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FLCN regulates transferrin receptor 1 transport and iron homeostasis

Birt–Hogg–Dubé (BHD) syndrome is a multiorgan disorder caused by inactivation of the folliculin (FLCN) protein. Previously, we identified FLCN as a binding protein of Rab11A, a key regulator of the endocytic recycling pathway. This finding implies that the abnormal localization of specific proteins...

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Detalles Bibliográficos
Autores principales:	Wang, Xiaojuan, Wu, Hanjie, Zhao, Lingling, Liu, Zeyao, Qi, Maozhen, Jin, Yaping, Liu, Wei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	American Society for Biochemistry and Molecular Biology 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995610/ https://www.ncbi.nlm.nih.gov/pubmed/33609526 http://dx.doi.org/10.1016/j.jbc.2021.100426

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