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Human tracheobronchial submucosal gland cells in culture.
Sommerhoff CP, Finkbeiner WE. Sommerhoff CP, et al. Among authors: finkbeiner we. Am J Respir Cell Mol Biol. 1990 Jan;2(1):41-50. doi: 10.1165/ajrcmb/2.1.41. Am J Respir Cell Mol Biol. 1990. PMID: 2306368
Role of CFTR in chloride secretion across human tracheal epithelium.
Shen BQ, Mrsny RJ, Finkbeiner WE, Widdicombe JH. Shen BQ, et al. Among authors: finkbeiner we. Am J Physiol. 1995 Nov;269(5 Pt 1):L561-6. doi: 10.1152/ajplung.1995.269.5.L561. Am J Physiol. 1995. PMID: 7491973
We have tested two hypotheses: 1) the cystic fibrosis transmembrane conductance regulator (CFTR) represents the predominant Cl conductance in the apical membrane of human tracheal epithelium, and 2) CFTR in this tissue is close to maximally activated under baseline conditi
We have tested two hypotheses: 1) the cystic fibrosis transmembrane conductance regulator (CFTR) represents the predominant Cl conduc
Flow-Cytometric Analysis and Purification of Airway Epithelial-Cell Subsets.
Bonser LR, Koh KD, Johansson K, Choksi SP, Cheng D, Liu L, Sun DI, Zlock LT, Eckalbar WL, Finkbeiner WE, Erle DJ. Bonser LR, et al. Among authors: finkbeiner we. Am J Respir Cell Mol Biol. 2021 Mar;64(3):308-317. doi: 10.1165/rcmb.2020-0149MA. Am J Respir Cell Mol Biol. 2021. PMID: 33196316 Free PMC article.
151 results