Papers associated with cement gland (and fn1)

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	16p12.1 Deletion Orthologs are Expressed in Motile Neural Crest Cells and are Important for Regulating Craniofacial Development in Xenopus laevis., Lasser M., Front Genet. January 1, 2022; 13 833083.
	Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
	Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.
	Hedgehog activity controls opening of the primary mouth., Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	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.
	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.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.
	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.
	Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.
	TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.
	Development of the primary mouth in Xenopus laevis., Dickinson AJ., Dev Biol. July 15, 2006; 295 (2): 700-13.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.
	Patterning and tissue movements in a novel explant preparation of the marginal zone of Xenopus laevis., Davidson LA., Gene Expr Patterns. July 1, 2004; 4 (4): 457-66.
	Xenopus Cyr61 regulates gastrulation movements and modulates Wnt signalling., Latinkic BV., Development. June 1, 2003; 130 (11): 2429-41.
	Xenopus ADAM 13 is a metalloprotease required for cranial neural crest-cell migration., Alfandari D, Alfandari D., Curr Biol. June 26, 2001; 11 (12): 918-30.
	A novel POZ/zinc finger protein, champignon, interferes with gastrulation movements in Xenopus., Goto T., Dev Dyn. May 1, 2001; 221 (1): 14-25.
	PACSIN2 is a regulator of the metalloprotease/disintegrin ADAM13., Cousin H., Dev Biol. November 1, 2000; 227 (1): 197-210.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	A role for Siamois in Spemann organizer formation., Fan MJ., Development. July 1, 1997; 124 (13): 2581-9.
	Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain., Landesman Y., Mech Dev. May 1, 1997; 63 (2): 199-209.
	ADAM 13: a novel ADAM expressed in somitic mesoderm and neural crest cells during Xenopus laevis development., Alfandari D, Alfandari D., Dev Biol. February 15, 1997; 182 (2): 314-30.
	Analysis of Dishevelled signalling pathways during Xenopus development., Sokol SY., Curr Biol. November 1, 1996; 6 (11): 1456-67.
	Specific modulation of ectodermal cell fates in Xenopus embryos by glycogen synthase kinase., Itoh K., Development. December 1, 1995; 121 (12): 3979-88.

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