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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...
Autores principales: | Chaya, Taro, Furukawa, Takahisa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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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 |
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