| 1 | CEP78, CORDHL
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| Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.
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| Nikopoulos K, Farinelli P, Giangreco B, Tsika C, Royer-Bertrand B, Mbefo MK, Bedoni N, Kjellström U, El Zaoui I, Di Gioia SA, Balzano S, Cisarova K, Messina A, Decembrini S, Plainis S, Blazaki SV, Khan MI, Micheal S, Boldt K, Ueffing M, Moulin AP, Cremers FP, Roepman R, Arsenijevic Y, Tsilimbaris MK, Andréasson S, Rivolta C.
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| Am J Hum Genet 99(3):770-6. doi: 10.1016/j.ajhg.2016.07.009.
2016
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| 2 | CEP78, CORDHL
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| Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
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| Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D.
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| Am J Hum Genet 99(3):777-84. doi: 10.1016/j.ajhg.2016.07.010.
2016
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| 3 | CEP78, PLK4
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| Cep78 is a new centriolar protein involved in Plk4-induced centriole overduplication.
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| Brunk K, Zhu M, Bärenz F, Kratz AS, Haselmann-Weiss U, Antony C, Hoffmann I.
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| J Cell Sci 129(14):2713-8. doi: 10.1242/jcs.184093. Epub 2016 May 31.
2016
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| 4 | CEP78
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| Low expression of centrosomal protein 78 (CEP78) is associated with poor prognosis of colorectal cancer patients.
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| Zhang M, Duan T, Wang L, Tang J, Luo R, Zhang R, Kang T.
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| Chin J Cancer 35(1):62. doi: 10.1186/s40880-016-0121-3.
2016
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| 5 | CEP78
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| CEP78 is mutated in a distinct type of Usher syndrome.
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| Fu Q, Xu M, Chen X, Sheng X, Yuan Z, Liu Y, Li H, Sun Z, Li H, Yang L, Wang K, Zhang F, Li Y, Zhao C, Sui R, Chen R.
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| J Med Genet Med Genet. 2016 Sep 14. pii: jmedgenet-2016-104166. doi: 10.1136/jmedgenet-2016-104166. [Epub ahead of print]
2016
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| 6 | CEP131, CEP152, CEP192, CEP27, CEP57, CEP63, CEP68, CEP70, CEP72, CEP76, CEP78, SASS6
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| Proteomic characterization of the human centrosome by protein correlation profiling.
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| Andersen JS, Wilkinson CJ, Mayor T, Mortensen P, Nigg EA, Mann M.
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| Nature 426(6966):570-4. 2003
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