Results 191 to 200 of about 459,657 (249)
Alpha-1 antitrypsin deficiency: genetics, clinical manifestations, AI prognostics, and advanced imaging in liver disease. [PDF]
Rajab I +9 more
europepmc +1 more source
Alpha-1 antitrypsin promotes re-epithelialization by regulating inflammation and migration. [PDF]
Farber I +18 more
europepmc +1 more source
Identification of an exosite at the neutrophil elastase/alpha-1-antitrypsin interface. [PDF]
Gangemi R +8 more
europepmc +1 more source
Alpha-1 antitrypsin in COVID-19 patients: a dual-center screening study in Malaysia. [PDF]
Musa N +9 more
europepmc +1 more source
Alpha-1 Antitrypsin Mediates Spontaneous Resolution of Acute Gouty Inflammation Via Inhibiting Caspase 3/GSDME-dependent Macrophage Pyroptosis. [PDF]
Li X +11 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Alpha-1 antitrypsin deficiency: a re-surfacing adult liver disorder.
Journal of Hepatology, 2021Alpha-1 antitrypsin deficiency (AATD) arises from mutations in the SERPINA1 gene encoding alpha-1 antitrypsin (AAT) that lead to AAT retention in the endoplasmic reticulum of hepatocytes, causing proteotoxic liver injury and loss-of-function lung disease.
M. Fromme +4 more
semanticscholar +1 more source
Alpha‐1‐Antitrypsin Deficiency
Clinical Liver Disease, 2022Content available: Author Audio Recording.
Anandini Suri +2 more
openaire +2 more sources
Alpha-1 Antitrypsin Deficiency
Journal of Insurance Medicine, 2015Alpha-1 antitrypsin deficiency is an inherited disorder that may cause severe lung and liver disease.
SK Kabra, Rakesh Lodha, Kana Jat
openaire +3 more sources
Alpha-1 Antitrypsin Deficiency
2023Alpha-1 antitrypsin (AAT) deficiency is a common monogenic disorder in which there is a strong founder effect of a single missense mutation in SERPINA1, the gene encoding this major circulating serum anti-protease that is normally expressed primarily in hepatocytes.
Alisha M, Gruntman +2 more
openaire +2 more sources

