Papers associated with rhombomere (and chrd.1)

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	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis., Ding Y., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.
	Nodal/Activin Pathway is a Conserved Neural Induction Signal in Chordates., Le Petillon Y., Nat Ecol Evol. August 1, 2017; 1 (8): 1192-1200.
	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.
	G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
	40LoVe and Samba are involved in Xenopus neural development and functionally distinct from hnRNP AB., Andreou M., PLoS One. January 1, 2014; 9 (1): e85026.
	FoxA4 favours notochord formation by inhibiting contiguous mesodermal fates and restricts anterior neural development in Xenopus embryos., Murgan S., PLoS One. January 1, 2014; 9 (10): e110559.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
	The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
	Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification., Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
	BMP antagonists and FGF signaling contribute to different domains of the neural plate in Xenopus., Wills AE., Dev Biol. January 15, 2010; 337 (2): 335-50.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	The role of the Spemann organizer in anterior-posterior patterning of the trunk., Jansen HJ., Mech Dev. January 1, 2007; 124 (9-10): 668-81.
	Neurotrophin receptor homolog (NRH1) proteins regulate mesoderm formation and apoptosis during early Xenopus development., Knapp D., Dev Biol. December 15, 2006; 300 (2): 554-69.
	Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.
	Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
	Xenopus Teashirt1 regulates posterior identity in brain and cranial neural crest., Koebernick K., Dev Biol. October 1, 2006; 298 (1): 312-26.
	Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis., Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
	Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
	Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.
	Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.
	MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.
	Pilot morpholino screen in Xenopus tropicalis identifies a novel gene involved in head development., Kenwrick S., Dev Dyn. February 1, 2004; 229 (2): 289-99.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	Xolloid-related: a novel BMP1/Tolloid-related metalloprotease is expressed during early Xenopus development., Dale L., Mech Dev. December 1, 2002; 119 (2): 177-90.
	The latent-TGFbeta-binding-protein-1 (LTBP-1) is expressed in the organizer and regulates nodal and activin signaling., Altmann CR., Dev Biol. August 1, 2002; 248 (1): 118-27.
	Transcription factor AP-2 is an essential and direct regulator of epidermal development in Xenopus., Luo T., Dev Biol. May 1, 2002; 245 (1): 136-44.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	Conserved cellular and molecular mechanisms in development., Giudice G., Cell Biol Int. January 1, 2001; 25 (11): 1081-90.
	A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1., Pera EM., Mech Dev. September 1, 2000; 96 (2): 183-95.
	Neuralization of the Xenopus embryo by inhibition of p300/ CREB-binding protein function., Kato Y., J Neurosci. November 1, 1999; 19 (21): 9364-73.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	Role of Xrx1 in Xenopus eye and anterior brain development., Andreazzoli M., Development. June 1, 1999; 126 (11): 2451-60.
	Induction and patterning of the neural crest, a stem cell-like precursor population., LaBonne C., J Neurobiol. August 1, 1998; 36 (2): 175-89.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	Differential regulation of chordin expression domains in mutant zebrafish., Miller-Bertoglio VE., Dev Biol. December 15, 1997; 192 (2): 537-50.
	Regulation of dorsal fate in the neuraxis by Wnt-1 and Wnt-3a., Saint-Jeannet JP., Proc Natl Acad Sci U S A. December 9, 1997; 94 (25): 13713-8.
	Xwnt-8 and lithium can act upon either dorsal mesodermal or neurectodermal cells to cause a loss of forebrain in Xenopus embryos., Fredieu JR., Dev Biol. June 1, 1997; 186 (1): 100-14.
	Drosophila short gastrulation induces an ectopic axis in Xenopus: evidence for conserved mechanisms of dorsal-ventral patterning., Schmidt J., Development. December 1, 1995; 121 (12): 4319-28.

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