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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Pubblicato in:BMB Rep
Autori principali: Kim, Hyunho, Sung, Jinmo, Kim, Hyunsuk, Ryu, Hyunjin, Park, Hayne Cho, Oh, Yun Kyu, Lee, Hyun-Seob, Oh, Kook-Hwan, Ahn, Curie
Natura: Artigo
Lingua:Inglês
Pubblicazione: Korean Society for Biochemistry and Molecular Biology 2019
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Articles
Accesso online: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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