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Circulating microRNA Associated to Different Stages of Liver Steatosis in Prader–Willi Syndrome and Non-Syndromic Obesity

Background: Prader–Willi syndrome (PWS) is a rare and poorly characterized disease. Recent genomic and transcriptomic studies contributed to elucidate the molecular bases of the syndrome. In this study, we characterized the expression of circulating miRNAs in patients with PWS compared to those with...

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Detalhes bibliográficos
Publicado no:J Clin Med
Main Authors: Pratama, Muhammad Yogi, Pascut, Devis, Tamini, Sofia, Minocci, Alessandro, Tiribelli, Claudio, Grugni, Graziano, Sartorio, Alessandro
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7230920/
https://ncbi.nlm.nih.gov/pubmed/32295264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9041123
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