Papers associated with skeleton (and tbx2)

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	The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development., Forman TE., J Dev Biol. August 27, 2021; 9 (3):
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	The positive transcriptional elongation factor (P-TEFb) is required for neural crest specification., Hatch VL., Dev Biol. August 15, 2016; 416 (2): 361-72.
	Xenopus Limb bud morphogenesis., Keenan SR., Dev Dyn. March 1, 2016; 245 (3): 233-43.
	Genetics, Morphology, Advertisement Calls, and Historical Records Distinguish Six New Polyploid Species of African Clawed Frog (Xenopus, Pipidae) from West and Central Africa., Evans BJ., PLoS One. December 16, 2015; 10 (12): e0142823.
	The NOTCH signaling pathway in normal and malignant blood cell production., Suresh S., J Cell Commun Signal. March 1, 2015; 9 (1): 5-13.
	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.
	MHC class I limits hippocampal synapse density by inhibiting neuronal insulin receptor signaling., Dixon-Salazar TJ., J Neurosci. August 27, 2014; 34 (35): 11844-56.
	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.
	Developmental expression and role of Kinesin Eg5 during Xenopus laevis embryogenesis., Fernández JP., Dev Dyn. April 1, 2014; 243 (4): 527-40.
	Scaling of dorsal-ventral patterning in the Xenopus laevis embryo., Ben-Zvi D., Bioessays. February 1, 2014; 36 (2): 151-6.
	A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A., Dis Model Mech. January 1, 2014; 7 (1): 119-28.
	Vestibular lesion-induced developmental plasticity in spinal locomotor networks during Xenopus laevis metamorphosis., Beyeler A., PLoS One. August 12, 2013; 8 (8): e71013.
	Unraveling new roles for serotonin receptor 2B in development: key findings from Xenopus., Ori M., Int J Dev Biol. January 1, 2013; 57 (9-10): 707-14.
	A homolog of Subtilisin-like Proprotein Convertase 7 is essential to anterior neural development in Xenopus., Senturker S., PLoS One. January 1, 2012; 7 (6): e39380.
	Histone deacetylases are required for amphibian tail and limb regeneration but not development., Taylor AJ., Mech Dev. January 1, 2012; 129 (9-12): 208-18.
	Molecular dynamics simulations of the Cx26 hemichannel: evaluation of structural models with Brownian dynamics., Kwon T., J Gen Physiol. November 1, 2011; 138 (5): 475-93.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	The cellular basis for animal regeneration., Tanaka EM., Dev Cell. July 19, 2011; 21 (1): 172-85.
	Peter Pan functions independently of its role in ribosome biogenesis during early eye and craniofacial cartilage development in Xenopus laevis., Bugner V., Development. June 1, 2011; 138 (11): 2369-78.
	Increased basal activity is a key determinant in the severity of human skeletal dysplasia caused by TRPV4 mutations., Loukin S., PLoS One. May 3, 2011; 6 (5): e19533.
	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.
	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.
	ZFP423 coordinates Notch and bone morphogenetic protein signaling, selectively up-regulating Hes5 gene expression., Masserdotti G., J Biol Chem. October 1, 2010; 285 (40): 30814-24.
	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.
	Gene structure, transcripts and calciotropic effects of the PTH family of peptides in Xenopus and chicken., Pinheiro PL., BMC Evol Biol. May 6, 2010; 10 373.
	FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development., Gessert S., Dev Biol. May 1, 2010; 341 (1): 222-35.
	Enzymatic regulation of pattern: BMP4 binds CUB domains of Tolloids and inhibits proteinase activity., Lee HX., Genes Dev. November 1, 2009; 23 (21): 2551-62.
	Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.
	Scaling of BMP gradients in Xenopus embryos., Francois P., Nature. September 3, 2009; 461 (7260): E1; discussion E2.
	Effects of activation of hedgehog signaling on patterning, growth, and differentiation in Xenopus froglet limb regeneration., Yakushiji N., Dev Dyn. August 1, 2009; 238 (8): 1887-96.
	Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
	The Wnt antagonists Frzb-1 and Crescent locally regulate basement membrane dissolution in the developing primary mouth., Dickinson AJ., Development. April 1, 2009; 136 (7): 1071-81.
	A protein scaffold plays matchmaker for chordin., Harland RM., Cell. September 5, 2008; 134 (5): 718-9.
	Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1., Suls A., Brain. July 1, 2008; 131 (Pt 7): 1831-44.
	Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9., Stone S., Genes Cells. July 1, 2007; 12 (7): 841-51.
	Runx2 is essential for larval hyobranchial cartilage formation in Xenopus laevis., Kerney R., Dev Dyn. June 1, 2007; 236 (6): 1650-62.
	Wnt/beta-catenin signaling controls Mespo expression to regulate segmentation during Xenopus somitogenesis., Wang J., Dev Biol. April 15, 2007; 304 (2): 836-47.
	Regeneration of the amphibian retina: role of tissue interaction and related signaling molecules on RPE transdifferentiation., Araki M., Dev Growth Differ. February 1, 2007; 49 (2): 109-20.
	Hoxa2 knockdown in Xenopus results in hyoid to mandibular homeosis., Baltzinger M., Dev Dyn. December 1, 2005; 234 (4): 858-67.
	A novel G protein-coupled receptor, related to GPR4, is required for assembly of the cortical actin skeleton in early Xenopus embryos., Tao Q, Tao Q., Development. June 1, 2005; 132 (12): 2825-36.
	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.
	[The role of Smads and related transcription factors in the signal transduction of bone morphogenetic protein inducing bone formation]., Xu XL., Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. September 1, 2003; 17 (5): 359-62.
	Coordination of BMP-3b and cerberus is required for head formation of Xenopus embryos., Hino J., Dev Biol. August 1, 2003; 260 (1): 138-57.
	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.
	Conserved expression control and shared activity between cognate T-box genes Tbx2 and Tbx3 in connection with Sonic hedgehog signaling during Xenopus eye development., Takabatake Y., Dev Growth Differ. August 1, 2002; 44 (4): 257-71.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	Neural induction takes a transcriptional twist., Bainter JJ., Dev Dyn. November 1, 2001; 222 (3): 315-27.
	Cloning, characterization, and tissue expression pattern of mouse Nma/BAMBI during odontogenesis., Knight C., J Dent Res. October 1, 2001; 80 (10): 1895-902.
	FGF-10 stimulates limb regeneration ability in Xenopus laevis., Yokoyama H., Dev Biol. May 1, 2001; 233 (1): 72-9.

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