The molecular basis of α1-antichymotrypsin deficiency in a heterozygote with liver and lung disease
- 31 December 1993
- journal article
- case report
- Published by Elsevier in Journal of Hepatology
- Vol. 18 (3) , 313-321
- https://doi.org/10.1016/s0168-8278(05)80275-2
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Mis-sense mutation of α1-antichymotrypsin gene associated with chronic lung diseaseThe Lancet, 1992
- Structure of Sindbis virus core protein reveals a chymotrypsin-like serine proteinase and the organization of the virionNature, 1991
- Crystal structure of cleaved human α1-antichymotrypsin at 2.7 å resolution and its comparison with other serpinsJournal of Molecular Biology, 1991
- Crystal structure of plakalbumin, a proteolytically nicked form of ovalbuminJournal of Molecular Biology, 1990
- Endoplasmic reticulum storage diseaseHistopathology, 1990
- The microheterogeneity of desialylated α1-antichymotrypsin: the occurrence of two amino-terminal isoforms, one lacking a His-Pro dipeptideBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1989
- Molecular evolution of serpins: homologous structure of the human .alpha.1-antichymotrypsin and .alpha.1-antitrypsin genesBiochemistry, 1987
- α1Antitrypsin Deficiency and Liver Cirrhosis in AdultsActa Medica Scandinavica, 1987
- Inactivation of bradykinin and kallidin by cathepsin G and mast cell chymaseBiochemical and Biophysical Research Communications, 1985
- Sequence homology between human .alpha.1-antichymotrypsin, .alpha.1-antitrypsin, and antithrombin IIIBiochemistry, 1983