Human Z α1 -antitrypsin accumulates intracellularly and stimulates lysosomal activity when synthesised in the Xenopus oocyte
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(85)80798-5/fullpdf
Reference16 articles.
1. The Electrophoretic α;1-Globulin Pattern of Serum in α;1-Antitrypsin Deficiency
2. Structural and functional characterization of the abnormal Z α1 -antitrypsin isolated from human liver
3. Translation and processing of normal (PiMM) and abnormal (PiZZ) human α1 -antitrypsin
4. α1-Antitrypsin retention by hepatocytes in deficient individuals
5. Xenopus oocytes can synthesise but do not secrete the Z variant of human α1 -antitrypsin
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1. Molecular Mechanisms Responsible for Increased Vulnerability of the Ageing Oocyte to Oxidative Damage;Oxidative Medicine and Cellular Longevity;2017
2. The Endosomal Protein-Sorting Receptor Sortilin Has a Role in Trafficking α-1 Antitrypsin;Genetics;2012-11-01
3. REVIEW: α1-Antitrypsin deficiency associated liver disease;Journal of Gastroenterology and Hepatology;1997-05
4. Molecular pathogenesis of liver disease in alpha1-antitrypsin deficiency;Hepatology;1996-12
5. Mutations Which Impede Loop/Sheet Polymerization Enhance the Secretion of Human α1-Antitrypsin Deficiency Variants;Journal of Biological Chemistry;1995-04
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