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The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium

Mutations in RPGRIP1L result in severe human diseases called ciliopathies. To unravel the molecular function of RPGRIP1L, we analyzed Rpgrip1l(−/−) mouse embryos, which display a ciliopathy phenotype and die, at the latest, around birth. In these embryos, cilia-mediated signaling was severely distur...

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Detalhes bibliográficos
Publicado no:J Cell Biol
Main Authors: Gerhardt, Christoph, Lier, Johanna Maria, Burmühl, Stephan, Struchtrup, Andreas, Deutschmann, Kathleen, Vetter, Maik, Leu, Tristan, Reeg, Sandra, Grune, Tilman, Rüther, Ulrich
Formato: Artigo
Idioma:Inglês
Publicado em: The Rockefeller University Press 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4494006/
https://ncbi.nlm.nih.gov/pubmed/26150391
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201408060
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