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1 d-type mice (n=6), we found less bacteria in postcapillary (60+/-6 versus 32+/-5 bacteria) and collec
2 nteract with adherent leukocytes in inflamed postcapillary and collecting venules.
3 ecommended to differentiate between isolated postcapillary and combined pre-/postcapillary pulmonary
4 ary pulmonary hypertension (IpcPH), combined postcapillary and precapillary (CpcPH), or exercise PH.
5 ith preserved ejection fraction and combined postcapillary and precapillary pulmonary hypertension we
6 ith preserved ejection fraction and combined postcapillary and precapillary pulmonary hypertension, w
7 ith preserved ejection fraction and combined postcapillary and precapillary pulmonary hypertension.
8 ations was caused by widespread adhesion and postcapillary blockage.
9 alciparum-infected erythrocytes (Pf-IRBC) in postcapillary brain endothelium is a hallmark of cerebra
10 diately improved after TAVI in patients with postcapillary combined (57.8+/-14.1 versus 50.4+/-17.3 m
11 helial venules, a compartment of specialized postcapillary endothelial cells that are characterized b
12 ed to epinephrine with increased adhesion to postcapillary endothelium in nude mice.
13 od cells (RBCs) and leukocytes as they enter postcapillary expansions, but the details of the fluid d
14                          We further simulate postcapillary flow of SS-RBC suspensions with different
15 de lymphocytes (LNCs) tethered and rolled in postcapillary high endothelial venules (HEVs) and to a l
16 left ventricular end-diastolic pressure into postcapillary (left ventricular end-diastolic pressure,
17 at parasitized erythrocytes can sequester in postcapillary microvessels of critical tissues such as t
18  of 433 (75%) patients and was predominantly postcapillary (n=269/325; 82%).
19  cohort of 255 patients with PH from pre and postcapillary pathogeneses was assembled from 2 centers.
20                                              Postcapillary PH is associated with a decreased survival
21                                              Postcapillary PH is generally associated with a diastoli
22                       Finally, patients with postcapillary PH were divided into isolated (n=220) and
23                                              Postcapillary PH with elevated vascular gradients and pu
24 n, and shorter life expectancy than isolated postcapillary PH.
25 ombination of mean PAP and mean PAWP defines postcapillary PH.
26 ose with HFpEF and combined precapillary and postcapillary PH.
27 his combination of criteria defines isolated postcapillary PH.
28 tality to physiological measures of pre- and postcapillary PH.
29 een isolated postcapillary and combined pre-/postcapillary pulmonary hypertension (Cpc-PH) in left he
30  is referred to as combined precapillary and postcapillary pulmonary hypertension (CpcPH).
31 (PH) is classified as precapillary, isolated postcapillary pulmonary hypertension (IpcPH), combined p
32 pulmonary arterial pressures versus isolated postcapillary pulmonary hypertension (P<0.05).
33                            Five patients had postcapillary pulmonary hypertension at rest.
34  arterial hypertension, and in patients with postcapillary pulmonary hypertension because of left hea
35 sion of various causes, including those with postcapillary pulmonary hypertension due to left heart d
36 lmonary capillary wedge pressure (PCWP) with postcapillary pulmonary hypertension even at rest, which
37 re than those with combined precapillary and postcapillary pulmonary hypertension HFpEF (n=31; intera
38                           The remainder have postcapillary pulmonary hypertension secondary to left v
39 es a subset of PH-LHD patients from isolated postcapillary pulmonary hypertension to Cpc-PH, which is
40 stcapillary pulmonary hypertension, combined postcapillary pulmonary hypertension, and pulmonary arte
41 ined 4 hemodynamic groups: control, isolated postcapillary pulmonary hypertension, combined postcapil
42 evere, degenerative AS have exercise-induced postcapillary pulmonary hypertension.
43 s in patients with combined precapillary and postcapillary pulmonary hypertension.
44 cular resistance, known as combined pre- and postcapillary pulmonary hypertension.
45 ich may classify Cpc-PH patients as isolated postcapillary pulmonary hypertension.
46 nt of left ventricular failure in those with postcapillary pulmonary hypertension; and hydroxyurea or
47 ACh was to induce a reduction in the pre- to postcapillary resistance ratio.
48 el flow past multiple adherent leukocytes in postcapillary size vessels.
49  increased leukocyte rolling and adhesion in postcapillary skin venules that were both inhibited afte
50 e circulation and reduced deposition in deep postcapillary vascular beds.
51 terations in sRBC/endothelium adhesion under postcapillary venular conditions.
52 was widespread basal plasma extravasation in postcapillary venular endothelia in NEP-/- mice, which w
53 V-CD8eNOSGFP (ECV-304 transfected cells) and postcapillary venular endothelial cells (CVEC).
54 926 (derived from human umbilical vein), and postcapillary venular endothelial cells (derived from bo
55 Duffy Ag expressed on RBCs, capillaries, and postcapillary venular endothelial cells binds selective
56 translocation and permeability properties of postcapillary venular endothelial cells.
57                                        Under postcapillary venular shear stress (1 dyne/cm2), sickle
58              Our results show that capillary-postcapillary venule diameter ratio, RBC configuration,
59 rs of vasoconstriction, edema formation, and postcapillary venule leakage, followed by ex vivo functi
60        The number of leukocytes in capillary-postcapillary venule units per 4-second image sequence (
61 d cells as they flow from a capillary into a postcapillary venule using a lattice Boltzmann approach.
62 We constructed composite models of the human postcapillary venule, combining ECs with PCs or PC-depos
63           In flow chamber experiments, under postcapillary venule-like flow conditions, the pretreatm
64 l endothelial inflammation at the collecting postcapillary venule.
65              Most of the leakage occurred in postcapillary venules (< 40-microns diameter), whereas m
66  of 478 microbubbles (13.6%) observed in six postcapillary venules 11 to 30 microm in diameter and 24
67 s and vascular permeability were measured in postcapillary venules after 4-hour and 1-hour reperfusio
68  TDLN cells began migrating across pulmonary postcapillary venules and first appeared within metastas
69 e blood were investigated in mouse cremaster postcapillary venules and in flow chambers coated with P
70 of neutrophils along the endothelial wall of postcapillary venules and integrin-mediated arrest.
71 ity begins in the superficial arterioles and postcapillary venules and progresses to the capillary be
72 ross HEVs is faster than across conventional postcapillary venules and requires a unique set of adhes
73  borders between endothelial cells that line postcapillary venules at that site.
74 ation of 40-kDa dextran from capillaries and postcapillary venules but had no effect on extravasation
75 ting leukocytes were labeled and observed in postcapillary venules for adhesion before and up to 120
76 l cells from human renal arteries as well as postcapillary venules from lymphoid tissue.
77 theless, the number of leukocytes rolling on postcapillary venules in an E-selectin-dependent manner
78 bone marrow (BM) endothelium and to inflamed postcapillary venules in an E-selectin-dependent manner.
79 phocyte-associated Ag tether on the walls of postcapillary venules in inflamed skin via interaction w
80 othelial venules (HEV) are specialized plump postcapillary venules in lymphoid tissues that support h
81  (PfEMP1) mediates parasite sequestration in postcapillary venules in P. falciparum malaria.
82 es can be found marginalized in the lumen of postcapillary venules in postmortem brain tissue derived
83 nd sialyl Lewis(x) (sLe(x)) to interact with postcapillary venules in the absence of PSGL-1.
84 ) increases clearance of macromolecules from postcapillary venules in the in situ oral mucosa and, if
85 duced neutrophil rolling and adhesion to the postcapillary venules in the mouse ears is significantly
86 , E-selectin, and ICAM-1 are up-regulated on postcapillary venules in the retina.
87  retinal perivascular macrophages resided on postcapillary venules in the superficial vascular plexus
88 eukocyte trafficking across mouse mesenteric postcapillary venules in vivo.
89 s required to sustain neutrophil adhesion in postcapillary venules in vivo.
90 arkedly reduced (>60%) leukocyte adhesion to postcapillary venules in wild type and Fpr1(-/-), but no
91 ting therapies evoke transdifferentiation of postcapillary venules into inflamed high-endothelial ven
92 Transendothelial migration of neutrophils in postcapillary venules is a key event in the inflammatory
93 d that the abundance of leukocyte rolling in postcapillary venules is due to interactions between red
94                    Plasma extravasation from postcapillary venules is one of the earliest steps of in
95 ncreased expression of P-selectin protein in postcapillary venules of all vital organs after trauma.
96 ks leukocyte extravasation in lung, skin and postcapillary venules of cremaster muscle.
97 s the leukocyte-endothelial cell adhesion in postcapillary venules of HCD mice.
98                         Leukocyte rolling in postcapillary venules of inflamed tissues is reduced in
99 ng and adhesion were measured in cremasteric postcapillary venules of septic and control rats using i
100 med soluble ICs are rapidly deposited in the postcapillary venules of the cremaster microcirculation,
101 nt microbeads flowing within mildly inflamed postcapillary venules of the cremaster muscle in vivo.
102 in vivo, studied by intravital microscopy in postcapillary venules of the cremaster muscle, was marke
103 dothelial Tie-2 results in leak formation in postcapillary venules of the inflamed cremaster muscle a
104 was restricted to focal areas of the retinal postcapillary venules of the inner vascular plexus.
105 s leukocyte-endothelial cell interactions in postcapillary venules of the mouse cremaster muscle.
106 yte-endothelial cell adhesion in cremasteric postcapillary venules of wild-type (WT) mice, CuZn-super
107 sed to monitor L/E and P/E adhesion in brain postcapillary venules of wild-type (WT), SOD1 transgenic
108 mber of adherent and emigrated leukocytes in postcapillary venules of WT HCD mice was significantly h
109 n is important in inflammation and occurs in postcapillary venules over a wide range of wall shear st
110 se model suggest that adherent leukocytes in postcapillary venules play a critical role in vaso-occlu
111          E-selectin and P-selectin on dermal postcapillary venules play critical roles in the migrati
112  that P-selectin and E-selectin expressed on postcapillary venules play overlapping roles in the recr
113 d leukocyte-endothelial cell interactions in postcapillary venules revealed that CXCL1-induced neutro
114 h endothelial venules (HEVs) are specialised postcapillary venules that specifically serve this funct
115 thelium may regulate neutrophil migration in postcapillary venules through the presentation of variou
116 ltered adhesive interactions within inflamed postcapillary venules under conditions of blood flow by
117  reveal that the basement membrane of dermal postcapillary venules undergoes changes in structure and
118                         Wall shear stress in postcapillary venules varies widely within and between t
119   Intravital video microscopy of cremasteric postcapillary venules was performed.
120                                              Postcapillary venules were dilated, and up to 70% of the
121                                     Tracheal postcapillary venules were visualized and leukocyte kine
122 hodamine-stained leukocytes were observed in postcapillary venules with analysis for adhesion and rol
123 ed a network of arterioles, capillaries, and postcapillary venules with continuous blood flow.
124 ntibody fluorescence intensity in submucosal postcapillary venules with the use of intravital microsc
125                     Intravital microscopy of postcapillary venules within the cremaster muscle of mic
126 ial permeability and leakage of albumin from postcapillary venules within the dura mater.
127  increased in the superficial arterioles and postcapillary venules, 2 weeks after the onset of diabet
128 sed luminally by endothelial cells that line postcapillary venules, a primary site of leukocyte recru
129 ed adhesion of leukocytes in capillaries and postcapillary venules, but no such adhesion in arteriole
130 about midway between terminal arterioles and postcapillary venules, challenging the classical concept
131  adhesion of leukocytes to discrete sites on postcapillary venules, followed by upregulation of adhes
132 mbranes that arise from inflamed venules and postcapillary venules, increase in size as the disease p
133 f leukocyte-endothelial cell interactions in postcapillary venules, leading to leukocyte recruitment
134       Neutrophil extravasation occurs across postcapillary venules, structures composed of endothelia
135 including endothelial cells of capillary and postcapillary venules, the epithelial cell of kidney col
136 r physiological shear stress consistent with postcapillary venules, we found a significant increase i
137  designed to approximate physiologic flow in postcapillary venules, we have characterized a rolling i
138                                           In postcapillary venules, where shear stress is approximate
139 ill offer an effective, direct access to the postcapillary venules, where the target event (leukocyte
140 eukocyte rolling and adherence in mesenteric postcapillary venules.
141 ma that tumor vessels arise exclusively from postcapillary venules.
142 erial/venous characteristics and derive from postcapillary venules.
143 re weeks exhibit an inflammatory response in postcapillary venules.
144  occur primarily via capillaries rather than postcapillary venules.
145 nomethyl-L-arginine (NMA) on skeletal muscle postcapillary venules.
146 rolling eosinophils, but not neutrophils, to postcapillary venules.
147 y designed to mimic physiologic flow through postcapillary venules.
148 ophages and erythrocytes) in capillaries and postcapillary venules.
149 leukocyte rolling and adhesion in mesenteric postcapillary venules.
150 rteries and veins, most arterioles, and some postcapillary venules.
151 utrophil emigration across murine mesenteric postcapillary venules.
152 ophil but not eosinophil rolling in inflamed postcapillary venules.
153 and in a flow system to mirror conditions at postcapillary venules.
154 hat activate leukocytes to transmigrate from postcapillary venules.
155 nd pericytes (PCs) that form the wall of the postcapillary venules.
156 deficient in in vivo crawling and TEM in the postcapillary venules.
157 o the relatively low-oxygen and low-velocity postcapillary venules.
158  and E-selectin-dependent adhesion in airway postcapillary venules.
159 selectins to roll and integrins to arrest in postcapillary venules.
160 ualize rolling of endogenous Tregs in dermal postcapillary venules.
161  pial vessels and in deep ascending cortical postcapillary venules.
162 y channels connecting terminal arterioles to postcapillary venules.
163 displayed on endothelial cells in intestinal postcapillary venules.
164 shear stress levels similar to that found in postcapillary venules.
165 tructure and increases leukocyte adhesion in postcapillary venules.
166 sults in vasculitic lesions predominantly in postcapillary venules.
167 enous malformations, and focal dilatation of postcapillary venules.
168  gap formation, and protein extravasation in postcapillary venules.
169 small lymphocytes for the endothelium of the postcapillary venules.
170 rolling effector and central memory cells in postcapillary venules.
171 e and continue to roll as elongated cells in postcapillary venules.
172 es as the main L-selectin ligand in inflamed postcapillary venules.
173 minants of the initiation of cell rolling in postcapillary venules.
174  in tissues that possess receptors for SP in postcapillary venules; (ii) liposome material in these t
175 ery catheterization with blood sampling from postcapillary (wedged balloon) and precapillary (unwedge

 
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