Year |
Citation |
Score |
2021 |
O'Toole GA, Crabbé A, Kümmerli R, LiPuma JJ, Bomberger JM, Davies JC, Limoli D, Phelan VV, Bliska JB, DePas WH, Dietrich LE, Hampton TH, Hunter R, Khursigara CM, Price-Whelan A, et al. Model Systems to Study the Chronic, Polymicrobial Infections in Cystic Fibrosis: Current Approaches and Exploring Future Directions. Mbio. e0176321. PMID 34544277 DOI: 10.1128/mBio.01763-21 |
0.575 |
|
2020 |
Flynn JM, Cameron LC, Wiggen TD, Dunitz JM, Harcombe WR, Hunter RC. Disruption of Cross-Feeding Inhibits Pathogen Growth in the Sputa of Patients with Cystic Fibrosis. Msphere. 5. PMID 32350096 DOI: 10.1128/mSphere.00343-20 |
0.307 |
|
2019 |
Glasser NR, Hunter RC, Liou TG, Newman DK. Refinement of metabolite detection in cystic fibrosis sputum reveals heme correlates with lung function decline. Plos One. 14: e0226578. PMID 31851705 DOI: 10.1371/Journal.Pone.0226578 |
0.475 |
|
2017 |
Flynn JM, Phan C, Hunter RC. 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. PMID 28507068 DOI: 10.1128/Iai.00182-17 |
0.313 |
|
2016 |
Choi HM, Calvert CR, Husain N, Huss D, Barsi JC, Deverman BE, Hunter RC, Kato M, Lee SM, Abelin AC, Rosenthal AZ, Akbari OS, Li Y, Hay BA, Sternberg PW, et al. Mapping a multiplexed zoo of mRNA expression. Development (Cambridge, England). 143: 3632-3637. PMID 27702788 DOI: 10.1242/Dev.140137 |
0.397 |
|
2016 |
Flynn JM, Niccum D, Dunitz JM, Hunter RC. Evidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease. Plos Pathogens. 12: e1005846. PMID 27548479 DOI: 10.1371/Journal.Ppat.1005846 |
0.319 |
|
2013 |
Hunter RC, Asfour F, Dingemans J, Osuna BL, Samad T, Malfroot A, Cornelis P, Newman DK. Ferrous iron is a significant component of bioavailable iron in cystic fibrosis airways. Mbio. 4. PMID 23963183 DOI: 10.1128/Mbio.00557-13 |
0.457 |
|
2013 |
Dietrich LE, Okegbe C, Price-Whelan A, Sakhtah H, Hunter RC, Newman DK. Bacterial community morphogenesis is intimately linked to the intracellular redox state. Journal of Bacteriology. 195: 1371-80. PMID 23292774 DOI: 10.1128/Jb.02273-12 |
0.608 |
|
2012 |
Hunter RC, Klepac-Ceraj V, Lorenzi MM, Grotzinger H, Martin TR, Newman DK. 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. PMID 22865623 DOI: 10.1165/Rcmb.2012-0088Oc |
0.51 |
|
2011 |
Doughty DM, Coleman ML, Hunter RC, Sessions AL, Summons RE, Newman DK. 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. PMID 21873238 DOI: 10.1073/Pnas.1104209108 |
0.611 |
|
2011 |
Reddy KC, Hunter RC, Bhatla N, Newman DK, Kim DH. Caenorhabditis elegans NPR-1-mediated behaviors are suppressed in the presence of mucoid bacteria. Proceedings of the National Academy of Sciences of the United States of America. 108: 12887-92. PMID 21768378 DOI: 10.1073/Pnas.1108265108 |
0.462 |
|
2010 |
Hunter RC, Newman DK. A putative ABC transporter, hatABCDE, is among molecular determinants of pyomelanin production in Pseudomonas aeruginosa. Journal of Bacteriology. 192: 5962-71. PMID 20870774 DOI: 10.1128/Jb.01021-10 |
0.529 |
|
2009 |
Welander PV, Hunter RC, Zhang L, Sessions AL, Summons RE, Newman DK. Hopanoids play a role in membrane integrity and pH homeostasis in Rhodopseudomonas palustris TIE-1. Journal of Bacteriology. 191: 6145-56. PMID 19592593 DOI: 10.1128/Jb.00460-09 |
0.625 |
|
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