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Expression and secretion of CXCL12 are enhanced in autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease (ADPKD), one of the most common human monogenic diseases (frequency of 1/1000-1/400), is characterized by numerous fluid-filled renal cysts (RCs). Inactivation of the PKD1 or PKD2 gene by germline and somatic mutations is necessary for cyst formation in A...
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| Publicado no: | BMB Rep |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Society for Biochemistry and Molecular Biology
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6675246/ https://ncbi.nlm.nih.gov/pubmed/31186083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5483/BMBRep.2019.52.7.112 |
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