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搜索结果时间表的表表示，每年搜索结果数量。

Year 结果数
2018 2
2019 1
2020 1
2022 1
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Pathological mucus and impaired mucus clearance in cystic fibrosis patients result from increased concentration, not altered pH.
Hill DB, Long RF,Kissner WJ, Atieh E, Garbarine IC, Markovetz MR, Fontana NC, Christy M, Habibpour M, Tarran R, Forest MG, Boucher RC, Button B. Hill DB等。在作者中：kissner wj. Eur Respir J. 2018 Dec 6;52(6):1801297. doi: 10.1183/13993003.01297-2018. Print 2018 Dec. Eur Respir J. 2018. PMID：30361244 Free PMC article.
Endotracheal tube mucus as a source of airway mucus for rheological study.
Markovetz MR, Subramani DB,Kissner WJ, Morrison CB, Garbarine IC, Ghio A, Ramsey KA, Arora H, Kumar P, Nix DB, Kumagai T, Krunkosky TM, Krause DC, Radicioni G, Alexis NE, Kesimer M, Tiemeyer M, Boucher RC, Ehre C, Hill DB. Markovetz MR, et al. Among authors:kissner wj. Am J Physiol Lung Cell Mol Physiol. 2019 Oct 1;317(4):L498-L509. doi: 10.1152/ajplung.00238.2019. Epub 2019 Aug 7. Am J Physiol Lung Cell Mol Physiol. 2019. PMID：31389736 Free PMC article.
Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosis.
Markovetz MR, Garbarine IC, Morrison CB,Kissner WJ, Seim I, Forest MG, Papanikolas MJ, Freeman R, Ceppe A, Ghio A, Alexis NE, Stick SM, Ehre C, Boucher RC, Esther CR, Muhlebach MS, Hill DB. Markovetz MR, et al. Among authors:kissner wj. J Cyst Fibros. 2022 Apr 15:S1569-1993(22)00097-2. doi: 10.1016/j.jcf.2022.04.008. Online ahead of print. J Cyst Fibros. 2022. PMID：35437233
Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice.
Hancock LA, Hennessy CE, Solomon GM, Dobrinskikh E, Estrella A, Hara N, Hill DB,Kissner WJ, Markovetz MR, Grove Villalon DE, Voss ME, Tearney GJ, Carroll KS, Shi Y, Schwarz MI, Thelin WR, Rowe SM, Yang IV, Evans CM, Schwartz DA. Hancock LA等。在作者中：kissner wj. Nat Commun. 2018 Dec 18;9(1):5363. doi: 10.1038/s41467-018-07768-9. Nat Commun. 2018. PMID：30560893 Free PMC article.