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]

open access: yesAnn Med Surg (Lond)
Rajab I   +9 more
europepmc   +1 more source

Alpha-1 antitrypsin promotes re-epithelialization by regulating inflammation and migration. [PDF]

open access: yesFront Immunol
Farber I   +18 more
europepmc   +1 more source

Identification of an exosite at the neutrophil elastase/alpha-1-antitrypsin interface. [PDF]

open access: yesFEBS J
Gangemi R   +8 more
europepmc   +1 more source

Alpha-1 antitrypsin in COVID-19 patients: a dual-center screening study in Malaysia. [PDF]

open access: yesAnn Saudi Med
Musa N   +9 more
europepmc   +1 more source

Alpha-1 antitrypsin deficiency: a re-surfacing adult liver disorder.

Journal of Hepatology, 2021
Alpha-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, 2022
Content available: Author Audio Recording.
Anandini Suri   +2 more
openaire   +2 more sources

Alpha-1 Antitrypsin Deficiency

Journal of Insurance Medicine, 2015
Alpha-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

2023
Alpha-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

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