Pathogenesis of liver disease in alpha1-antitrypsin deficiency
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1994.tb13198.x/fullpdf
Reference32 articles.
1. Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis.
2. Species- and tissue-specific expression of human alpha 1-antitrypsin in transgenic mice.
3. Elastase regulates the synthesis of its inhibitor, alpha 1-proteinase inhibitor, and exaggerates the defect in homozygous PiZZ alpha 1 PI deficiency.
4. The Electrophoretic α;1-Globulin Pattern of Serum in α;1-Antitrypsin Deficiency
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1. Development and analytical validation of an enzyme-linked immunosorbent assay (ELISA) for the measurement of alpha1-proteinase inhibitor in serum and faeces from cats;Research in Veterinary Science;2012-10
2. Differential expression of liver proteins between obesity-prone and obesity-resistant rats in response to a high-fat diet;British Journal of Nutrition;2011-05-03
3. Molekulare Ursachen von Störungen des hepatogastroenterologischen Systems bei Neugeborenen;Molekularmedizinische Grundlagen von fetalen und neonatalen Erkrankungen;2005
4. Chronic liver disease in heterozygous α1-antitrypsin deficiency PiZ;Journal of Hepatology;2000-12
5. An overview of proteinase inhibitors;J VET INTERN MED;1999
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