Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Courtney E, Price"'
Autor:
Courtney E. Price, Rebecca A. Valls, Alexis R. Ramsey, Nicole A. Loeven, Jane T. Jones, Kaitlyn E. Barrack, Joseph D. Schwartzman, Darlene B. Royce, Robert A. Cramer, Juliette C. Madan, Benjamin D. Ross, James Bliska, George A. O'Toole
Publikováno v:
mBio, Vol 15, Iss 2 (2024)
ABSTRACT Persons with cystic fibrosis (CF), starting in early life, show intestinal microbiome dysbiosis characterized in part by a decreased relative abundance of the genus Bacteroides. Bacteroides is a major producer of the intestinal short chain f
Externí odkaz:
https://doaj.org/article/6a530a3789b44d7fa6ae1050050a8bac
Autor:
Courtney E. Price, Thomas H. Hampton, Rebecca A. Valls, Kaitlyn E. Barrack, George A. O’Toole, Juliette C. Madan, Modupe O. Coker
Publikováno v:
mSphere, Vol 8, Iss 4 (2023)
ABSTRACT Cystic fibrosis (CF) is a heritable disease that causes altered physiology at mucosal sites; these changes result in chronic infections in the lung, significant gastrointestinal complications as well as dysbiosis of the gut microbiome, altho
Externí odkaz:
https://doaj.org/article/aa0b0337d724452394ed04389ec97a6d
Autor:
Kareen Cortes, Courtney E. Price, Katherine Cook, Nada Naguib, George A. O'Toole, Stefan Katharios, Jack Kirsch, Mark W. Grinstaff, Katherine Hohl
Publikováno v:
ACS Biomaterials Science & Engineering. 7:4362-4370
Currently, no dressings are utilized after removal of polyps during a colonoscopy rendering these tissue sites susceptible to bleeding, sepsis, and perfusion. We report the design specifications, synthesis, and ex vivo evaluation of in situ polymeriz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26010d52b811f48a905efa02ee70c71a
https://doi.org/10.1021/acsbiomaterials.1c00549
https://doi.org/10.1021/acsbiomaterials.1c00549
Autor:
Rebecca A. Valls, Thomas H. Hampton, Courtney E. Price, Kaitlyn E. Barrack, George A. O’Toole, Modupe O. Coker, Juliette C. Madan
The gut-lung axis describes the interaction between microbiota in the gut and health status of the airway, whereby there is a bidirectional relationship facilitated by systemic transport of microbially-derived metabolites and immune factors. Cystic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfbe1bb53b38873413ce2ff24245fe46
https://doi.org/10.1101/2022.08.06.503028
https://doi.org/10.1101/2022.08.06.503028
Autor:
Courtney E. Price, Thomas H. Hampton, Rebecca A. Valls, Kaitlyn E. Barrack, George A. O’Toole, Juliette C. Madan, Modupe O. Coker
Cystic Fibrosis is a heritable disease that causes altered physiology at mucosal sites; these changes result in chronic infection in the lung, significant gastrointestinal complications as well as dysbiosis of the gut microbiome, although the latter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7147a7b291777d3478ba0eca6ab3c927
https://doi.org/10.1101/2022.05.27.493808
https://doi.org/10.1101/2022.05.27.493808
Autor:
Courtney E. Price, Rebecca A. Valls, Alexis R. Ramsey, Nicole A. Loeven, Jane T. Jones, Kaitlyn E. Barrack, Joseph D Schwartzman, Darlene B. Royce, Robert A. Cramer, Juliette C. Madan, Benjamin D. Ross, James Bliska, George A. O’Toole
Persons with cystic fibrosis, starting in early life, have intestinal microbiome dysbiosis characterized in part by a decreased relative abundance of the genus Bacteroides. Bacteroides is a major producer of the intestinal short chain fatty acid (SCF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::743a378e8c97be22c21ae56ce26ee2c8
https://doi.org/10.1101/2022.01.05.475125
https://doi.org/10.1101/2022.01.05.475125
Autor:
Courtney E. Price, George A. O'Toole
Publikováno v:
Journal of Bacteriology
Cystic fibrosis (CF) is a heritable, multiorgan disease that impacts all tissues that normally express cystic fibrosis transmembrane conductance regulator (CFTR) protein. While the importance of the airway microbiota has long been recognized, the int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2e418d0f6d8a406a7cee6c89478f7ae
https://doi.org/10.1128/jb.00311-21
https://doi.org/10.1128/jb.00311-21
Autor:
Katherine, Cook, Nada, Naguib, Courtney E, Price, Stefan, Katharios, Jack, Kirsch, Kareen, Cortes, Katherine, Hohl, George A, O'Toole, Mark W, Grinstaff
Publikováno v:
ACS Biomater Sci Eng
Currently, no dressings are utilized after removal of polyps during a colonoscopy rendering these tissue sites susceptible to bleeding, sepsis, and perfusion. We report the design specifications, synthesis, and ex vivo evaluation of in situ polymeriz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0327893941e876577e3ce7c80408042
https://pubmed.ncbi.nlm.nih.gov/34342427
https://pubmed.ncbi.nlm.nih.gov/34342427
Autor:
George A. O'Toole, Courtney E. Price, Dominique H. Limoli, Vanessa V. Phelan, Dustin G. Brown
Publikováno v:
J Bacteriol
Cystic fibrosis (CF) patients chronically infected with bothPseudomonas aeruginosaandStaphylococcus aureushave worse health outcomes than patients who are mono-infected with eitherP. aeruginosaorS. aureus. We showed previously that mucoid strains ofP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07e02a692b7a455ab25b979065605b7a
https://europepmc.org/articles/PMC7099135/
https://europepmc.org/articles/PMC7099135/
Autor:
John A. Dessaint, Lisa A. Moulton, Ana Martínez del Campo, Molly A Williams, Juliette C. Madan, George A. O'Toole, Margaret R. Karagas, Todd A. MacKenzie, Shuyu Hao, Lily Ting, Brian J. Aldrich, Margaret F. Guill, Diana Chernikova, Hilary G. Morrison, Katherine M. Antosca, Irene H. Yuan, Edward J. Stewart, Dana B. Dorman, Courtney E. Price, Kathryn L. Ruoff, Mitchell L. Drumm, Lynn M. Feenan, Natalie R. Sontag, Kewei Li
Publikováno v:
Journal of Bacteriology. 201
Previous work from our group indicated an association between the gastrointestinal microbiota of infants with cystic fibrosis (CF) and airway disease in this population. Here we report that stool microbiota of infants with CF demonstrates an altered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e0286a1242c018973bcded7976cf0b
https://doi.org/10.1128/jb.00274-19
https://doi.org/10.1128/jb.00274-19