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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Bibliografische gegevens
Gepubliceerd in:PLoS Genet
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Public Library of Science 2015
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4635004/
https://ncbi.nlm.nih.gov/pubmed/26540106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005627
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