Results 1 - 10 of 10 results
Rab11fip5 regulates telencephalon development via ephrinB1 recycling. , Yoon J, Garo J, Lee M, Sun J, Hwang YS, Daar IO ., Development. February 2, 2021; 148 (3):
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos. , Lichtig H, Artamonov A, Polevoy H, Reid CD, Bielas SL, Frank D ., Front Physiol. January 1, 2020; 11 75.
Interplay of TRIM2 E3 Ubiquitin Ligase and ALIX/ESCRT Complex: Control of Developmental Plasticity During Early Neurogenesis. , Lokapally A, Neuhaus H , Herfurth J, Hollemann T ., Cells. January 1, 2020; 9 (7):
Alteration of the Retinoid Acid- CBP Signaling Pathway in Neural Crest Induction Contributes to Enteric Nervous System Disorder. , Li C, Hu R, Hou N, Wang Y, Wang Z, Yang T, Gu Y, He M, Shi Y , Chen J , Song W, Li T., Front Pediatr. January 1, 2018; 6 382.
Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment. , Schietroma C, Parain K , Estivalet A, Aghaie A, Boutet de Monvel J, Picaud S, Sahel JA, Perron M , El-Amraoui A, Petit C., J Cell Biol. January 1, 2017; 216 (6): 1849-1864.
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.
Ascl1 phospho-status regulates neuronal differentiation in a Xenopus developmental model of neuroblastoma. , Wylie LA, Hardwick LJ , Papkovskaia TD, Thiele CJ, Philpott A ., Dis Model Mech. May 1, 2015; 8 (5): 429-41.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y , Thomsen GH ., Development. October 1, 2014; 141 (19): 3740-51.
A dominant-negative form of the E3 ubiquitin ligase Cullin-1 disrupts the correct allocation of cell fate in the neural crest lineage. , Voigt J , Papalopulu N ., Development. February 1, 2006; 133 (3): 559-68.
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. , Stancheva I , Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR ., Mol Cell. August 1, 2003; 12 (2): 425-35.