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1 scular endothelial-cell proliferation of the capillary bed.
2 od supply with no increase from a peripheral capillary bed.
3 iameter before the blood enters the alveolar capillary bed.
4 the effective shunting of blood through its capillary bed.
5 lar dilation, increasing blood flow into the capillary bed.
6 pread of proinflammatory signals in the lung capillary bed.
7 apid and heterogeneous BBB disruption in the capillary bed.
8 postcapillary venules and progresses to the capillary bed.
9 arteriovenous shunt), without an intervening capillary bed.
10 ), representing a simple in vitro model of a capillary bed.
11 eakage occurred from a small fraction of the capillary bed.
12 mit transmission of systemic pressure to the capillary bed.
13 riovenous connections without an intervening capillary bed.
14 effects of uniform filling of the pulmonary capillary bed.
15 f control is peripheral resistance in tissue capillary beds.
16 uctural elements surrounding glomerulus-like capillary beds.
17 lation that was associated with disorganized capillary beds.
18 oles and "downstream" propagation into local capillary beds.
19 he preferential targeting of newly generated capillary beds.
20 c BL, was found between capillaries in dense capillary beds.
21 vessels is crucial for morphogenesis of the capillary beds.
22 ed at high microvascular pressures in intact capillary beds.
23 1.99.25 induced PLVAP expression in the deep capillary bed and enabled extravasation of small and lar
24 nary artery pressure closer to the pulmonary capillary bed and LA pressure closer to the venoatrial j
25 dothelial Ca2+ conduction occurs in the lung capillary bed and that Cx43-containing gap junctions med
26 Immunofluorescence to anti-ET-1 within the capillary bed and veins of the retina in diabetic insuli
27 perience shear forces equivalent to those in capillary beds and are made to flow through capillary-li
28 and demarginated from microfluidic models of capillary beds and veins, respectively, increased after
29 ral inlet vessel, branched into an extensive capillary bed, and coalesced into a single outlet vessel
30 abilize the enzyme, localize LpL in specific capillary beds, and route lipoprotein lipids to the unde
31 include reduction in vessel number, loss of capillary beds, and the formation of hemorrhagic vascula
32 retinal neovascularization, formation of new capillary beds, and the presence of new blood vessels ab
33 leukocytes adhere to solid surfaces, such as capillary beds, and the subsequent migration through the
34 distribution differences in tumor-associated capillary bed at different stages of disease progression
36 particle local accessibility to flow area of capillary beds by co-circulating red blood cells (RBC).
37 We demonstrate that for RBCs entering the capillary bed close to the cortical surface (< 400 mum)
38 imately 7.5% in venous blood leaving the CNS capillary bed compared to arterial blood, indicating eff
39 viously unknown role for Abeta in regulating capillary bed density, providing new insight into the no
40 se effects were dose-dependent and increased capillary bed density, though there was no effect on lar
41 tudy, EMBs consisting of an afferent artery, capillary beds, efferent vein, and surrounding parenchym
42 d the existing wealth of knowledge regarding capillary bed formation, studies for the development of
47 he liver may be a simple strategy to protect capillary beds in the retina and in other peripheral tis
48 eyes induced neovascularization in multiple capillary beds, including those not responsive to VEGF a
49 r or not the developmental stage of the deep capillary bed is critical for occurrence of neovasculari
51 asmodium falciparum-infected erythrocytes in capillary beds is a characteristic feature of severe mal
52 tween arteries and veins without intervening capillary beds is the primary pathology of arteriovenous
53 of erythrocytes, and entrapment in the lung capillary bed, largely due to their poor biocompatibilit
55 lets are released from megakaryocytes in the capillary bed of the lung, this concept has not been uni
56 provide evidence for platelet release in the capillary bed of the lungs during stimulated as well as
57 ascularization that originates from the deep capillary bed of the retina and grows into the subretina
58 strate new vessels originating from the deep capillary bed of the retina that extend beneath the phot
59 neovascularization originated from the deep capillary bed of the retina, but it was more extensive a
62 rth, there was increased density of the deep capillary bed on postnatal day (P) 11 that returned to n
66 ith sprouts from retinal vessels in the deep capillary bed seen on P14 and vessels reaching the subre
70 ystemic venous blood to bypass the pulmonary capillary bed through anatomic right-to-left shunts.
71 yloid-beta (Abeta) across the human cerebral capillary bed to determine whether transport into the bl
72 en proposed to expose parts of the pulmonary capillary bed to high pressure and vascular injury in hi
73 and mesangium associated with the glomerular capillary bed to maintain filtration barrier function.
76 -brain barrier (BBB) was observed across the capillary bed with the small molecule fluorescein, conco
77 nd marginal epithelial cell barriers and the capillary bed within the stria vascularis of the S1P(2)
78 higher number of non-anastomotic vessels and capillary beds within the matrix predisposes these regio
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