Papers associated with ethmoid bone

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	Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders., Wyatt BH., Genesis. February 1, 2021; 59 (1-2): e23394.
	CAMSAP3 facilitates basal body polarity and the formation of the central pair of microtubules in motile cilia., Robinson AM., Proc Natl Acad Sci U S A. June 16, 2020; 117 (24): 13571-13579.
	Effect of nano-encapsulation of β-carotene on Xenopus laevis embryos development (FETAX)., Battistoni M., Toxicol Rep. January 1, 2020; 7 510-519.
	E-cigarette aerosol exposure can cause craniofacial defects in Xenopus laevis embryos and mammalian neural crest cells., Kennedy AE., PLoS One. September 8, 2017; 12 (9): e0185729.
	Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.
	A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.
	Temporal and spatial expression analysis of peripheral myelin protein 22 (Pmp22) in developing Xenopus., Tae HJ., Gene Expr Patterns. January 1, 2015; 17 (1): 26-30.
	Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus., Tahir R., Mech Dev. August 1, 2014; 133 91-104.
	The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.
	The protein kinase MLTK regulates chondrogenesis by inducing the transcription factor Sox6., Suzuki T., Development. August 1, 2012; 139 (16): 2988-98.
	Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes., Kennedy AE., Dev Biol. May 1, 2012; 365 (1): 229-40.
	Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.
	Expression analysis of Runx3 and other Runx family members during Xenopus development., Park BY., Gene Expr Patterns. June 1, 2010; 10 (4-5): 159-66.
	The mych gene is required for neural crest survival during zebrafish development., Hong SK., PLoS One. April 9, 2008; 3 (4): e2029.
	Xenopus embryos lacking specific isoforms of the corepressor SMRT develop abnormal heads., Malartre M., Dev Biol. April 15, 2006; 292 (2): 333-43.
	Hoxa2 knockdown in Xenopus results in hyoid to mandibular homeosis., Baltzinger M., Dev Dyn. December 1, 2005; 234 (4): 858-67.
	Activin A induces craniofacial cartilage from undifferentiated Xenopus ectoderm in vitro., Furue M., Proc Natl Acad Sci U S A. November 26, 2002; 99 (24): 15474-9.
	Ectopic Hoxa2 induction after neural crest migration results in homeosis of jaw elements in Xenopus., Pasqualetti M., Development. December 1, 2000; 127 (24): 5367-78.
	Development of the ethmoidal structures of the endocranium in the anuran Pipa pipa., Roček Z., J Morphol. June 1, 1989; 200 (3): 301-319.
	Neural crest development in the Xenopus laevis embryo, studied by interspecific transplantation and scanning electron microscopy., Sadaghiani B., Dev Biol. November 1, 1987; 124 (1): 91-110.

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