Papers associated with nucleus (and pomc)

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	Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS., Kim E., Sci Rep. March 22, 2019; 9 (1): 5025.
	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.
	Identification of domains within the V-ATPase accessory subunit Ac45 involved in V-ATPase transport and Ca2+-dependent exocytosis., Jansen EJ., J Biol Chem. August 10, 2012; 287 (33): 27537-46.
	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.
	The role of brain-derived neurotrophic factor in the regulation of cell growth and gene expression in melanotrope cells of Xenopus laevis., Jenks BG., Gen Comp Endocrinol. July 1, 2012; 177 (3): 315-21.
	The origins and evolution of vertebrate metamorphosis., Laudet V., Curr Biol. September 27, 2011; 21 (18): R726-37.
	ERK-regulated double cortin-like kinase (DCLK)-short phosphorylation and nuclear translocation stimulate POMC gene expression in endocrine melanotrope cells., Kuribara M., Endocrinology. June 1, 2011; 152 (6): 2321-9.
	Plasticity of melanotrope cell regulations in Xenopus laevis., Roubos EW., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.
	Ultrastructural and neurochemical architecture of the pituitary neural lobe of Xenopus laevis., van Wijk DC., Gen Comp Endocrinol. September 1, 2010; 168 (2): 293-301.
	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.
	The dynamic properties of intermediate filaments during organelle transport., Chang L., J Cell Sci. August 15, 2009; 122 (Pt 16): 2914-23.
	COP-binding sites in p24delta2 are necessary for proper secretory cargo biosynthesis., Strating JR., Int J Biochem Cell Biol. July 1, 2009; 41 (7): 1619-27.
	Pituitary adenylate cyclase-activating polypeptide regulates brain-derived neurotrophic factor exon IV expression through the VPAC1 receptor in the amphibian melanotrope cell., Kidane AH., Endocrinology. August 1, 2008; 149 (8): 4177-82.
	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.
	Disparate effects of p24alpha and p24delta on secretory protein transport and processing., Strating JR., PLoS One. August 8, 2007; 2 (8): e704.
	Plasticity in the melanotrope neuroendocrine interface of Xenopus laevis., Jenks BG., Neuroendocrinology. January 1, 2007; 85 (3): 177-85.
	Transgene expression of prion protein induces crinophagy in intermediate pituitary cells., van Rosmalen JW., Dev Neurobiol. January 1, 2007; 67 (1): 81-96.
	Expression and physiological regulation of BDNF receptors in the neuroendocrine melanotrope cell of Xenopus laevis., Kidane AH., Gen Comp Endocrinol. January 1, 2007; 153 (1-3): 176-81.
	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.
	Calcium influx through voltage-operated calcium channels is required for proopiomelanocortin protein expression in Xenopus melanotropes., van den Hurk MJ., Ann N Y Acad Sci. April 1, 2005; 1040 494-7.
	Neuronal, neurohormonal, and autocrine control of Xenopus melanotrope cell activity., Roubos EW., Ann N Y Acad Sci. April 1, 2005; 1040 172-83.
	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.
	Multiple control and dynamic response of the Xenopus melanotrope cell., Kolk SM., Comp Biochem Physiol B Biochem Mol Biol. May 1, 2002; 132 (1): 257-68.
	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.
	Expression of salmon corticotropin-releasing hormone precursor gene in the preoptic nucleus in stressed rainbow trout., Ando H., Gen Comp Endocrinol. January 1, 1999; 113 (1): 87-95.
	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.
	Characterization of the genomic corticotropin-releasing factor (CRF) gene from Xenopus laevis: two members of the CRF family exist in amphibians., Stenzel-Poore MP., Mol Endocrinol. October 1, 1992; 6 (10): 1716-24.
	Correlated onset and patterning of proopiomelanocortin gene expression in embryonic Xenopus brain and pituitary., Hayes WP., Development. November 1, 1990; 110 (3): 747-57.
	Immunohistochemical localization of beta-endorphin-like material in the urodele and anuran amphibian tissues., Vethamany-Globus S., Gen Comp Endocrinol. August 1, 1989; 75 (2): 271-9.
	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.
	The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis., Eagleson GW., J Embryol Exp Morphol. June 1, 1986; 95 1-14.
	Evidence for corticotropin releasing factor (CRF) synthesis in the preoptic nucleus of Xenopus laevis tadpoles: a preliminary report based on lesion experiments., Notenboom CD., Cell Tissue Res. June 11, 1976; 169 (1): 23-31.

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