The deficiency of α1-antitrypsin (AAT) is secondary to misfolding and polymerization of the abnormal Z-AAT in liver cells and is associated with lung emphysema. Alveolar macrophages (AMs) produce AAT; however, it is not known whether Z-AAT can polymerize in AMs, further decreasing lung AAT and promoting lung inflammation. Our intention was to investigate whether AAT polymerizes in human AMs and to study the possible relation between polymerization and degree of lung inflammation
Chronic Obstructive Pulmonary Disease (COPD) is a respiratory disease characterized by chronic infla...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
Background: Alpha-1 antitrypsin is the main inhibitor of neutrophil elastase in the lung. Although i...
The deficiency of α1-antitrypsin (AAT) is secondary to misfolding and polymerization of the abnormal...
Background: The deficiency of \u3b11-antitrypsin (AAT) is secondary to misfolding and polymerization...
The molecular mechanisms that cause emphysema are complex but most theories suggest that an excess o...
Background: {alpha}1-Antitrypsin (AAT)-Z deficiency is a risk factor for the development of COPD. Co...
Background Animal models using intratracheal instillation show that elastase, unopposed by α1-antitr...
Alpha-1-Antitrypsin (AAT) is a protein of the SERPINA1 gene. A single amino acid mutation (Lys342Glu...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
α1-antitrypsin deficiency is the most widely recognised genetic disorder causing chronic obstructive...
The severe, early onset emphysema that occurs in patients with circulating deficiency of α1-antitryp...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
The emphysema of al-antitrypsin (alAT) deficiency is concep-tualized to result from insufficient alA...
Alpha-1 antitrypsin (AAT) acts as an important neutrophil elastase inhibitor in the lung. Although t...
Chronic Obstructive Pulmonary Disease (COPD) is a respiratory disease characterized by chronic infla...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
Background: Alpha-1 antitrypsin is the main inhibitor of neutrophil elastase in the lung. Although i...
The deficiency of α1-antitrypsin (AAT) is secondary to misfolding and polymerization of the abnormal...
Background: The deficiency of \u3b11-antitrypsin (AAT) is secondary to misfolding and polymerization...
The molecular mechanisms that cause emphysema are complex but most theories suggest that an excess o...
Background: {alpha}1-Antitrypsin (AAT)-Z deficiency is a risk factor for the development of COPD. Co...
Background Animal models using intratracheal instillation show that elastase, unopposed by α1-antitr...
Alpha-1-Antitrypsin (AAT) is a protein of the SERPINA1 gene. A single amino acid mutation (Lys342Glu...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
α1-antitrypsin deficiency is the most widely recognised genetic disorder causing chronic obstructive...
The severe, early onset emphysema that occurs in patients with circulating deficiency of α1-antitryp...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
The emphysema of al-antitrypsin (alAT) deficiency is concep-tualized to result from insufficient alA...
Alpha-1 antitrypsin (AAT) acts as an important neutrophil elastase inhibitor in the lung. Although t...
Chronic Obstructive Pulmonary Disease (COPD) is a respiratory disease characterized by chronic infla...
Alpha1-antitrypsin (AAT) deficiency is a hereditary disorder associated with reduced AAT plasma leve...
Background: Alpha-1 antitrypsin is the main inhibitor of neutrophil elastase in the lung. Although i...