Papers associated with tail region (and sst.1)

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	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	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.
	Targeted search for scaling genes reveals matrixmetalloproteinase 3 as a scaler of the dorsal-ventral pattern in Xenopus laevis embryos., Orlov EE., Dev Cell. January 10, 2022; 57 (1): 95-111.e12.
	Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
	Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney., Zhang B., Development. March 22, 2018; 145 (6):
	Identification of novel cis-regulatory elements of Eya1 in Xenopus laevis using BAC recombineering., Maharana SK., Sci Rep. November 3, 2017; 7 (1): 15033.
	Mesodermal origin of median fin mesenchyme and tail muscle in amphibian larvae., Taniguchi Y., Sci Rep. June 18, 2015; 5 11428.
	Migratory and adhesive properties of Xenopus laevis primordial germ cells in vitro., Dzementsei A., Biol Open. December 15, 2013; 2 (12): 1279-87.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	The hypoxia factor Hif-1α controls neural crest chemotaxis and epithelial to mesenchymal transition., Barriga EH., J Cell Biol. May 27, 2013; 201 (5): 759-76.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	Paralysis and delayed Z-disc formation in the Xenopus tropicalis unc45b mutant dicky ticker., Geach TJ., BMC Dev Biol. January 22, 2010; 10 75.
	Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.
	Identification of a novel uromodulin-like gene related to predator-induced bulgy morph in anuran tadpoles by functional microarray analysis., Mori T., PLoS One. June 16, 2009; 4 (6): e5936.
	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.
	p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.
	Wnt5 signaling in vertebrate pancreas development., Kim HJ., BMC Biol. October 24, 2005; 3 23.
	Elucidating the origins of the vascular system: a fate map of the vascular endothelial and red blood cell lineages in Xenopus laevis., Mills KR., Dev Biol. May 15, 1999; 209 (2): 352-68.
	Expression pattern of the winged helix factor XFD-11 during Xenopus embryogenesis., Köster M., Mech Dev. August 1, 1998; 76 (1-2): 169-73.
	Inhibition of Xbra transcription activation causes defects in mesodermal patterning and reveals autoregulation of Xbra in dorsal mesoderm., Conlon FL., Development. August 1, 1996; 122 (8): 2427-35.
	The Xenopus homologue of Otx2 is a maternal homeobox gene that demarcates and specifies anterior body regions., Pannese M., Development. March 1, 1995; 121 (3): 707-20.
	The distribution of fibronectin and tenascin along migratory pathways of the neural crest in the trunk of amphibian embryos., Epperlein HH., Development. August 1, 1988; 103 (4): 743-56.

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