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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Ren Fail
Päätekijät: Sannomiya, Yuya, Kaseda, Shota, Kamura, Misato, Yamamoto, Hiroshi, Yamada, Hiroyuki, Inamoto, Masataka, Kuwazuru, Jun, Niino, Saki, Shuto, Tsuyoshi, Suico, Mary Ann, Kai, Hirofumi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Taylor & Francis 2021
Aiheet:
Laboratory Study
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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