Papers associated with anatomical region (and not)

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	Tissue-specific expression of carbohydrate sulfotransferases drives keratan sulfate biosynthesis in the notochord and otic vesicles of Xenopus embryos., Yasuoka Y., Front Cell Dev Biol. January 1, 2023; 11 957805.
	ARVCF catenin controls force production during vertebrate convergent extension., Huebner RJ., Dev Cell. May 9, 2022; 57 (9): 1119-1131.e5.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
	Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis., Lee H, Lee H., Antioxidants (Basel). December 12, 2020; 9 (12):
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	Comprehensive RNA-Seq analysis of notochord-enriched genes induced during Xenopus tropicalis tail resorption., Nakajima K., Gen Comp Endocrinol. February 1, 2020; 287 113349.
	The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	A unique role of thyroid hormone receptor β in regulating notochord resorption during Xenopus metamorphosis., Nakajima K., Gen Comp Endocrinol. June 1, 2019; 277 66-72.
	Shared evolutionary origin of vertebrate neural crest and cranial placodes., Horie R., Nature. August 1, 2018; 560 (7717): 228-232.
	Transcriptomics of dorso-ventral axis determination in Xenopus tropicalis., Monteiro RS., Dev Biol. July 15, 2018; 439 (2): 69-79.
	Head formation requires Dishevelled degradation that is mediated by March2 in concert with Dapper1., Lee H, Lee H., Development. April 10, 2018; 145 (7):
	RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
	Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
	hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus., Prager A., Dev Biol. October 1, 2017; 430 (1): 188-201.
	interleukin-11 induces and maintains progenitors of different cell lineages during Xenopus tadpole tail regeneration., Tsujioka H., Nat Commun. September 8, 2017; 8 (1): 495.
	Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	Early neural ectodermal genes are activated by Siamois and Twin during blastula stages., Klein SL., Genesis. May 1, 2015; 53 (5): 308-20.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	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.
	Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	High-resolution analysis of gene activity during the Xenopus mid-blastula transition., Collart C., Development. May 1, 2014; 141 (9): 1927-39.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
	Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.
	Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation., Hara Y., Dev Biol. October 15, 2013; 382 (2): 482-95.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	β-Arrestin 1 mediates non-canonical Wnt pathway to regulate convergent extension movements., Kim GH., Biochem Biophys Res Commun. May 31, 2013; 435 (2): 182-7.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
	Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos., Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling., Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	Long-distance signals are required for morphogenesis of the regenerating Xenopus tadpole tail, as shown by femtosecond-laser ablation., Mondia JP., PLoS One. January 1, 2011; 6 (9): e24953.
	Xenopus furry contributes to release of microRNA gene silencing., Goto T., Proc Natl Acad Sci U S A. November 9, 2010; 107 (45): 19344-9.
	Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.
	Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway., Luxardi G., Development. February 1, 2010; 137 (3): 417-26.
	Comparison of Lim1 expression in embryos of frogs with different modes of reproduction., Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.
	Identification and gastrointestinal expression of Xenopus laevis FoxF2., McLin VA., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
	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.
	Bestrophin genes are expressed in Xenopus development., Onuma Y., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.
	The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets., Lee C, Lee C, Lee C., Dev Dyn. June 1, 2009; 238 (6): 1480-91.

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