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Summary Anatomy Item Literature (334) Expression Attributions Wiki
XB-ANAT-1566

Papers associated with suprachiasmatic nucleus (and pomc)

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Ancient origins and evolutionary conservation of intracellular and neural signaling pathways engaged by the leptin receptor., Cui MY., Endocrinology. November 1, 2014; 155 (11): 4202-14.


Pituitary melanotrope cells of Xenopus laevis are of neural ridge origin and do not require induction by the infundibulum., Eagleson GW., Gen Comp Endocrinol. August 1, 2012; 178 (1): 116-22.            


Plasticity of melanotrope cell regulations in Xenopus laevis., Roubos EW., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.    


Brain distribution and evidence for both central and neurohormonal actions of cocaine- and amphetamine-regulated transcript peptide in Xenopus laevis., Roubos EW., J Comp Neurol. April 1, 2008; 507 (4): 1622-38.                  


Plasticity in the melanotrope neuroendocrine interface of Xenopus laevis., Jenks BG., Neuroendocrinology. January 1, 2007; 85 (3): 177-85.


Localisation and physiological regulation of corticotrophin-releasing factor receptor 1 mRNA in the Xenopus laevis brain and pituitary gland., Calle M., J Neuroendocrinol. October 1, 2006; 18 (10): 797-805.


Effect of starvation on Fos and neuropeptide immunoreactivities in the brain and pituitary gland of Xenopus laevis., Calle M., Gen Comp Endocrinol. July 1, 2006; 147 (3): 237-46.        


Evidence that urocortin I acts as a neurohormone to stimulate alpha MSH release in the toad Xenopus laevis., Calle M., Dev Biol. April 8, 2005; 1040 (1-2): 14-28.              


Neuronal, neurohormonal, and autocrine control of Xenopus melanotrope cell activity., Roubos EW., Ann N Y Acad Sci. April 1, 2005; 1040 172-83.


Ion transport across Xenopus alveolar epithelium is regulated by extracellular ATP, UTP and adenosine., Fronius M., Respir Physiol Neurobiol. January 15, 2004; 139 (2): 133-44.


Alpha-melanophore-stimulating hormone in the brain, cranial placode derivatives, and retina of Xenopus laevis during development in relation to background adaptation., Kramer BM., J Comp Neurol. January 27, 2003; 456 (1): 73-83.                  


Distribution of pro-opiomelanocortin and its peptide end products in the brain and hypophysis of the aquatic toad, Xenopus laevis., Tuinhof R., Cell Tissue Res. May 1, 1998; 292 (2): 251-65.


Background adaptation by Xenopus laevis: a model for studying neuronal information processing in the pituitary pars intermedia., Roubos EW., Comp Biochem Physiol A Physiol. November 1, 1997; 118 (3): 533-50.


Physiologically induced Fos expression in the hypothalamo-hypophyseal system of Xenopus laevis., Ubink R., Neuroendocrinology. June 1, 1997; 65 (6): 413-22.


Central control of melanotrope cells of Xenopus laevis., Tuinhof R., Eur J Morphol. August 1, 1994; 32 (2-4): 307-10.


Involvement of retinohypothalamic input, suprachiasmatic nucleus, magnocellular nucleus and locus coeruleus in control of melanotrope cells of Xenopus laevis: a retrograde and anterograde tracing study., Tuinhof R., Neuroscience. July 1, 1994; 61 (2): 411-20.

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