Ryan Hunter
Affiliations: | University of Minnesota, Twin Cities, Minneapolis, MN |
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"Ryan Hunter"
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| O'Toole GA, Crabbé A, Kümmerli R, et al. (2021) Model Systems to Study the Chronic, Polymicrobial Infections in Cystic Fibrosis: Current Approaches and Exploring Future Directions. Mbio. e0176321 |
| Flynn JM, Cameron LC, Wiggen TD, et al. (2020) Disruption of Cross-Feeding Inhibits Pathogen Growth in the Sputa of Patients with Cystic Fibrosis. Msphere. 5 |
| Glasser NR, Hunter RC, Liou TG, et al. (2019) Refinement of metabolite detection in cystic fibrosis sputum reveals heme correlates with lung function decline. Plos One. 14: e0226578 |
| Flynn JM, Phan C, Hunter RC. (2017) Genome-wide survey of Pseudomonas aeruginosa PA14 reveals a role for the glyoxylate pathway and extracellular proteases in the utilization of mucin. Infection and Immunity |
| Choi HM, Calvert CR, Husain N, et al. (2016) Mapping a multiplexed zoo of mRNA expression. Development (Cambridge, England). 143: 3632-3637 |
| Flynn JM, Niccum D, Dunitz JM, et al. (2016) Evidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease. Plos Pathogens. 12: e1005846 |
| Hunter RC, Asfour F, Dingemans J, et al. (2013) Ferrous iron is a significant component of bioavailable iron in cystic fibrosis airways. Mbio. 4 |
| Dietrich LE, Okegbe C, Price-Whelan A, et al. (2013) Bacterial community morphogenesis is intimately linked to the intracellular redox state. Journal of Bacteriology. 195: 1371-80 |
| Hunter RC, Klepac-Ceraj V, Lorenzi MM, et al. (2012) Phenazine content in the cystic fibrosis respiratory tract negatively correlates with lung function and microbial complexity. American Journal of Respiratory Cell and Molecular Biology. 47: 738-45 |
| Doughty DM, Coleman ML, Hunter RC, et al. (2011) The RND-family transporter, HpnN, is required for hopanoid localization to the outer membrane of Rhodopseudomonas palustris TIE-1. Proceedings of the National Academy of Sciences of the United States of America. 108: E1045-51 |