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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):
Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1. , Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
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.
Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning. , Steventon B ., Dev Biol. July 1, 2012; 367 (1): 55-65.
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.
EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis. , Li Y., Biol Cell. February 17, 2010; 102 (5): 277-92.
Pleiotropic effects in Eya3 knockout mice. , Söker T., BMC Dev Biol. June 23, 2008; 8 118.
Regulation of otic vesicle and hair cell stereocilia morphogenesis by Ena/ VASP-like ( Evl) in Xenopus. , Wanner SJ., J Cell Sci. August 1, 2007; 120 (Pt 15): 2641-51.
Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus. , Chen JA ., Mech Dev. March 1, 2005; 122 (3): 307-31.