Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Laura T Fee"'
Autor:
Laura T. Fee, Debananda Gogoi, Michael E. O’Brien, Emer McHugh, Michelle Casey, Ciara Gough, Mark Murphy, Ann M. Hopkins, Tomás P. Carroll, Noel G. McElvaney, Emer P. Reeves
Publikováno v:
Biomedicines, Vol 9, Iss 12, p 1925 (2021)
Alpha-1 antitrypsin (AAT) deficiency (AATD) is characterized by increased risk for emphysema, chronic obstructive pulmonary disease (COPD), vasculitis, and wound-healing impairment. Neutrophils play a central role in the pathogenesis of AATD. Dysregu
Externí odkaz:
https://doaj.org/article/fd3974a57e8e4a62945b8c22bb67bc45
Autor:
Michael Henry, Cormac McCarthy, Emer P. Reeves, Paula Meleady, Oliver J. McElvaney, Karen McQuillan, Mark Logan, Mark P Murphy, Noel G. McElvaney, Michael Emmet O'Brien, Tomás P. Carroll, Niall Browne, Laura T. Fee
Publikováno v:
Thorax
IntroductionAlpha-1 antitrypsin (AAT) deficiency (AATD) is associated with early onset emphysema. The aim of this study was to investigate whether AAT binding to plasma constituents could regulate their activation, and in AATD, exploit this binding e
Autor:
Hamad Alkandari, Andrew Woodsmith, Mansour A. Alkhunaizi, Tomás P. Carroll, Layali Aldaihani, Siobhán E Lee, Alessandro N Franciosi, Laura T Fee, Noel G. McElvaney
Publikováno v:
COPD. 18(1)
The ZZ genotype of alpha-1 antitrypsin deficiency (AATD) is strongly associated with COPD, even in never-smokers. Moderate AATD genotypes (MZ and SZ) have been shown to increase the severity of COPD in smokers. In this comparative study, we examine t
Publikováno v:
Journal of Inflammation Research
Alpha-1 antitrypsin (AAT) is the most abundant serine protease inhibitor circulating in the blood. AAT deficiency (AATD) is an autosomal codominant condition affecting an estimated 3.4 million individuals worldwide. The clinical disease associated wi
Autor:
Geraldine M. McCarthy, Douglas J. Veale, Paul O'Connell, Dermot Kenny, Eimear Dunne, Danielle M Dunlea, Emer P. Reeves, David J. L. Hunt, Carl Orr, Tomás P. Carroll, Ursula Fearon, Laura T. Fee, Noel G. McElvaney, Cormac McCarthy
Publikováno v:
Arthritis & Rheumatology. 69:1576-1579
Objective To examine the prevalence of α1-antitrypsin deficiency (AATD) in rheumatoid arthritis (RA), and to determine whether AATD is associated with higher levels of rheumatoid factor (RF), antinuclear antibodies (ANAs), and anti–citrullinated p
Autor:
M.E. O'Brien, Tomás P. Carroll, Danielle M Dunlea, Laura T. Fee, Karen McQuillan, N.G. McElvaney, Emer P. Reeves, M. Molloy, Oliver J. McElvaney
Publikováno v:
B101. ADVANCES IN COPD PATHOGENESIS.
Autor:
Emer P. Reeves, Jonathan Shum, M Emmett O'Brien, Noel G. McElvaney, Tomás P. Carroll, Kevin Pennycooke, Catherine O'Connor, P Mark Logan, Laura T. Fee
Publikováno v:
COPD: Journal of Chronic Obstructive Pulmonary Disease. 12:2-9
Individuals with Alpha-1 antitrypsin deficiency (AATD) have mutations in the SERPINA1 gene causing genetic susceptibility to early onset lung and liver disease that may result in premature death. Environmental interactions have a significant impact i
Autor:
Cormac, McCarthy, Carl, Orr, Laura T, Fee, Tomás P, Carroll, Danielle M, Dunlea, David J L, Hunt, Eimear, Dunne, Paul, O'Connell, Geraldine, McCarthy, Dermot, Kenny, Ursula, Fearon, Douglas J, Veale, Emer P, Reeves, Noel G, McElvaney
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 69(8)
To examine the prevalence of αRF, ANAs, and ACPAs were measured by standard immunoturbidimetry, immunofluorescence assay, and enzyme-linked immunosorbent assay, respectively. Characterization of AAT phenotypes was performed by isoelectric focusing a
Autor:
Oisín F. McElvaney, Noel G. McElvaney, M. Emmet O’Brien, Laura T. Fee, Seshma Ramsawak, Kevin Molloy, Tomás P. Carroll, BlairMurray, Catherine O'Connor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acd2849f5377841e9be194ca3026e767
https://doi.org/10.5772/58602
https://doi.org/10.5772/58602
Autor:
Ilaria Ferrarotti, Stefania Ottaviani, Catherine O'Connor, Patrick O'Brien, Maurizio Luisetti, Tomás P. Carroll, Gerry McElvaney, Laura T. Fee
Publikováno v:
C25. CHRONIC OBSTRUCTIVE PULMONARY DISEASE: UPDATES ON EPIDEMIOLOGY AND CLINICAL PHENOTYPES.
AAT deficiency (AATD) results from mutations in the SERPINA1 gene, classically presenting with early-onset emphysema and liver disease. The most common mutation responsible for AATD is the Z mutation. AAT deficiency is under-diagnosed and prolonged d