Proteome profiling identifies circulating biomarkers associated with hepatic steatosis in subjects with Prader-Willi syndrome

INTRODUCTION: Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by loss of expression of paternal chromosome 15q11.2-q13 genes. Individuals with PWS exhibit unique physical, endocrine, and metabolic traits associated with severe obesity. Identifying liver steatosis in PWS is chall...

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Detalles Bibliográficos
Autores principales: Pascut, Devis, Giraudi, Pablo J., Banfi, Cristina, Ghilardi, Stefania, Tiribelli, Claudio, Bondesan, Adele, Caroli, Diana, Minocci, Alessandro, Grugni, Graziano, Sartorio, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684934/
https://www.ncbi.nlm.nih.gov/pubmed/38034016
http://dx.doi.org/10.3389/fendo.2023.1254778

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684934/
https://www.ncbi.nlm.nih.gov/pubmed/38034016
http://dx.doi.org/10.3389/fendo.2023.1254778

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