pEGFP-mCep290 Citations (2)

Originally described in: Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome.
Valente EM, Silhavy JL, Brancati F, Barrano G, Krishnaswami SR, Castori M, Lancaster MA, Boltshauser E, Boccone L, Al-Gazali L, Fazzi E, Signorini S, Louie CM, Bellacchio E, Bertini E, Dallapiccola B, Gleeson JG Nat Genet. 2006 Jun . 38(6):623-5. PubMed Journal

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Articles Citing pEGFP-mCep290

Articles
CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base. Wang WJ, Tay HG, Soni R, Perumal GS, Goll MG, Macaluso FP, Asara JM, Amack JD, Tsou MF. Nat Cell Biol. 2013 Jun;15(6):591-601. doi: 10.1038/ncb2739. Epub 2013 May 5. PubMed
NPHP proteins are binding partners of nucleoporins at the base of the primary cilium. Blasius TL, Takao D, Verhey KJ. PLoS One. 2019 Sep 25;14(9):e0222924. doi: 10.1371/journal.pone.0222924. eCollection 2019. PubMed

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