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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.
The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx. , Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
Molecular anatomy of placode development in Xenopus laevis. , Schlosser G ., Dev Biol. July 15, 2004; 271 (2): 439-66.
The Iroquois family of genes: from body building to neural patterning. , Cavodeassi F., Development. August 1, 2001; 128 (15): 2847-55.