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Summary Anatomy Item Literature (955) Expression Attributions Wiki
XB-ANAT-3351

Papers associated with thalamus (and lhx1)

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Xenopus leads the way: Frogs as a pioneering model to understand the human brain., Exner CRT., Genesis. February 1, 2021; 59 (1-2): e23405.          


Amphibian thalamic nuclear organization during larval development and in the adult frog Xenopus laevis: Genoarchitecture and hodological analysis., Morona R., J Comp Neurol. October 1, 2020; 528 (14): 2361-2403.                                                                


Gene expression analysis of developing cell groups in the pretectal region of Xenopus laevis., Morona R., J Comp Neurol. March 1, 2017; 525 (4): 715-752.                                            


Probing forebrain to hindbrain circuit functions in Xenopus., Kelley DB., Genesis. January 1, 2017; 55 (1-2):           


Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.                      


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.                                    


The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.          


Comparative expression analysis of cysteine-rich intestinal protein family members crip1, 2 and 3 during Xenopus laevis embryogenesis., Hempel A., Int J Dev Biol. January 1, 2014; 58 (10-12): 841-9.                                              


Characterization of the hypothalamus of Xenopus laevis during development. I. The alar regions., Domínguez L., J Comp Neurol. March 1, 2013; 521 (4): 725-59.                                                  


Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.                          


The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C., BMC Dev Biol. January 31, 2011; 11 5.              


Contexts for dopamine specification by calcium spike activity in the CNS., Velázquez-Ulloa NA., J Neurosci. January 5, 2011; 31 (1): 78-88.                    


Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.                                  


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.                    


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.                    


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.


XIPOU 2, a noggin-inducible gene, has direct neuralizing activity., Witta SE., Development. March 1, 1995; 121 (3): 721-30.                


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.              


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.              

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