Papers associated with proximal (and myod1)

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	Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs., Bredeson JV., Nat Commun. January 17, 2024; 15 (1): 579.
	Purine Biosynthesis Pathways Are Required for Myogenesis in Xenopus laevis., Duperray M., Cells. September 28, 2023; 12 (19):
	The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos., Massé K., Commun Biol. October 7, 2021; 4 (1): 1158.
	Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5., Maerker M., Nat Commun. September 16, 2021; 12 (1): 5482.
	Wnt-inducible Lrp6-APEX2 interacting proteins identify ESCRT machinery and Trk-fused gene as components of the Wnt signaling pathway., Colozza G., Sci Rep. December 9, 2020; 10 (1): 21555.
	The SNPs in myoD gene from normal muscle developing individuals have no effect on muscle mass., Ding S., BMC Genet. September 2, 2019; 20 (1): 72.
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS., Cell Rep. February 3, 2015; 10 (4): 527-36.
	Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
	The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	Interrogating transcriptional regulatory sequences in Tol2-mediated Xenopus transgenics., Loots GG., PLoS One. July 1, 2013; 8 (7): e68548.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	Transcriptional regulation of mesoderm genes by MEF2D during early Xenopus development., Kolpakova A., PLoS One. January 1, 2013; 8 (7): e69693.
	Skeletal muscle regeneration in Xenopus tadpoles and zebrafish larvae., Rodrigues AM., BMC Dev Biol. February 27, 2012; 12 9.
	Involvement of the eukaryotic initiation factor 6 and kermit2/gipc2 in Xenopus laevis pronephros formation., Tussellino M., Int J Dev Biol. January 1, 2012; 56 (5): 357-62.
	Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.
	Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.
	Role of Tbx2 in defining the territory of the pronephric nephron., Cho GS., Development. February 1, 2011; 138 (3): 465-74.
	Tissue-specific expression of Sarcoplasmic/Endoplasmic Reticulum Calcium ATPases (ATP2A/SERCA) 1, 2, 3 during Xenopus laevis development., Pegoraro C., Gene Expr Patterns. January 1, 2011; 11 (1-2): 122-8.
	XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
	Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
	Coordination of cell polarity during Xenopus gastrulation., Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.
	The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	Limb regeneration in Xenopus laevis froglet., Suzuki M, Suzuki M., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.
	Cooperative non-cell and cell autonomous regulation of Nodal gene expression and signaling by Lefty/Antivin and Brachyury in Xenopus., Cha YR., Dev Biol. February 15, 2006; 290 (2): 246-64.
	Spatio-temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis., Della Gaspera B., Dev Dyn. February 1, 2006; 235 (2): 524-9.
	Characteristics of initiation and early events for muscle development in the Xenopus limb bud., Satoh A., Dev Dyn. December 1, 2005; 234 (4): 846-57.
	XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
	Muscle formation in regenerating Xenopus froglet limb., Satoh A., Dev Dyn. June 1, 2005; 233 (2): 337-46.
	neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia., Ma Q., Neuron. March 1, 1998; 20 (3): 469-82.
	Activation of the cardiac alpha-actin promoter depends upon serum response factor, Tinman homologue, Nkx-2.5, and intact serum response elements., Chen CY., Dev Genet. January 1, 1996; 19 (2): 119-30.
	The regulation of MyoD gene expression: conserved elements mediate expression in embryonic axial muscle., Asakura A., Dev Biol. October 1, 1995; 171 (2): 386-98.

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