Alport syndrome: Proteomic analysis identifies early molecular pathway alterations in Col4a3 knock out mice

AIM: Alport syndrome (AS) is the second most common hereditary kidney disease caused by mutations in collagen IV genes. Patients present with microhaematuria that progressively leads to proteinuria and end stage renal disease. Currently, no specific treatment exists for AS. Using mass spectrometry b...

Descripción completa

Detalles Bibliográficos
Autores principales: Nicolaou, Orthodoxia, Kousios, Andreas, Sokratous, Kleitos, Potamiti, Louiza, Koniali, Lola, Neophytou, George, Papacharalampous, Revekka, Zanti, Maria, Ioannou, Kyriakos, Hadjisavvas, Andreas, Stingl, Christoph, Luider, Theo M., Kyriacou, Kyriacos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754404/
https://www.ncbi.nlm.nih.gov/pubmed/32743880
http://dx.doi.org/10.1111/nep.13764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754404/
https://www.ncbi.nlm.nih.gov/pubmed/32743880
http://dx.doi.org/10.1111/nep.13764

Ejemplares similares