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Samuel I Miller

Showing results (131-140 of 161) with videos related to

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Plos Pathogens|January 15, 2010
Nutrient availability as a mechanism for selection of antibiotic tolerant Pseudomonas aeruginosa within the CF airwayLucas R Hoffman, Anthony R Richardson, Laura S Houston, et al.
Journal of Clinical Gastroenterology|December 29, 2016
Clinical and Fecal Microbial Changes With Diet Therapy in Active Inflammatory Bowel DiseaseDavid L Suskind, Stanley A Cohen, Mitchell J Brittnacher, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 2, 2013
Escherichia coli dysbiosis correlates with gastrointestinal dysfunction in children with cystic fibrosisLucas R Hoffman, Christopher E Pope, Hillary S Hayden, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 2018
Adaptation of commensal proliferating <i>Escherichia coli</i> to the intestinal tract of young children with cystic fibrosisSusana Matamouros, Hillary S Hayden, Kyle R Hager, et al.
Nature Structural & Molecular Biology|April 28, 2009
A conserved structural motif mediates formation of the periplasmic rings in the type III secretion systemThomas Spreter, Calvin K Yip, Sarah Sanowar, et al.
Infection and Immunity|September 20, 2006
Lack of in vitro and in vivo recognition of Francisella tularensis subspecies lipopolysaccharide by Toll-like receptorsAdeline M Hajjar, Megan D Harvey, Scott A Shaffer, et al.
Scientific Reports|March 5, 2016
Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosisOhad Manor, Roie Levy, Christopher E Pope, et al.
BMC Microbiology|September 16, 2021
Infants with cystic fibrosis have altered fecal functional capacities with potential clinical and metabolic consequencesAlexander Eng, Hillary S Hayden, Christopher E Pope, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2006
Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patientsEric E Smith, Danielle G Buckley, Zaining Wu, et al.
Molecular Microbiology|November 29, 2013
A divergent Pseudomonas aeruginosa palmitoyltransferase essential for cystic fibrosis-specific lipid AIyarit Thaipisuttikul, Lauren E Hittle, Ramesh Chandra, et al.
Pageof 17

Showing results (131-140 of 161) with videos related to

Sort By:
Pageof 17
Plos Pathogens|January 15, 2010
Nutrient availability as a mechanism for selection of antibiotic tolerant Pseudomonas aeruginosa within the CF airwayLucas R Hoffman, Anthony R Richardson, Laura S Houston, et al.
Journal of Clinical Gastroenterology|December 29, 2016
Clinical and Fecal Microbial Changes With Diet Therapy in Active Inflammatory Bowel DiseaseDavid L Suskind, Stanley A Cohen, Mitchell J Brittnacher, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 2, 2013
Escherichia coli dysbiosis correlates with gastrointestinal dysfunction in children with cystic fibrosisLucas R Hoffman, Christopher E Pope, Hillary S Hayden, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 2018
Adaptation of commensal proliferating <i>Escherichia coli</i> to the intestinal tract of young children with cystic fibrosisSusana Matamouros, Hillary S Hayden, Kyle R Hager, et al.
Nature Structural & Molecular Biology|April 28, 2009
A conserved structural motif mediates formation of the periplasmic rings in the type III secretion systemThomas Spreter, Calvin K Yip, Sarah Sanowar, et al.
Infection and Immunity|September 20, 2006
Lack of in vitro and in vivo recognition of Francisella tularensis subspecies lipopolysaccharide by Toll-like receptorsAdeline M Hajjar, Megan D Harvey, Scott A Shaffer, et al.
Scientific Reports|March 5, 2016
Metagenomic evidence for taxonomic dysbiosis and functional imbalance in the gastrointestinal tracts of children with cystic fibrosisOhad Manor, Roie Levy, Christopher E Pope, et al.
BMC Microbiology|September 16, 2021
Infants with cystic fibrosis have altered fecal functional capacities with potential clinical and metabolic consequencesAlexander Eng, Hillary S Hayden, Christopher E Pope, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2006
Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patientsEric E Smith, Danielle G Buckley, Zaining Wu, et al.
Molecular Microbiology|November 29, 2013
A divergent Pseudomonas aeruginosa palmitoyltransferase essential for cystic fibrosis-specific lipid AIyarit Thaipisuttikul, Lauren E Hittle, Ramesh Chandra, et al.
Pageof 17