Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling

Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting many tissues. Individual genes can be linked to ciliopathies with dramatically different phenotypes, suggesting that genetic modifiers may participate in their pathogenesis. The ciliary transition zone c...

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Detalles Bibliográficos
Autores principales: Yee, Laura E., Garcia-Gonzalo, Francesc R., Bowie, Rachel V., Li, Chunmei, Kennedy, Julie K., Ashrafi, Kaveh, Blacque, Oliver E., Leroux, Michel R., Reiter, Jeremy F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635004/
https://www.ncbi.nlm.nih.gov/pubmed/26540106
http://dx.doi.org/10.1371/journal.pgen.1005627

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635004/
https://www.ncbi.nlm.nih.gov/pubmed/26540106
http://dx.doi.org/10.1371/journal.pgen.1005627

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