Alpha-1 antitrypsin (A1AT) is the most abundant serine protease inhibitor in human blood and exerts important anti-inflammatory and immune-modulatory effects. In combination with smoking or other long-term noxious exposures such as occupational dust and fumes, genetic A1AT deficiency can cause chronic obstructive pulmonary disease, a condition with elevated cardiovascular risk. The effects of A1AT deficiency on cardiovascular risk have hardly been studied today
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
BACKGROUND AND AIMS Alpha-1 antitrypsin (A1AT) is the most abundant serine protease inhibitor in hu...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
hereditary condition that is passed on from parents to their children through genes. This condition ...
Abstract From the discovery that alpha-1 antitrypsin (AAT) was an effective inhibitor of neutrophil ...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Danielle M Dunlea, Laura T Fee, Thomas McEnery, Noel G McElvaney, Emer P Reeves Irish Centre for Gen...
More than fifty years ago the observation that absence of the \u3b11 band from protein electrophores...
Alpha1-antitrypsin (AAT) is one of the major inhibitors involved in protease/antiprotease homeostasi...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...
BACKGROUND AND AIMS Alpha-1 antitrypsin (A1AT) is the most abundant serine protease inhibitor in hu...
Alpha-1 antitrypsin (A1AT) is a serine anti-protease produced chiefly by the liver. A1AT deficiency ...
hereditary condition that is passed on from parents to their children through genes. This condition ...
Abstract From the discovery that alpha-1 antitrypsin (AAT) was an effective inhibitor of neutrophil ...
Alpha-1-antitrypsin deficiency (AATD) is a hereditary disorder that is characterized by a low serum ...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circula...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
Alpha-1 antitrypsin deficiency (AATD) is an inherited disorder characterized by low serum levels of ...
Danielle M Dunlea, Laura T Fee, Thomas McEnery, Noel G McElvaney, Emer P Reeves Irish Centre for Gen...
More than fifty years ago the observation that absence of the \u3b11 band from protein electrophores...
Alpha1-antitrypsin (AAT) is one of the major inhibitors involved in protease/antiprotease homeostasi...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
To the Editor: PiZZ (Glu342Lys) alpha-1 antitrypsin deficiency (A1ATD) is a typical genetic risk ...
Alpha-1-antitrypsin (AAT) is a glycoprotein synthesised in the liver. Its main role is to protect lu...
Abstract Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emp...