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Post-translational modification enzymes as key regulators of ciliary protein trafficking

Primary cilia are evolutionarily conserved microtubule-based organelles that protrude from the surface of almost all cell types and decode a variety of extracellular stimuli. Ciliary dysfunction causes human diseases named ciliopathies, which span a wide range of symptoms, such as developmental and...

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Detalles Bibliográficos
Autores principales: Chaya, Taro, Furukawa, Takahisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423421/
https://www.ncbi.nlm.nih.gov/pubmed/33681987
http://dx.doi.org/10.1093/jb/mvab024