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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
DIPA-family coiled-coils bind conserved isoform-specific head domain of p120-catenin family: potential roles in hydrocephalus and heterotopia. , Markham NO., Mol Biol Cell. September 1, 2014; 25 (17): 2592-603.
Down's-syndrome-related kinase Dyrk1A modulates the p120-catenin-Kaiso trajectory of the Wnt signaling pathway. , Hong JY., J Cell Sci. February 1, 2012; 125 (Pt 3): 561-9.
ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus. , Tran HT., Dev Dyn. December 1, 2011; 240 (12): 2680-7.
Kazrin, and its binding partners ARVCF- and delta-catenin, are required for Xenopus laevis craniofacial development. , Cho K., Dev Dyn. December 1, 2011; 240 (12): 2601-12.
Xenopus Kazrin interacts with ARVCF-catenin, spectrin and p190B RhoGAP, and modulates RhoA activity and epithelial integrity. , Cho K., J Cell Sci. December 1, 2010; 123 (Pt 23): 4128-44.
Inhibition of cell adhesion by xARVCF indicates a regulatory function at the plasma membrane. , Reintsch WE., Dev Dyn. September 1, 2008; 237 (9): 2328-41.
Vertebrate development requires ARVCF and p120 catenins and their interplay with RhoA and Rac. , Fang X., J Cell Biol. April 1, 2004; 165 (1): 87-98.
Isolation and characterization of XKaiso, a transcriptional repressor that associates with the catenin Xp120(ctn) in Xenopus laevis. , Kim SW., J Biol Chem. March 8, 2002; 277 (10): 8202-8.
Xarvcf, Xenopus member of the p120 catenin subfamily associating with cadherin juxtamembrane region. , Paulson AF., J Biol Chem. September 29, 2000; 275 (39): 30124-31.