Llwytho...

The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development

Ciliopathies represent a growing group of human genetic diseases whose etiology lies in defects in ciliogenesis or ciliary function. Given the established entity of renal–retinal ciliopathies, we have been examining the role of cilia-localized proteins mutated in retinitis pigmentosa (RP) in regulat...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Hurd, Toby, Zhou, Weibin, Jenkins, Paul, Liu, Chia-Jen, Swaroop, Anand, Khanna, Hemant, Martens, Jeffrey, Hildebrandt, Friedhelm, Margolis, Ben
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2010
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2957320/
https://ncbi.nlm.nih.gov/pubmed/20729296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq355
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