highest calcium/magnesium ADPase activity ratio, 2.8-fold higher than that of wild
50 rthermore, these mutations decreased maximal ADPase activity for both the soluble and membrane-bound
51 ing activity (>90%) and completely devoid of ADPase activity, along with a similar extent of inhibiti
53 Ps) were counted in serial cross-sections of ADPase flat-embedded retinas of air-reared control 8-, 1
55 hibitor, diadenosine pentaphosphate, reduced ADPase activity by more than 70% on both epithelial surf
58 restored the ability to form dimers and the ADPase activity, further indicating that the nucleotidas
61 the ATPase activity but less than 50% of the ADPase activity, converting the enzyme into an ADPase wi
64 ction with antisense oligonucleotides, total ADPase activity fell from 26.0 +/- 3.1 in control cultur
65 or SOR-recovered animals were analyzed using ADPase stained or fluorescein-labeled dextran infused re
68 Endothelial cell CD39, an ecto-enzyme with ADPase and ATPase activities, rapidly metabolizes ATP an
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