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1 reciprocal accumulation of these Abs in the peripheral circulation).
2 and higher Ly6C(Low)-expressing monocytes in peripheral circulation.
3 f SCID and was found to lack NK cells in his peripheral circulation.
4 t promotes rapid mobilization of CEPs to the peripheral circulation.
5 igher in the pleural compartment than in the peripheral circulation.
6 ascent eosinophils from bone marrow into the peripheral circulation.
7 ors and in breast tumor cells present in the peripheral circulation.
8 corresponding increase of human cells in the peripheral circulation.
9 cytokines would recruit donor cells into the peripheral circulation.
10 e liver in 16 of the 35 patients, but not in peripheral circulation.
11 r treatment mobilizes OC precursors into the peripheral circulation.
12 al after it can no longer be detected in the peripheral circulation.
13 e of appearance of ingested nutrients in the peripheral circulation.
14 ins, are also present in soluble form in the peripheral circulation.
15 hysiological euglycaemia on the state of the peripheral circulation.
16 uration, and survival of erythrocytes in the peripheral circulation.
17 drugs and sex differences, and detectable in peripheral circulation.
18 ebral autonomic activation compared with the peripheral circulation.
19 microglia), the neurovascular unit, and the peripheral circulation.
20 s the brain from toxic substances within the peripheral circulation.
21 traits that are routinely measurable in the peripheral circulation.
22 hormone glucagon-like peptide (GLP)-1 in the peripheral circulation.
23 and exchange interface between the brain and peripheral circulation.
24 l egress from the bone marrow niche into the peripheral circulation.
25 ges at the blood-brain barrier and/or in the peripheral circulation.
26 n was greater in the retina but lower in the peripheral circulation.
27 he local site of infection compared with the peripheral circulation.
28 old mobilization in leukemic blasts into the peripheral circulation.
29 rkedly reduced but detectable B cells in the peripheral circulation.
30 he tumor draining lymph nodes but not in the peripheral circulation.
31 ecreases in these NKT cell parameters in the peripheral circulation.
32 ogical Abeta and IgM concentrations found in peripheral circulation.
33 d NO-dependent vasodilator mechanisms in the peripheral circulation.
34 D8(+) T cells, were rapidly decreased in the peripheral circulation.
35 bited profound T cell lymphocytopenia in the peripheral circulation.
36 IGF-1R+CD4+CD3+ cells as those found in the peripheral circulation.
37 ss of infected B cells from lymph nodes into peripheral circulation.
38 mobilization of myeloid lineage cells to the peripheral circulation.
39 ethanol levels in the coronary sinus and the peripheral circulation.
40 endothelium-dependent vasodilation in human peripheral circulation.
41 as selection in the thymus and homing in the peripheral circulation.
42 testinal beta-glucosidases for uptake to the peripheral circulation.
43 cocaine can inhibit NE reuptake in the human peripheral circulation.
44 to permit sequestration of parasites in the peripheral circulation.
45 rauma may induce mobilization of CEPs to the peripheral circulation.
46 -forming units-granulocyte-macrophage to the peripheral circulation.
47 parasite stage found in large numbers in the peripheral circulation.
48 e blood flow towards the brain and away from peripheral circulations.
49 ercentage of surface IgM(dim) B cells in the peripheral circulation (0.08% compared with 5-20% in hea
51 ization or augment EPC mobilization into the peripheral circulation after injury in endothelial nitri
52 increased deformability and reappear in the peripheral circulation, allowing uptake by mosquitoes.
53 rogenitor (MPP) cells in the bone marrow and peripheral circulation, an increase in populations of ea
54 cocaine can inhibit NE reuptake in the human peripheral circulation and (b) whether the NE-mediated p
55 luble receptor, sTNFp55) is increased in the peripheral circulation and amniotic fluid of women with
56 ssing cells mobilize PMNs and HSPCs into the peripheral circulation and are therapeutically useful fo
57 ro culture method, low parasite densities in peripheral circulation and asynchronous parasite develop
59 d in the bone marrow can be mobilized to the peripheral circulation and can colonize endothelial flow
61 mparisons are made to recent advances in the peripheral circulation and current gaps in our knowledge
62 (Ang II) is a potent vasoconstrictor in the peripheral circulation and has been implicated in many c
63 Cs are mobilized from the bone marrow to the peripheral circulation and home to the sites of new vess
65 em or progenitor cells were increased in the peripheral circulation and incorporated into the site of
66 lts demonstrated that BMSCs can recruit from peripheral circulation and participate in wound healing
67 n magnocellular cells that supply AVP to the peripheral circulation and project to limbic structures
69 ered to be the recruitment of cells from the peripheral circulation and the re-entry of mature cells
70 sulin balance between the hepatic portal and peripheral circulations and thereby avoid the complicati
71 rom the lungs to the tissue but forms in the peripheral circulation, and (iii) SNO-Hb and S-nitrosoth
72 a complex interplay of cardiac remodelling, peripheral circulation, and concomitant features includi
73 are able to leave the lymph node, enter the peripheral circulation, and migrate to the s.c. immuniza
74 , we examined etanet, central haemodynamics, peripheral circulation, and peripheral factors (skeletal
75 ities of ventilatory control, the lungs, the peripheral circulation, and skeletal muscle appear to co
76 nt a predominant cell source of IL-11 in the peripheral circulation, and the percentage of IL-11(+)CD
77 owever, did not correlate with levels in the peripheral circulation, and there were no T cells or an
78 ent of occlusive disease in the coronary and peripheral circulations, and traditional pharmacotherape
79 elevant, since elevated anandamide levels in peripheral circulation are associated with spontaneous p
80 dulates the balance of T cell subsets in the peripheral circulation as well as multiple inflammatory
83 ific CD8(+) T cells can be maintained in the peripheral circulation at high frequency in the absence
85 CD8+ cells and decreased NK1.1+ cells in the peripheral circulation at the time of transplantation.
86 tes are the predominant asexual stage in the peripheral circulation but are rarely investigated in th
87 c cardiovascular disease in the coronary and peripheral circulations but not the cerebrovasculature.
88 LSP and RAG-1+ ELP were both present in the peripheral circulation, but RAG-1+ ELP had no exact coun
89 , injected labeled MSCs had cleared from the peripheral circulation by 15 minutes after injection.
90 ngent selection either in the bone marrow or peripheral circulation by deletion, induction of anergy,
91 E degeneration, BMCs were mobilized into the peripheral circulation by granulocyte-colony stimulating
92 T cells, the predominant yd T cell subset in peripheral circulation, by mechanisms independent of tum
93 ence to show that injecting insulin into the peripheral circulation bypasses first-pass hepatic insul
94 on triggered by exposure of TNF-alpha in the peripheral circulation can aggravate the accumulation of
95 t appears that BMCs, when mobilized into the peripheral circulation, can home to focal areas of RPE d
97 ained release of platelets directly into the peripheral circulation during both fetal and adult life
98 ted Lewis rats, but could be measured in the peripheral circulation during small bowel allograft reje
99 expressing granulocytes were obtained in the peripheral circulation during the early posttransplant p
101 parating the central nervous system from the peripheral circulation, ensuring brain homeostasis and f
102 NGFR+/TK+ donor lymphocytes persisted in the peripheral circulation for 6 months in both syngeneic an
103 nts had persistent donor class II DNA in the peripheral circulation for at least 1 year after transpl
105 erotic occlusive disease in the coronary and peripheral circulations; however, long-term results are
107 and oxytocin (OT) levels in the IPS and the peripheral circulation in nine normal volunteers, before
108 n be mobilized from the bone marrow into the peripheral circulation in response to a number of stimul
109 er over time and failed to mobilize into the peripheral circulation in response to cytokine stimulati
110 ashion to attenuate its own release into the peripheral circulation in response to increased plasma o
112 s HPT progenitor cells from the HPT into the peripheral circulation in the hemolymph and strongly red
113 r's disease (AD), whether immune proteins in peripheral circulation influence the rate of amyloid-bet
114 dy suggest that fetal cells migrate from the peripheral circulation into multiple organs in women wit
115 n of the thymus, a low CD3 percentage in the peripheral circulation is also associated with a CD8(low
118 ole of the renin-angiotensin system (RAS) in peripheral circulation is well characterized, we still l
119 erial tissue and hydraulic resistance in the peripheral circulation jointly impact haemodynamics as M
120 metabolic dysfunction and upon release into peripheral circulation may exacerbate pathophysiology co
121 erve activity seems to act opposingly to the peripheral circulation, mediated at least in part by cha
122 clusion, an adequate insulin delivery in the peripheral circulation, obtained by islet transplantatio
123 es more CD4(+) T cells than basophils in the peripheral circulation of filaria-infected patients, the
125 e, the presence of normal blood cells in the peripheral circulation of neonatal and adult sph/sph mic
126 that KLK4-specific CD4 T cells exist in the peripheral circulation of normal male donors and the ide
127 to muscarinic stimulation is impaired in the peripheral circulation of patients with congestive heart
128 ulating tumor cells (CTCs) isolated from the peripheral circulation of patients with metastatic color
129 specific CD8+ T cells were determined in the peripheral circulation of patients with squamous cell ca
130 y, IL-10 must either access the CNS from the peripheral circulation or be delivered directly to it by
131 ar proteins not previously identified in the peripheral circulation or have functional roles relevant
132 ic, with the capacity to enter skin from the peripheral circulation, patrol within tissue, and migrat
133 of high-avidity autoreactive T cells in the peripheral circulation, perhaps due to this capability o
134 to the delivery of viable platelets into the peripheral circulation (peripheral platelet mass turnove
135 t displace the parasite from the deep to the peripheral circulation, promoting its elimination at the
136 (patrolling) monocytes in the heart and the peripheral circulation provides evidence that the massiv
137 monstrate that overexpression of SDF1 in the peripheral circulation results in the mobilization of he
138 tor cells (EPCs) from the bone marrow to the peripheral circulation (see the related article beginnin
139 s that the MUC1 alpha chain is shed into the peripheral circulation, sequesters circulating antitande
140 termine the proportion of each subset in the peripheral circulation, spleen, and bronchotracheal lymp
141 is found more commonly in the liver than in peripheral circulation, suggesting a tissue-specific loc
142 ighlight recent experimental findings in the peripheral circulation that have added valuable insight
143 otective interface between the brain and the peripheral circulation that maintains the extracellular
144 As thymocytes leave the thymus and enter the peripheral circulation, the expression of CXCR4 is again
145 r necrosis factor-alpha (TNF-alpha) in their peripheral circulation, the structural and functional ef
148 to the recruitment of mature cells from the peripheral circulation to the development of airway eosi
150 ves a redistribution of blood flow away from peripheral circulations towards essential vascular beds,
152 xtracellular osmotic conditions found in the peripheral circulation vs. the bone marrow could dictate
153 hocytes subsequently traffic to the lungs or peripheral circulation, we compared the immune responses
154 ve of neutrophils that are released into the peripheral circulation where they traverse to sites of i
155 CR4 interaction and releases BM PCs into the peripheral circulation, where the mobilized cells are re
156 one of the major antigen presenting cells in peripheral circulation, which are chronically exposed to
157 ecially relevant to pain caused by issues of peripheral circulation, which is commonly observed in di
158 and HIV-positive patients compared with the peripheral circulation with a focus on myeloid cells and
159 s (OCs), CD34+ cells were mobilized into the peripheral circulation with granulocyte colony-stimulati
160 thesized that elevation of SDF1 level in the peripheral circulation would result in mobilization of p