Papers associated with pars intermedia

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	Background adaptation and synapse plasticity in the pars intermedia of Xenopus laevis., Berghs CA., Neuroscience. February 1, 1996; 70 (3): 833-41.
	Immunohistochemical investigation of gamma-aminobutyric acid ontogeny and transient expression in the central nervous system of Xenopus laevis tadpoles., Barale E., J Comp Neurol. April 29, 1996; 368 (2): 285-94.
	Acetylcholine autoexcites the release of proopiomelanocortin-derived peptides from melanotrope cells of Xenopus laevis via an M1 muscarinic receptor., Van Strien FJ., Endocrinology. October 1, 1996; 137 (10): 4298-307.
	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.
	Forebrain differentiation and axonogenesis in amphibians: I. Differentiation of the suprachiasmatic nucleus in relation to background adaptation behavior., Eagleson GW., Brain Behav Evol. January 1, 1998; 52 (1): 23-36.
	Identification of suprachiasmatic melanotrope-inhibiting neurons in Xenopus laevis: a confocal laser-scanning microscopy study., Ubink R., J Comp Neurol. July 20, 1998; 397 (1): 60-8.
	Serotonergic innervation of the pituitary pars intermedia of xenopus laevis., Ubink R., J Neuroendocrinol. March 1, 1999; 11 (3): 211-9.
	Endogenous production of nitric oxide and effects of nitric oxide and superoxide on melanotrope functioning in the pituitary pars intermedia of Xenopus laevis., Allaerts W., Nitric Oxide. February 1, 2000; 4 (1): 15-28.
	Functional organization of the suprachiasmatic nucleus of Xenopus laevis in relation to background adaptation., Kramer BM., J Comp Neurol. April 9, 2001; 432 (3): 346-55.
	Dynamics and plasticity of peptidergic control centres in the retino-brain-pituitary system of Xenopus laevis., Kramer BM., Microsc Res Tech. August 1, 2001; 54 (3): 188-99.
	Relationships between CB1 cannabinoid receptors and pituitary endocrine cells in Xenopus laevis: an immunohistochemical study., Cesa R., Gen Comp Endocrinol. January 1, 2002; 125 (1): 17-24.
	Evidence that brain-derived neurotrophic factor acts as an autocrine factor on pituitary melanotrope cells of Xenopus laevis., Kramer BM., Endocrinology. April 1, 2002; 143 (4): 1337-45.
	Differential distribution of melatonin receptors in the pituitary gland of Xenopus laevis., Wiechmann AF., Anat Embryol (Berl). March 1, 2003; 206 (4): 291-9.
	Differential distribution and regulation of expression of synaptosomal-associated protein of 25 kDa isoforms in the Xenopus pituitary gland and brain., Kolk SM., Neuroscience. January 1, 2004; 128 (3): 531-43.
	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.
	Plasticity in the melanotrope neuroendocrine interface of Xenopus laevis., Jenks BG., Neuroendocrinology. January 1, 2007; 85 (3): 177-85.
	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.
	Distribution pattern of neuropeptide Y in the brain, pituitary and olfactory system during the larval development of the toad Rhinella arenarum (Amphibia: Anura)., Heer T., Anat Histol Embryol. April 1, 2009; 38 (2): 89-95.
	Using transgenic animal models in neuroendocrine research: lessons from Xenopus laevis., Scheenen WJ., Ann N Y Acad Sci. April 1, 2009; 1163 296-307.
	Dynamics of glucocorticoid and mineralocorticoid receptors in the Xenopus laevis pituitary pars intermedia., Roubos EW., Ann N Y Acad Sci. April 1, 2009; 1163 292-5.
	About a snail, a toad, and rodents: animal models for adaptation research., Roubos EW., Front Endocrinol (Lausanne). January 1, 2010; 1 4.
	A proteome map of the pituitary melanotrope cell activated by black-background adaptation of Xenopus laevis., Bart D., Proteomics. February 1, 2010; 10 (3): 574-80.
	Plasticity of melanotrope cell regulations in Xenopus laevis., Roubos EW., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.
	Extracellular-signal regulated kinase regulates production of pro-opiomelanocortin in pituitary melanotroph cells., Kuribara M., J Neuroendocrinol. March 1, 2011; 23 (3): 261-8.
	Angiogenesis in the intermediate lobe of the pituitary gland alters its structure and function., Tanaka S., Gen Comp Endocrinol. May 1, 2013; 185 10-8.
	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.

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