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Summary Anatomy Item Literature (1547) Expression Attributions Wiki
XB-ANAT-14

Papers associated with diencephalon (and sst.1)

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Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.                                


Transcriptome profiles of metamorphosis in the ornamented pygmy frog Microhyla fissipes clarify the functions of thyroid hormone receptors in metamorphosis., Zhao L., Sci Rep. June 2, 2016; 6 27310.            


Patterns of hypothalamic regionalization in amphibians and reptiles: common traits revealed by a genoarchitectonic approach., Domínguez L., Front Neuroanat. February 3, 2015; 9 3.                


Characterization of the hypothalamus of Xenopus laevis during development. II. The basal regions., Domínguez L., J Comp Neurol. April 1, 2014; 522 (5): 1102-31.                                      


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.                                                  


Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.                


Ontogenetic distribution of the transcription factor nkx2.2 in the developing forebrain of Xenopus laevis., Domínguez L., Front Neuroanat. March 2, 2011; 5 11.            


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


Development of the vomeronasal amygdala in anuran amphibians: hodological, neurochemical, and gene expression characterization., Moreno N., J Comp Neurol. August 20, 2007; 503 (6): 815-31.


Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.                


Basal ganglia organization in amphibians: chemoarchitecture., Marín O., J Comp Neurol. March 16, 1998; 392 (3): 285-312.                      


Neural induction and patterning in embryos deficient in FGF signaling., Godsave SF., Int J Dev Biol. February 1, 1997; 41 (1): 57-65.        


Expression of a new G protein-coupled receptor X-msr is associated with an endothelial lineage in Xenopus laevis., Devic E., Mech Dev. October 1, 1996; 59 (2): 129-40.        


Immunocytochemical analysis of proenkephalin-derived peptides in the amphibian hypothalamus and optic tectum., Merchenthaler I., Dev Biol. July 28, 1987; 416 (2): 219-27.    


Cerebrospinal fluid-contacting neurons and other somatostatin-immunoreactive perikarya in brains of tadpoles of Xenopus laevis., Blähser S., Cell Tissue Res. January 1, 1982; 224 (3): 693-7.

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