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

Internet

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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