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1 d with disease are present in both nasal and tracheal epithelium.
2 e, with virus located in the pneumocytes and tracheal epithelium.
3 ent neurons that project specifically to the tracheal epithelium.
4 lung epithelial differentiation in embryonic tracheal epithelium.
5 nd found to exceed 50% in SO2-injured murine tracheal epithelium.
6 ogenitors differentiate toward esophageal or tracheal epithelium.
7 ted to, but distinct from, that expressed in tracheal epithelium.
8 for the establishment and maintenance of the tracheal epithelium.
9 the presumptive Sox2+ esophageal and Nkx2-1+ tracheal epithelium.
10 r time, we lesioned small areas of the mouse tracheal epithelium (1 to 12 cells) using a femtosecond
11 cally, we followed the regeneration of mouse tracheal epithelium after ablation of luminal cells by i
12 rin at the basolateral surfaces of migrating tracheal epithelium, and the reorganization of cell-cell
13 s, when CRCs from ectocervical epithelium or tracheal epithelium are placed in an air-liquid interfac
14  14 and was associated with complete loss of tracheal epithelium by day 14.
15 ndent chloride channel described recently in tracheal epithelium, Ca-CC.
16 tein Gpr177 (also known as Wntless) in mouse tracheal epithelium causes a significant reduction in th
17 sitive chloride secretory response in murine tracheal epithelium could be measured if the calcium-dep
18 age relationships in the naphthalene-injured tracheal epithelium demonstrated that two multipotential
19 h single cell RNA-sequencing analysis of the tracheal epithelium from smokers and non-smokers, we gen
20  of Pseudomonas aeruginosa (PA) in nasal and tracheal epithelium has recently been shown to involve t
21 factor-induced transdifferentiation of early tracheal epithelium into respiratory epithelium.
22               We found that the steady-state tracheal epithelium is maintained by two progenitor cell
23  bodies and apical and basal surfaces of the tracheal epithelium normally move in concert as new bran
24                                       In the tracheal epithelium of all conditional mutants there are
25  intestinal epithelium of the fly and in the tracheal epithelium of mice exhibit transient activation
26 ion was found in either squamous metaplastic tracheal epithelium or in sections of human lung tumors.
27 rom improper stratification of the embryonic tracheal epithelium or the abnormal trachealis muscle.
28                   Additionally, in the adult tracheal epithelium, SOX21 inhibits basal to ciliated ce
29 ted by reverse transcription-PCR in neonatal tracheal epithelium, suggesting that other family member
30 la FGF ortholog branchless in the developing tracheal epithelium, suggesting that the function of the
31 lycyclic aromatic hydrocarbons to the canine tracheal epithelium, the purpose of the current study wa
32  evident by the capacity to reconstitute the tracheal epithelium through seven generations of seconda
33  lung mesenchyme can reprogram embryonic rat tracheal epithelium to express a distal lung phenotype.
34                         Day-13 embryonic rat tracheal epithelium was separated from its mesenchyme, e
35 lung, RBD-1 mRNA expression localized to the tracheal epithelium while RBD-2 was expressed in alveola
36 n IAVs (hIAVs) showed that they infected the tracheal epithelium with various efficiencies depending