Mechanistic complement of autosomal dominant polycystic kidney disease: the role of aquaporins
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00109-024-02446-4.pdf
Reference137 articles.
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2. Willey CJ, Blais JD, Hall AK, Krasa HB, Makin AJ, Czerwiec FS (2017) Prevalence of autosomal dominant polycystic kidney disease in the European Union. Nephrol Dial Transplant 32:1356–1363. https://doi.org/10.1093/ndt/gfw240
3. Guay-Woodford LM (2003) Murine models of polycystic kidney disease: molecular and therapeutic insights. Am J Physiol Renal Physiol 285:F1034–F1049. https://doi.org/10.1152/ajprenal.00195.2003
4. Song X, Di Giovanni V, He N, Wang K, Ingram A, Rosenblum ND, Pei Y (2009) Systems biology of autosomal dominant polycystic kidney disease (Adpkd): computational identification of gene expression pathways and integrated regulatory networks. Hum Mol Genet 18:2328–2343. https://doi.org/10.1093/hmg/ddp165
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