Expression of mRNA for type IV collagen α1, α5 and α6 chains by cultured dermal fibroblasts from patients with X-linked Alport syndrome
- 31 August 1998
- journal article
- Published by Elsevier in Matrix Biology
- Vol. 17 (4) , 279-291
- https://doi.org/10.1016/s0945-053x(98)90081-6
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- There Is Temporal and Spatial Expression of α1 (IV), α2 (IV), α5 (IV), α6 (IV) Collagen Chains and β1 Integrins During the Development of the Basal Lamina in an “In Vitro” Skin ModelJournal of Investigative Dermatology, 1997
- Characterization of α1(IV) Collagen Mutations in Caenorhabditis elegans and the Effects of α1 and α2(IV) Mutations on Type IV Collagen DistributionThe Journal of cell biology, 1997
- Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis.Journal of Clinical Investigation, 1997
- Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distributionKidney International, 1995
- A monoclonal antibody marker for Alport syndrome identifies the Alport antigen as the α5 chain of type IV collagenKidney International, 1994
- Identification of Mutations in the COL4A5 Collagen Gene in Alport SyndromeScience, 1990
- Identification of variant Alport phenotypes using an Alport-specific antibody probeKidney International, 1989
- Basement membrane collagen in the kidney: Regional localization of novel chains related to collagen IVKidney International, 1989
- Extracellular matrix proteins of human epidermal keratinocytes and feeder 3T3 cells.The Journal of cell biology, 1982
- Fibroblast selection in sclerodermaArthritis & Rheumatism, 1982