Papers associated with tadpole (and tgfb1)

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	Knockdown of NeuroD2 leads to seizure-like behaviour, brain neuronal hyperactivity and a leaky blood-brain barrier in a Xenopus laevis tadpole model of DEE75., Banerjee S., Genetics. May 24, 2024;
	Impaired negative feedback and death following acute stress in glucocorticoid receptor knockout Xenopus tropicalis tadpoles., Paul B., Gen Comp Endocrinol. September 15, 2022; 326 114072.
	Foxm1 regulates neural progenitor fate during spinal cord regeneration., Pelzer D., EMBO Rep. September 6, 2021; 22 (9): e50932.
	TGF-β1 signaling is essential for tissue regeneration in the Xenopus tadpole tail., Nakamura M., Biochem Biophys Res Commun. August 6, 2021; 565 91-96.
	Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs., Aztekin C., Development. June 1, 2021; 148 (11):
	Model systems for regeneration: Xenopus., Phipps LS., Development. March 19, 2020; 147 (6):
	The myeloid lineage is required for the emergence of a regeneration-permissive environment following Xenopus tail amputation., Aztekin C., Development. February 5, 2020; 147 (3):
	More Than Just a Bandage: Closing the Gap Between Injury and Appendage Regeneration., Kakebeen AD., Front Physiol. January 1, 2019; 10 81.
	Pitx1 regulates cement gland development in Xenopus laevis through activation of transcriptional targets and inhibition of BMP signaling., Jin Y., Dev Biol. May 1, 2018; 437 (1): 41-49.
	ZC4H2 stabilizes Smads to enhance BMP signalling, which is involved in neural development in Xenopus., Ma P., Open Biol. August 1, 2017; 7 (8):
	Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.
	Transducing bioelectric signals into epigenetic pathways during tadpole tail regeneration., Tseng AS., Anat Rec (Hoboken). October 1, 2012; 295 (10): 1541-51.
	Transgenic analysis of signaling pathways required for Xenopus tadpole spinal cord and muscle regeneration., Lin G., Anat Rec (Hoboken). October 1, 2012; 295 (10): 1532-40.
	Tissue-specific alternative splicing of Tak1 is conserved in deuterostomes., Venables JP., Mol Biol Evol. January 1, 2012; 29 (1): 261-9.
	TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	DRAGON, a bone morphogenetic protein co-receptor., Samad TA., J Biol Chem. April 8, 2005; 280 (14): 14122-9.
	Comparative functional analysis of rat TGF-beta1 and Xenopus laevis TGF-beta5 promoters suggest differential regulations., Goswami MT., J Mol Evol. July 1, 2003; 57 (1): 44-51.
	Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor., Bell E., Development. April 1, 2003; 130 (7): 1381-9.
	Gene profiling during neural induction in Xenopus laevis: regulation of BMP signaling by post-transcriptional mechanisms and TAB3, a novel TAK1-binding protein., Muñoz-Sanjuán I., Development. December 1, 2002; 129 (23): 5529-40.
	Molecular cloning and expression study of Xenopus latent TGF-beta binding protein-1 (LTBP-1)., Quarto N., Gene. May 15, 2002; 290 (1-2): 53-61.
	Origins of inner ear sensory organs revealed by fate map and time-lapse analyses., Kil SH., Dev Biol. May 15, 2001; 233 (2): 365-79.
	Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth factor-beta receptors., Souchelnytskyi S., J Biol Chem. September 25, 1998; 273 (39): 25364-70.
	Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos., Joseph EM., Development. July 1, 1998; 125 (14): 2677-85.
	Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins., Sparrow DB., Mech Dev. February 1, 1998; 71 (1-2): 151-63.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Misexpression of chick Vg1 in the marginal zone induces primitive streak formation., Shah SB., Development. December 1, 1997; 124 (24): 5127-38.
	Smad5 induces ventral fates in Xenopus embryo., Suzuki A., Dev Biol. April 15, 1997; 184 (2): 402-5.
	A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C., Development. February 1, 1997; 124 (4): 827-37.
	An ascidian homologue of vertebrate BMPs-5-8 is expressed in the midline of the anterior neuroectoderm and in the midline of the ventral epidermis of the embryo., Miya T., Mech Dev. July 1, 1996; 57 (2): 181-90.
	Mothers against dpp encodes a conserved cytoplasmic protein required in DPP/TGF-beta responsive cells., Newfeld SJ., Development. July 1, 1996; 122 (7): 2099-108.
	A truncated bone morphogenetic protein receptor affects dorsal-ventral patterning in the early Xenopus embryo., Suzuki A., Proc Natl Acad Sci U S A. October 25, 1994; 91 (22): 10255-9.
	Transforming growth factor beta (TGF beta) is produced by and influences the proliferative response of Xenopus laevis lymphocytes., Haynes L., Dev Immunol. January 1, 1993; 3 (3): 223-30.

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