Dietary ω-3 Fatty Acid Supplementation Improves Murine Sickle Cell Bone Disease and Reprograms Adipogenesis

Sickle cell disease (SCD) is a genetic disorder of hemoglobin, leading to chronic hemolytic anemia and multiple organ damage. Among chronic organ complications, sickle cell bone disease (SBD) has a very high prevalence, resulting in long-term disability, chronic pain and fractures. Here, we evaluate...

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Auteurs principaux:	Maria Teresa Valenti, Alessandro Mattè, Enrica Federti, Mark Puder, Lorenzo Anez-Bustillos, Michela Deiana, Samuele Cheri, Arianna Minoia, Carlo Brugnara, Maria Luisa Di Paolo, Luca Dalle Carbonare, Lucia De Franceschi
Format:	Artigo
Langue:	Inglês
Publié:	MDPI AG 2021-05-01
Collection:	Antioxidants
Sujets:	sickle cell disease bone histomorphometry osteogenesis adipogenesis miRNAs
Accès en ligne:	https://www.mdpi.com/2076-3921/10/5/799
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