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The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. , Schwenty-Lara J., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.
Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome. , Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
Hedgehog activity controls opening of the primary mouth. , Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.
The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning. , Schlosser G ., Dev Biol. May 1, 2014; 389 (1): 98-119.
Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning. , Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos. , Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.
The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning. , Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.