Papers associated with lhx3

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	In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C, Saint-Jeannet JP., Dev Biol. February 1, 2024; 506 20-30.
	Conservatism and variability of gene expression profiles among homeologous transcription factors in Xenopus laevis., Watanabe M, Yasuoka Y, Mawaribuchi S, Kuretani A, Ito M, Kondo M, Ochi H, Ogino H, Fukui A, Taira M, Kinoshita T., Dev Biol. June 15, 2017; 426 (2): 301-324.
	Insights into electrosensory organ development, physiology and evolution from a lateral line-enriched transcriptome., Modrell MS, Lyne M, Carr AR, Zakon HH, Buckley D, Campbell AS, Davis MC, Micklem G, Baker CV., Elife. March 27, 2017; 6
	Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus., Thélie A, Desiderio S, Hanotel J, Quigley I, Van Driessche B, Rodari A, Borromeo MD, Kricha S, Lahaye F, Croce J, Cerda-Moya G, Ordoño Fernandez J, Bolle B, Lewis KE, Sander M, Pierani A, Schubert M, Johnson JE, Kintner CR, Pieler T, Van Lint C, Henningfeld KA, Bellefroid EJ, Van Campenhout C., Development. October 1, 2015; 142 (19): 3416-28.
	Nkx6 genes pattern the frog neural plate and Nkx6.1 is necessary for motoneuron axon projection., Dichmann DS, Harland RM., Dev Biol. January 15, 2011; 349 (2): 378-86.
	Contexts for dopamine specification by calcium spike activity in the CNS., Velázquez-Ulloa NA, Spitzer NC, Dulcis D., J Neurosci. January 5, 2011; 31 (1): 78-88.
	Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy., Ymlahi-Ouazzani Q, J Bronchain O, Paillard E, Ballagny C, Chesneau A, Jadaud A, Mazabraud A, Pollet N., Neurogenetics. February 1, 2010; 11 (1): 27-40.
	Evolutionary origins of blastoporal expression and organizer activity of the vertebrate gastrula organizer gene lhx1 and its ancient metazoan paralog lhx3., Yasuoka Y, Kobayashi M, Kurokawa D, Akasaka K, Saiga H, Taira M., Development. June 1, 2009; 136 (12): 2005-14.
	Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ, Aruga J., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.
	Conserved regulatory elements establish the dynamic expression of Rpx/HesxI in early vertebrate development., Chou SJ, Hermesz E, Hatta T, Feltner D, El-Hodiri HM, Jamrich M, Mahon K., Dev Biol. April 15, 2006; 292 (2): 533-45.
	Identification of target genes for the Xenopus Hes-related protein XHR1, a prepattern factor specifying the midbrain-hindbrain boundary., Takada H, Hattori D, Kitayama A, Ueno N, Taira M., Dev Biol. July 1, 2005; 283 (1): 253-67.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I, Yamamoto N, Mochizuki T, Ohmori SY, Taira M., Development. September 1, 2003; 130 (17): 4161-75.
	Ectodermal patterning in vertebrate embryos., Sasai Y, De Robertis EM., Dev Biol. February 1, 1997; 182 (1): 5-20.
	Molecular cloning, structure, and chromosomal localization of the mouse LIM/homeobox gene Lhx5., Bertuzzi S, Sheng HZ, Copeland NG, Gilbert DJ, Jenkins NA, Taira M, Dawid IB, Westphal H., Genomics. September 1, 1996; 36 (2): 234-9.
	Expression pattern of the murine LIM class homeobox gene Lhx3 in subsets of neural and neuroendocrine tissues., Zhadanov AB, Bertuzzi S, Taira M, Dawid IB, Westphal H., Dev Dyn. April 1, 1995; 202 (4): 354-64.
	Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues., Taira M, Hayes WP, Otani H, Dawid IB., Dev Biol. September 1, 1993; 159 (1): 245-56.

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