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Review
. 2012 Feb;139(3):443-8.
doi: 10.1242/dev.050054.

Cilia in vertebrate development and disease

Affiliations
Review

Cilia in vertebrate development and disease

Edwin C Oh et al. Development. 2012 Feb.

Abstract

Through the combined study of model organisms, cell biology, cell signaling and medical genetics we have significantly increased our understanding of the structure and functions of the vertebrate cilium. This ancient organelle has now emerged as a crucial component of certain signaling and sensory perception pathways in both developmental and homeostatic contexts. Here, we provide a snapshot of the structure, function and distribution of the vertebrate cilium and of the pathologies that are associated with its dysfunction.

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References

    1. Andersen J. S., Wilkinson C. J., Mayor T., Mortensen P., Nigg E. A., Mann M. (2003). Proteomic characterization of the human centrosome by protein correlation profiling. Nature 426, 570–574 - PubMed
    1. Avidor-Reiss T., Maer A. M., Koundakjian E., Polyanovsky A., Keil T., Subramaniam S., Zuker C. S. (2004). Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis. Cell 117, 527–539 - PubMed
    1. Badano J. L., Mitsuma N., Beales P. L., Katsanis N. (2006). The ciliopathies: an emerging class of human genetic disorders. Annu. Rev. Genomics Hum. Genet. 7, 125–148 - PubMed
    1. Baker K., Beales P. L. (2009). Making sense of cilia in disease: the human ciliopathies. Am. J. Med. Genet. C Semin. Med. Genet. 151C, 281–295 - PubMed
    1. Berbari N. F., Lewis J. S., Bishop G. A., Askwith C. C., Mykytyn K. (2008). Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia. Proc. Natl. Acad. Sci. USA 105, 4242–4246 - PMC - PubMed

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