α1-Antichymotrypsin Mutations In Patients With Chronic Obstructive Pulmonary Disease
Main Authors: | Andrew J. Sandford, Tabassum Chagani, Tracey D. Weir, Peter D. Parè |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
1998-01-01
|
Series: | Disease Markers |
Online Access: | http://dx.doi.org/10.1155/1998/867620 |
Similar Items
-
Plasma levels of alpha1-antichymotrypsin and secretory leukocyte proteinase inhibitor in healthy and chronic obstructive pulmonary disease (COPD) subjects with and without severe α1-antitrypsin deficiency
by: Sveger Tomas, et al.
Published: (2007-01-01) -
Alpha₁-antichymotrypsin : conformational transitions and disease
by: Gooptu, Bibekbrata
Published: (2000) -
Topical delivery of alpha1-Antichymotrypsin for wound healing
by: Schmidt, Roland
Published: (2005) -
Urinary alpha1-antichymotrypsin: a biomarker of prion infection.
by: Gino Miele, et al.
Published: (2008-01-01) -
Soluble selectins and highly fucosylated ?1-antichymotrypsin in rheumatoid arthritis patients
by: Anna Olewicz-Gawlik, et al.
Published: (2015-03-01)