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1 FAZ area was enlarged at the DCP (P = .001).
2 FAZ area was significantly correlated with foveal pit ar
3 FAZ area, point thickness of central fovea, central 1-mm
4 FAZ area, vessel area density (VAD), vessel length densi
5 FAZ diameters measured by UHR-AO-OCT and entoptic imagin
6 FAZ enlargement rates were higher in the more advanced i
7 FAZ from maize tortillas is positively related to the ex
8 FAZ was determined with a dual-isotope tracer ratio tech
9 FAZ was measured on days 2-3 and 51-52; meal-specific AZ
10 FAZ-based analysis revealed statistically significant di
11 tly associated were age (r = 0.33, P = .03), FAZ area (r = 0.45, P = .02), and central retinal thickn
12 omparison were testing for the presence of a FAZ, noting distinct features in the capillary pattern,
14 that TbSAS-4 associates with six additional FAZ tip proteins, and depletion of TbSAS-4 disrupts the
16 n was found between logMAR visual acuity and FAZ area in both the superficial (rho = 0.29; P < 0.01)
21 re not interchangeable regarding VD, FD, and FAZ for both the superficial and deep capillary plexus.
25 ved between the peripheral leakage index and FAZ area, but only in eyes that were laser naive (r = 0.
26 cally labeled with zinc stable isotopes, and FAZ was determined with a dual-isotope-tracer ratio tech
30 Z enlargement ranges from 5%-10% of baseline FAZ area per year in eyes with established ischemia.
32 ative relation (P < 0.001) was found between FAZ and both dietary phytate and the phytate:zinc molar
34 ith age (P = 0.026) such that for a constant FAZ area, an increase in patient age was associated with
39 weighing, the total absorbed zinc (TAZ) from FAZ x diet zinc, and the exchangeable zinc pool size (EZ
40 ferences between diabetic and normal eyes in FAZ area (superficial and deep layers), perimeter (super
46 gote form disrupts the elongation of the new FAZ filament, generating cells with a shorter FAZ associ
50 ichment of these FAZ tip proteins at the new FAZ tip, suggesting a role of TbSAS-4 in maintaining the
51 o-like kinase and aurora B kinase to the new FAZ tip, thus revealing the mechanistic role of CIF2 in
54 Two masked graders performed measurements of FAZ dimensions including area, perimeter, and maximum ho
57 significant difference (P < .05) in terms of FAZ perimeter, surface, and major axis and a not statist
61 nsumption of zinc-fortified foods may reduce FAZ, zinc fortification at the levels studied positively
63 the initial absorption studies; mean (+/-SD) FAZ values were 0.341 +/- 0.111, 0.237 +/- 0.052, and 0.
66 AZ filament, generating cells with a shorter FAZ associated with a longer unattached flagellum and re
67 cells with long free flagella and a shorter FAZ, accompanied by repositioning of the basal body, the
68 erver agreement was high for all superficial FAZ measurements (ICC >/=0.90) but did not meet the lowe
74 22 of 70 of the capillary loops defining the FAZ were visible in the optimal frame of the capillary p
76 izing contour was manually placed inside the FAZ of the smoothed image and iteratively moved by the s
81 pvOCT provides accurate measurements of the FAZ area and its morphology and a volumetric perfusion m
83 n of TbSAS-4 in regulating the length of the FAZ filament to control basal body positioning and life
84 S-4 is concentrated at the distal tip of the FAZ filament, and depletion of TbSAS-4 in the trypomasti
85 and pvOCT, the measured average areas of the FAZ from two healthy subjects were below 0.22 mm(2), and
88 technique for automated segmentation of the FAZ using images from fundus fluorescein angiography (FF
90 ression analysis showed that the area of the FAZ was significantly correlated with VA in DR and RVO (
92 vertical collateral vessels, the area of the FAZ, and order of vessel branching in greater detail tha
98 he bilobe, rather assembly of the EGJ on the FAZ:ER, which is coupled to the flagellar cytoskeleton,
99 ensities in the zone immediately outside the FAZ were calculated and the variation in density as a fu
100 r zone (FAZ) and vasculature surrounding the FAZ were performed on the automatically generated en fac
101 n of many of the capillaries proximal to the FAZ, including those of average size based on published
103 ted from retinal thickness data, whereas the FAZ was manually segmented by two observers to extract e
104 ing results obtained by the program with the FAZ boundaries manually delineated by medical retina spe
106 of TbSAS-4 disrupts the enrichment of these FAZ tip proteins at the new FAZ tip, suggesting a role o
108 s also highly variable between persons, with FAZ area ranging from 0.05 to 1.05 mm(2) and FAZ diamete
110 needed on the fractional absorption of zinc (FAZ) and absorbed zinc (AZ) during prolonged exposure to
111 n between the fractional absorption of zinc (FAZ) and the phytate content and phytate:zinc molar rati
112 o measure the fractional absorption of zinc (FAZ) and to estimate the total quantity of absorbed zinc
113 o measure the fractional absorption of zinc (FAZ) in human milk and CF by dual-isotope ratios in urin
115 th the postnuclear flagellar adherence zone (FAZ), and closely juxtaposed to corresponding Golgi clus
116 the length of the flagellum attachment zone (FAZ) filament, a specialized cytoskeletal structure requ
117 aligned with the flagellar attachment zone (FAZ) indicating nucleation on the FAZ-associated ER (FAZ
119 nd nucleating the flagellum attachment zone (FAZ), which adheres the flagellum to the cell surface.
127 uantified include the foveal avascular zone (FAZ) area, peripheral ischemic index, peripheral leakage
130 ntitative data on the foveal avascular zone (FAZ) features and the total vascular and avascular surfa
131 ify the size of their foveal avascular zone (FAZ) from the entoptic view, whereas only 22 of 70 of th
132 l dimension (FD), and foveal avascular zone (FAZ) of superficial and deep capillary plexus in healthy
134 capillary network and foveal avascular zone (FAZ) were extracted using video and image analysis algor
135 sels, the size of the foveal avascular zone (FAZ), and degree of vessel branching were compared betwe
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