Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Cameron B. Morrison"'
Autor:
Matthew R. Markovetz, Ian C. Garbarine, Cameron B. Morrison, William J. Kissner, Ian Seim, M. Gregory Forest, Micah J. Papanikolas, Ronit Freeman, Agathe Ceppe, Andrew Ghio, Neil E. Alexis, Stephen M. Stick, Camille Ehre, Richard C. Boucher, Charles R. Esther, Marianne S. Muhlebach, David B. Hill
Publikováno v:
Journal of Cystic Fibrosis. 21:959-966
Mucus hyperconcentration in cystic fibrosis (CF) lung disease is marked by increases in both mucin and DNA concentration. Additionally, it has been shown that half of the mucins present in bronchial alveolar lavage fluid (BALF) from preschool-aged CF
Autor:
Yuzhi Chen, Charlotte A Love, Jason D. Surratt, Camille Ehre, Elise Hickman, Yael-Natalie Escobar, Meghan E. Rebuli, Cameron B. Morrison, Ilona Jaspers
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
In the United States, millions of adults use electronic cigarettes (e-cigs), and a majority of these users are former or current cigarette smokers. It is unclear, whether prior smoking status affects biological responses induced by e-cigs. In this st
Autor:
Takafumi Kato, Giorgia Radicioni, Micah J. Papanikolas, Georgi V. Stoychev, Matthew R. Markovetz, Kazuhiro Aoki, Melody Porterfield, Kenichi Okuda, Selene M. Barbosa Cardenas, Rodney C. Gilmore, Cameron B. Morrison, Camille Ehre, Kimberlie A. Burns, Kristen K. White, Tara A. Brennan, Henry P. Goodell, Holly Thacker, Henry T. Loznev, Lawrence J. Forsberg, Takahide Nagase, Michael Rubinstein, Scott H. Randell, Michael Tiemeyer, David B. Hill, Mehmet Kesimer, Wanda K. O’Neal, Stephen T. Ballard, Ronit Freeman, Brian Button, Richard C. Boucher
Publikováno v:
Science Advances. 8
Cystic fibrosis (CF) is characterized by abnormal transepithelial ion transport. However, a description of CF lung disease pathophysiology unifying superficial epithelial and submucosal gland (SMG) dysfunctions has remained elusive. We hypothesized t
Autor:
Kimberlie A. Burns, Brian Button, Richard C. Boucher, Micah J. Papanikolas, Stephen T. Ballard, Lawrence J. Forsberg, Giorgia Radicioni, Kenichi Okuda, Michael Rubinstein, Henry P. Goodell, David B. Hill, Henry T. Loznev, Takafumi Kato, Kristen K. White, Rodney C. Gilmore, Takahide Nagase, Mehmet Kesimer, Selene Margarita Barbosa Cardenas, Matthew R. Markovetz, Holly Thacker, Ronit Freeman, Scott H. Randell, Michael Tiemeyer, Cameron B. Morrison, Mindy Porterfield, Camille Ehre, Wanda K. O'Neal, Georgi Stoychev, Kazuhiro Aoki
Cystic fibrosis (CF) is characterized by abnormal transepithelial ion transport. However, a description of CF lung disease pathophysiology unifying superficial epithelial and submucosal gland (SMG) dysfunctions has remained elusive. We hypothesized t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f7ad9fe184ed86e58f8c8f68362e0a5
https://doi.org/10.1101/2021.09.22.461306
https://doi.org/10.1101/2021.09.22.461306
Autor:
Yu Mikami, Troy D. Rogers, Lawrence E. Ostrowski, Ling Sun, Richard C. Boucher, Scott H. Randell, Cameron B. Morrison, Camille Ehre, Patrick R. Sears, Barbara R. Grubb, Takafumi Kato
Publikováno v:
Am J Respir Cell Mol Biol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c40c6b9ee4eb9515d584950a2d7ba11
https://europepmc.org/articles/PMC8456889/
https://europepmc.org/articles/PMC8456889/
Autor:
Matthew R. Markovetz, Samir N. P. Kelada, Troy D. Rogers, Lauren J. Donoghue, Camille Ehre, Barbara R. Grubb, Cameron B. Morrison, David B. Hill, Brian Button, Kathryn M. McFadden
Airway mucociliary clearance (MCC) is required for host defense and often diminished in chronic lung diseases. Effective clearance depends upon coordinated actions of the airway epithelium and a mobile mucus layer. Dysregulation of the primary secret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a74fb84c4b7c601e88cbb693511553a
https://doi.org/10.1101/2020.06.17.155846
https://doi.org/10.1101/2020.06.17.155846
Publikováno v:
Pediatr Pulmonol
Cystic fibrosis (CF) is both the most common and most lethal genetic disease in the Caucasian population. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and is characterized by the accumulation of thi
Autor:
Matthew R. Markovetz, Jimmy Liao, Camille Ehre, Wanda K. O'Neal, Cameron B. Morrison, Kendall M. Shaffer, Nancy L. Quinney, Lisa C. Morton, Jason A. Wykoff, Alexis Flen, David B. Hill, M. Delion, Mehmet Kesimer, Martina Gentzsch, Mitchell L. Drumm, Shuyu Hao, Kenza C Araba
Publikováno v:
Eur Respir J
QuestionCystic fibrosis (CF) is characterised by the accumulation of viscous adherent mucus in the lungs. While several hypotheses invoke a direct relationship with cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction (i.e. acidic a
Autor:
Camille Ehre, Tadahiro Kumagai, David B. Nix, Giorgia Radicioni, Harendra Arora, Neil E. Alexis, William J. Kissner, Michael Tiemeyer, Kathryn A. Ramsey, Ian C. Garbarine, Cameron B. Morrison, Richard C. Boucher, Priya A. Kumar, Mehmet Kesimer, Duncan C. Krause, David B. Hill, Andrew J. Ghio, Thomas M. Krunkosky, Durai B. Subramani, Matthew R. Markovetz
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
Muco-obstructive lung diseases (MOLDs), like cystic fibrosis and chronic obstructive pulmonary disease, affect a spectrum of subjects globally. In MOLDs, the airway mucus becomes hyperconcentrated, increasing osmotic and viscoelastic moduli and impai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7381fe9b8d723d21762e6b01f3d3176a
https://europepmc.org/articles/PMC6842913/
https://europepmc.org/articles/PMC6842913/
Autor:
Ian C. Garbarine, Stephen M. Stick, Lidija Turkovic, B. Thelin, Ian Seim, M. Delion, Matthew R. Markovetz, Marianne S. Muhlebach, Matthew C. Wolfgang, Charles R. Esther, Richard C. Boucher, Juan R. Sabater, Camille Ehre, David B. Hill, Kathryn A. Ramsey, Sarath Ranganathan, Bryan Zorn, D. Villalon, Mark Gregory Forest, Arest Cf, Cameron B. Morrison
Publikováno v:
A108. PATHOPHYSIOLOGY IN DIFFUSE PARENCHYMAL LUNG DISEASES.