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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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Hurd, Toby, Zhou, Weibin, Jenkins, Paul, Liu, Chia-Jen, Swaroop, Anand, Khanna, Hemant, Martens, Jeffrey, Hildebrandt, Friedhelm, Margolis, Ben
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Oxford University Press 2010
Θέματα:
Διαθέσιμο Online: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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