Results 101 to 110 of about 3,462 (201)
A1AT is ineffective on endogenous caspase-1 activation in cell-free system.
Caspase-1 activity was measured in cell-free lysates from THP-1 monocytes. Cell-free lysates in a hypotonic buffer were placed at 4 or 30°C for 1 hour with or without A1AT (2.5 mg/mL). Same concentration of BSA was used as control. Caspase-1 activity was
Srabani Mitra (259173) +3 more
core +1 more source
ROC Analysis of Diagnostic Performance Utilizing Serum Antiproteases in Cancer Patients
Assessment of the accuracy of diagnostic procedures is made independent of diagnostic criteria by means of a receiver-operating-characteristics (ROC) curve. We performed ROC analysis for the major serum antiproteases: alpha-1-antitrypsin (A1AT) and alpha-
J. Millán +6 more
doaj +1 more source
We inserted the sequence coding for the cytoplasmic portion of the human MET receptor into an 18-kb genomic fragment containing the entire human A1AT gene (encoding alpha-1-antitrypsin).
AMICONE, Laura +11 more
core +1 more source
Objective: The clinical, functional, radiological and genotypic descriptions of patients with an alpha-1 antitrypsin (A1AT) gene mutation in a referral center for COPD in Brazil.
Manuela Brisot Felisbino +5 more
doaj +1 more source
A1AT does not influence IL-18 processing and release through the activation of caspase-1.
THP-1 cells and human monocytes were pre-treated with A1AT (2.5 mg/mL) for 1 h followed by LPS 1 μg/ml for 30 minutes, and then triggered with ATP 5 mM for another 30 minutes to determine the release of IL-18 and caspase-1.
Srabani Mitra (259173) +3 more
core +1 more source
Gene targeted therapeutics for liver disease in alpha-1 antitrypsin deficiency
Caitriona McLean*, Catherine M Greene*, Noel G McElvaneyRespiratory Research Division, Dept. Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin 9, Ireland; *Each of these authors contributed equally ...
Caitriona McLean +2 more
doaj
Mice were infected with PA as described in Materials and Methods, and treated at 2 h post PA infection with A1AT. After 1 day of PA infection, mice (n = 6 mice/group) were sacrificed to determine inflammation (A, B, C, D) and PA load (E, F) in ...
Di Jiang (258208) +4 more
core +1 more source
Mice were infected with Pseudomonas aeruginosa (PA) as described in Materials and Methods, and treated at 2 hr, 1 day and 3 day post PA infection with A1AT.
Di Jiang (258208) +4 more
core +1 more source
Mice were infected with PA as described in Materials and Methods, and treated at 2 hr, 1 day and 3 day post PA infection with A1AT. After 3 days of PA infection, mice (n = 6–7 mice/group) were sacrificed to determine inflammation (A, B, C, D) and PA load
Di Jiang (258208) +4 more
core +1 more source

