TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia development
Author:
Funder
U.S. Department of Health & Human Services | NIH | National Eye Institute
U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s42003-024-06867-2.pdf
Reference64 articles.
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2. Barlan, K. & Gelfand, V. I. Microtubule-based transport and the distribution, tethering, and organization of organelles. Cold Spring Harbor. Perspect. Biol. https://doi.org/10.1101/cshperspect.a025817 (2017).
3. Janke, C. & Magiera, M. M. The tubulin code and its role in controlling microtubule properties and functions. Nat. Rev. Mol. Cell Biol. 21, 307–326 (2020).
4. Roll-Mecak, A. The tubulin code in microtubule dynamics and information encoding. Dev. Cell 54, 7–20 (2020).
5. Breuss, M. et al. Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities. Cell Rep. 2, 1554–1562 (2012).
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