The molecular basis of α1-antichymotrypsin deficiency in a heterozygote with liver and lung disease-Reference-Cited by-同舟云学术

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The molecular basis of α1-antichymotrypsin deficiency in a heterozygote with liver and lung disease

Published:1993-01 Issue:3 Volume:18 Page:313-321
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Faber Jakob-Peter,Poller Wolfgang,Olek Klaus,Baumann Ulrich,Carlson Joyce,Lindmark Bertil,Eriksson Sten

Publisher

Elsevier BV

Subject

Hepatology

Reference40 articles.

1. Human α1-antichymotrypsin: Interaction with chymotrypsin-like proteinases;Travis;J Biol Chem,1978

2. Characterisierung von α1-X-Glykoprotein als Chymotrypsin-Inhibitor des Humanplasmas;Heimburger;Clin Chim Acta,1965

3. Human α1-antichymotrypsin: Purification and properties;Travis;J Biol Chem,1978

4. α1-Antichymotrypsin;Berninger;J Med,1985

5. Evidence that alveolar macrophages can synthesize and secrete α1-antichymotrypsin;Burnett;Am Rev Respir Dis,1984

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