Endoplasmic Reticulum Stress Activation in Alport Syndrome Varies Between Genotype and Cell Type

Alport syndrome is a hereditary progressive chronic kidney disease caused by mutations in type IV collagen genes COL4A3/4/5. X-linked Alport syndrome (XLAS) is caused by mutations in the COL4A5 gene and is the most common form of Alport syndrome. A strong correlation between the type of COL4A5 mutat...

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Detalles Bibliográficos
Autores principales: Wang, Cong, Liang, Shenghui, Xing, Shijia, Xu, Ke, Xiao, Huijie, Deng, Haiyue, Wang, Xiaoyuan, Chen, Liangyi, Ding, Jie, Wang, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025644/
https://www.ncbi.nlm.nih.gov/pubmed/32117450
http://dx.doi.org/10.3389/fgene.2020.00036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025644/
https://www.ncbi.nlm.nih.gov/pubmed/32117450
http://dx.doi.org/10.3389/fgene.2020.00036

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