Papers associated with brain (and lhx1)

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	The LIM domain-containing homeo box gene Xlim-1 is expressed specifically in the organizer region of Xenopus gastrula embryos., Taira M., Genes Dev. March 1, 1992; 6 (3): 356-66.
	Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues., Taira M., Dev Biol. September 1, 1993; 159 (1): 245-56.
	Expression patterns of the murine LIM class homeobox gene lim1 in the developing brain and excretory system., Fujii T., Dev Dyn. January 1, 1994; 199 (1): 73-83.
	Embryonic expression of Lim-1, the mouse homolog of Xenopus Xlim-1, suggests a role in lateral mesoderm differentiation and neurogenesis., Barnes JD., Dev Biol. January 1, 1994; 161 (1): 168-78.
	Expression of the LIM class homeobox gene Xlim-1 in pronephros and CNS cell lineages of Xenopus embryos is affected by retinoic acid and exogastrulation., Taira M., Development. June 1, 1994; 120 (6): 1525-36.
	XIPOU 2, a noggin-inducible gene, has direct neuralizing activity., Witta SE., Development. March 1, 1995; 121 (3): 721-30.
	A dominant negative bone morphogenetic protein 4 receptor causes neuralization in Xenopus ectoderm., Xu RH., Biochem Biophys Res Commun. July 6, 1995; 212 (1): 212-9.
	The LIM class homeobox gene lim5: implied role in CNS patterning in Xenopus and zebrafish., Toyama R., Dev Biol. August 1, 1995; 170 (2): 583-93.
	The LIM homeodomain protein Lim-1 is widely expressed in neural, neural crest and mesoderm derivatives in vertebrate development., Karavanov AA., Int J Dev Biol. April 1, 1996; 40 (2): 453-61.
	Molecular cloning, structure, and chromosomal localization of the mouse LIM/homeobox gene Lhx5., Bertuzzi S., Genomics. September 1, 1996; 36 (2): 234-9.
	Expression of murine Lhx5 suggests a role in specifying the forebrain., Sheng HZ., Dev Dyn. February 1, 1997; 208 (2): 266-77.
	Frzb-1 is a secreted antagonist of Wnt signaling expressed in the Spemann organizer., Leyns L., Cell. March 21, 1997; 88 (6): 747-56.
	Cerberus-like is a secreted factor with neutralizing activity expressed in the anterior primitive endoderm of the mouse gastrula., Belo JA., Mech Dev. November 1, 1997; 68 (1-2): 45-57.
	Differential expression of non-muscle myosin heavy chain genes during Xenopus embryogenesis., Bhatia-Dey N., Mech Dev. November 1, 1998; 78 (1-2): 33-6.
	Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development., Gómez-Skarmeta JL., Mech Dev. January 1, 1999; 80 (1): 15-27.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	Synergism between Pax-8 and lim-1 in embryonic kidney development., Carroll TJ., Dev Biol. October 1, 1999; 214 (1): 46-59.
	Maternal cold inducible RNA binding protein is required for embryonic kidney formation in Xenopus laevis., Peng Y., FEBS Lett. September 29, 2000; 482 (1-2): 37-43.
	A role for Xlim-1 in pronephros development in Xenopus laevis., Chan TC., Dev Biol. December 15, 2000; 228 (2): 256-69.
	A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.
	Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation., Lamar E., Development. April 1, 2001; 128 (8): 1335-46.
	The LIM-homeodomain gene family in the developing Xenopus brain: conservation and divergences with the mouse related to the evolution of the forebrain., Bachy I., J Neurosci. October 1, 2001; 21 (19): 7620-9.
	Synthesis and release of activin and noggin by cultured human amniotic epithelial cells., Koyano S., Dev Growth Differ. April 1, 2002; 44 (2): 103-12.
	Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney., Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	The Xenopus receptor tyrosine kinase Xror2 modulates morphogenetic movements of the axial mesoderm and neuroectoderm via Wnt signaling., Hikasa H., Development. November 1, 2002; 129 (22): 5227-39.
	The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	LIM-homeodomain genes as developmental and adult genetic markers of Xenopus forebrain functional subdivisions., Moreno N., J Comp Neurol. April 19, 2004; 472 (1): 52-72.
	Regulation of Otx2 expression and its functions in mouse epiblast and anterior neuroectoderm., Kurokawa D., Development. July 1, 2004; 131 (14): 3307-17.
	Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.
	LIM-homeodomain genes as territory markers in the brainstem of adult and developing Xenopus laevis., Moreno N., J Comp Neurol. May 9, 2005; 485 (3): 240-54.
	The Vg1-related protein Gdf3 acts in a Nodal signaling pathway in the pre-gastrulation mouse embryo., Chen C., Development. January 1, 2006; 133 (2): 319-29.
	Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
	Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.
	Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.
	Embryogenesis and laboratory maintenance of the foam-nesting túngara frogs, genus Engystomops (= Physalaemus)., Romero-Carvajal A., Dev Dyn. June 1, 2009; 238 (6): 1444-54.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Comparison of Lim1 expression in embryos of frogs with different modes of reproduction., Venegas-Ferrín M., Int J Dev Biol. January 1, 2010; 54 (1): 195-202.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Evolutionary origin of the Otx2 enhancer for its expression in visceral endoderm., Kurokawa D., Dev Biol. June 1, 2010; 342 (1): 110-20.
	Contexts for dopamine specification by calcium spike activity in the CNS., Velázquez-Ulloa NA., J Neurosci. January 5, 2011; 31 (1): 78-88.
	Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.
	Dynamic in vivo binding of transcription factors to cis-regulatory modules of cer and gsc in the stepwise formation of the Spemann-Mangold organizer., Sudou N., Development. May 1, 2012; 139 (9): 1651-61.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.
	Variation in the schedules of somite and neural development in frogs., Sáenz-Ponce N., Proc Natl Acad Sci U S A. December 11, 2012; 109 (50): 20503-7.

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