Papers associated with muscle (and tgfb1)

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	Downregulation of Yap1 during limb regeneration results in defective bone formation in axolotl., Bay S., Dev Biol. June 2, 2023; 500 31-39.
	Acute multidrug delivery via a wearable bioreactor facilitates long-term limb regeneration and functional recovery in adult Xenopus laevis., Murugan NJ., Sci Adv. January 28, 2022; 8 (4): eabj2164.
	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):
	Genome-wide transcriptomics analysis identifies sox7 and sox18 as specifically regulated by gata4 in cardiomyogenesis., Afouda BA., Dev Biol. February 1, 2018; 434 (1): 108-120.
	Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy., Freyermuth F., Nat Commun. April 11, 2016; 7 11067.
	A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome., Rienhoff HY., Am J Med Genet A. August 1, 2013; 161A (8): 2040-6.
	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.
	R-spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis Kazanskaya O, Glinka A, del BarcoBarrantes I, Stannek P, Niehrs C, Wu W, Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Heidelberg, Germany., Koeneman KS., Urol Oncol. January 1, 2009; 27 (1):
	Schwann cells promote synaptogenesis at the neuromuscular junction via transforming growth factor-beta1., Feng Z., J Neurosci. September 24, 2008; 28 (39): 9599-609.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Regulation of the Xenopus Xsox17alpha(1) promoter by co-operating VegT and Sox17 sites., Howard L., Dev Biol. October 15, 2007; 310 (2): 402-15.
	BMP-4 and Noggin signaling modulate dorsal fin and somite development in the axolotl trunk., Epperlein HH., Dev Dyn. September 1, 2007; 236 (9): 2464-74.
	Evolution of Na,K-ATPase beta m-subunit into a coregulator of transcription in placental mammals., Pestov NB., Proc Natl Acad Sci U S A. July 3, 2007; 104 (27): 11215-20.
	ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.
	Left-right lineage analysis of AV cushion tissue in normal and laterality defective Xenopus hearts., Ramsdell AF., Anat Rec A Discov Mol Cell Evol Biol. December 1, 2005; 287 (2): 1176-82.
	Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
	Interplay between the tumor suppressor p53 and TGF beta signaling shapes embryonic body axes in Xenopus., Takebayashi-Suzuki K., Development. September 1, 2003; 130 (17): 3929-39.
	Uncommitted Xenopus blastula cells can be directed to uniform muscle gene expression by gradient interpretation and a community effect., Standley HJ., Int J Dev Biol. December 1, 2002; 46 (8): 993-8.
	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.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	BIP, a BRAM-interacting protein involved in TGF-beta signalling, regulates body length in Caenorhabditis elegans., Sugawara K., Genes Cells. July 1, 2001; 6 (7): 599-606.
	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.
	BMP-binding modules in chordin: a model for signalling regulation in the extracellular space., Larraín J., Development. February 1, 2000; 127 (4): 821-30.
	Sequence and expression of myoglianin, a novel Drosophila gene of the TGF-beta superfamily., Lo PC., Mech Dev. August 1, 1999; 86 (1-2): 171-5.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	Identification of two Smad4 proteins in Xenopus. Their common and distinct properties., Masuyama N., J Biol Chem. April 23, 1999; 274 (17): 12163-70.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Drosophila dSmad2 and Atr-I transmit activin/TGFbeta signals., Das P., Genes Cells. February 1, 1999; 4 (2): 123-34.
	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.
	Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.
	XTrR-I is a TGFbeta receptor and overexpression of truncated form of the receptor inhibits axis formation and dorsalising activity., Mahony D., Mech Dev. July 1, 1998; 75 (1-2): 95-105.
	Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos., Joseph EM., Development. July 1, 1998; 125 (14): 2677-85.
	Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis., Nakayama T., Genes Cells. June 1, 1998; 3 (6): 387-94.
	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.
	The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds., Armes NA., Development. October 1, 1997; 124 (19): 3797-804.
	Xnr4: a Xenopus nodal-related gene expressed in the Spemann organizer., Joseph EM., Dev Biol. April 15, 1997; 184 (2): 367-72.
	A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C., Development. February 1, 1997; 124 (4): 827-37.
	Combinatorial signalling by Xwnt-11 and Xnr3 in the organizer epithelium., Glinka A., Mech Dev. December 1, 1996; 60 (2): 221-31.
	A Xenopus nodal-related gene that acts in synergy with noggin to induce complete secondary axis and notochord formation., Lustig KD., Development. October 1, 1996; 122 (10): 3275-82.
	BMP-like signals are required after the midblastula transition for blood cell development., Zhang C., Dev Genet. January 1, 1996; 18 (3): 267-78.
	Anti-dorsalizing morphogenetic protein is a novel TGF-beta homolog expressed in the Spemann organizer., Moos M., Development. December 1, 1995; 121 (12): 4293-301.
	A nodal-related gene defines a physical and functional domain within the Spemann organizer., Smith WC., Cell. July 14, 1995; 82 (1): 37-46.
	Sequential expression of acetylcholine receptor isoforms in mesodermalized Xenopus animal caps., Reuer Q., Dev Biol. November 1, 1994; 166 (1): 323-30.
	[The effect of microinjection of anti-TGF beta-1 antibodies on the early development of Xenopus laevis]., Shou WN., Shi Yan Sheng Wu Xue Bao. June 1, 1992; 25 (2): 123-37.
	Injected Wnt RNA induces a complete body axis in Xenopus embryos., Sokol S., Cell. November 15, 1991; 67 (4): 741-52.

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