Papers associated with stria terminalis (and odc1)

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	A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.
	Expression pattern of bcar3, a downstream target of Gata2, and its binding partner, bcar1, during Xenopus development., Green YS., Gene Expr Patterns. January 1, 2016; 20 (1): 55-62.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	GATA2 regulates Wnt signaling to promote primitive red blood cell fate., Mimoto MS., Dev Biol. November 1, 2015; 407 (1): 1-11.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	miR-34/449 control apical actin network formation during multiciliogenesis through small GTPase pathways., Chevalier B., Nat Commun. September 18, 2015; 6 8386.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	Comparative expression analysis of pfdn6a and tcp1α during Xenopus development., Marracci S., Int J Dev Biol. January 1, 2015; 59 (4-6): 235-40.
	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.
	Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos., Chatfield J., Development. June 1, 2014; 141 (12): 2429-40.
	A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis., Dubaissi E., Development. April 1, 2014; 141 (7): 1514-25.
	IRE1α is essential for Xenopus pancreas development., Yuan L., J Biomed Res. March 1, 2014; 28 (2): 123-31.
	Xenopus embryonic epidermis as a mucociliary cellular ecosystem to assess the effect of sex hormones in a non-reproductive context., Castillo-Briceno P., Front Zool. February 6, 2014; 11 (1): 9.
	Differential expression of arid5b isoforms in Xenopus laevis pronephros., Le Bouffant R., Int J Dev Biol. January 1, 2014; 58 (5): 363-8.
	Xenopus cadherin 5 is specifically expressed in endothelial cells of the developing vascular system., Neuhaus H., Int J Dev Biol. January 1, 2014; 58 (1): 51-6.
	Retinoic acid-activated Ndrg1a represses Wnt/β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification., Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.
	β-Adrenergic signaling promotes posteriorization in Xenopus early development., Mori S., Dev Growth Differ. April 1, 2013; 55 (3): 350-8.
	Expression of pluripotency factors in larval epithelia of the frog Xenopus: evidence for the presence of cornea epithelial stem cells., Perry KJ., Dev Biol. February 15, 2013; 374 (2): 281-94.
	Suv4-20h histone methyltransferases promote neuroectodermal differentiation by silencing the pluripotency-associated Oct-25 gene., Nicetto D., PLoS Genet. January 1, 2013; 9 (1): e1003188.
	Expression of xSDF-1α, xCXCR4, and xCXCR7 during gastrulation in Xenopus laevis., Mishra SK., Int J Dev Biol. January 1, 2013; 57 (1): 95-100.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.
	The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.
	Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos., Canning CA., Dev Dyn. August 1, 2011; 240 (8): 1958-63.
	MiR-124 regulates early neurogenesis in the optic vesicle and forebrain, targeting NeuroD1., Liu K., Nucleic Acids Res. April 1, 2011; 39 (7): 2869-79.
	The secreted integrin ligand nephronectin is necessary for forelimb formation in Xenopus tropicalis., Abu-Daya A., Dev Biol. January 15, 2011; 349 (2): 204-12.
	Expression of Transposable Elements in Neural Tissues during Xenopus Development., Faunes F., PLoS One. January 1, 2011; 6 (7): e22569.
	XIer2 is required for convergent extension movements during Xenopus development., Hong SK., Int J Dev Biol. January 1, 2011; 55 (10-12): 917-21.
	Expression analysis of Runx3 and other Runx family members during Xenopus development., Park BY., Gene Expr Patterns. June 1, 2010; 10 (4-5): 159-66.
	FoxG1 and TLE2 act cooperatively to regulate ventral telencephalon formation., Roth M., Development. May 1, 2010; 137 (9): 1553-62.
	Xenopus Bsx links daily cell cycle rhythms and pineal photoreceptor fate., D'Autilia S., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6352-7.
	A non-enzymatic function of 17beta-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival., Rauschenberger K., EMBO Mol Med. February 1, 2010; 2 (2): 51-62.
	Identification and developmental expression of Xenopus laevis SUMO proteases., Wang Y., PLoS One. December 11, 2009; 4 (12): e8462.
	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.
	Xenopus Wntless and the retromer complex cooperate to regulate XWnt4 secretion., Kim H., Mol Cell Biol. April 1, 2009; 29 (8): 2118-28.
	N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
	Expression of Xenopus tropicalis HNF6/Onecut-1., Haworth KE., Int J Dev Biol. January 1, 2009; 53 (1): 159-62.
	The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos., Stubbs JL., Nat Genet. December 1, 2008; 40 (12): 1454-60.
	GATA4 and GATA5 are essential for heart and liver development in Xenopus embryos., Haworth KE., BMC Dev Biol. July 28, 2008; 8 74.
	FoxM1-driven cell division is required for neuronal differentiation in early Xenopus embryos., Ueno H., Development. June 1, 2008; 135 (11): 2023-30.
	The myocardin-related transcription factor, MASTR, cooperates with MyoD to activate skeletal muscle gene expression., Meadows SM., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1545-50.
	The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.
	Xenopus cDNA microarray identification of genes with endodermal organ expression., Park EC., Dev Dyn. June 1, 2007; 236 (6): 1633-49.
	Expression analysis of IGFBP-rP10, IGFBP-like and Mig30 in early Xenopus development., Kuerner KM., Dev Dyn. October 1, 2006; 235 (10): 2861-7.
	Xenopus embryos lacking specific isoforms of the corepressor SMRT develop abnormal heads., Malartre M., Dev Biol. April 15, 2006; 292 (2): 333-43.
	Mxi1 is essential for neurogenesis in Xenopus and acts by bridging the pan-neural and proneural genes., Klisch TJ., Dev Biol. April 15, 2006; 292 (2): 470-85.
	Developmental expression of Shisa-2 in Xenopus laevis., Silva AC., Int J Dev Biol. January 1, 2006; 50 (6): 575-9.
	A novel G protein-coupled receptor, related to GPR4, is required for assembly of the cortical actin skeleton in early Xenopus embryos., Tao Q, Tao Q., Development. June 1, 2005; 132 (12): 2825-36.

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