Papers associated with ventral (and dlx5)

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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.
	Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.
	Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):
	Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.
	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):
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	Identification of new regulators of embryonic patterning and morphogenesis in Xenopus gastrulae by RNA sequencing., Popov IK., Dev Biol. June 15, 2017; 426 (2): 429-441.
	Thyroid Hormone-Induced Activation of Notch Signaling is Required for Adult Intestinal Stem Cell Development During Xenopus Laevis Metamorphosis., Hasebe T., Stem Cells. April 1, 2017; 35 (4): 1028-1039.
	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 ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	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.
	Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.
	ΔNp63 is regulated by BMP4 signaling and is required for early epidermal development in Xenopus., Tríbulo C., Dev Dyn. February 1, 2012; 241 (2): 257-69.
	Combinatorial roles for BMPs and Endothelin 1 in patterning the dorsal-ventral axis of the craniofacial skeleton., Alexander C., Development. December 1, 2011; 138 (23): 5135-46.
	Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR., Sato S., Dev Biol. August 1, 2010; 344 (1): 158-71.
	Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis., Illes JC., Dev Dyn. January 1, 2009; 238 (1): 194-203.
	Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1., Herr P., Development. May 1, 2008; 135 (10): 1813-22.
	Evidences for tangential migrations in Xenopus telencephalon: developmental patterns and cell tracking experiments., Moreno N., Dev Neurobiol. March 1, 2008; 68 (4): 504-20.
	An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
	Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes., von Bubnoff A., Dev Biol. May 15, 2005; 281 (2): 210-26.
	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.
	Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.
	Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor., Brugmann SA., Development. December 1, 2004; 131 (23): 5871-81.
	Dlx proteins position the neural plate border and determine adjacent cell fates., Woda JM., Development. January 1, 2003; 130 (2): 331-42.
	Defining pallial and subpallial divisions in the developing Xenopus forebrain., Bachy I., Mech Dev. September 1, 2002; 117 (1-2): 163-72.
	Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.
	A BMP-inducible gene, dlx5, regulates osteoblast differentiation and mesoderm induction., Miyama K., Dev Biol. April 1, 1999; 208 (1): 123-33.
	Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos., Fredieu JR., Dev Biol. June 1, 1997; 186 (1): 100-14.
	Expression of murine Lhx5 suggests a role in specifying the forebrain., Sheng HZ., Dev Dyn. February 1, 1997; 208 (2): 266-77.
	Patterns of distal-less gene expression and inductive interactions in the head of the direct developing frog Eleutherodactylus coqui., Fang H., Dev Biol. October 10, 1996; 179 (1): 160-72.
	Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals., Papalopulu N., Development. March 1, 1993; 117 (3): 961-75.

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