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The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains. , Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation. , Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.
Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development. , Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
The neural border: Induction, specification and maturation of the territory that generates neural crest cells. , Pla P., Dev Biol. December 1, 2018; 444 Suppl 1 S36-S46.
Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates. , Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development. , Neilson KM ., Dev Biol. January 15, 2017; 421 (2): 171-182.
Evolutionarily conserved role for SoxC genes in neural crest specification and neuronal differentiation. , Uy BR., Dev Biol. January 15, 2015; 397 (2): 282-92.
Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm. , Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
Yes-associated protein 65 ( YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. , Gee ST ., PLoS One. January 1, 2011; 6 (6): e20309.
Mechanisms driving neural crest induction and migration in the zebrafish and Xenopus laevis. , Klymkowsky MW ., Cell Adh Migr. January 1, 2010; 4 (4): 595-608.
Xenopus Sox3 activates sox2 and geminin and indirectly represses Xvent2 expression to induce neural progenitor formation at the expense of non-neural ectodermal derivatives. , Rogers CD., Mech Dev. January 1, 2009; 126 (1-2): 42-55.
Identification of neural genes using Xenopus DNA microarrays. , Shin Y ., Dev Dyn. February 1, 2005; 232 (2): 432-44.
Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. , Brugmann SA ., Development. December 1, 2004; 131 (23): 5871-81.