Alpha-1 antitrypsin deficiency (A1AD) is an inherited condition that often leads to emphysema that is associated with breathing difficulties. Current therapies for this condition are expensive and invasive, or only address the symptoms (such as shortness of breath) instead of addressing the underlying cause. Through this project, a research question will be pursued that will aim to improve identification of potential new therapies. Candidate therapies include low molecular weight compounds that may inhibit human neutrophil elastase (HNE), the enzyme that degrades the elastic component in the lungs leading to the breathing difficulties associated with A1AD. The approach is to determine whether commercially available kits utilizing different...
Introduction: Chronic respiratory diseases such as COPD, bronchiectasis and cystic fibrosis (CF), ar...
Human neutrophil elastase (HNE) has been identified as a potential therapeutic target for the discov...
Inherited or "acquired" deficiency of alpha 1-antitrypsin (believed to be the cause of pulmonary emp...
Alpha-1 antitrypsin deficiency (A1AD) is an inherited condition that often leads to emphysema that i...
Alpha-1-antitrypsin deficiency (A1AD) is a disorder inherited through certain genotypes and is in ab...
BACKGROUND Alpha-1-antitrypsin (A1AT) deficiency is the only recognised genetic risk factor for chro...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
Introduction: Neutrophil elastase (NE) is a 29kDa serine protease released from the azurophilic gran...
Alpha-1 antitrypsin deficiency (AATD) is a protein conformational disease with the most common cause...
AbstractAlpha-1 antitrypsin deficiency is linked with an increased risk of suffering from lung emphy...
Introduction: Little is known about protease, anti-protease markers in chronic obstructive pulmonary...
Abstract: Alpha-1 antitrypsin (AAT) functions primarily to inhibit neutrophil elastase, and its defi...
International audienceINTRODUCTION: Alpha-1 antitrypsin, secreted by the liver, inhibits neutrophil ...
α1 Antitrypsin deficiency (AATD) increases the risk of chronic obstructive pulmonary disease (COPD),...
Alpha1-antitrypsin deficiency (AATD) is a genetic disorder characterized by reduced serum levels of ...
Introduction: Chronic respiratory diseases such as COPD, bronchiectasis and cystic fibrosis (CF), ar...
Human neutrophil elastase (HNE) has been identified as a potential therapeutic target for the discov...
Inherited or "acquired" deficiency of alpha 1-antitrypsin (believed to be the cause of pulmonary emp...
Alpha-1 antitrypsin deficiency (A1AD) is an inherited condition that often leads to emphysema that i...
Alpha-1-antitrypsin deficiency (A1AD) is a disorder inherited through certain genotypes and is in ab...
BACKGROUND Alpha-1-antitrypsin (A1AT) deficiency is the only recognised genetic risk factor for chro...
Alpha-1 antitrypsin (AAT) deficiency remains an underrecognized genetic disease with predominantly p...
Introduction: Neutrophil elastase (NE) is a 29kDa serine protease released from the azurophilic gran...
Alpha-1 antitrypsin deficiency (AATD) is a protein conformational disease with the most common cause...
AbstractAlpha-1 antitrypsin deficiency is linked with an increased risk of suffering from lung emphy...
Introduction: Little is known about protease, anti-protease markers in chronic obstructive pulmonary...
Abstract: Alpha-1 antitrypsin (AAT) functions primarily to inhibit neutrophil elastase, and its defi...
International audienceINTRODUCTION: Alpha-1 antitrypsin, secreted by the liver, inhibits neutrophil ...
α1 Antitrypsin deficiency (AATD) increases the risk of chronic obstructive pulmonary disease (COPD),...
Alpha1-antitrypsin deficiency (AATD) is a genetic disorder characterized by reduced serum levels of ...
Introduction: Chronic respiratory diseases such as COPD, bronchiectasis and cystic fibrosis (CF), ar...
Human neutrophil elastase (HNE) has been identified as a potential therapeutic target for the discov...
Inherited or "acquired" deficiency of alpha 1-antitrypsin (believed to be the cause of pulmonary emp...