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2 sequential events, spontaneous emphysema and bronchioalveolar adenocarcinoma were developed as a resu
5 a, acute lymphoblastic leukemia, meningioma, bronchioalveolar carcinoma, basal cell carcinoma, and ca
6 ression patterns from histologically defined bronchioalveolar carcinoma, squamous cell carcinoma, and
8 t case-controlled clinical studies show that bronchioalveolar carcinomas (BAC) are correlated with sm
10 e, mimicking the cellular composition of the bronchioalveolar compartment as defined by single-cell R
11 he putative bronchoalveolar stem cell at the bronchioalveolar duct junction as a cancer cell of origi
15 tential to differentiate into all major lung bronchioalveolar epithelium cell types in homeostasis or
17 ive, single center study comparing levels of bronchioalveolar lavage (BAL) and serum HA and the HA im
18 Replication-competent virus was detected in bronchioalveolar lavage (BAL) macrophages beyond 6 month
19 ected animals were increased in frequency in bronchioalveolar lavage and decreased in lymph nodes, co
20 c lung compliance and injury scores, reduced bronchioalveolar lavage cell counts and cytokine levels,
22 enase, or hospitalization for pneumonia with bronchioalveolar lavage demonstrating Pneumocystis jirov
23 tein, showed increased concentration in both bronchioalveolar lavage fluid (BALF) and blood of doxycy
24 nhibitory factor (MIF) in serum, sputum, and bronchioalveolar lavage fluid (BALF) from asthmatic pati
28 inflammation, neutrophil predominance in the bronchioalveolar lavage fluid, and enhanced airway mucus
29 levels, defined as adenosine levels found in bronchioalveolar lavage fluid, were determined in mouse
30 n of interleukin-6 was steadily increased in bronchioalveolar lavage fluid, which activated the oncog
32 induced in the lungs and cells derived from bronchioalveolar lavage of cotton rats infected with RSV
33 the lung and assessment of leukocytes in the bronchioalveolar lavage revealed that neutrophil numbers
34 tionally similar to those recovered from the bronchioalveolar lavage, based on ex vivo cytokine produ
36 nse to respiratory virus infections, both in bronchioalveolar lavages from COVID-19 patients and in p
37 established a three-dimensional (3D) murine bronchioalveolar lung organoid (BALO) model that allows
38 (2020) report a murine lung stem cell-based bronchioalveolar organoid system and provide insights in
39 IgG, monocytes, B cells and T cells into the bronchioalveolar space combined with expansion of CD69(+
40 ibitor aurothiomalate inhibits Kras-mediated bronchioalveolar stem cell expansion and lung tumor grow
41 ed the frequency and activity of multipotent bronchioalveolar stem cells (BASCs) and bronchiolar prog
42 s such as label retention and harboring rare bronchioalveolar stem cells (BASCs) in terminal bronchio
43 ulates the temporal appearance and number of bronchioalveolar stem cells (BASCs) in the lung, its abs
44 rts a growing narrative-a rare population of bronchioalveolar stem cells (BASCs) that can contribute
45 pansion and self-organization of FACS-sorted bronchioalveolar stem cells (BASCs) upon co-culture with
46 ndothelial cells and distal lung stem cells, bronchioalveolar stem cells (BASCs), to probe the instru
48 CS-isolated populations, we demonstrate that bronchioalveolar stem cells and club cells are the likel
50 h a defect in the ability of Prkci-deficient bronchioalveolar stem cells to undergo Kras-mediated exp
52 opment was preceded by aberrant expansion of bronchioalveolar stem/progenitor and alveolar type II (A
53 in the kidney capsule produce differentiated bronchioalveolar tissue, while retaining self-renewal, a