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The role of discoidin domain receptor 2 in the renal dysfunction of alport syndrome mouse model
Alport syndrome (AS) is a hereditary glomerular nephritis caused by mutation in one of the type IV collagen genes α3/α4/α5 that encode the heterotrimer COL4A3/4/5. Failure to form a heterotrimer due to mutation leads to the dysfunction of the glomerular basement membrane, and end-stage renal disease...
Tallennettuna:
| Julkaisussa: | Ren Fail |
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| Päätekijät: | , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Taylor & Francis
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7971217/ https://ncbi.nlm.nih.gov/pubmed/33706638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/0886022X.2021.1896548 |
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