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Summary Expression Phenotypes Gene Literature (10) GO Terms (10) Nucleotides (132) Proteins (51) Interactants (94) Wiki
XB--979544

Papers associated with ccno



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Fosl1 is vital to heart regeneration upon apex resection in adult Xenopus tropicalis., Wu HY, Zhou YM, Liao ZQ, Zhong JW, Liu YB, Zhao H, Liang CQ, Huang RJ, Park KS, Feng SS, Zheng L, Cai DQ, Qi XF., NPJ Regen Med. June 29, 2021; 6 (1): 36.                    

Xenopus to the rescue: A model to validate and characterize candidate ciliopathy genes., Rao VG, Kulkarni SS., Genesis. February 1, 2021; 59 (1-2): e23414.  

TRRAP is a central regulator of human multiciliated cell formation., Wang Z, Plasschaert LW, Aryal S, Renaud NA, Yang Z, Choo-Wing R, Pessotti AD, Kirkpatrick ND, Cochran NR, Carbone W, Maher R, Lindeman A, Russ C, Reece-Hoyes J, McAllister G, Hoffman GR, Roma G, Jaffe AB., J Cell Biol. June 4, 2018; 217 (6): 1941-1955.                        

The aryl hydrocarbon receptor controls cyclin O to promote epithelial multiciliogenesis., Villa M, Crotta S, Dingwell KS, Hirst EM, Gialitakis M, Ahlfors H, Smith JC, Stockinger B, Wack A., Nat Commun. August 24, 2016; 7 12652.            

Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis., Amirav I, Wallmeier J, Loges NT, Menchen T, Pennekamp P, Mussaffi H, Abitbul R, Avital A, Bentur L, Dougherty GW, Nael E, Lavie M, Olbrich H, Werner C, Kintner C, Omran H, Israeli PCD Consortium Investigators., Hum Mutat. April 1, 2016; 37 (4): 396-405.

MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia., Boon M, Wallmeier J, Ma L, Loges NT, Jaspers M, Olbrich H, Dougherty GW, Raidt J, Werner C, Amirav I, Hevroni A, Abitbul R, Avital A, Soferman R, Wessels M, O'Callaghan C, Chung EM, Rutman A, Hirst RA, Moya E, Mitchison HM, Van Daele S, De Boeck K, Jorissen M, Kintner C, Cuppens H, Omran H., Nat Commun. July 22, 2014; 5 4418.

Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia., Wallmeier J, Al-Mutairi DA, Chen CT, Loges NT, Pennekamp P, Menchen T, Ma L, Shamseldin HE, Olbrich H, Dougherty GW, Werner C, Alsabah BH, Köhler G, Jaspers M, Boon M, Griese M, Schmitt-Grohé S, Zimmermann T, Koerner-Rettberg C, Horak E, Kintner C, Alkuraya FS, Omran H., Nat Genet. June 1, 2014; 46 (6): 646-51.

Simultaneous in vitro characterisation of DNA deaminase function and associated DNA repair pathways., Franchini DM, Incorvaia E, Rangam G, Coker HA, Petersen-Mahrt SK., PLoS One. December 9, 2013; 8 (12): e82097.                

Uracil DNA N-glycosylase promotes assembly of human centromere protein A., Zeitlin SG, Chapados BR, Baker NM, Tai C, Slupphaug G, Wang JY., PLoS One. March 2, 2011; 6 (3): e17151.                        

Xenopus CENP-A assembly into chromatin requires base excision repair proteins., Zeitlin SG, Patel S, Kavli B, Slupphaug G., DNA Repair (Amst). July 12, 2005; 4 (7): 760-72.

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