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1 cally sensitive nerve endings in the trachea/bronchus.
2 genetic changes in cells exfoliating in the bronchus.
3 ting a 5-F balloon catheter into a secondary bronchus.
4 achea, and the other, of the left upper lobe bronchus.
5 of an organized epithelial cell layer in the bronchus.
6 infiltrate occurring distal to an obstructed bronchus.
7 onstriction and proliferation in the primary bronchus.
8 xamined in purified HLMCs and isolated human bronchus.
9 expiratory collapse was calculated for each bronchus.
10 th muscle-positive cells of human trachea or bronchus.
11 receptive fields in the trachea or main stem bronchus.
12 the distal trachea, the carina, and the main bronchus.
13 acheobronchial damage at the carina and main bronchus.
14 observed vs expected cases included lung and bronchus (-24 940 cases; 95% CI, -28 936 to -20 944 case
15 ts with 54 telescoping anastomoses (30 right bronchus, 24 left bronchus) were retrospectively reviewe
16 28.1% for gynecological, 24.9% for lung and bronchus, 24.9% for sarcoma, 21.0% for genitourinary, an
18 irway lavage (PAL) of the isolated left main bronchus and bronchoalveolar lavage (BAL; bronchial frac
19 ed vascular compression of the proximal left bronchus and distal trachea, and the other, of the left
23 c heart disease (IHD), stroke, and tracheal, bronchus and lung cancer-specific disability adjusted li
30 pase-1 expression in human airway epithelium bronchus and primary cells, (2) characterized NLRP3 infl
32 revealed DeltaNp63alpha expression in normal bronchus and squamous carcinomas but not in normal lung
35 roduced by complete obstruction of one lobar bronchus, and (3) VA/Q inequality (n = 8) created by par
39 and anus (male, 3.3; female, 3.0); trachea, bronchus, and lung (male, 3.3; female, 7.5); and brain a
42 and 2014, including 5656423 due to tracheal, bronchus, and lung cancer; 2484476 due to colon and rect
43 value of approximately 5, included trachea, bronchus, and lung, at 0.52 (95% CI, 0.21-0.82); stomach
44 r and biliary; pancreatic; larynx; tracheal, bronchus, and lung; malignant skin melanoma; nonmelanoma
45 the rectum, rectosigmoid, and anus; trachea, bronchus, and lung; skin; and connective tissues (all si
46 on with stenosis in the right superior lobar bronchus, and there was an outflow of yellow viscous spu
48 of granulomas and instead generate inducible bronchus associated lymphoid structures, and robust anti
49 characterized by lymphoid hyperplasia of the bronchus-associated lymphoid tissue (BALT) and infiltrat
53 n lung grafts and accumulated within induced bronchus-associated lymphoid tissue (BALT) of tolerant m
55 odels of acute rejection in lung allografts, bronchus-associated lymphoid tissue (BALT) plays a major
58 c organ donors aged 0-13 years, we show that bronchus-associated lymphoid tissue (BALT), containing B
59 athologic changes including the expansion of bronchus-associated lymphoid tissue (BALT), goblet cell
60 ymphatic growth was restricted to regions of bronchus-associated lymphoid tissue (BALT), where VEGF-C
63 ults in significant recruitment of inducible bronchus-associated lymphoid tissue (iBALT) as well as C
64 ukin-1alpha (IL-1alpha) and caused inducible bronchus-associated lymphoid tissue (iBALT) formation in
67 induction in myeloid cells in the inducible bronchus-associated lymphoid tissue (iBALT) likely contr
69 tertiary lymphoid tissues, such as inducible bronchus-associated lymphoid tissue (iBALT), form in non
72 mice, but some pathologies such as enhanced bronchus-associated lymphoid tissue and bronchiolitis ob
73 ses were retained, including vaccine-induced bronchus-associated lymphoid tissue and CD8(+) effector
74 T cell proliferation, induction of inducible bronchus-associated lymphoid tissue and correlates of ba
80 ne expression assays to evaluate the role of bronchus-associated lymphoid tissue in pulmonary hyperte
82 afts results in temporary reductions of both bronchus-associated lymphoid tissue size and abundance o
87 y defined cellular accumulations include the bronchus-associated lymphoid tissue, cryptopatches, and
88 ged mice disrupted smoking-related inducible bronchus-associated lymphoid tissue, induced regeneratio
89 ction of Foxp3(+) regulatory T cell-enriched bronchus-associated lymphoid tissue, which suppresses lo
90 y chemokines and the appearance of inducible bronchus-associated lymphoid tissue-like structures in t
92 hallenge and were activated within inducible bronchus-associated lymphoid tissues (iBALTs), resident
95 y (always right upper lobe second-generation bronchus) at baseline, after 2 wk, and again after 8 wk
98 ; 95% CI, 70.08-92.45; P < .001) and lung or bronchus cancer (24.99 per 100 000; 95% CI, 21.57-28.40;
99 tributions of known risk factors to lung and bronchus cancer (LBC) mortality rates in the conterminou
100 01) and a 58.9% higher incidence of lung and bronchus cancer (mean [SD], 92.4 [41.6] per 100 000; 95%
104 difference in relative survival for lung and bronchus cancer patients is examined using data from pop
105 primary diagnoses of breast cancer, lung or bronchus cancer, or melanoma and control patients who we
106 atients with IMD and breast cancer, lung and bronchus cancer, or melanoma, 57% of patients were women
110 assigned to 3 groups: (1) AAV9-PD-L1 via the bronchus during static cold storage, (2) no-virus contro
111 uding bladder, prostate, female breast, lung/bronchus, endometrial, colon, non-Hodgkin lymphoma, panc
112 he dorsal and ventral aspects of the primary bronchus, especially before branch formation, inhibiting
113 acentral lesion (target overlapping proximal bronchus) experienced a possible treatment-related grade
115 ml for normal human mesenchymal cells, human bronchus fibroblasts and human airway smooth muscle cell
116 l blocker was placed into the left main stem bronchus for lung isolation and application of continuou
117 n of balloon-tip catheters into the bleeding bronchus for tamponade of the hemorrhagic artery, protec
118 ions caused by separation of the invaginated bronchus from the recipient bronchus were seen in 16 ana
121 py analyses revealed that the decellularized bronchus graft was well integrated with native tissue an
122 ependent contractions of guinea pig isolated bronchus, however, thrombin (3-300 nM) was a weak spasmo
123 ecal swabs and mucosal scraping samples from bronchus, ileum, and colon were collected approximately
126 yzed, including trachea, left and right main bronchus, intermediate bronchus, left and right upper lo
127 onchus (RMB), left main bronchus, (LMB), and bronchus intermedius (BI), and the mean percentage of ex
128 edetermined levels (aortic arch, carina, and bronchus intermedius) to confirm ECAC (>50% reduction in
130 s 30.9% with end expiration (P < .0001); and bronchus intermedius, 57.5% with dynamic expiration vers
132 [IRR], 1.70; P < .01), carcinoma of the lung/bronchus (IRR, 1.58; P < .01), non-Hodgkin lymphoma (IRR
133 tion of ACE2 and TMPRSS2 with smoking in the bronchus is due to their high expression in goblet cells
134 , left and right main bronchus, intermediate bronchus, left and right upper lobe, and left lower lobe
135 for the right main bronchus (RMB), left main bronchus, (LMB), and bronchus intermedius (BI), and the
137 x) was significantly higher in the left main bronchus (mean, 2.7) than in the right (mean, 2.3) (P <
139 supracarinal trachea (n = 9; 45%), the right bronchus (n = 4; 20%), and the cervical trachea (n = 3;
140 nary arteries before and after left mainstem bronchus occlusion (LMBO) in mice with and without a con
141 nd during hypoxia produced by left main stem bronchus occlusion (LMBO) in mice with and without a tar
142 tance (LPVR) before and during left mainstem bronchus occlusion (LMBO) was measured in mice with and
143 did not impair the ability of left mainstem bronchus occlusion to increase left pulmonary vascular r
144 vascular resistance induced by left mainstem bronchus occlusion, was markedly impaired in animals ven
146 ic acid was instilled into the left mainstem bronchus of TLR4-defective (both C3H/HeJ and congenic C.
148 for malignant neoplasms of digestive organs, bronchus or lung, melanoma of skin, and urinary tract wh
150 significantly higher at the carina and main bronchus (p <.01; Kruskal-Wallis test followed by Dunn's
152 cross 5 types of cancer: cancers of the lung/bronchus, prostate, female breast, colorectum, and liver
153 roptic bronchoscopy, with isolated left main bronchus proximal airway lavage (PAL) and bronchoalveola
155 aller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with heal
156 , gastrectomy, liver/biliary resection, lung/bronchus resection, pancreatectomy, proctectomy, prostat
157 created by partial obstruction of one lobar bronchus resulting in a bimodal VA/Q distribution with 1
158 rced-expiratory CT images for the right main bronchus (RMB), left main bronchus, (LMB), and bronchus
159 d and neck, gynecological, thyroid, lung and bronchus, sarcoma, genitourinary, melanoma, hematologica
160 Purpose To characterize the hyperintense bronchus sign (HBS) in in vivo fetal MRI of congenital l
162 l impact on SARS-CoV-2 infection, but in the bronchus, smoking may lead to higher viral loads and mor
163 cancer incidence rates (overall- and lung or bronchus-specific) were examined using the Ohio Cancer I
164 ved in patients with cancers of the lung and bronchus (standardized mortality ratio [SMR] = 5.74; 95%
165 ously defined smoking-induced genes from the bronchus suggested that smoking had a similar effect on
166 scopy was performed using the superDimension/Bronchus system consisting of electromagnetic board, pos
167 navigation bronchoscopy using superDimension/Bronchus System is a novel method to increase diagnostic
168 y larger in diameter than the left main-stem bronchus, though the latter was longer and straighter.
169 osures and 10 common cancers (i.e., lung and bronchus, thyroid, colorectal, kidney and renal pelvis,
172 ammac(-/-) mice undergoing heterotopic human bronchus transplantation and reconstitution with allogen
173 zed mouse models of heterotopic subcutaneous bronchus transplantation imitate the in vivo development
175 deficient mice receiving heterotopic porcine bronchus transplants, and major histocompatibility compl
176 erges from the dorsal surface of the primary bronchus via monopodial branching to form the conducting
177 was oversewn and a fistula to the right main bronchus was closed by means of an autologous pericardia
179 specimens, we found that the right main-stem bronchus was consistently larger in diameter than the le
180 tient, stent placement in the left main stem bronchus was needed to relieve left lung atelectasis.
181 al window was created and the decellularized bronchus was transplanted into the defect in a porcine m
182 ic ganglia neurons on the guinea pig primary bronchus were analyzed, and the procedure for localizing
186 pithelial cells of airways, particularly the bronchus, where high expression of SCGB3A2 is found.