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Matrix Metalloproteinase Dysregulation in the Stria Vascularis of Mice with Alport Syndrome : Implications for Capillary Basement Membrane Pathology
Alport syndrome results from mutations in genes encoding collagen α3(IV), α4(IV), or α5(IV) and is characterized by progressive glomerular disease associated with a high-frequency sensorineural hearing loss. Earlier studies of a gene knockout mouse model for Alport syndrome noted thickening of stria...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Investigative Pathology
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1606400/ https://ncbi.nlm.nih.gov/pubmed/15855646 |
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