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Anaerobic bacteria cultured from cystic fibrosis airways correlate to milder disease: a multisite study.
Muhlebach MS, Hatch JE, Einarsson GG, McGrath SJ, Gilipin DF, Lavelle G, Mirkovic B, Murray MA, McNally P, Gotman N, Davis Thomas S, Wolfgang MC, Gilligan PH, McElvaney NG, Elborn JS, Boucher RC, Tunney MM. Muhlebach MS, et al. Eur Respir J. 2018 Jul 11;52(1):1800242. doi: 10.1183/13993003.00242-2018. Print 2018 Jul. Eur Respir J. 2018. PMID: 29946004 Free PMC article.
Use of culture and molecular analysis to determine the effect of antibiotic treatment on microbial community diversity and abundance during exacerbation in patients with cystic fibrosis.
Tunney MM, Klem ER, Fodor AA, Gilpin DF, Moriarty TF, McGrath SJ, Muhlebach MS, Boucher RC, Cardwell C, Doering G, Elborn JS, Wolfgang MC. Tunney MM, et al. Among authors: boucher rc. Thorax. 2011 Jul;66(7):579-84. doi: 10.1136/thx.2010.137281. Epub 2011 Jan 26. Thorax. 2011. PMID: 21270069
Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children.
Muhlebach MS, Zorn BT, Esther CR, Hatch JE, Murray CP, Turkovic L, Ranganathan SC, Boucher RC, Stick SM, Wolfgang MC. Muhlebach MS, et al. Among authors: boucher rc. PLoS Pathog. 2018 Jan 18;14(1):e1006798. doi: 10.1371/journal.ppat.1006798. eCollection 2018 Jan. PLoS Pathog. 2018. PMID: 29346420 Free PMC article.
Cystic Fibrosis Airway Mucus Hyperconcentration Produces a Vicious Cycle of Mucin, Pathogen, and Inflammatory Interactions that Promotes Disease Persistence.
Batson BD, Zorn BT, Radicioni G, Livengood SS, Kumagai T, Dang H, Ceppe A, Clapp PW, Tunney M, Elborn JS, McElvaney NG, Muhlebach MS, Boucher RC, Tiemeyer M, Wolfgang MC, Kesimer M. Batson BD, et al. Am J Respir Cell Mol Biol. 2022 Aug;67(2):253-265. doi: 10.1165/rcmb.2021-0359OC. Am J Respir Cell Mol Biol. 2022. PMID: 35486871 Free PMC article.
934 results