Papers associated with primary germ layer (and cat.2)

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	ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia., Walentek P., Dev Biol. December 15, 2015; 408 (2): 292-304.
	Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.
	The conserved barH-like homeobox-2 gene barhl2 acts downstream of orthodentricle-2 and together with iroquois-3 in establishment of the caudal forebrain signaling center induced by Sonic Hedgehog., Juraver-Geslin HA., Dev Biol. December 1, 2014; 396 (1): 107-20.
	Sterol carrier protein 2 regulates proximal tubule size in the Xenopus pronephric kidney by modulating lipid rafts., Cerqueira DM., Dev Biol. October 1, 2014; 394 (1): 54-64.
	Nuclearization of β-catenin in ectodermal precursors confers organizer-like ability to induce endomesoderm and pattern a pluteus larva., Byrum CA., Evodevo. November 4, 2013; 4 (1): 31.
	Different thresholds of Wnt-Frizzled 7 signaling coordinate proliferation, morphogenesis and fate of endoderm progenitor cells., Zhang Z., Dev Biol. June 1, 2013; 378 (1): 1-12.
	Jun N-terminal kinase maintains tissue integrity during cell rearrangement in the gut., Dush MK., Development. April 1, 2013; 140 (7): 1457-66.
	A chimera carrying the functional domain of the orphan protein SLC7A14 in the backbone of SLC7A2 mediates trans-stimulated arginine transport., Jaenecke I., J Biol Chem. August 31, 2012; 287 (36): 30853-60.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Roles of ADAM13-regulated Wnt activity in early Xenopus eye development., Wei S., Dev Biol. March 1, 2012; 363 (1): 147-54.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.
	Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.
	Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses., Hurle B., BMC Evol Biol. January 24, 2011; 11 23.
	The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling., Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Syndecan-1 regulates BMP signaling and dorso-ventral patterning of the ectoderm during early Xenopus development., Olivares GH., Dev Biol. May 15, 2009; 329 (2): 338-49.
	Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus., Mir A., Dev Biol. March 1, 2008; 315 (1): 161-72.
	Peroxisome biogenesis occurs in late dorsal-anterior structures in the development of Xenopus laevis., Cooper CA., Dev Dyn. December 1, 2007; 236 (12): 3554-61.
	Xenopus galectin-VIa shows highly specific expression in cement glands and is regulated by canonical Wnt signaling., Michiue T., Gene Expr Patterns. October 1, 2007; 7 (8): 852-7.
	Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.
	A cell cycle arrest is necessary for bottle cell formation in the early Xenopus gastrula: integrating cell shape change, local mitotic control and mesodermal patterning., Kurth T., Mech Dev. December 1, 2005; 122 (12): 1251-65.
	The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system., Huang X., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
	Protection of Xenopus laevis embryos against alcohol-induced delayed gut maturation and growth retardation by peroxiredoxin 5 and catalase., Peng Y., J Mol Biol. July 16, 2004; 340 (4): 819-27.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	Distinct enhancer elements control Hex expression during gastrulation and early organogenesis., Rodriguez TA., Dev Biol. June 15, 2001; 234 (2): 304-16.
	Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.
	Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif., Germain S., Genes Dev. February 15, 2000; 14 (4): 435-51.
	Essential role of CREB family proteins during Xenopus embryogenesis., Lutz B., Mech Dev. October 1, 1999; 88 (1): 55-66.
	Differential expression of two skeletal muscle beta-tropomyosin mRNAs during Xenopus laevis development., Gaillard C., Int J Dev Biol. March 1, 1999; 43 (2): 175-8.
	Opl: a zinc finger protein that regulates neural determination and patterning in Xenopus., Kuo JS., Development. August 1, 1998; 125 (15): 2867-82.
	Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.
	X-MyT1, a Xenopus C2HC-type zinc finger protein with a regulatory function in neuronal differentiation., Bellefroid EJ., Cell. December 27, 1996; 87 (7): 1191-202.
	Maternal beta-catenin establishes a 'dorsal signal' in early Xenopus embryos., Wylie C., Development. October 1, 1996; 122 (10): 2987-96.
	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.
	DNA sequences mediating the transcriptional response of the Mix.2 homeobox gene to mesoderm induction., Vize PD., Dev Biol. July 10, 1996; 177 (1): 226-31.
	Activation of Xenopus MyoD transcription by members of the MEF2 protein family., Wong MW., Dev Biol. December 1, 1994; 166 (2): 683-95.
	Distinct elements of the xsna promoter are required for mesodermal and ectodermal expression., Mayor R., Development. November 1, 1993; 119 (3): 661-71.
	XASH-3, a novel Xenopus achaete-scute homolog, provides an early marker of planar neural induction and position along the mediolateral axis of the neural plate., Zimmerman K., Development. September 1, 1993; 119 (1): 221-32.
	Interactions between Xwnt-8 and Spemann organizer signaling pathways generate dorsoventral pattern in the embryonic mesoderm of Xenopus., Christian JL., Genes Dev. January 1, 1993; 7 (1): 13-28.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.
	The comparative distribution of xenopsin- and neurotensin-like immunoreactivity in Xenopus laevis and rat tissues., Goedert M., Dev Biol. August 13, 1984; 308 (2): 273-80.
	Melatonin content of cat cerebrospinal fluid and blood following intravenous injection of melatonin as measured by Xenopus laevis skin melanophore test., Kovács L., Acta Physiol Acad Sci Hung. January 1, 1975; 46 (1): 33-6.

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