Bone health in autosomal dominant polycystic kidney disease (ADPKD) patients after kidney transplantation

ADPKD is caused by pathogenic variants in PKD1 or PKD2, encoding polycystin-1 and -2 proteins. Polycystins are expressed in osteoblasts and chondrocytes in animal models, and loss of function is associated with low bone mineral density (BMD) and volume. However, it is unclear whether these variants...

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Detalles Bibliográficos
Autores principales: Zubidat, Dalia, Hanna, Christian, Randhawa, Amarjyot K., Smith, Byron H., Chedid, Maroun, Kaidbay, Daniel-Hasan N., Nardelli, Luca, Mkhaimer, Yaman G., Neal, Reem M., Madsen, Charles D., Senum, Sarah R., Gregory, Adriana V., Kline, Timothy L., Zoghby, Ziad M., Broski, Stephen M., Issa, Naim S., Harris, Peter C., Torres, Vicente E., Sfeir, Jad G., Chebib, Fouad T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Full Length Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842864/
https://www.ncbi.nlm.nih.gov/pubmed/36659900
http://dx.doi.org/10.1016/j.bonr.2023.101655

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842864/
https://www.ncbi.nlm.nih.gov/pubmed/36659900
http://dx.doi.org/10.1016/j.bonr.2023.101655

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