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1 perfused juxtamedullary nephron preparation, interlobular and afferent arteriolar diameter responses
2 12-DIHETE, had no effect on diameters of the interlobular and afferent arterioles at concentrations u
4 nM, 11,12-EET increased the diameters of the interlobular and afferent arterioles by 18 +/- 2% (N = 1
8 e control diameter, whereas the diameters of interlobular and arcuate arteries declined to 50%+/-12%
9 here a significant difference between small (interlobular and bile ductules) and large (intrahepatic
10 gradients of development (i.e. early to late interlobular and posterior to anterior, respectively).
11 reshly isolated from afferent arterioles and interlobular arteries averaging between 10 to 40 microns
12 usside (SNP) increased the diameter of renal interlobular arteries preconstricted with phenylephrine
13 ETHODS AND Sprague-Dawley rat interlobar and interlobular arteries were examined in terms of superoxi
14 ithelial cells and endothelial cells of some interlobular arteries, in parallel with SODD, during acu
18 e three-dimensional (3D) architecture of the interlobular bile duct during cholestasis, we used 3D co
19 e each of a portal vein, hepatic artery, and interlobular bile duct numbered 11 +/- 6 per biopsy (ran
23 ly by chronic non-suppurative destruction of interlobular bile ducts leading to advanced fibrosis, ci
24 ffusion in individual bile canaliculi and in interlobular bile ducts of intact livers in living mice,
25 Notably, on average there were 2.3 +/- 2.2 interlobular bile ducts per portal tract, compared to 2.
26 PDC-E2 monoclonal antibody (mAb) C355.1, the interlobular bile ducts showed typical aberrant apical s
28 disease characterized by the destruction of interlobular bile ducts, leading to cholestasis and live
32 disease characterized by the destruction of interlobular biliary ductules, which progressively leads
33 or protein was detected in interalveolar and interlobular connective tissue cells adjacent to glandul
34 We show a highly reproducible sequence of interlobular duct remodeling, where cholangiocyte prolif
36 was expressed in the glandular alveolar and interlobular ductal cells in the lacrimal gland and all
37 toring the luminal pH of isolated guinea-pig interlobular ducts after microinjection of an extracellu
38 yte growth factor likely collects within the interlobular ducts and becomes a component in normal tea
47 acteristics: the intercalated, intralobular, interlobular, intralobar, interlobar, and main excretory
48 significantly more intralobular (P < 0.001), interlobular (P < 0.05), and total pancreatic fat (P < 0
52 , reticular or granular opacities (thickened interlobular septa and ground-glass opacities at CT), cy
54 es enlarge and approach each other along the interlobular septa, causing a fine reticular pattern on
55 d ASIR-HD images for small anatomic details (interlobular septa, centrilobular region, and small bron
56 revealed lymphadenopathy, nodules, thickened interlobular septa, focal consolidation, reticular opaci
57 solidation or reticular) patterns, thickened interlobular septa, vascular enlargement, air bronchogra
61 e-in-bud pattern (accuracy, 93% vs 78%-80%), interlobular septal thickening (accuracy, 78%-83% vs 61%
62 The predominant HRCT presentation of PAP was interlobular septal thickening (ILST;100%) and ground gl
63 omy visible on thin-section CT scans include interlobular septal thickening and diseases with periphe
64 nant HRCT presentation of idiopathic PAP was interlobular septal thickening and ground glass opacitie
66 ; interquartile range, 23-38 years) and more interlobular septal thickening and mediastinal lymphaden
68 nd-glass opacity or airspace consolidation), interlobular septal thickening, and gastric distention a
69 consisting of multifocal opacity and smooth interlobular septal thickening, possibly with small effu
72 bubble sign, peribronchovascular thickening, interlobular thickening, and number of involved lobes 4
73 n associated with autism, and the cerebellar interlobular variation in Spry3 expression coincident wi