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Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP, Jourdeuil K, Neilson KM , Majumdar HD, Moody SA ., Development. September 1, 2021; 148 (17):
Molecular mechanisms of hearing loss in Nager syndrome. , Maharana SK , Saint-Jeannet JP ., Dev Biol. August 1, 2021; 476 200-208.
TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis. , Chen M, Amado N, Tan J, Reis A, Ge M, Abreu JG , He X ., Elife. September 14, 2020; 9
The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. , Schwenty-Lara J, Nehl D, Borchers A ., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.
microRNAs associated with early neural crest development in Xenopus laevis. , Ward NJ, Green D, Higgins J, Dalmay T, Münsterberg A, Moxon S, Wheeler GN ., BMC Genomics. January 18, 2018; 19 (1): 59.
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome. , Devotta A, Juraver-Geslin H , Gonzalez JA, Hong CS , Saint-Jeannet JP ., Dev Biol. July 15, 2016; 415 (2): 371-382.
Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus. , Thélie A, Desiderio S, Hanotel J, Quigley I , Van Driessche B, Rodari A, Borromeo MD, Kricha S, Lahaye F, Croce J, Cerda-Moya G, Ordoño Fernandez J, Bolle B, Lewis KE , Sander M, Pierani A, Schubert M, Johnson JE, Kintner CR , Pieler T , Van Lint C, Henningfeld KA , Bellefroid EJ , Van Campenhout C., Development. October 1, 2015; 142 (19): 3416-28.
Phosphorylation of Dishevelled by protein kinase RIPK4 regulates Wnt signaling. , Huang X , McGann JC, Liu BY, Hannoush RN, Lill JR, Pham V, Newton K, Kakunda M, Liu J , Yu C, Hymowitz SG, Hongo JA, Wynshaw-Boris A, Polakis P, Harland RM , Dixit VM., Science. March 22, 2013; 339 (6126): 1441-5.