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1 nsion of anastomotic connectivity within the capillary bed.
2 lar dilation, increasing blood flow into the capillary bed.
3 apid and heterogeneous BBB disruption in the capillary bed.
4 eakage occurred from a small fraction of the capillary bed.
5 scular endothelial-cell proliferation of the capillary bed.
6 od supply with no increase from a peripheral capillary bed.
7 iameter before the blood enters the alveolar capillary bed.
8  the effective shunting of blood through its capillary bed.
9 pread of proinflammatory signals in the lung capillary bed.
10  postcapillary venules and progresses to the capillary bed.
11 arteriovenous shunt), without an intervening capillary bed.
12 ), representing a simple in vitro model of a capillary bed.
13 s lactate from the glucose received from its capillary bed.
14 mit transmission of systemic pressure to the capillary bed.
15 riovenous connections without an intervening capillary bed.
16  effects of uniform filling of the pulmonary capillary bed.
17  entering the penetrating arterioles and the capillary bed.
18  transition zone and distal pericytes of the capillary bed.
19 poxia and hyperoxia in the different retinal capillary beds.
20  kidney vasculature induce specialization of capillary beds.
21 f control is peripheral resistance in tissue capillary beds.
22 uctural elements surrounding glomerulus-like capillary beds.
23 lation that was associated with disorganized capillary beds.
24 oles and "downstream" propagation into local capillary beds.
25 he preferential targeting of newly generated capillary beds.
26 c BL, was found between capillaries in dense capillary beds.
27  vessels is crucial for morphogenesis of the capillary beds.
28 ed at high microvascular pressures in intact capillary beds.
29 ulature including penetrating arterioles and capillary beds.
30 pillary flow while protecting the downstream capillary bed and brain tissue from adverse pressure flu
31 1.99.25 induced PLVAP expression in the deep capillary bed and enabled extravasation of small and lar
32 nary artery pressure closer to the pulmonary capillary bed and LA pressure closer to the venoatrial j
33 dothelial Ca2+ conduction occurs in the lung capillary bed and that Cx43-containing gap junctions med
34          The endothelial cell network in the capillary bed and the arterial and venous vessels provid
35   Immunofluorescence to anti-ET-1 within the capillary bed and veins of the retina in diabetic insuli
36 estream dark-field imaging in the sublingual capillary bed and videocapillaroscopy at the nailfold.
37 perience shear forces equivalent to those in capillary beds and are made to flow through capillary-li
38          We find that activation of TRPA1 in capillary beds and post-arteriole transitional segments
39 flow, including potential contributions from capillary beds and surrounding tissue.
40 and demarginated from microfluidic models of capillary beds and veins, respectively, increased after
41 olar input, establishing the backbone of the capillary bed, and 2) short-range sprouts that contribut
42 ral inlet vessel, branched into an extensive capillary bed, and coalesced into a single outlet vessel
43 bodies and processes cover around 90% of the capillary bed, and here we show that these cells play a
44 abilize the enzyme, localize LpL in specific capillary beds, and route lipoprotein lipids to the unde
45  include reduction in vessel number, loss of capillary beds, and the formation of hemorrhagic vascula
46 retinal neovascularization, formation of new capillary beds, and the presence of new blood vessels ab
47 leukocytes adhere to solid surfaces, such as capillary beds, and the subsequent migration through the
48                                 We find that capillary beds are more susceptible to occlusions than t
49  mice, we identifed pericytes throughout the capillary bed as key drivers of an immune reactive oxyge
50 distribution differences in tumor-associated capillary bed at different stages of disease progression
51  to allow complete filling of the myocardial capillary bed by microbubbles.
52 particle local accessibility to flow area of capillary beds by co-circulating red blood cells (RBC).
53    We demonstrate that for RBCs entering the capillary bed close to the cortical surface (< 400 mum)
54 imately 7.5% in venous blood leaving the CNS capillary bed compared to arterial blood, indicating eff
55 viously unknown role for Abeta in regulating capillary bed density, providing new insight into the no
56 se effects were dose-dependent and increased capillary bed density, though there was no effect on lar
57                        This implies that the capillary bed dominates the hydrodynamic resistance of b
58  cells can spread to organs beyond the first capillary bed downstream from the primary tumor.
59 tudy, EMBs consisting of an afferent artery, capillary beds, efferent vein, and surrounding parenchym
60     Control cells became lodged in the first capillary bed encountered in the tail, whereas cells ove
61 d the existing wealth of knowledge regarding capillary bed formation, studies for the development of
62 tly to the stria vascularis and protects its capillary bed from high perfusion pressure.
63   vILC3s are distributed broadly in alveolar capillary beds from which inhaled pathogens enter the lu
64                                          The capillary bed in muscle and spinal cord was normal in pr
65 kidney, and more prominent congestion in the capillary beds in the lungs and heart.
66 he nerve fiber layer and only contributes to capillary beds in the neck of the nerve head.
67 he liver may be a simple strategy to protect capillary beds in the retina and in other peripheral tis
68 s through the regression and regeneration of capillary beds in the skin, indicating that tissue regen
69  eyes induced neovascularization in multiple capillary beds, including those not responsive to VEGF a
70 r or not the developmental stage of the deep capillary bed is critical for occurrence of neovasculari
71 natal days 5 and 7, the period when the deep capillary bed is developing.
72 asmodium falciparum-infected erythrocytes in capillary beds is a characteristic feature of severe mal
73 tween arteries and veins without intervening capillary beds is the primary pathology of arteriovenous
74  of erythrocytes, and entrapment in the lung capillary bed, largely due to their poor biocompatibilit
75  layers and the most delayed response in the capillary bed of layer I.
76 lets are released from megakaryocytes in the capillary bed of the lung, this concept has not been uni
77 provide evidence for platelet release in the capillary bed of the lungs during stimulated as well as
78 ascularization that originates from the deep capillary bed of the retina and grows into the subretina
79 strate new vessels originating from the deep capillary bed of the retina that extend beneath the phot
80  neovascularization originated from the deep capillary bed of the retina, but it was more extensive a
81                 This primarily occurs in the capillary beds of muscle and adipose tissue.
82       We hypothesized that bulk perfusion in capillary beds of the large mammalian heart not only enh
83 rth, there was increased density of the deep capillary bed on postnatal day (P) 11 that returned to n
84 s blood to bypass gas exchange and pulmonary capillary bed processing.
85 ich source blood from pial arterioles to the capillary bed, profoundly impact perfusion throughout ne
86                                    Synthetic capillary beds, randomly- and radially-oriented, and opt
87 dividual RBC trajectories reveal that in the capillary bed RBCs preferentially move in plane.
88 phs and vector representations for the dense capillary bed remains a bottleneck in many applications.
89 hains of hemoglobin when deoxygenated within capillary beds, resulting in sickle-shaped red blood cel
90                               The glomerular capillary bed seems to contribute to all subtypes of rTx
91 ith sprouts from retinal vessels in the deep capillary bed seen on P14 and vessels reaching the subre
92              The astrocytes accompanying the capillary bed showed a redistribution in the glaucomatou
93                  The choriocapillaris is the capillary bed supporting the metabolism of photoreceptor
94              The glomerulus is a specialized capillary bed that is involved in urine production and B
95              The density and architecture of capillary beds that form within a tissue depend on many
96 ferences, on the fluid flow across the tumor capillary bed, the lymphatic drainage, and the IFP.
97 ystemic venous blood to bypass the pulmonary capillary bed through anatomic right-to-left shunts.
98 yloid-beta (Abeta) across the human cerebral capillary bed to determine whether transport into the bl
99 en proposed to expose parts of the pulmonary capillary bed to high pressure and vascular injury in hi
100 and mesangium associated with the glomerular capillary bed to maintain filtration barrier function.
101 stitial fluid flow as might occur to connect capillary beds to venules or lymphatics.
102             Development and integrity of the capillary bed was examined in skeletal muscle and spinal
103  microfluidic device mimicking the pulmonary capillary bed, we show that the dynamics of THP1 monocyt
104                          Pericytes reside in capillary beds where they share a basement membrane with
105 ation, circulating tumour cells (CTCs) enter capillary beds, where they experience mechanical constri
106 -brain barrier (BBB) was observed across the capillary bed with the small molecule fluorescein, conco
107 ar abnormalities in the superficial and deep capillary bed with worse retinopathy as measured on the
108 nd marginal epithelial cell barriers and the capillary bed within the stria vascularis of the S1P(2)
109 higher number of non-anastomotic vessels and capillary beds within the matrix predisposes these regio

 
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