KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling.
Molecular Medicine Reports
Hu, Lingyu L; Chen, Li L; Yang, Liu L; Ye, Zi Z; Huang, Wenhuan W; Li, Xinxin X; Liu, Qing Q; Qiu, Junlu J; Ding, Xiaofeng X
Escolano, Amelia A; Steichen, Jon M JM; Dosenovic, Pia P; Kulp, Daniel W DW; Golijanin, Jovana J; Sok, Devin D; Freund, Natalia T NT; Gitlin, Alexander D AD; Oliveira, Thiago T; Araki, Tatsuya T; Lowe, Sarina S; Chen, Spencer T ST; Heinemann, Jennifer J; Yao, Kai-Hui KH; Georgeson, Erik E; Saye-Francisco, Karen L KL; Gazumyan, Anna A; Adachi, Yumiko Y; Kubitz, Michael M; Burton, Dennis R DR; Schief, William R WR; Nussenzweig, Michel C MC