Papers associated with posterior (and cat.2)

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	Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders., Kaiyrzhanov R., Brain. April 4, 2024; 147 (4): 1436-1456.
	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.
	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.
	The need of MMP-2 on the sperm surface for Xenopus fertilization: its role in a fast electrical block to polyspermy., Iwao Y., Mech Dev. November 1, 2014; 134 80-95.
	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.
	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.
	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.
	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.
	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.
	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.
	Essential role of CREB family proteins during Xenopus embryogenesis., Lutz B., Mech Dev. October 1, 1999; 88 (1): 55-66.
	Opl: a zinc finger protein that regulates neural determination and patterning in Xenopus., Kuo JS., Development. August 1, 1998; 125 (15): 2867-82.
	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.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.

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