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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.
Mcrs1 interacts with Six1 to influence early craniofacial and otic development. , Neilson KM ., Dev Biol. November 1, 2020; 467 (1-2): 39-50.
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.
sox4 and sox11 function during Xenopus laevis eye development. , Cizelsky W., PLoS One. July 1, 2013; 8 (7): e69372.
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.
Grainyhead-like 3, a transcription factor identified in a microarray screen, promotes the specification of the superficial layer of the embryonic epidermis. , Chalmers AD ., Mech Dev. September 1, 2006; 123 (9): 702-18.
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.