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1 ed numbers of lymphocytes and neutrophils in bronchoalveolar lavage.
2 All patients underwent bronchoalveolar lavage.
3 Twenty-three ventilated patients underwent bronchoalveolar lavage.
4 derwent spirometry, chest x-ray study, and a bronchoalveolar lavage.
5 g surfactant membranes isolated from porcine bronchoalveolar lavage.
6 olating large numbers of cells by whole-lung bronchoalveolar lavage.
7 ant SP-D and captured native SP-D from human bronchoalveolar lavage.
8 r infiltration, and E. coli colony counts in bronchoalveolar lavage.
9 els of Aspergillus and total fungus in their bronchoalveolar lavage.
10 from the baseline value until 2 hours after bronchoalveolar lavage and became similar to the baselin
12 or cigarette smoke for 22 weeks followed by bronchoalveolar lavage and lung and cardiac tissue analy
14 ion model, IL-10-producing CD4(+) T cells in bronchoalveolar lavage and lung were significantly decre
15 ition of ADAM10 reduces sEphrin-B2 levels in bronchoalveolar lavage and prevents lung fibrosis in mic
18 We found that levels of inflammation in the bronchoalveolar lavage and the lung, as well as levels o
21 the lung, proinflammatory cytokine levels in bronchoalveolar lavage, and alveolar capillary leakage.
27 bacterial burden in the lungs, blood, liver, bronchoalveolar lavage, and spleens of mice at 24 h post
28 tinocyte chemoattractant, and neutrophils in bronchoalveolar lavage; and mortality, mucus obstruction
29 BAFF levels were also higher in blood and bronchoalveolar lavage B cells in patients with COPD ver
31 tegrated study of human small airway tissue, bronchoalveolar lavage (BAL) and an experimental murine
32 bit AHR, increased numbers of eosinophils in bronchoalveolar lavage (BAL) and increased collagen cont
33 he diagnostic yield and complication rate of bronchoalveolar lavage (BAL) and lung biopsy in the eval
35 a methacholine test, airway inflammation in bronchoalveolar lavage (BAL) and lung tissue, and total
36 e expression and activity were determined in bronchoalveolar lavage (BAL) and lungs of human donors a
38 ort study; 72 consented to bronchoscopy with bronchoalveolar lavage (BAL) and transbronchial biopsies
39 Conventional methods to identify HBEC in bronchoalveolar lavage (BAL) and wash (BW) have throughp
41 cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells and leukocytes of sar
42 was to investigate the expression of iNOS in bronchoalveolar lavage (BAL) cells and tissue from centr
44 esponsiveness (AHR) to inhaled methacholine, bronchoalveolar lavage (BAL) cytokine levels, and lung h
47 perimental model of allergic asthma, matched bronchoalveolar lavage (BAL) fluid and plasma were colle
48 igatus Its performance has been validated on bronchoalveolar lavage (BAL) fluid and serum specimens,
52 elial growth factor (VEGF) levels in hamster bronchoalveolar lavage (BAL) fluid early after intranasa
53 A gene sequencing was performed on acellular bronchoalveolar lavage (BAL) fluid from 30 subjects infe
54 ic bead array, and L-ficolin was measured in bronchoalveolar lavage (BAL) fluid from lung transplant
57 We found that bleomycin injury increases the bronchoalveolar lavage (BAL) fluid levels of ATX protein
58 mesenteric lymph nodes (MLNs), jejunum, and bronchoalveolar lavage (BAL) fluid of healthy and SIV-in
60 Prospective real-time testing of serum and bronchoalveolar lavage (BAL) fluid pools from positive a
61 rometry based proteome analysis of acellular bronchoalveolar lavage (BAL) fluid samples on an observa
62 respiratory tract disease, 72 paired NP and bronchoalveolar lavage (BAL) fluid specimen sets, mostly
67 responses, we hypothesized that MV, found in bronchoalveolar lavage (BAL) fluids (BALF) of LTR at CLA
68 igated M. tuberculosis-specific responses in bronchoalveolar lavage (BAL) from persons with latent M.
73 d their binding to TIMP-1, -2, -3, and -4 in bronchoalveolar lavage (BAL) of lung transplant recipien
74 mplicated in the pathogenesis of ACR) in the bronchoalveolar lavage (BAL) of lung transplant recipien
75 r flow cytometry in digested lung tissue and bronchoalveolar lavage (BAL) simultaneously, 6 h after e
76 ng flow cytometry and a multiplex assay with bronchoalveolar lavage (BAL) specimens (n = 68) from 52
81 ergic patients underwent SAC, and cells from bronchoalveolar lavage (BAL) were collected after 24 hou
82 SCFA levels in anaerobic supernatants and bronchoalveolar lavage (BAL) were determined by gas chro
83 The predominant macrophages harvested by bronchoalveolar lavage (BAL), alveolar macrophages (AMs)
84 flux of neutrophils and macrophages into the bronchoalveolar lavage (BAL), and human CD45(+) cells in
86 D4 and CD8 T cell immune responses in blood, bronchoalveolar lavage (BAL), and tracheobronchial lymph
87 linically indicated fiberoptic bronchoscopy, bronchoalveolar lavage (BAL), endobronchial brushings, a
91 aeruginosa, P. aeruginosa) were analyzed in bronchoalveolar lavage (BAL); and alveolar SGLT1 was ana
92 Oral washes (OW), induced sputa (IS), and bronchoalveolar lavages (BAL) were collected from 56 par
93 6S rRNA sequencing data from oral washes and bronchoalveolar lavages (BALs) obtained from HIV-uninfec
94 subjects had symptom scores, spirometry, and bronchoalveolar lavage before and after rhinovirus-induc
97 Ag85A-specific CD4 T cells were detected in bronchoalveolar lavage cells from both groups and respon
99 nsistent with this, 14-HDoHE was detected in bronchoalveolar lavage cells of mild to moderate asthmat
100 e marrow progenitors, blood neutrophils, and bronchoalveolar lavage cells to initiate and complete an
101 At baseline and after hyperoxia exposure, bronchoalveolar lavage cytokine levels were unchanged in
102 expression of PD-1 and PD-L1 on systemic and bronchoalveolar lavage-derived cells of subjects with sa
103 increased, and protein concentration in the bronchoalveolar lavage diminished, showing the impact of
105 niae infection was diagnosed on the basis of bronchoalveolar lavage eosinophilia and blood findings.
106 b induced a rise in circulating eosinophils, bronchoalveolar lavage eosinophilia, and eosinophil pero
108 ions to perform bronchoscopic airway survey, bronchoalveolar lavage, esophageal pH monitoring, and a
109 tracellular vesicles (EVs) are detectable in bronchoalveolar lavage fluid (BALF) and culture medium o
111 im of this study was to analyze cytokines in bronchoalveolar lavage fluid (BALF) and explore predicti
112 infected with Streptococcus pneumoniae, and bronchoalveolar lavage fluid (BALF) and lung CFU values
113 d temporal kinetics of GT and bmGT in serum, bronchoalveolar lavage fluid (BALF) and lungs of A. fumi
114 s the overlap in metabolites between matched bronchoalveolar lavage fluid (BALF) and plasma, identifi
116 -type lymphocytes were assessed in lungs and bronchoalveolar lavage fluid (BALF) by multiparametric f
118 understanding of the proinflammatory role of bronchoalveolar lavage fluid (BALF) exosomes in patients
120 etabolic profiling of serum, lung tissue and bronchoalveolar lavage fluid (BALF) from a non-lethal mo
121 identification of two biomarkers present in bronchoalveolar lavage fluid (BALF) from chlorine gas ex
122 y flow cytometry on neutrophils in blood and bronchoalveolar lavage fluid (BALF) from mechanically ve
123 with human MSCs when stimulated with LPS or bronchoalveolar lavage fluid (BALF) from patients with A
124 cytomegalovirus (HCMV) DNA detection in the bronchoalveolar lavage fluid (BALF) indicates HCMV repli
125 ive to air-exposed controls, ozone increased bronchoalveolar lavage fluid (BALF) protein, a marker of
128 d higher levels of Th2 and Th17 cytokines in bronchoalveolar lavage fluid (BALF), accompanied by an i
129 4, 17, 21, 25, or 33 d after exposure, SpO2, bronchoalveolar lavage fluid (BALF), and histologic anal
130 mpared with WT mice, with fewer cells in Wsh bronchoalveolar lavage fluid (BALF), despite similar lev
132 utum (n = 128), tracheal aspirates (n = 71), bronchoalveolar lavage fluid (n = 152), pleural fluid (n
134 lmost 10-fold-higher bacterial burden in the bronchoalveolar lavage fluid 3 h following infection.
135 2 ligands was significantly increased in the bronchoalveolar lavage fluid 48 hours after segmental al
136 PM2.5 increased neutrophil numbers and KC in bronchoalveolar lavage fluid and caused slight peribronc
137 Higher levels of Th2 cytokines were found in bronchoalveolar lavage fluid and draining lymph node cel
138 ikingly reduced numbers of leukocytes in the bronchoalveolar lavage fluid and lower expression of inf
139 ine expression in ILC2s and TH2 cells in the bronchoalveolar lavage fluid and lung tissue were assess
141 nd primary lung monocytes/macrophages, mouse bronchoalveolar lavage fluid and lung tissues, and AHR i
143 SM reduces inflammatory cell accumulation in bronchoalveolar lavage fluid and proinflammatory cytokin
144 We detected the presence of PRELP in human bronchoalveolar lavage fluid and showed that PRELP can b
146 l counts with increased extracellular DNA in bronchoalveolar lavage fluid as well as in lung tissue,
147 n reduced the immunosuppressive functions of bronchoalveolar lavage fluid cells, inhibited bone marro
148 s extracted from endobronchial brushings and bronchoalveolar lavage fluid collected from 39 asthmatic
150 eduction of eosinophil and T cell numbers in bronchoalveolar lavage fluid compared with those in dilu
151 tion and IL-17A/F production in the lung and bronchoalveolar lavage fluid compared with wild-type mic
152 iduals with cystic fibrosis underwent annual bronchoalveolar lavage fluid examination, and chest comp
155 17A, neutrophil counts, and total protein in bronchoalveolar lavage fluid from acute respiratory dist
159 was consistently inhibited by treatment with bronchoalveolar lavage fluid from inhibitory kappaB kina
160 vo, histone-C1INH complexes were detected in bronchoalveolar lavage fluid from patients with acute re
161 we found significant elevation of IL-17A in bronchoalveolar lavage fluid from patients with ARDS, an
162 he protein expression patterns in plasma and bronchoalveolar lavage fluid from patients with ARDS.
163 nase activities were quantified in serum and bronchoalveolar lavage fluid from patients with CF, asth
164 pulmonary eosinophilia were measured in the bronchoalveolar lavage fluid from patients with mild ast
165 F-specific IgG is elevated in both serum and bronchoalveolar lavage fluid from Rasgrp1-deficient mice
167 ry inflammation, eosinophilia, and increased bronchoalveolar lavage fluid IL-4 and IL-5, whereas adop
168 s, angiotensin-converting enzyme activity in bronchoalveolar lavage fluid increased 3.2-fold in elder
169 es in lung epithelial cell proliferation and bronchoalveolar lavage fluid levels of keratinocyte grow
171 ded throughout the study day, and plasma and bronchoalveolar lavage fluid markers of inflammation wer
173 m asthmatic and control lung tissue, (ii) in bronchoalveolar lavage fluid obtained from non-severe an
174 cytokines, chemokines, and growth factors in bronchoalveolar lavage fluid of 20 stable patients, 20 p
175 P-ribosyl-HNP-(ornithine) were isolated from bronchoalveolar lavage fluid of a patient with idiopathi
176 cells in lymph nodes, peripheral blood, and bronchoalveolar lavage fluid of AGMs and rhesus macaques
177 1) levels were significantly elevated in the bronchoalveolar lavage fluid of all mice infected with C
179 we report that SOCS3 protein was elevated in bronchoalveolar lavage fluid of both virus- and bacteria
182 oxidase were more frequently detected in the bronchoalveolar lavage fluid of lung transplant patients
183 of desialylated MUC1-ED were elevated in the bronchoalveolar lavage fluid of mechanically ventilated
184 f RAGE was determined in protein, serum, and bronchoalveolar lavage fluid of mice and lungs and serum
185 identify host proteins contained within the bronchoalveolar lavage fluid of mice that are cleaved an
188 resulted in hypovirulence, while analysis of bronchoalveolar lavage fluid revealed that tumor necrosi
189 istress syndrome 1, we used paired serum and bronchoalveolar lavage fluid samples obtained within 48
191 ynthase similarly attenuated the increase in bronchoalveolar lavage fluid SOCS3 noted in lungs of mic
192 ption factor GATA3 and intracellular IL-4 in bronchoalveolar lavage fluid T cells, but expression of
193 ith severe asthma had increased HA levels in bronchoalveolar lavage fluid that correlated with pulmon
194 ther report that intra-alveolar coagulation (bronchoalveolar lavage fluid thrombin-antithrombin compl
195 ressive alveolar neutrocytosis and increased bronchoalveolar lavage fluid tumor necrosis factor-alpha
197 gillus species, Streptococcus pneumoniae) in bronchoalveolar lavage fluid was associated with clinica
200 had a separate donor; however, pretransplant bronchoalveolar lavage fluid was only available from the
203 Bacterial counts in homogenized lungs and bronchoalveolar lavage fluid were decreased after cranbe
204 While total and differential cell counts in bronchoalveolar lavage fluid were similar between the Sy
205 urement and polymorphonuclear recruitment in bronchoalveolar lavage fluid), and lethality were evalua
206 ity in lymphoid tissues and Th2 responses in bronchoalveolar lavage fluid), they also accumulate func
207 The specimens (5 cerebrospinal fluid, 7 bronchoalveolar lavage fluid, 5 plasma, 2 serum, and 1 n
208 chronic rhinosinusitis (CRS), as well as in bronchoalveolar lavage fluid, after segmental allergen c
209 d lower total cell counts and neutrophils in bronchoalveolar lavage fluid, and had earlier influx of
210 nd disaturated PC in lung tissue homogenate, bronchoalveolar lavage fluid, and lung LB was increased
211 were sensitized and challenged with OVA and bronchoalveolar lavage fluid, and the lungs were collect
212 and nonlymphoid tissues, including lung and bronchoalveolar lavage fluid, as measured by H2-Db NP366
213 d tumor-promoting cyto-/chemokine profile in bronchoalveolar lavage fluid, decreased TLR2/4 expressio
214 fferential cell counts were performed on the bronchoalveolar lavage fluid, followed by histological a
215 und significantly elevated total proteins in bronchoalveolar lavage fluid, higher parasitemia and tis
216 ase-9 and proinflammatory mediator levels in bronchoalveolar lavage fluid, ii) lung parenchymal leuko
218 fected myeloid cells were detected in blood, bronchoalveolar lavage fluid, lungs, spleen, and brain,
220 tained pulmonary or systemic health effects, bronchoalveolar lavage fluid, serum metabolic and inflam
222 increased the numbers of eosinophils in the bronchoalveolar lavage fluid, while simultaneously decre
236 d with the concentration of total protein in bronchoalveolar lavage fluids (BALF) from patients with
238 ncreased ATP concentrations were reported in bronchoalveolar lavage fluids of asthmatic patients.
239 The concentration of CXCL12 in plasma and bronchoalveolar lavage fluids was quantified by ELISA.
242 uction compared to normal lung, as did human bronchoalveolar lavage following lipopolysaccharide inst
243 d, induced sputum, endobronchial biopsy, and bronchoalveolar lavage for flow cytometry and multiplex-
248 ial alarmins were measured longitudinally in bronchoalveolar lavages from lung transplant recipients
251 L-1alpha positively correlated with elevated bronchoalveolar lavage IL-8 levels (r(2) = 0.6095, p < 0
255 arance from the lungs, cytokine secretion in bronchoalveolar lavage, lung antimicrobial peptide expre
256 llergic airway inflammation was evaluated by bronchoalveolar lavage, lung histology, serology, gene e
257 , PAR, lactate dehydrogenase and proteins in bronchoalveolar lavage, lung weight gain, perivascular e
260 increases than downwind fine/ultrafine PM in bronchoalveolar lavage neutrophils, eosinophils, and lac
262 ll as 16S ribosomal RNA sequencing data from bronchoalveolar lavage obtained as part of the COMET-IPF
263 NA and host total RNA were isolated from 203 bronchoalveolar lavages obtained from 112 patients post-
264 NA and host total RNA were isolated from 189 bronchoalveolar lavages obtained from 116 patients post
265 rleukin-1 alpha (IL-1alpha) was increased in bronchoalveolar lavage of lung transplant recipients gro
266 des of the biculture and was also present in bronchoalveolar lavage of lung transplantation patients.
267 ive HC3-HA structures were also found in the bronchoalveolar lavage of naive mice and were observed o
268 was also demonstrated in vivo by challenging bronchoalveolar lavage of SET-M33-treated mice with LPS,
269 % male) with pulmonary nocardiosis proved by bronchoalveolar lavage or biopsy were reviewed by two ex
270 ; 54.3% male) with idiopathic PAP (proved by bronchoalveolar lavage or biopsy) were reviewed by two e
271 marker of PARP activation) and IL-6, in the bronchoalveolar lavage or the lung tissue, and histology
273 oneal (p = 0.037), systemic (p = 0.019), and bronchoalveolar lavage (p = 0.011) quantitative bacteria
274 ukin-17A was strongly associated with higher bronchoalveolar lavage percent neutrophils (p < 0.001) a
275 gonist resulted in a 59% and 91% increase in bronchoalveolar lavage protein and LDH, respectively.
276 ression resulted in reduced edema formation (bronchoalveolar lavage protein concentration and lung hi
278 ially in patients with severe asthma in whom bronchoalveolar lavage regulatory T-cell numbers were al
279 ximal and distal airways (bronchial wash and bronchoalveolar lavage, respectively), as well as mucosa
281 l or immunocompromised or fail to improve, a bronchoalveolar lavage sample FARP (BAL FARP) is perform
282 y evaluating both upper airway and acellular bronchoalveolar lavage samples from 49 subjects from thr
283 have previously demonstrated that acellular bronchoalveolar lavage samples from half of the healthy
284 and BAFF expression in B cells in blood and bronchoalveolar lavage samples from the same subject gro
286 pression of FXIII mRNA and protein levels in bronchoalveolar lavage samples obtained before and after
287 tes for the galactomannan assay in serum and bronchoalveolar lavage samples were 61.3% and 57.1%, res
288 The genome yield from tracheal aspirates and bronchoalveolar lavage samples were similar (P = .1174).
289 terium tuberculosis (MTB) mRNA in sputum and bronchoalveolar lavage samples, in a substantial proport
293 r lavage percent neutrophils (p < 0.001) and bronchoalveolar lavage total protein (p < 0.01) in acute
294 r (CD95) and programmed death-1, but similar bronchoalveolar lavage viral loads as control subjects.
299 is factor-alpha concentrations were lower in bronchoalveolar lavage, whereas the concentrations of th
300 was associated with IFN-gamma expression in bronchoalveolar lavage, while inducing its expression in
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