Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Theresa A, Laguna"'
Autor:
Monica E. Kruk, Subina Mehta, Kevin Murray, LeeAnn Higgins, Katherine Do, James E. Johnson, Reid Wagner, Chris H. Wendt, John B. O’Connor, J. Kirk Harris, Theresa A. Laguna, Pratik D. Jagtap, Timothy J. Griffin
Publikováno v:
mSystems, Vol 9, Iss 7 (2024)
ABSTRACT Airway microbiota are known to contribute to lung diseases, such as cystic fibrosis (CF), but their contributions to pathogenesis are still unclear. To improve our understanding of host-microbe interactions, we have developed an integrated a
Externí odkaz:
https://doaj.org/article/e36a430e5a754b0e804f12b6ccd9536c
Autor:
Ana Gabriela Soares Silva, Fernanda Dias de Paula, Nelson Rannieri Tirone, Maria Theresa Cerávolo Laguna Abreu
Publikováno v:
Revista Brasileira de Extensão Universitária, Vol 14, Iss 3 (2023)
No Brasil, jovens de 18 anos ao participarem dos tiros de guerra (TG) são convidados a realizarem atividades junto à comunidade, entre elas, a realização da doação de sangue (DS). Esta ação, entretanto, muitas vezes é um ato único na vida d
Externí odkaz:
https://doaj.org/article/53ce96ab9b5d414f85d8235ef99f8c92
Autor:
John B. O’Connor, Brandie D. Wagner, J. Kirk Harris, Daniel N. Frank, Diana E. Clabots, Theresa A. Laguna
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
IntroductionAirway infection and inflammation lead to the progression of obstructive lung disease in persons with cystic fibrosis (PWCF). However, cystic fibrosis (CF) fungal communities, known drivers of CF pathophysiology, remain poorly understood
Externí odkaz:
https://doaj.org/article/6c4c54828ce34dc581befcf5b9402f63
Autor:
John B. O’Connor, Madison Mottlowitz, Monica E. Kruk, Alan Mickelson, Brandie D. Wagner, Jonathan Kirk Harris, Christine H. Wendt, Theresa A. Laguna
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
The leading cause of morbidity and mortality in cystic fibrosis (CF) is progressive lung disease secondary to chronic airway infection and inflammation; however, what drives CF airway infection and inflammation is not well understood. By providing a
Externí odkaz:
https://doaj.org/article/13f9151e0ea34ab487fd3db7683c1514
Autor:
John B O'Connor, Madison M Mottlowitz, Brandie D Wagner, Kathleen L Boyne, Mark J Stevens, Charles E Robertson, Jonathan K Harris, Theresa A Laguna
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0257838 (2021)
RationaleChronic airway infection and inflammation resulting in progressive, obstructive lung disease is the leading cause of morbidity and mortality in cystic fibrosis. Understanding the lower airway microbiota across the ages can provide valuable i
Externí odkaz:
https://doaj.org/article/d0321265d8184464ad546af551bcee45
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
Newborn screening for cystic fibrosis is universal across the United States; however, each state chooses the method by which they screen. Illinois employs a two-step process which includes the measurement of the immunoreactive trypsinogen followed by
Externí odkaz:
https://doaj.org/article/a06628ba75f2499581fa9dcae44e726c
Autor:
Theresa A. Laguna, Cynthia B. Williams, Myra G. Nunez, Cole Welchlin-Bradford, Catherine E. Moen, Cavan S. Reilly, Chris H. Wendt
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background There are urgent needs for clinically relevant biomarkers to identify children with cystic fibrosis (CF) at risk for more progressive lung disease and to serve as outcome measures for clinical trials. Our objective was to investig
Externí odkaz:
https://doaj.org/article/b32dcc037e1940a5b7902b7b7dba7302
Autor:
Meghan E. McGarry, Elizabeth R. Gibb, Theresa A. Laguna, Brian P. O'Sullivan, Gregory S. Sawicki, Jeffery T. Zobell
Publikováno v:
Pediatric Pulmonology. 58:1595-1597
Autor:
Alexander L Bisch, Courtney M Wheatley, Sarah E Baker, Elizabeth R Peitzman, Erik H Van Iterson, Theresa A Laguna, Wayne J Morgan, Eric M Snyder
Publikováno v:
Clinical Medicine Insights: Circulatory, Respiratory and Pulmonary Medicine, Vol 13 (2019)
Background: Cystic fibrosis (CF) is a genetic disease affecting multiple organ systems of the body and is characterized by mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR). Previous work has shown that a
Externí odkaz:
https://doaj.org/article/8eef6bf0bf7647a4a12c2b67f9fc2f52
Autor:
John Palla, Santosh Thapa, Alamelu Venkatachalam, Jessica K. Runge, Theresa A. Laguna, Ruth Ann Luna
Background: Hispanic people with cystic fibrosis (CF) have decreased life expectancy and earlier acquisition of Pseudomonas aeruginosa compared to non-Hispanic white individuals with CF. Racial and ethnic differences in the airway microbiome of CF ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::721a55263c63db0cc515ca1c7723df6e
https://doi.org/10.22541/au.167411529.91637649/v1
https://doi.org/10.22541/au.167411529.91637649/v1