Disruption of Disulfide Bonds Is Responsible for Impaired Secretion in Human Complement Factor H Deficiency
Open Access
- 1 April 1999
- journal article
- Published by Elsevier
- Vol. 274 (17) , 11782-11788
- https://doi.org/10.1074/jbc.274.17.11782
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Role of 26S proteasome and HRD genes in the degradation of 3-hydroxy-3-methylglutaryl-CoA reductase, an integral endoplasmic reticulum membrane protein.Molecular Biology of the Cell, 1996
- Localization of the Disulfide Bond Involved in Post-translational Processing of Glycosylasparaginase and Disrupted by a Mutation in the Finnish-type AspartylglycosaminuriaJournal of Biological Chemistry, 1995
- Complement factor H and related proteins: an expanding family of complement-regulatory proteins?Immunology Today, 1994
- Solution Structure of a Pair of Complement Modules by Nuclear Magnetic ResonanceJournal of Molecular Biology, 1993
- Accelerated secretion of human lysozyme with a disulfide bond mutationEuropean Journal of Biochemistry, 1992
- Hereditary, Complete Deficiency of Complement Factor H Associated with Recurrent Meningococcal DiseaseScandinavian Journal of Immunology, 1989
- COMPLEMENT DEFICIENCIES IN PATIENTS OVER TEN YEARS OLD WITH MENINGOCOCCAL DISEASE DUE TO UNCOMMON SEROGROUPSThe Lancet, 1989
- Structure-function relationships of the complement componentsImmunology Today, 1989
- Role of disulfide bonds in folding and secretion of human lysozyme in saccharomycescerevisiaeBiochemical and Biophysical Research Communications, 1988
- Lectin-binding sites as markers of Golgi subcompartments: proximal-to-distal maturation of oligosaccharides.The Journal of cell biology, 1983