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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
Npr3 regulates neural crest and cranial placode progenitors formation through its dual function as clearance and signaling receptor. , Devotta A., Elife. May 10, 2023; 12
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation. , Jourdeuil K., Front Cell Dev Biol. January 1, 2023; 11 1274788.
Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development. , Tavares ALP., Development. September 1, 2021; 148 (17):
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):
In vivo confinement promotes collective migration of neural crest cells. , Szabó A., J Cell Biol. June 6, 2016; 213 (5): 543-55.
E-cadherin is required for cranial neural crest migration in Xenopus laevis. , Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development. , Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling. , Watanabe T., Genesis. October 1, 2014; .
RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm. , Janesick A ., Development. March 1, 2012; 139 (6): 1213-24.
Pleiotropic effects in Eya3 knockout mice. , Söker T., BMC Dev Biol. June 23, 2008; 8 118.