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

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