Papers associated with limb (and tbxt)

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	RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis., Wong S., EMBO Mol Med. May 8, 2023; 15 (5): e17078.
	Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR., Sempou E., Nat Commun. November 5, 2022; 13 (1): 6681.
	Normal Table of Xenopus development: a new graphical resource., Zahn N., Development. July 15, 2022; 149 (14):
	A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.
	Evolution of Somite Compartmentalization: A View From Xenopus., Della Gaspera B., Front Cell Dev Biol. January 1, 2021; 9 790847.
	The secreted BMP antagonist ERFE is required for the development of a functional circulatory system in Xenopus., Melchert J., Dev Biol. March 15, 2020; 459 (2): 138-148.
	Cdc42 Effector Protein 3 Interacts With Cdc42 in Regulating Xenopus Somite Segmentation., Kho M., Front Physiol. January 1, 2019; 10 542.
	A transition from SoxB1 to SoxE transcription factors is essential for progression from pluripotent blastula cells to neural crest cells., Buitrago-Delgado E., Dev Biol. December 15, 2018; 444 (2): 50-61.
	Cells from subcutaneous tissues contribute to scarless skin regeneration in Xenopus laevis froglets., Otsuka-Yamaguchi R., Dev Dyn. August 1, 2017; 246 (8): 585-597.
	Ascl1 represses the mesendoderm induction in Xenopus., Min Z., Acta Biochim Biophys Sin (Shanghai). November 1, 2016; 48 (11): 1006-1015.
	Small C-terminal Domain Phosphatase 3 Dephosphorylates the Linker Sites of Receptor-regulated Smads (R-Smads) to Ensure Transforming Growth Factor β (TGFβ)-mediated Germ Layer Induction in Xenopus Embryos., Sun G., J Biol Chem. July 10, 2015; 290 (28): 17239-49.
	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.
	Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos., Chatfield J., Development. June 1, 2014; 141 (12): 2429-40.
	Highly efficient targeted mutagenesis in axolotl using Cas9 RNA-guided nuclease., Flowers GP., Development. May 1, 2014; 141 (10): 2165-71.
	An essential role for transcription before the MBT in Xenopus laevis., Skirkanich J., Dev Biol. September 15, 2011; 357 (2): 478-91.
	The roles of maternal Vangl2 and aPKC in Xenopus oocyte and embryo patterning., Cha SW., Development. September 1, 2011; 138 (18): 3989-4000.
	Snail2 controls mesodermal BMP/Wnt induction of neural crest., Shi J., Development. August 1, 2011; 138 (15): 3135-45.
	XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.
	Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo., Lim JW., Development. January 1, 2011; 138 (1): 33-44.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	The function of heterodimeric AP-1 comprised of c-Jun and c-Fos in activin mediated Spemann organizer gene expression., Lee SY., PLoS One. January 1, 2011; 6 (7): e21796.
	Delta-Notch signaling is involved in the segregation of the three germ layers in Xenopus laevis., Revinski DR., Dev Biol. March 15, 2010; 339 (2): 477-92.
	Tissue-Tissue Interaction-Triggered Calcium Elevation Is Required for Cell Polarization during Xenopus Gastrulation., Shindo A., PLoS One. February 2, 2010; 5 (2): e8897.
	Xwnt8 directly initiates expression of labial Hox genes., In der Rieden PM., Dev Dyn. January 1, 2010; 239 (1): 126-39.
	PRDC regulates placode neurogenesis in chick by modulating BMP signalling., Kriebitz NN., Dev Biol. December 15, 2009; 336 (2): 280-92.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Rab5-mediated endocytosis of activin is not required for gene activation or long-range signalling in Xenopus., Hagemann AI., Development. August 1, 2009; 136 (16): 2803-13.
	Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.
	Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation., Haremaki T., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	Tsukushi cooperates with VG1 to induce primitive streak and Hensen's node formation in the chick embryo., Ohta K., Development. October 1, 2006; 133 (19): 3777-86.
	CDMP1/GDF5 has specific processing requirements that restrict its action to joint surfaces., Thomas JT., J Biol Chem. September 8, 2006; 281 (36): 26725-33.
	Hex acts with beta-catenin to regulate anteroposterior patterning via a Groucho-related co-repressor and Nodal., Zamparini AL., Development. September 1, 2006; 133 (18): 3709-22.
	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.
	Interaction between X-Delta-2 and Hox genes regulates segmentation and patterning of the anteroposterior axis., Peres JN., Mech Dev. April 1, 2006; 123 (4): 321-33.
	XBP1 forms a regulatory loop with BMP-4 and suppresses mesodermal and neural differentiation in Xenopus embryos., Cao Y, Cao Y., Mech Dev. January 1, 2006; 123 (1): 84-96.
	Novel Daple-like protein positively regulates both the Wnt/beta-catenin pathway and the Wnt/JNK pathway in Xenopus., Kobayashi H., Mech Dev. October 1, 2005; 122 (10): 1138-53.
	Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer., Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.
	Sirenomelia in Bmp7 and Tsg compound mutant mice: requirement for Bmp signaling in the development of ventral posterior mesoderm., Zakin L., Development. May 1, 2005; 132 (10): 2489-99.
	R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
	Amphibian in vitro heart induction: a simple and reliable model for the study of vertebrate cardiac development., Ariizumi T., Int J Dev Biol. September 1, 2003; 47 (6): 405-10.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor., Yokota C., Development. May 1, 2003; 130 (10): 2199-212.
	FGFR4 signaling is a necessary step in limb muscle differentiation., Marics I., Development. October 1, 2002; 129 (19): 4559-69.
	eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis., Fisher ME, Fisher ME., Development. March 1, 2002; 129 (6): 1307-15.
	Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes., Charbonnier F., J Biol Chem. January 11, 2002; 277 (2): 1139-47.
	Determinants of T box protein specificity., Conlon FL., Development. October 1, 2001; 128 (19): 3749-58.
	XCL-2 is a novel m-type calpain and disrupts morphogenetic movements during embryogenesis in Xenopus laevis., Cao Y., Dev Growth Differ. October 1, 2001; 43 (5): 563-71.
	FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.

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