Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 May 21;12(2):129-133.
doi: 10.2478/jtim-2024-0005. eCollection 2024 Apr.

Progress in therapeutic targets on podocyte for Alport syndrome

Qimin Zheng  1   2 , Xiangchen Gu  1   2 , John Cijiang He  3 , Jingyuan Xie  1   2
Affiliations

Progress in therapeutic targets on podocyte for Alport syndrome

Qimin Zheng et al. J Transl Int Med. .
No abstract available

Keywords: Alport syndrome; podocyte; therapeutic targets.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest None declared.

Figures

Figure 1
Figure 1
Pathogenic mechanisms of intrinsic cells and basement membrane in glomerulus of Alport syndrome. Created with BioRender.
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

References

    1. Gibson J, Fieldhouse R, Chan MMY, Sadeghi-Alavijeh O, Burnett L, Izzi V. Prevalence Estimates of Predicted Pathogenic COL4A3-COL4A5 Variants in a Population Sequencing Database and Their Implications for Alport Syndrome. J Am Soc Nephrol. 2021;32:2273. et al. –. - PMC - PubMed
    1. Kashtan CE, Ding J, Garosi G, Heidet L, Massella L, Nakanishi K. Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group. Kidney Int. 2018;93:1045. et al. –. - PubMed
    1. Li Y, Groopman EE, D’Agati V, Prakash S, Zhang J, Mizerska-Wasiak M. Type IV Collagen Mutations in Familial IgA Nephropathy. Kidney Int Rep. 2020;5:1075. et al. –. - PMC - PubMed
    1. Xie J, Wu X, Ren H, Wang W, Wang Z, Pan X. COL4A3 mutations cause focal segmental glomerulosclerosis. J Mol Cell Biol. 2014;6:498. et al. –. - PubMed
    1. Wang Y, Zhang J, Zhao Y, Wang S, Zhang J, Han Q. COL4A3 Gene Variants and Diabetic Kidney Disease in MODY. Clin J Am Soc Nephrol. 2018;13:1162. et al. –. - PMC - PubMed

LinkOut - more resources