Papers associated with hypothalamus (and pomc)

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	cyp21a2 Knockout Tadpoles Survive Metamorphosis Despite Low Corticosterone., Paul B., Endocrinology. November 14, 2022; 164 (1):
	Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS., Kim E., Sci Rep. March 22, 2019; 9 (1): 5025.
	Melanocortin Receptor 4 Signaling Regulates Vertebrate Limb Regeneration., Zhang M., Dev Cell. August 20, 2018; 46 (4): 397-409.e5.
	Spatial and temporal expression profiles of urocortin 3 mRNA in the brain of the chicken (Gallus gallus)., Grommen SVH., J Comp Neurol. August 1, 2017; 525 (11): 2583-2591.
	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.
	Expression of orexin receptors in the pituitary., Kaminski T., Vitam Horm. January 1, 2012; 89 61-73.
	Plasticity of melanotrope cell regulations in Xenopus laevis., Roubos EW., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.
	The organization of CRF neuronal pathways in toads: Evidence that retinal afferents do not contribute significantly to tectal CRF content., Carr JA., Brain Behav Evol. January 1, 2010; 76 (1): 71-86.
	About a snail, a toad, and rodents: animal models for adaptation research., Roubos EW., Front Endocrinol (Lausanne). January 1, 2010; 1 4.
	Neurochemistry and plasticity of the median eminence and neural pituitary lobe in relation to background adaptation of Xenopus laevis., van Wijk DC., Ann N Y Acad Sci. April 1, 2009; 1163 524-7.
	Evolutionarily conserved glucocorticoid regulation of corticotropin-releasing factor expression., Yao M., Endocrinology. May 1, 2008; 149 (5): 2352-60.
	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.
	Structural and functional conservation of vertebrate corticotropin-releasing factor genes: evidence for a critical role for a conserved cyclic AMP response element., Yao M., Endocrinology. May 1, 2007; 148 (5): 2518-31.
	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.
	Expression and hypophysiotropic actions of corticotropin-releasing factor in Xenopus laevis., Boorse GC., Gen Comp Endocrinol. July 1, 2004; 137 (3): 272-82.
	Roles of corticotropin-releasing factor, neuropeptide Y and corticosterone in the regulation of food intake in Xenopus laevis., Crespi EJ., J Neuroendocrinol. March 1, 2004; 16 (3): 279-88.
	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.
	Immunohistochemical localization and biochemical characterization of two novel decapeptides derived from POMC-A in the trout hypothalamus., Tollemer H., Cell Tissue Res. March 1, 1999; 295 (3): 409-17.
	Cloning and expression of two proopiomelanocortin mRNAs in the common carp (Cyprinus carpio L.)., Arends RJ., Mol Cell Endocrinol. August 25, 1998; 143 (1-2): 23-31.
	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.
	Sauvagine and TRH differentially stimulate proopiomelanocortin biosynthesis in the Xenopus laevis intermediate pituitary., Dotman CH., Neuroendocrinology. August 1, 1997; 66 (2): 106-13.
	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.
	Correlated onset and patterning of proopiomelanocortin gene expression in embryonic Xenopus brain and pituitary., Hayes WP., Development. November 1, 1990; 110 (3): 747-57.
	Immunocytochemical analysis of proenkephalin-derived peptides in the amphibian hypothalamus and optic tectum., Merchenthaler I., Dev Biol. July 28, 1987; 416 (2): 219-27.
	Immunocytochemical localization and spatial relation to the adenohypophysis of a somatostatin-like and a corticotropin-releasing factor-like peptide in the brain of four amphibian species., Olivereau M., Cell Tissue Res. February 1, 1987; 247 (2): 317-24.
	An NPY-like peptide may function as MSH-release inhibiting factor in Xenopus laevis., Verburg-van Kemenade BM., Peptides. January 1, 1987; 8 (1): 61-7.
	The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis., Eagleson GW., J Embryol Exp Morphol. June 1, 1986; 95 1-14.

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