Type IV collagen: structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis.
Open Access
- 1 December 1993
- journal article
- review article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 268 (35) , 26033-26036
- https://doi.org/10.1016/s0021-9258(19)74270-7
Abstract
No abstract availableThis publication has 65 references indexed in Scilit:
- Identification of Four Novel Mutations in the COL4A5 Gene of Patients with Alport SyndromeGenomics, 1993
- Colocalization of the genes for the α3(IV) and α4(IV) chains of type IV collagen to chromosome 2 bands q35–q37Genomics, 1992
- Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndromeGenomics, 1991
- Basement membrane collagen in the kidney: Regional localization of novel chains related to collagen IVKidney International, 1989
- Diffuse leiomyomatosis in alport syndromeThe Journal of Pediatrics, 1988
- Complete primary structure of the α1‐chain of human basement membrane (type IV) collagenFEBS Letters, 1987
- Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.Journal of Clinical Investigation, 1987
- COOH-terminal propeptides of the major human procollagensJournal of Molecular Biology, 1987
- Increased glycosylation of glomerular basement membrane collagen in diabetesBiochemical and Biophysical Research Communications, 1980
- Isolation of a collagen from basement membranes containing three identical α-chainsBiochemical and Biophysical Research Communications, 1971