Zobrazeno 1 - 10
of 225
pro vyhledávání: '"Carroll E. Cross"'
Autor:
Maret G. Traber, Carroll E. Cross
Publikováno v:
Antioxidants & Redox Signaling. 38:775-791
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28e98ffdc473da9ba3cc8470813d6bbf
https://doi.org/10.1089/ars.2022.0212
https://doi.org/10.1089/ars.2022.0212
Autor:
Maret G. Traber, Scott W. Leonard, Vihas T. Vasu, Brian M. Morrissey, Huangshu (John) Lei, Jeffrey Atkinson, Carroll E. Cross
Publikováno v:
Nutrients; Volume 14; Issue 18; Pages: 3717
Nutrients, vol 14, iss 18
Nutrients, vol 14, iss 18
Background: Numerous abnormalities in cystic fibrosis (CF) could influence tocopherol absorption, transportation, storage, metabolism and excretion. We hypothesized that the oxidative distress due to inflammation in CF increases vitamin E utilization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca962d0c529904f1bb90a0b82eab76a9
https://doi.org/10.3390/nu14183717
https://doi.org/10.3390/nu14183717
Autor:
Brian M. Morrissey, Michele A. La Merrill, Carroll E. Cross, Sean Ott, Keri A. Hayakawa, Tamara Kadir, Jason P. Eiserich
Publikováno v:
Free Radical Biology and Medicine. 129:146-154
Rationale Cystic fibrosis (CF) patients are known to produce cyanide (CN-) although challenges exist in determinations of total levels, the precise bioactive levels, and specificity of its production by CF microflora, especially P. aeruginosa. Our ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c019d0ab7e4bbd39d4a48a0dc5e19739
https://doi.org/10.1016/j.freeradbiomed.2018.09.007
https://doi.org/10.1016/j.freeradbiomed.2018.09.007
Autor:
Brooks Kuhn, David Z. Silberstein, Somen Nandi, Karen A. McDonald, Carroll E. Cross, Hal S. Padgett, Matthew J. McNulty
Publikováno v:
Free radical biologymedicine. 163
Alpha-1 antitrypsin deficiency (A1ATD) is an autosomal recessive disease characterized by low plasma levels of A1AT, a serine protease inhibitor representing the most abundant circulating antiprotease normally present at plasma levels of 1–2 g/L. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a797b3a2e2786f35fbfbd93be73a2cf
https://pubmed.ncbi.nlm.nih.gov/33279618
https://pubmed.ncbi.nlm.nih.gov/33279618
Autor:
James K. Stoller, Gerard M. Turino, Shandra L Knight, Kenneth S. Goodman, James M. Stocks, Mark L. Brantly, Jeffrey Teckman, C Strange, Carroll E. Cross, Douglas K. Hogarth, Michael Campos, Robert A. Sandhaus
Publikováno v:
Chronic obstructive pulmonary diseases (Miami, Fla.), vol 3, iss 3
Background: The diagnosis and clinical management of adults with alpha-1 antitrypsin deficiency (AATD) have been the subject of ongoing debate, ever since the publication of the first American Thoracic Society guideline statement in 1989.1 In 2003, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f330366f19edda8a5c9da4751ce284
https://doi.org/10.15326/jcopdf.3.3.2015.0182
https://doi.org/10.15326/jcopdf.3.3.2015.0182
Autor:
Carroll E. Cross
Publikováno v:
Postgraduate medicine. 76(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::981c7508342af20c52ebe6d4dc6cfbdd
https://pubmed.ncbi.nlm.nih.gov/27224539
https://pubmed.ncbi.nlm.nih.gov/27224539
Autor:
Carroll E. Cross, Amir A. Zeki
Neutrophil extracellular traps (NETs) formation was initially linked with host defence and extracellular killing of pathogens. However, recent studies have highlighted their inflammatory potential. Oxidized low density lipoprotein (oxLDL) has been im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d9e344a89ab00c3ead527f6cf1800c
https://europepmc.org/articles/PMC6020148/
https://europepmc.org/articles/PMC6020148/
Publikováno v:
Annals of the New York Academy of Sciences. 1259:1-9
Cystic fibrosis (CF) is associated with abnormal lipid metabolism, intense respiratory tract (RT) infection, and inflammation, eventually resulting in lung tissue destruction and respiratory failure. The CF RT inflammatory milieu, as reflected by air
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f801151c23d8c440cd09bbd1fece2b6
https://doi.org/10.1111/j.1749-6632.2012.06580.x
https://doi.org/10.1111/j.1749-6632.2012.06580.x
Autor:
Anna L.P. Chapman, Brian M. Morrissey, Maya Juarez, Carroll E. Cross, Vihas T. Vasu, Chin-Shang Li, Jessica S. Houghton, Jason P. Eiserich
Publikováno v:
Journal of Cystic Fibrosis. 9:84-92
BackgroundDecreased expired nitric oxide (eNO) is commonly observed in cystic fibrosis (CF) patients and is usually explained by dysregulation of NO synthase (NOS) isoforms in respiratory tract epithelium. Later stages of this disease are accompanied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5747bbcc59d094b135611a0c7d092a8
https://doi.org/10.1016/j.jcf.2009.10.001
https://doi.org/10.1016/j.jcf.2009.10.001
Publikováno v:
Molecular Nutrition & Food Research. 54:693-709
Rodents fed alpha-tocopherol (alphaT)-depleted diets develop neuromuscular deficits. Unequivocal role of alphaT in the prevention of these deficits is confounded by possible neurotoxic oxidant products generated, ex vivo in alphaT-depleted diets. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe4c8b146e6e60531110a07c33d8cca
https://doi.org/10.1002/mnfr.200900575
https://doi.org/10.1002/mnfr.200900575