Differences in circulating microRNA signature in Prader–Willi syndrome and non-syndromic obesity

Prader–Willi syndrome (PWS) represents the most common genetic-derived obesity disorder caused by the loss of expression of genes located on the paternal chromosome 15q11.2-q13. The PWS phenotype shows peculiar physical, endocrine and metabolic characteristics compared to those observed in non-syndr...

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Vydáno v:Endocr Connect
Hlavní autoři: Pascut, Devis, Tamini, Sofia, Bresolin, Silvia, Giraudi, Pablo, Basso, Giuseppe, Minocci, Alessandro, Tiribelli, Claudio, Grugni, Graziano, Sartorio, Alessandro
Médium: Artigo
Jazyk:Inglês
Vydáno: Bioscientifica Ltd 2018
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6240145/
https://ncbi.nlm.nih.gov/pubmed/30352401
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-18-0329
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