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Androgen receptor activation induces senescence in thyroid cancer cells

Primary carnitine deficiency PCD is a rare genetic disease caused by mutations in the SLC22A5 gene, which leads to dysfunction of the carnitine transporter OCTN2, thereby hindering the entry of carnitine from the blood into cells and the reabsorption of carnitine by the kidneys

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doi: 10.1038/sj.ejcn.1602594 80 EslamparastTZamaniFHekmatdoostASharafkhahMEghtesadSMalekzadehRet al

[DOI] [PMC free article] [PubMed] [Google Scholar] 56.Setoyama D, Lee HY, Moon JS, Tian J, Kang YE, Lee JH, et al