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1 nd protein levels were highly upregulated in bronchoalveolar cells and fluid after allergen challenge
2  2287 significantly decreased esophageal and bronchoalveolar eosinophilia but only when given as a th
3 ermeability, lung histology, AFC, and plasma/bronchoalveolar fluid measurements of proinflammatory cy
4 ated with sRAGE levels in the plasma and the bronchoalveolar fluid of acid-injured mice (Spearman's r
5 d anti-inflammatory cytokines (IL-10) in the bronchoalveolar fluid, and IL-2 and IFN-gamma cytokines
6  serum IgG antibodies as well as vaginal and bronchoalveolar IgA antibodies.
7 ntral and peripheral airway remodelling, and bronchoalveolar inflammation were assessed.
8                           Cells recovered by bronchoalveolar lavage (BAL) after imaging were stained
9 tegrated study of human small airway tissue, bronchoalveolar lavage (BAL) and an experimental murine
10 bit AHR, increased numbers of eosinophils in bronchoalveolar lavage (BAL) and increased collagen cont
11 he diagnostic yield and complication rate of bronchoalveolar lavage (BAL) and lung biopsy in the eval
12                                              Bronchoalveolar lavage (BAL) and lung tissue were examin
13  a methacholine test, airway inflammation in bronchoalveolar lavage (BAL) and lung tissue, and total
14 e expression and activity were determined in bronchoalveolar lavage (BAL) and lungs of human donors a
15                              We investigated bronchoalveolar lavage (BAL) and serum samples from pati
16 ort study; 72 consented to bronchoscopy with bronchoalveolar lavage (BAL) and transbronchial biopsies
17     Conventional methods to identify HBEC in bronchoalveolar lavage (BAL) and wash (BW) have throughp
18 cDNA library derived from mRNA isolated from bronchoalveolar lavage (BAL) cells and leukocytes of sar
19 was to investigate the expression of iNOS in bronchoalveolar lavage (BAL) cells and tissue from centr
20                              Using blood and bronchoalveolar lavage (BAL) cells from normal control s
21 esponsiveness (AHR) to inhaled methacholine, bronchoalveolar lavage (BAL) cytokine levels, and lung h
22 ) and nearly 7-fold more active TGF-beta1 in bronchoalveolar lavage (BAL) fluid (BALF).
23 phil and bacterial counts were determined in bronchoalveolar lavage (BAL) fluid and blood.
24 perimental model of allergic asthma, matched bronchoalveolar lavage (BAL) fluid and plasma were colle
25 igatus Its performance has been validated on bronchoalveolar lavage (BAL) fluid and serum specimens,
26  and production of inflammatory cytokines in bronchoalveolar lavage (BAL) fluid and the lungs.
27 ormed in nasopharyngeal aspirates (NPAs) and bronchoalveolar lavage (BAL) fluid before HCT.
28              (1,3)beta-D-glucan detection in bronchoalveolar lavage (BAL) fluid by Fungitell assay ai
29 elial growth factor (VEGF) levels in hamster bronchoalveolar lavage (BAL) fluid early after intranasa
30 A gene sequencing was performed on acellular bronchoalveolar lavage (BAL) fluid from 30 subjects infe
31 ic bead array, and L-ficolin was measured in bronchoalveolar lavage (BAL) fluid from lung transplant
32                          Unlike blood ILC2s, bronchoalveolar lavage (BAL) fluid ILC2s from asthmatic
33                                  We examined bronchoalveolar lavage (BAL) fluid leukocytes, cytokines
34 We found that bleomycin injury increases the bronchoalveolar lavage (BAL) fluid levels of ATX protein
35  mesenteric lymph nodes (MLNs), jejunum, and bronchoalveolar lavage (BAL) fluid of healthy and SIV-in
36 nsus sequences of viruses collected from the bronchoalveolar lavage (BAL) fluid of the animals.
37 rometry based proteome analysis of acellular bronchoalveolar lavage (BAL) fluid samples on an observa
38  respiratory tract disease, 72 paired NP and bronchoalveolar lavage (BAL) fluid specimen sets, mostly
39           We analyzed 46 clinically obtained bronchoalveolar lavage (BAL) fluid specimens from sympto
40                                              Bronchoalveolar lavage (BAL) fluid was assessed for tota
41      Using a cutoff of >/=2% eosinophilia in bronchoalveolar lavage (BAL) fluid, chronic lung allogra
42 manifestation, so we evaluated biomarkers in bronchoalveolar lavage (BAL) fluid.
43 responses, we hypothesized that MV, found in bronchoalveolar lavage (BAL) fluids (BALF) of LTR at CLA
44 igated M. tuberculosis-specific responses in bronchoalveolar lavage (BAL) from persons with latent M.
45          We measured mtDNA concentrations in bronchoalveolar lavage (BAL) from subjects with and with
46           ALI was quantified by weight loss, bronchoalveolar lavage (BAL) inflammatory cell number, c
47                                  We assessed bronchoalveolar lavage (BAL) inflammatory cell numbers,
48 ls (MSCs) in the terminal airways-alveoli by bronchoalveolar lavage (BAL) of human adult lungs.
49 d their binding to TIMP-1, -2, -3, and -4 in bronchoalveolar lavage (BAL) of lung transplant recipien
50 r flow cytometry in digested lung tissue and bronchoalveolar lavage (BAL) simultaneously, 6 h after e
51 ng flow cytometry and a multiplex assay with bronchoalveolar lavage (BAL) specimens (n = 68) from 52
52      However, no CMV DNA threshold exists in bronchoalveolar lavage (BAL) to differentiate pneumonia
53                             Six hours later, bronchoalveolar lavage (BAL) was collected for leukocyte
54          Airway responsiveness was assessed, bronchoalveolar lavage (BAL) was performed, and lung cel
55 s of CD4(+) T and B cells in the spleens and bronchoalveolar lavage (BAL) were also observed.
56 ergic patients underwent SAC, and cells from bronchoalveolar lavage (BAL) were collected after 24 hou
57    SCFA levels in anaerobic supernatants and bronchoalveolar lavage (BAL) were determined by gas chro
58     The predominant macrophages harvested by bronchoalveolar lavage (BAL), alveolar macrophages (AMs)
59 flux of neutrophils and macrophages into the bronchoalveolar lavage (BAL), and human CD45(+) cells in
60                           Subjects underwent bronchoalveolar lavage (BAL), and peripheral whole blood
61 D4 and CD8 T cell immune responses in blood, bronchoalveolar lavage (BAL), and tracheobronchial lymph
62 linically indicated fiberoptic bronchoscopy, bronchoalveolar lavage (BAL), endobronchial brushings, a
63 t computed tomography, and bronchoscopy with bronchoalveolar lavage (BAL).
64 ated with proinflammatory cytokines in human bronchoalveolar lavage (BAL).
65  by an accumulation of CD4(+) T cells in the bronchoalveolar lavage (BAL).
66  aeruginosa, P. aeruginosa) were analyzed in bronchoalveolar lavage (BAL); and alveolar SGLT1 was ana
67 oneal (p = 0.037), systemic (p = 0.019), and bronchoalveolar lavage (p = 0.011) quantitative bacteria
68  in several proinflammatory cytokines in the bronchoalveolar lavage and in serum.
69 ortant cellular sources of IL-5 and IL-13 in bronchoalveolar lavage and lung tissue.
70 ion model, IL-10-producing CD4(+) T cells in bronchoalveolar lavage and lung were significantly decre
71 ition of ADAM10 reduces sEphrin-B2 levels in bronchoalveolar lavage and prevents lung fibrosis in mic
72                                              Bronchoalveolar lavage and pulmonary function tests were
73                       Double-stranded RNA in bronchoalveolar lavage and serum samples following lung
74  We found that levels of inflammation in the bronchoalveolar lavage and the lung, as well as levels o
75                                              Bronchoalveolar lavage and tissues were sampled for myco
76 ermate control animals through evaluation of bronchoalveolar lavage and tissues.
77    BAFF levels were also higher in blood and bronchoalveolar lavage B cells in patients with COPD ver
78 subjects had symptom scores, spirometry, and bronchoalveolar lavage before and after rhinovirus-induc
79                  Following silica treatment, bronchoalveolar lavage cell infiltrates decreased in fem
80                                              Bronchoalveolar lavage cell mRNA levels of iNOS or iNOS
81  Ag85A-specific CD4 T cells were detected in bronchoalveolar lavage cells from both groups and respon
82              At two independent study sites, bronchoalveolar lavage cells from donors with latent tub
83 nsistent with this, 14-HDoHE was detected in bronchoalveolar lavage cells of mild to moderate asthmat
84 e marrow progenitors, blood neutrophils, and bronchoalveolar lavage cells to initiate and complete an
85  increased, and protein concentration in the bronchoalveolar lavage diminished, showing the impact of
86       This activation phenotype indicated by bronchoalveolar lavage eosinophil surface markers, as we
87 niae infection was diagnosed on the basis of bronchoalveolar lavage eosinophilia and blood findings.
88 b induced a rise in circulating eosinophils, bronchoalveolar lavage eosinophilia, and eosinophil pero
89                Before mepolizumab treatment, bronchoalveolar lavage eosinophils had more surface IL-3
90 tracellular vesicles (EVs) are detectable in bronchoalveolar lavage fluid (BALF) and culture medium o
91                                 Lung tissue, bronchoalveolar lavage fluid (BALF) and draining lymph n
92 im of this study was to analyze cytokines in bronchoalveolar lavage fluid (BALF) and explore predicti
93  infected with Streptococcus pneumoniae, and bronchoalveolar lavage fluid (BALF) and lung CFU values
94 d temporal kinetics of GT and bmGT in serum, bronchoalveolar lavage fluid (BALF) and lungs of A. fumi
95 s the overlap in metabolites between matched bronchoalveolar lavage fluid (BALF) and plasma, identifi
96                                 BORT reduced bronchoalveolar lavage fluid (BALF) and tissue eosinophi
97 -type lymphocytes were assessed in lungs and bronchoalveolar lavage fluid (BALF) by multiparametric f
98                           Bacterial burdens, bronchoalveolar lavage fluid (BALF) cell counts, cell ty
99 understanding of the proinflammatory role of bronchoalveolar lavage fluid (BALF) exosomes in patients
100                                   We studied bronchoalveolar lavage fluid (BALF) from 36 patients wit
101 etabolic profiling of serum, lung tissue and bronchoalveolar lavage fluid (BALF) from a non-lethal mo
102  identification of two biomarkers present in bronchoalveolar lavage fluid (BALF) from chlorine gas ex
103 y flow cytometry on neutrophils in blood and bronchoalveolar lavage fluid (BALF) from mechanically ve
104  with human MSCs when stimulated with LPS or bronchoalveolar lavage fluid (BALF) from patients with A
105  cytomegalovirus (HCMV) DNA detection in the bronchoalveolar lavage fluid (BALF) indicates HCMV repli
106 ive to air-exposed controls, ozone increased bronchoalveolar lavage fluid (BALF) protein, a marker of
107                               Neutrophils in bronchoalveolar lavage fluid (BALF) served as markers of
108             In parallel, adenosine levels in bronchoalveolar lavage fluid (BALF) were increased by ap
109 d higher levels of Th2 and Th17 cytokines in bronchoalveolar lavage fluid (BALF), accompanied by an i
110 4, 17, 21, 25, or 33 d after exposure, SpO2, bronchoalveolar lavage fluid (BALF), and histologic anal
111 mpared with WT mice, with fewer cells in Wsh bronchoalveolar lavage fluid (BALF), despite similar lev
112              Lung function measurements, and bronchoalveolar lavage fluid (BALF), serum, and lungs we
113 utum (n = 128), tracheal aspirates (n = 71), bronchoalveolar lavage fluid (n = 152), pleural fluid (n
114 ns and polymorphonuclear cell recruitment in bronchoalveolar lavage fluid (p<0.05 for both).
115 2 ligands was significantly increased in the bronchoalveolar lavage fluid 48 hours after segmental al
116 PM2.5 increased neutrophil numbers and KC in bronchoalveolar lavage fluid and caused slight peribronc
117 Higher levels of Th2 cytokines were found in bronchoalveolar lavage fluid and draining lymph node cel
118 ikingly reduced numbers of leukocytes in the bronchoalveolar lavage fluid and lower expression of inf
119 ine expression in ILC2s and TH2 cells in the bronchoalveolar lavage fluid and lung tissue were assess
120 ical studies and biochemical measurements in bronchoalveolar lavage fluid and lung tissue.
121 nd primary lung monocytes/macrophages, mouse bronchoalveolar lavage fluid and lung tissues, and AHR i
122                   NETs were also measured in bronchoalveolar lavage fluid and plasma from lung transp
123 SM reduces inflammatory cell accumulation in bronchoalveolar lavage fluid and proinflammatory cytokin
124   We detected the presence of PRELP in human bronchoalveolar lavage fluid and showed that PRELP can b
125                                No changes in bronchoalveolar lavage fluid angiotensin-converting enzy
126 l counts with increased extracellular DNA in bronchoalveolar lavage fluid as well as in lung tissue,
127 n reduced the immunosuppressive functions of bronchoalveolar lavage fluid cells, inhibited bone marro
128 s extracted from endobronchial brushings and bronchoalveolar lavage fluid collected from 39 asthmatic
129                                  Analysis of bronchoalveolar lavage fluid collected from human patien
130 eduction of eosinophil and T cell numbers in bronchoalveolar lavage fluid compared with those in dilu
131 iduals with cystic fibrosis underwent annual bronchoalveolar lavage fluid examination, and chest comp
132                        Our findings validate bronchoalveolar lavage fluid exosomal shuttle RNA as a s
133                                              Bronchoalveolar lavage fluid from 23 lean, 12 overweight
134 17A, neutrophil counts, and total protein in bronchoalveolar lavage fluid from acute respiratory dist
135                                              Bronchoalveolar lavage fluid from Ad-MD-2s mice transfer
136                                           In bronchoalveolar lavage fluid from human lung transplant
137                                           In bronchoalveolar lavage fluid from humans with ARDS, gut-
138 was consistently inhibited by treatment with bronchoalveolar lavage fluid from inhibitory kappaB kina
139 vo, histone-C1INH complexes were detected in bronchoalveolar lavage fluid from patients with acute re
140  we found significant elevation of IL-17A in bronchoalveolar lavage fluid from patients with ARDS, an
141 he protein expression patterns in plasma and bronchoalveolar lavage fluid from patients with ARDS.
142 nase activities were quantified in serum and bronchoalveolar lavage fluid from patients with CF, asth
143  pulmonary eosinophilia were measured in the bronchoalveolar lavage fluid from patients with mild ast
144 F-specific IgG is elevated in both serum and bronchoalveolar lavage fluid from Rasgrp1-deficient mice
145                                Additionally, bronchoalveolar lavage fluid from this group of hepSTAT3
146 ry inflammation, eosinophilia, and increased bronchoalveolar lavage fluid IL-4 and IL-5, whereas adop
147 s, angiotensin-converting enzyme activity in bronchoalveolar lavage fluid increased 3.2-fold in elder
148 es in lung epithelial cell proliferation and bronchoalveolar lavage fluid levels of keratinocyte grow
149                                              Bronchoalveolar lavage fluid LT levels were increased in
150                                   Similarly, bronchoalveolar lavage fluid obtained from human volunte
151 m asthmatic and control lung tissue, (ii) in bronchoalveolar lavage fluid obtained from non-severe an
152 cytokines, chemokines, and growth factors in bronchoalveolar lavage fluid of 20 stable patients, 20 p
153 P-ribosyl-HNP-(ornithine) were isolated from bronchoalveolar lavage fluid of a patient with idiopathi
154  cells in lymph nodes, peripheral blood, and bronchoalveolar lavage fluid of AGMs and rhesus macaques
155 1) levels were significantly elevated in the bronchoalveolar lavage fluid of all mice infected with C
156            OSM levels were also increased in bronchoalveolar lavage fluid of allergic asthmatic patie
157 we report that SOCS3 protein was elevated in bronchoalveolar lavage fluid of both virus- and bacteria
158           As we found ILC3-like cells in the bronchoalveolar lavage fluid of individuals with asthma,
159 -promoting cytokines and chemokines into the bronchoalveolar lavage fluid of Lipa(-/-) mice.
160 oxidase were more frequently detected in the bronchoalveolar lavage fluid of lung transplant patients
161 of desialylated MUC1-ED were elevated in the bronchoalveolar lavage fluid of mechanically ventilated
162 f RAGE was determined in protein, serum, and bronchoalveolar lavage fluid of mice and lungs and serum
163  identify host proteins contained within the bronchoalveolar lavage fluid of mice that are cleaved an
164 lenge, and eosinophils were increased in the bronchoalveolar lavage fluid of wild-type mice.
165  HDM, elevated the levels of chemerin in the bronchoalveolar lavage fluid of WT mice.
166 resulted in hypovirulence, while analysis of bronchoalveolar lavage fluid revealed that tumor necrosi
167 istress syndrome 1, we used paired serum and bronchoalveolar lavage fluid samples obtained within 48
168                   Endobronchial biopsies and bronchoalveolar lavage fluid samples were collected from
169 ynthase similarly attenuated the increase in bronchoalveolar lavage fluid SOCS3 noted in lungs of mic
170 ption factor GATA3 and intracellular IL-4 in bronchoalveolar lavage fluid T cells, but expression of
171 ith severe asthma had increased HA levels in bronchoalveolar lavage fluid that correlated with pulmon
172 ther report that intra-alveolar coagulation (bronchoalveolar lavage fluid thrombin-antithrombin compl
173 ressive alveolar neutrocytosis and increased bronchoalveolar lavage fluid tumor necrosis factor-alpha
174                                              Bronchoalveolar lavage fluid was analyzed for inflammato
175 gillus species, Streptococcus pneumoniae) in bronchoalveolar lavage fluid was associated with clinica
176                                              Bronchoalveolar lavage fluid was collected from 23 stero
177                                              Bronchoalveolar lavage fluid was collected from patients
178 had a separate donor; however, pretransplant bronchoalveolar lavage fluid was only available from the
179                    Elevated levels of Cif in bronchoalveolar lavage fluid were correlated with lower
180 third MR imaging examination, eosinophils in bronchoalveolar lavage fluid were counted.
181    Bacterial counts in homogenized lungs and bronchoalveolar lavage fluid were decreased after cranbe
182  While total and differential cell counts in bronchoalveolar lavage fluid were similar between the Sy
183 urement and polymorphonuclear recruitment in bronchoalveolar lavage fluid), and lethality were evalua
184 ity in lymphoid tissues and Th2 responses in bronchoalveolar lavage fluid), they also accumulate func
185      The specimens (5 cerebrospinal fluid, 7 bronchoalveolar lavage fluid, 5 plasma, 2 serum, and 1 n
186  chronic rhinosinusitis (CRS), as well as in bronchoalveolar lavage fluid, after segmental allergen c
187 d lower total cell counts and neutrophils in bronchoalveolar lavage fluid, and had earlier influx of
188 nd disaturated PC in lung tissue homogenate, bronchoalveolar lavage fluid, and lung LB was increased
189  were sensitized and challenged with OVA and bronchoalveolar lavage fluid, and the lungs were collect
190  and nonlymphoid tissues, including lung and bronchoalveolar lavage fluid, as measured by H2-Db NP366
191 d tumor-promoting cyto-/chemokine profile in bronchoalveolar lavage fluid, decreased TLR2/4 expressio
192 fferential cell counts were performed on the bronchoalveolar lavage fluid, followed by histological a
193 und significantly elevated total proteins in bronchoalveolar lavage fluid, higher parasitemia and tis
194 ase-9 and proinflammatory mediator levels in bronchoalveolar lavage fluid, ii) lung parenchymal leuko
195                 Remodeling factors in murine bronchoalveolar lavage fluid, lung tissue, or human nasa
196 fected myeloid cells were detected in blood, bronchoalveolar lavage fluid, lungs, spleen, and brain,
197 ay and analyses of the injury markers in the bronchoalveolar lavage fluid, respectively.
198 tained pulmonary or systemic health effects, bronchoalveolar lavage fluid, serum metabolic and inflam
199                                 In serum and bronchoalveolar lavage fluid, total anti-IAV IgG and IgA
200  increased the numbers of eosinophils in the bronchoalveolar lavage fluid, while simultaneously decre
201 llikrein (KLK) 5 and KLK14, were assessed in bronchoalveolar lavage fluid.
202 lung while also reducing LPA 18:2 content in bronchoalveolar lavage fluid.
203 sed the production of TNF-alpha and MIP-2 in bronchoalveolar lavage fluid.
204  of increased macrophages and eosinophils in bronchoalveolar lavage fluid.
205 creased the numbers of inflammatory cells in bronchoalveolar lavage fluid.
206 ed in tissue extracts, nasal secretions, and bronchoalveolar lavage fluid.
207 ung epithelial cells and readily detected in bronchoalveolar lavage fluid.
208 1) with the percentage of eosinophils in the bronchoalveolar lavage fluid.
209 rase chain reaction using RNA extracted from bronchoalveolar lavage fluid.
210  release from lung epithelium as detected in bronchoalveolar lavage fluid.
211 in (TSLP), IL-9, and IL-13, but not IL-5, in bronchoalveolar lavage fluid.
212     Recruited eosinophils were enumerated in bronchoalveolar lavage fluid.
213 the macrophage chemoattractant MCP-1 in lung bronchoalveolar lavage fluid.
214 d with the concentration of total protein in bronchoalveolar lavage fluids (BALF) from patients with
215                                              Bronchoalveolar lavage fluids from ozone-treated rats re
216 ncreased ATP concentrations were reported in bronchoalveolar lavage fluids of asthmatic patients.
217    The concentration of CXCL12 in plasma and bronchoalveolar lavage fluids was quantified by ELISA.
218           The assay is validated for testing bronchoalveolar lavage fluids, replacing the requirement
219  0.00003), and similar results were found in bronchoalveolar lavage fluids.
220 uction compared to normal lung, as did human bronchoalveolar lavage following lipopolysaccharide inst
221 d, induced sputum, endobronchial biopsy, and bronchoalveolar lavage for flow cytometry and multiplex-
222                       AMs were obtained from bronchoalveolar lavage from healthy donors or patients w
223                      AMs were recovered from bronchoalveolar lavage from healthy subjects and patient
224                                              Bronchoalveolar lavage from mice expressing CAIKKbeta mi
225  leukocytes, macrophages, and neutrophils in bronchoalveolar lavage from O3-exposed mice.
226                               Interestingly, bronchoalveolar lavage IL-6, interferon gamma-induced pr
227 L-1alpha positively correlated with elevated bronchoalveolar lavage IL-8 levels (r(2) = 0.6095, p < 0
228                                We found that bronchoalveolar lavage interleukin-17A was strongly asso
229                     OVA-induced increases in bronchoalveolar lavage lymphocytes, eosinophils, IL-13,
230                                              Bronchoalveolar lavage macrophages were stimulated in vi
231 increases than downwind fine/ultrafine PM in bronchoalveolar lavage neutrophils, eosinophils, and lac
232  cell therapy groups, despite a reduction in bronchoalveolar lavage neutrophils.
233 ll as 16S ribosomal RNA sequencing data from bronchoalveolar lavage obtained as part of the COMET-IPF
234 rleukin-1 alpha (IL-1alpha) was increased in bronchoalveolar lavage of lung transplant recipients gro
235 des of the biculture and was also present in bronchoalveolar lavage of lung transplantation patients.
236 ive HC3-HA structures were also found in the bronchoalveolar lavage of naive mice and were observed o
237 was also demonstrated in vivo by challenging bronchoalveolar lavage of SET-M33-treated mice with LPS,
238 % male) with pulmonary nocardiosis proved by bronchoalveolar lavage or biopsy were reviewed by two ex
239  marker of PARP activation) and IL-6, in the bronchoalveolar lavage or the lung tissue, and histology
240 phenotype and function of T lymphocytes from bronchoalveolar lavage or the peripheral blood.
241 ukin-17A was strongly associated with higher bronchoalveolar lavage percent neutrophils (p < 0.001) a
242 gonist resulted in a 59% and 91% increase in bronchoalveolar lavage protein and LDH, respectively.
243 ression resulted in reduced edema formation (bronchoalveolar lavage protein concentration and lung hi
244        Incubating control cells with disease bronchoalveolar lavage recapitulated the aberrant functi
245 ially in patients with severe asthma in whom bronchoalveolar lavage regulatory T-cell numbers were al
246                      Blood, bone marrow, and bronchoalveolar lavage sample analyses from juvenile and
247 l or immunocompromised or fail to improve, a bronchoalveolar lavage sample FARP (BAL FARP) is perform
248 y evaluating both upper airway and acellular bronchoalveolar lavage samples from 49 subjects from thr
249  have previously demonstrated that acellular bronchoalveolar lavage samples from half of the healthy
250  and BAFF expression in B cells in blood and bronchoalveolar lavage samples from the same subject gro
251                                              Bronchoalveolar lavage samples from Ugandan patients wit
252 pression of FXIII mRNA and protein levels in bronchoalveolar lavage samples obtained before and after
253 tes for the galactomannan assay in serum and bronchoalveolar lavage samples were 61.3% and 57.1%, res
254 terium tuberculosis (MTB) mRNA in sputum and bronchoalveolar lavage samples, in a substantial proport
255                                       Serial bronchoalveolar lavage specimens were ultracentrifuged t
256                                      We used bronchoalveolar lavage to identify and characterize huma
257 r lavage percent neutrophils (p < 0.001) and bronchoalveolar lavage total protein (p < 0.01) in acute
258 r (CD95) and programmed death-1, but similar bronchoalveolar lavage viral loads as control subjects.
259               Three days after instillation, bronchoalveolar lavage was performed and plastic-adheren
260 asis of chest CT findings, bronchoscopy with bronchoalveolar lavage was performed.
261              E. coli colony-forming units in bronchoalveolar lavage were reduced in both cell therapy
262          Notably, Ag-specific T cells in the bronchoalveolar lavage were sustained at approximately 5
263 the lung, proinflammatory cytokine levels in bronchoalveolar lavage, and alveolar capillary leakage.
264 ovided induced sputum, endobronchial biopsy, bronchoalveolar lavage, and blood samples.
265          Eosinophils were examined in blood, bronchoalveolar lavage, and endobronchial biopsies 48 ho
266 ects underwent phlebotomy, sputum induction, bronchoalveolar lavage, and endobronchial biopsy.
267 h assessment by means of forced oscillation, bronchoalveolar lavage, and histologic analysis.
268          Silica-induced SPP1 in lung tissue, bronchoalveolar lavage, and serum increased more in male
269 bacterial burden in the lungs, blood, liver, bronchoalveolar lavage, and spleens of mice at 24 h post
270 ions to perform bronchoscopic airway survey, bronchoalveolar lavage, esophageal pH monitoring, and a
271                                       Blood, bronchoalveolar lavage, large proximal and small distal
272                                       Blood, bronchoalveolar lavage, large proximal, and small distal
273 arance from the lungs, cytokine secretion in bronchoalveolar lavage, lung antimicrobial peptide expre
274 llergic airway inflammation was evaluated by bronchoalveolar lavage, lung histology, serology, gene e
275 , PAR, lactate dehydrogenase and proteins in bronchoalveolar lavage, lung weight gain, perivascular e
276 ximal and distal airways (bronchial wash and bronchoalveolar lavage, respectively), as well as mucosa
277 is factor-alpha concentrations were lower in bronchoalveolar lavage, whereas the concentrations of th
278  was associated with IFN-gamma expression in bronchoalveolar lavage, while inducing its expression in
279 expression of PD-1 and PD-L1 on systemic and bronchoalveolar lavage-derived cells of subjects with sa
280 ed numbers of lymphocytes and neutrophils in bronchoalveolar lavage.
281                       All patients underwent bronchoalveolar lavage.
282   Twenty-three ventilated patients underwent bronchoalveolar lavage.
283 derwent spirometry, chest x-ray study, and a bronchoalveolar lavage.
284 g surfactant membranes isolated from porcine bronchoalveolar lavage.
285 olating large numbers of cells by whole-lung bronchoalveolar lavage.
286 ant SP-D and captured native SP-D from human bronchoalveolar lavage.
287 r infiltration, and E. coli colony counts in bronchoalveolar lavage.
288 els of Aspergillus and total fungus in their bronchoalveolar lavage.
289 tinocyte chemoattractant, and neutrophils in bronchoalveolar lavage; and mortality, mucus obstruction
290    Oral washes (OW), induced sputa (IS), and bronchoalveolar lavages (BAL) were collected from 56 par
291 6S rRNA sequencing data from oral washes and bronchoalveolar lavages (BALs) obtained from HIV-uninfec
292 ial alarmins were measured longitudinally in bronchoalveolar lavages from lung transplant recipients
293 sed eosinophil and neutrophil populations in bronchoalveolar lavages from mice with asthma.
294 NA and host total RNA were isolated from 203 bronchoalveolar lavages obtained from 112 patients post-
295 NA and host total RNA were isolated from 189 bronchoalveolar lavages obtained from 116 patients post
296               A similar pattern was seen for bronchoalveolar lymphocytes, but with quadruple the magn
297            Furthermore, obese mice had fewer bronchoalveolar macrophages and regulatory T cells durin
298        Only fluticasone/salmeterol decreased bronchoalveolar neutrophilia (p = 0.03) to the same exte
299    Mif(-/-) mice demonstrated an increase in bronchoalveolar protein (48%) and lactate dehydrogenase
300  platelet-leukocyte complex formation in the bronchoalveolar space.

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