Papers associated with sensory system (and sox9)

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	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
	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.
	Recognition of H2AK119ub plays an important role in RSF1-regulated early Xenopus development., Parast SM., Front Cell Dev Biol. January 1, 2023; 11 1168643.
	Ash2l, an obligatory component of H3K4 methylation complexes, regulates neural crest development., Mohammadparast S., Dev Biol. December 1, 2022; 492 14-24.
	The homeodomain transcription factor Ventx2 regulates respiratory progenitor cell number and differentiation timing during Xenopus lung development., Rankin SA, Rankin SA., Dev Growth Differ. September 1, 2022; 64 (7): 347-361.
	Influence of Sox protein SUMOylation on neural development and regeneration., Chang KC., Neural Regen Res. March 1, 2022; 17 (3): 477-481.
	Function of chromatin modifier Hmgn1 during neural crest and craniofacial development., Ihewulezi C., Genesis. October 1, 2021; 59 (10): e23447.
	Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease., Getwan M., Proc Natl Acad Sci U S A. September 28, 2021; 118 (39):
	Mapping single-cell atlases throughout Metazoa unravels cell type evolution., Tarashansky AJ., Elife. May 4, 2021; 10
	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):
	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	Adaptive correction of craniofacial defects in pre-metamorphic Xenopus laevis tadpoles involves thyroid hormone-independent tissue remodeling., Pinet K., Development. July 22, 2019; 146 (14):
	In vivo topology converts competition for cell-matrix adhesion into directional migration., Bajanca F., Nat Commun. April 3, 2019; 10 (1): 1518.
	Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
	Physiological effects of KDM5C on neural crest migration and eye formation during vertebrate development., Kim Y., Epigenetics Chromatin. December 6, 2018; 11 (1): 72.
	Gap junction protein Connexin-43 is a direct transcriptional regulator of N-cadherin in vivo., Kotini M., Nat Commun. September 21, 2018; 9 (1): 3846.
	Dkk2 promotes neural crest specification by activating Wnt/β-catenin signaling in a GSK3β independent manner., Devotta A., Elife. July 23, 2018; 7
	Xenopus ADAM19 regulates Wnt signaling and neural crest specification by stabilizing ADAM13., Li J., Development. April 4, 2018; 145 (7):
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	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.
	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.
	Apolipoprotein C-I mediates Wnt/Ctnnb1 signaling during neural border formation and is required for neural crest development., Yokota C., Int J Dev Biol. January 1, 2017; 61 (6-7): 415-425.
	Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome., Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
	Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin., Gouignard N., Dis Model Mech. June 1, 2016; 9 (6): 607-20.
	Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.
	Genes regulated by potassium channel tetramerization domain containing 15 (Kctd15) in the developing neural crest., Wong TC., Int J Dev Biol. January 1, 2016; 60 (4-6): 159-66.
	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.
	COUP-TFs and eye development., Tang K., Biochim Biophys Acta. February 1, 2015; 1849 (2): 201-9.
	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.
	A novel function for Egr4 in posterior hindbrain development., Bae CJ., Sci Rep. January 12, 2015; 5 7750.
	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.
	Identification of distal enhancers for Six2 expression in pronephros., Suzuki N., Int J Dev Biol. January 1, 2015; 59 (4-6): 241-6.
	Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
	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.
	Par3 controls neural crest migration by promoting microtubule catastrophe during contact inhibition of locomotion., Moore R., Development. December 1, 2013; 140 (23): 4763-75.
	Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.
	Lamellipodin and the Scar/WAVE complex cooperate to promote cell migration in vivo., Law AL., J Cell Biol. November 25, 2013; 203 (4): 673-89.
	Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
	Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.
	SUMOylated SoxE factors recruit Grg4 and function as transcriptional repressors in the neural crest., Lee PC., J Cell Biol. September 3, 2012; 198 (5): 799-813.
	The protein kinase MLTK regulates chondrogenesis by inducing the transcription factor Sox6., Suzuki T., Development. August 1, 2012; 139 (16): 2988-98.
	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.
	The LIM adaptor protein LMO4 is an essential regulator of neural crest development., Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
	Mustn1 is essential for craniofacial chondrogenesis during Xenopus development., Gersch RP., Gene Expr Patterns. January 1, 2012; 12 (3-4): 145-53.
	Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration., Love NR., BMC Dev Biol. November 15, 2011; 11 70.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.
	Sox9 function in craniofacial development and disease., Lee YH, Lee YH., Genesis. April 1, 2011; 49 (4): 200-8.
	Activity of the RhoU/Wrch1 GTPase is critical for cranial neural crest cell migration., Fort P., Dev Biol. February 15, 2011; 350 (2): 451-63.
	Serotonin 2B receptor signaling is required for craniofacial morphogenesis and jaw joint formation in Xenopus., Reisoli E., Development. September 1, 2010; 137 (17): 2927-37.

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