Papers associated with proximal (and sox3)

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	Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution., Hossain N., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
	The dorsal blastopore lip is a source of signals inducing planar cell polarity in the Xenopus neural plate., Mancini P., Biol Open. July 15, 2021; 10 (7):
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	A hindbrain-repressive Wnt3a/Meis3/Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation., Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.
	Xenopus laevis insulin receptor substrate IRS-1 is important for eye development., Bugner V., Dev Dyn. July 1, 2011; 240 (7): 1705-15.
	Evolution of non-coding regulatory sequences involved in the developmental process: reflection of differential employment of paralogous genes as highlighted by Sox2 and group B1 Sox genes., Kamachi Y., Proc Jpn Acad Ser B Phys Biol Sci. January 1, 2009; 85 (2): 55-68.
	XSip1 neuralizing activity involves the co-repressor CtBP and occurs through BMP dependent and independent mechanisms., van Grunsven LA., Dev Biol. June 1, 2007; 306 (1): 34-49.
	The HMG-box mitochondrial transcription factor xl-mtTFA binds DNA as a tetramer to activate bidirectional transcription., Antoshechkin I., EMBO J. June 2, 1997; 16 (11): 3198-206.

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