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1 on of TNF-alpha and MIP-2 in bronchoalveolar lavage fluid.
2 cylcarnitines are detectable in normal human lavage fluid.
3 nia were observed in blood, dermis, and lung lavage fluid.
4 crophages and eosinophils in bronchoalveolar lavage fluid.
5 ers of inflammatory cells in bronchoalveolar lavage fluid.
6 racts, nasal secretions, and bronchoalveolar lavage fluid.
7 ells and readily detected in bronchoalveolar lavage fluid.
8 ion using RNA extracted from bronchoalveolar lavage fluid.
9 entage of eosinophils in the bronchoalveolar lavage fluid.
10 triene (cysLT) levels were measured in nasal lavage fluid.
11 ssociated with increased IL-17 production in lavage fluid.
12 nd cytokine concentration in bronchoalveolar lavage fluid.
13 nfiltration and interleukin-5 (IL-5) in lung lavage fluid.
14 rophages were detected in bronchial alveolar lavage fluid.
15 sinophils were enumerated in bronchoalveolar lavage fluid.
16 ng epithelium as detected in bronchoalveolar lavage fluid.
17 and IL-13, but not IL-5, in bronchoalveolar lavage fluid.
18 ammatory cell numbers in the bronchoalveolar lavage fluid.
19 Cells were counted in bronchoalveolar lavage fluid.
20 in saliva correlates with levels in vaginal lavage fluid.
21 IL-33, and eotaxin levels in bronchoalveolar lavage fluid.
22 eduction in Th2 cytokines in bronchoalveolar lavage fluid.
23 lular necrosis, in cell-free bronchoalveolar lavage fluid.
24 d Th1 and Th2 cytokines were analyzed in the lavage fluid.
25 hemoattractant MCP-1 in lung bronchoalveolar lavage fluid.
26 increase in the levels of CCL4 in peritoneal lavage fluid.
27 s, and lower cytokine levels in the alveolar lavage fluid.
28 and KLK14, were assessed in bronchoalveolar lavage fluid.
29 reducing LPA 18:2 content in bronchoalveolar lavage fluid.
30 tion and after culture with broncho-alveolar lavage fluid.
31 imilar results were found in bronchoalveolar lavage fluids.
32 3 measured by ELISA in their bronchoalveolar lavage fluids.
34 gnificantly increased in the bronchoalveolar lavage fluid 48 hours after segmental allergen challenge
35 ns (5 cerebrospinal fluid, 7 bronchoalveolar lavage fluid, 5 plasma, 2 serum, and 1 nasopharyngeal as
38 nusitis (CRS), as well as in bronchoalveolar lavage fluid, after segmental allergen challenge in alle
39 ncreased ALI (as assessed by bronchoalveolar lavage fluid albumin concentration) in both NADPH oxidas
40 ith sHLA-G concentrations in bronchoalveolar lavage fluid among asthmatic subjects with an asthmatic
41 ammatory cytokines and eosinophil numbers in lavage fluid and augmented the histopathologic evidence
42 neutrophil numbers and KC in bronchoalveolar lavage fluid and caused slight peribronchiolar inflammat
43 ges in inflammatory cells in bronchoalveolar lavage fluid and cytokine expression in lung tissue.
45 Th2 cytokines were found in bronchoalveolar lavage fluid and draining lymph node cells of Nur77-KO m
46 nt inflammation in blood and bronchoalveolar lavage fluid and exacerbations despite high systemic cor
47 DM, the levels of PGP in the bronchoalveolar lavage fluid and infiltration of neutrophils into the lu
48 le reproductive tract tissue, cervicovaginal lavage fluid and its intracellular metabolite (TFV dipho
49 numbers of leukocytes in the bronchoalveolar lavage fluid and lower expression of inflammatory chemok
56 phocytes, and macrophages in bronchoalveolar lavage fluid and lungs; inflammatory cell infiltrates in
57 ociated with lower lymphocyte percentages in lavage fluid and marginally lower plasma cortisol concen
58 NETs were also measured in bronchoalveolar lavage fluid and plasma from lung transplant patients wi
59 d in BOS versus normal lung tissues and both lavage fluid and plasma HA concentrations were increased
61 mmatory cell accumulation in bronchoalveolar lavage fluid and proinflammatory cytokines levels in lun
63 e presence of PRELP in human bronchoalveolar lavage fluid and showed that PRELP can be found in alveo
64 rophilic inflammation in the bronchoalveolar lavage fluid and Th1, Th2, and Th17 inflammation in the
65 ear leukocytes (PMNs) in the bronchoalveolar lavage fluid and the wet-to-dry lung weight ratio, a mea
66 s the major MMP found in the bronchoalveolar lavage fluids and bronchial biopsies from patients with
67 e detected in nasal wash and bronchoalveolar lavage fluids and in sera from mice intranasally inocula
68 uced accumulation of IL-6 in bronchoalveolar lavage fluids and NADPH oxidase (NOX) 2 and NOX4 protein
70 morphonuclear recruitment in bronchoalveolar lavage fluid), and lethality were evaluated in a pneumon
71 gher amounts of IL-17 in the bronchoalveolar lavage fluid, and (iii) more neutrophils in the lungs th
73 ll counts and neutrophils in bronchoalveolar lavage fluid, and had earlier influx of macrophages.
74 content and cell count in bronchial alveolar lavage fluid, and increased Evans Blue dye infiltration
75 C in lung tissue homogenate, bronchoalveolar lavage fluid, and lung LB was increased significantly in
77 odies was measured in tissue extracts, nasal lavage fluid, and sera by using multiplex bead arrays an
78 and challenged with OVA and bronchoalveolar lavage fluid, and the lungs were collected for assessing
79 emokines eotaxin and CCL2 in bronchoalveolar lavage fluid; and decreased pulmonary inflammation, as w
80 ater than 20% lymphocytes in bronchoalveolar lavage fluid; and three had findings on surgical lung bi
82 creased extracellular DNA in bronchoalveolar lavage fluid as well as in lung tissue, confirming the p
83 tissues, including lung and bronchoalveolar lavage fluid, as measured by H2-Db NP366 and PA224 tetra
84 oglobulin E were measured in bronchoalveolar lavage fluid at baseline and 24 h after allergen instill
85 s), and IgE were measured in bronchoalveolar lavage fluid at baseline and 24 hours after allergen ins
86 greater drug levels in lung, bronchoalveolar lavage fluid (BAL), and plasma compared to conventional
89 eased concentration in both bronchioalveolar lavage fluid (BALF) and blood of doxycycline-treated CCS
90 cles (EVs) are detectable in bronchoalveolar lavage fluid (BALF) and culture medium of lung epithelia
92 was to analyze cytokines in bronchoalveolar lavage fluid (BALF) and explore predicting factors of se
93 treptococcus pneumoniae, and bronchoalveolar lavage fluid (BALF) and lung CFU values were determined.
94 ics of GT and bmGT in serum, bronchoalveolar lavage fluid (BALF) and lungs of A. fumigatus-infected c
95 metabolites between matched bronchoalveolar lavage fluid (BALF) and plasma, identifies the degree of
96 ssess airway inflammation in bronchoalveolar lavage fluid (BALF) and Th2 responses in lung explants a
98 s were assessed in lungs and bronchoalveolar lavage fluid (BALF) by multiparametric flow cytometry.
100 characterized by increased broncho-alveolar lavage fluid (BALF) cells and cytokines (IL-6 and TNF-al
101 ed lung bacterial clearance, bronchoalveolar lavage fluid (BALF) characterization, lung histology, lu
102 ity decreased by 80% in COPD bronchoalveolar lavage fluid (BALF) due to serine protease cleavage, pri
103 the proinflammatory role of bronchoalveolar lavage fluid (BALF) exosomes in patients with sarcoidosi
105 ng of serum, lung tissue and bronchoalveolar lavage fluid (BALF) from a non-lethal mouse model with i
106 ne profiles were measured in bronchoalveolar lavage fluid (BALF) from children with CF (n = 57; 6.1 +
107 of two biomarkers present in bronchoalveolar lavage fluid (BALF) from chlorine gas exposed mice.
108 on neutrophils in blood and bronchoalveolar lavage fluid (BALF) from mechanically ventilated patient
110 mmation and cytokines in the bronchoalveolar lavage fluid (BALF) in a murine model of allergic asthma
111 (HCMV) DNA detection in the bronchoalveolar lavage fluid (BALF) indicates HCMV replication in the pu
112 h the observation that local bronchoalveolar lavage fluid (BALF) levels of vitamin D are severely def
114 ed controls, ozone increased bronchoalveolar lavage fluid (BALF) protein, a marker of lung permeabili
117 A04-neutralizing activity of bronchoalveolar lavage fluid (BALF) was observed following secondary CA0
120 arallel, adenosine levels in bronchoalveolar lavage fluid (BALF) were increased by approximately 3-fo
121 of Th2 and Th17 cytokines in bronchoalveolar lavage fluid (BALF), accompanied by an increment in tran
123 e levels in spleen cells and bronchoalveolar lavage fluid (BALF), and cellular distribution in BALF w
124 r 33 d after exposure, SpO2, bronchoalveolar lavage fluid (BALF), and histologic analyses were perfor
125 mber of cells and macrophages in bronchiolar lavage fluid (BALF), as well infiltrating inflammatory c
126 ice, with fewer cells in Wsh bronchoalveolar lavage fluid (BALF), despite similar levels of cytokines
127 g function measurements, and bronchoalveolar lavage fluid (BALF), serum, and lungs were collected on
129 ntent in MMP active forms of bronchoalveolar lavage fluids (BALf) from male C57BL/6 mice exposed to u
130 ntration of total protein in bronchoalveolar lavage fluids (BALF) from patients with sepsis-related a
131 activation, was detected in bronchoalveolar lavage fluids (BALF) in a macrophage- and neutrophil-dep
133 spiratory distress syndrome broncho-alveolar lavage fluid by 60%, whereas serum amyloid P replenishme
134 eased lung injury scores and bronchoalveolar lavage fluid cell numbers in control but not TREK-1-defi
136 rease in lung injury scores, bronchoalveolar lavage fluid cell numbers, and cellular apoptosis and a
138 munosuppressive functions of bronchoalveolar lavage fluid cells, inhibited bone marrow cell transendo
140 ing cellular accumulation in bronchoalveolar lavage fluid, collagen levels, and histologic changes.
141 endobronchial brushings and bronchoalveolar lavage fluid collected from 39 asthmatic patients and 19
143 nophil and T cell numbers in bronchoalveolar lavage fluid compared with those in diluent-treated or c
144 F production in the lung and bronchoalveolar lavage fluid compared with wild-type mice, without chang
148 eumonia demonstrated cytotoxic activity, and lavage fluid contained amyloid molecules, including olig
149 y inflammation and function, bronchoalveolar lavage fluid cytokine levels, and flow cytometry of lung
150 Outcome measures included: bronchoalveolar lavage fluid cytology to assess airway eosinophilia, pul
151 kines interleukin-5 (IL-5) and IL-13 in lung lavage fluid, decreased regulatory T cell-associated FOX
152 g cyto-/chemokine profile in bronchoalveolar lavage fluid, decreased TLR2/4 expression and NF-kappaB
153 tive microbiology applied to bronchoalveolar lavage fluid derived from infected segments proved an in
154 the proinflammatory role of bronchoalveolar lavage fluid-derived exosomes in asthmatic progression,
155 use, human CD49d(+) PMNs isolated from nasal lavage fluid during a viral respiratory tract infection
156 d dramatically increased in broncho-alveolar lavage fluid during acute respiratory distress syndrome.
157 frequency was significantly higher in nasal lavage fluid during acute respiratory symptoms in all su
158 okines and chemokines in the bronchoalveolar lavage fluid, enhanced bronchoalveolar cellular influx,
160 n important mediator in resolving tissue and lavage fluid eosinophilia in allergic mouse models.
161 ssed, the inflammatory cell content in nasal lavage fluids estimated, and the activation pattern of p
162 ic fibrosis underwent annual bronchoalveolar lavage fluid examination, and chest computed tomography.
165 counts were performed on the bronchoalveolar lavage fluid, followed by histological analysis of lung
167 Siglec-F ligand activity in bronchoalveolar lavage fluid fractions containing polymeric secreted muc
170 counts, and total protein in bronchoalveolar lavage fluid from acute respiratory distress syndrome 1.
175 inhibited by treatment with bronchoalveolar lavage fluid from inhibitory kappaB kinase beta transact
176 significantly higher in the bronchoalveolar lavage fluid from OVA/OVA than OVA/PBS mice and were una
177 H complexes were detected in bronchoalveolar lavage fluid from patients with acute respiratory distre
178 icant elevation of IL-17A in bronchoalveolar lavage fluid from patients with ARDS, and rIL-17A direct
180 were quantified in serum and bronchoalveolar lavage fluid from patients with CF, asthmatic patients,
181 ophilia were measured in the bronchoalveolar lavage fluid from patients with mild asthma 48 hours aft
182 s elevated in both serum and bronchoalveolar lavage fluid from Rasgrp1-deficient mice; 4) GM-CSF-spec
184 tokines were compared in the bronchoalveolar lavage fluid from WT and SP-D(-/-) mice after C. neoform
185 veolar epithelial cells with bronchoalveolar lavage fluids from ARDS patients drove betaENaC internal
188 as non-ventilated controls' broncho-alveolar lavage fluid had no effect on fibrocyte differentiation.
189 ate surfactant isolated from LCAD(-/-) mouse lavage fluid had significantly reduced phospholipid cont
190 y elevated total proteins in bronchoalveolar lavage fluid, higher parasitemia and tissue parasite bur
191 ines in lung homogenates and bronchoalveolar lavage fluid; however, PMN recruitment in mice treated w
192 lammatory mediator levels in bronchoalveolar lavage fluid, ii) lung parenchymal leukocyte counts and
193 eosinophilia, and increased bronchoalveolar lavage fluid IL-4 and IL-5, whereas adoptive transfer of
196 uction was attenuated in the bronchoalveolar lavage fluid in all factor-deficient mice compared with
197 solute neutrophil numbers in bronchoalveolar lavage fluid in GSTM1+ but not GSTM1null asthmatics.
198 inflammatory protein-2 in bronchial alveolar lavage fluids in LPS-injured lung compared with wild-typ
199 onverting enzyme activity in bronchoalveolar lavage fluid increased 3.2-fold in elderly when compared
201 spiratory distress syndrome broncho-alveolar lavage fluid inhibited by 71% (55-94) fibrocyte differen
202 delayed (6-8 hr) increase in bronchoalveolar lavage fluid interleukin-6 concentration (p < 0.001) and
203 ation sufficiently decreased bronchoalveolar lavage fluid levels of IFN-gamma at day 7 postinfluenza
204 as associated with increased bronchoalveolar lavage fluid levels of IL-10 and TGF-beta and decreased
205 elial cell proliferation and bronchoalveolar lavage fluid levels of keratinocyte growth factor were o
206 in a remarkable increase in bronchoalveolar lavage fluid levels of LPA enriched in polyunsaturated 2
207 s in infiltrating neutrophils (23% and 68%), lavage fluid levels of TNF-alpha (70% and 80%), and the
209 ne levels were determined in bronchoalveolar lavage fluid, lung homogenates and lung mononuclear cell
210 Remodeling factors in murine bronchoalveolar lavage fluid, lung tissue, or human nasal polyp tissue w
211 ells were detected in blood, bronchoalveolar lavage fluid, lungs, spleen, and brain, demonstrating th
212 cells was increased in lung, bronchoalveolar lavage fluid, lymph nodes, and blood of allergic COX-2(-
213 he study day, and plasma and bronchoalveolar lavage fluid markers of inflammation were measured.
214 on, including cell counts in bronchoalveolar lavage fluid, mucin production, ASM mass, and subepithel
215 tracheal aspirates (n = 71), bronchoalveolar lavage fluid (n = 152), pleural fluid (n = 76), cerebral
216 G (sHLA-G) concentrations in bronchoalveolar lavage fluid (n = 36) and plasma (n = 57) from adult ast
219 ught to compare MP types and levels in nasal lavage fluids (NLFs) from controls and patients with chr
222 control lung tissue, (ii) in bronchoalveolar lavage fluid obtained from non-severe and severe asthmat
223 ifferential counts were evaluated from nasal lavage fluid obtained from wild-type and IL-17A-deficien
224 ng could detect somatic mutations in uterine lavage fluid obtained from women undergoing hysteroscopy
225 kines, and growth factors in bronchoalveolar lavage fluid of 20 stable patients, 20 patients sufferin
226 rnithine) were isolated from bronchoalveolar lavage fluid of a patient with idiopathic pulmonary fibr
227 nodes, peripheral blood, and bronchoalveolar lavage fluid of AGMs and rhesus macaques (in which CD4 d
228 ignificantly elevated in the bronchoalveolar lavage fluid of all mice infected with C. neoformans Del
229 evels were also increased in bronchoalveolar lavage fluid of allergic asthmatic patients after segmen
230 tion driver mutations were identified in the lavage fluid of approximately half of the women without
231 tly, the IL-22 expression in bronchoalveolar lavage fluid of asthmatic patients inversely correlated
232 OCS3 protein was elevated in bronchoalveolar lavage fluid of both virus- and bacteria-infected mice,
234 e isolated and detected from bronchoalveolar lavage fluid of control and asthmatic mice and were quan
235 ned that cells collected from the peritoneal lavage fluid of E. faecalis-infected mice showed reduced
237 found ILC3-like cells in the bronchoalveolar lavage fluid of individuals with asthma, we suggest that
239 e frequently detected in the bronchoalveolar lavage fluid of lung transplant patients diagnosed with
240 MUC1-ED were elevated in the bronchoalveolar lavage fluid of mechanically ventilated patients with P.
241 mined in protein, serum, and bronchoalveolar lavage fluid of mice and lungs and serum of human donors
242 5-HT levels are increased in bronchoalveolar lavage fluid of mice and people with asthma after allerg
243 of B20-treated cells and in bronchoalveolar lavage fluid of mice exposed to B20 were approximately 2
244 ophils, and cytokines in the bronchoalveolar lavage fluid of mice than its mutant counterpart 7 days
245 roteins contained within the bronchoalveolar lavage fluid of mice that are cleaved and/or processed b
249 he level of ATX exoenzyme in bronchoalveolar lavage fluids of human patients with asthma subjected to
250 5-HT levels were measured in bronchoalveolar lavage fluid or serum of animals with AAI and in human a
253 from eyelid skin and peritoneal and uterine lavage fluid provide unprecedented opportunities to diss
255 say is validated for testing bronchoalveolar lavage fluids, replacing the requirement for culture and
257 spiratory distress syndrome broncho-alveolar lavage fluid restored their full inhibitory effect.
258 Cytologic examination of bronchial alveolar lavage fluid revealed a high proportion of lipid-laden m
259 virulence, while analysis of bronchoalveolar lavage fluid revealed that tumor necrosis factor alpha (
260 onventional culture by using bronchoalveolar lavage fluid samples from patients with underlying respi
261 1, we used paired serum and bronchoalveolar lavage fluid samples obtained within 48 hours of acute r
262 Endobronchial biopsies and bronchoalveolar lavage fluid samples were collected from 13 GSTM1+ and 1
264 or systemic health effects, bronchoalveolar lavage fluid, serum metabolic and inflammatory end point
265 y attenuated the increase in bronchoalveolar lavage fluid SOCS3 noted in lungs of mice challenged wit
266 nt, was significantly increased in LCAD(-/-) lavage fluid, suggesting increased epithelial permeabili
267 A3 and intracellular IL-4 in bronchoalveolar lavage fluid T cells, but expression of the TH17 transcr
268 a had increased HA levels in bronchoalveolar lavage fluid that correlated with pulmonary function and
269 tissues and Th2 responses in bronchoalveolar lavage fluid), they also accumulate functions normally a
270 intra-alveolar coagulation (bronchoalveolar lavage fluid thrombin-antithrombin complex levels) and P
271 histopathologic changes and bronchoalveolar lavage fluid total protein (endothelial permeability) an
273 .03) and a minor increase in bronchoalveolar lavage fluid tumor necrosis factor-alpha were observed (
274 neutrocytosis and increased bronchoalveolar lavage fluid tumor necrosis factor-alpha, interleukin-6,
276 alyzed for immune cell subsets, and alveolar lavage fluid was analyzed for ILC2-derived cytokines.
278 Streptococcus pneumoniae) in bronchoalveolar lavage fluid was associated with clinically significant
281 One day after treatment, bronchoalveolar lavage fluid was collected to determine differential cel
283 onor; however, pretransplant bronchoalveolar lavage fluid was only available from the donor for patie
285 g, the median log10 HIV copies/milliliter of lavage fluid was significantly lower in men with ART-ind
287 Elevated levels of Cif in bronchoalveolar lavage fluid were correlated with lower levels of 15-epi
289 nts in homogenized lungs and bronchoalveolar lavage fluid were decreased after cranberry proanthocyan
290 cytokines and chemokines in bronchoalveolar lavage fluid were measured by enzyme-linked immunosorben
291 iquots of blood, sputum, and bronchoalveolar lavage fluid were obtained from asthma subjects for medi
292 21, levels of neutrophils and macrophages in lavage fluid were reduced by 49% and increased by 287%,
293 crobial burdens in the organs and peritoneal lavage fluid were similar between mono- and coinfected a
294 differential cell counts in bronchoalveolar lavage fluid were similar between the Syk(flox/flox) and
295 s adenosine levels found in bronchioalveolar lavage fluid, were determined in mouse models of resolva
296 f T cells and neutrophils in bronchoalveolar lavage fluid, whereas expression of Foxp3 and IL-2 and n
297 s and reduce neutrophilia in bronchoalveolar lavage fluid, while IL-6 increases rapidly following LPS
298 umbers of eosinophils in the bronchoalveolar lavage fluid, while simultaneously decreasing the percen
299 Cytologic examination of bronchial alveolar lavage fluid with oil red O staining is a useful diagnos
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