Ethnic differences in the occurrence of the M1(ala213) haplotype of alpha-1-antitrypsin in asthmatic and non-asthmatic black and white South Africans
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04008.x/fullpdf
Reference23 articles.
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2. Molecular basis of alpha-1-antitrypsin deficiency;Brantly;Am J Med,1988
3. The role of platelet-activating factor in inflammation;Camussi;Clin Immunol Immunopathol,1990
4. Synthesis and release of platelet-activating factor is inhibited by plasma α1-proteinase inhibitor or α1-anticriymotrypsin and is stimulated by proteinases;Camussi;J Exp Med,1988
5. Human alpha-1-antitrypsin: Carbohydrate attachment and sequence homology;Carrell;FEBS Lett,1981
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1. Historical role of alpha-1-antitrypsin deficiency in respiratory and hepatic complications;Gene;2016-09
2. Differences in the prevalence of a TaqI RFLP in the 3‘ flanking region of the α1-proteinase inhibitor gene between asthmatic and non-asthmatic black and white South Africans;Clinical Genetics;2008-06-28
3. A case of systemic nodular panniculitis associated with M1 (Val213) Z phenotype of α1-protease inhibitor;International Journal of Dermatology;2008-06-28
4. Alpha 1 antitrypsin polymorphism in the tunisian population with special reference to pulmonary disease;Pathologie Biologie;2008-05
5. Polymorphisms in the SERPINA1 Gene and the Risk of Chronic Obstructive Pulmonary Disease in a Korean Population;Tuberculosis and Respiratory Diseases;2008
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