Alpha1-antitrypsin genotypes in patients with chronic pancreatitis. Scand J Gastroenterol 2002; 37: 356 - 359H. Witt, A. Kage, W. Luck, and M. Becker, "𝛼1-antitrypsin genotypes in patients with chronic pancreatitis," Scandinavian Journal of Gastroenterology, vol. 37, no. 3, pp. 356-...
Alpha-1 antitrypsin levels and genotypes in children with primary spontaneous pneumothoraxPleural Disease/Pneumothorax PostersSESSION TYPE: Poster PresentationsPRESENTED ON: Saturday, March 22, 2014 at 01:15 PM - 02:15 PMPURPOSE: A recent series of case reports in children links Primary Spontaneous ...
Some deficient alpha 1 antitrypsin (AAT) genotypes seem to be associated with asthma development. The objective of this study was to analyze the distribution of AAT genotypes in asthmatic patients allergic to house dust mites (HDM), and to asses a possible association between these genotypes and...
Molecular Confirmation of α1-Antitrypsin Genotypes in Newborn Dried Blood Specimens Deficiency of 伪 1 -antitrypsin (伪 1 AT), a common hereditary disorder of Caucasians, is associated with an increased risk for early-onset chronic obstruc... WC Spence,JE Morris,K Pass,... - 《Biochemical ...
alpha-1 antitrypsin deficiency (AATD) is based on patients with the PI*ZZ or PI*Znull genotypes, who have a severe deficiency in alpha-1 antitrypsin (AAT), with plasma levels < 11 µM (< 52 mg/dL) compared with the normal range of 19–47 µM (102–254 mg/dL) [1]. ...
Deficiency of Alpha-1-antitrypsin (AAT) can be a genetic condition that increases the risk of developing liver, lung and possibly gastrointestinal disease. Since many autistic children also have gastrointestinal disorders, this study was designed to measure serum concentration of AAT and establish AAT...
PURPOSE: A protein or peptide fused body with enhanced half life in the body is provided to enhance half life(T1/2) in the blood by maintaining persistence in the body.;CONSTITUTION: A protein or peptide fused body with enhanced half-life is obtained by binding alpha-1 antitrypsin with phys...
Alpha-1 Antitrypsin Genotypes in Breast Cancer Patients Proteolytic enzymes play a significant role in malignancy including, loss of growth regulation, invasiveness and metastases forA1ATion. Alpha-1 antit-rypsi... EAZ Jalal,SD Hakam,NM Khalid - 《Journal of Health Science》 被引量: 6发表: 200...
Alpha 1 Antitrypsin Alpha-1-antitrypsin deficiency (A1ATD): What is A1AT? A1AT is a serine protease inhibitor secreted primarily in liver parenchymal cells and to a lesser extent in macrophages. It protects tissues from enzymes of inflammatory cells by inactivating especially neutrophil elastase (...
Alpha-1-antitrypsin deficiency (AATD) is a rare genetic disorder associated with the development of liver and lung disease. AAT is a 52-kD glycoprotein, produced mainly by hepatocytes and secreted into the blood. Agglomeration of the AAT-protein in hepatocytes can result in liver disease. Exposur...