Papers associated with melanotrope (and pomc)

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	A slow and a fast secretory compartment of POMC-derived peptides in the neurointermediate lobe of the amphibian Xenopus laevis., Van Zoest ID., Comp Biochem Physiol C Comp Pharmacol Toxicol. January 1, 1990; 96 (1): 199-203.
	Coordinated expression of 7B2 and alpha MSH in the melanotrope cells of Xenopus laevis. An immunocytochemical and in situ hybridization study., Ayoubi TA., Cell Tissue Res. May 1, 1991; 264 (2): 329-34.
	Dynamics of cyclic-AMP efflux in relation to alpha-MSH secretion from melanotrope cells of Xenopus laevis., de Koning HP., Life Sci. January 1, 1992; 51 (21): 1667-73.
	Evolutionary conservation of the 14-3-3 protein., Martens GJ., Biochem Biophys Res Commun. May 15, 1992; 184 (3): 1456-9.
	Transcriptional and posttranscriptional regulation of the proopiomelanocortin gene in the pars intermedia of the pituitary gland of Xenopus laevis., Ayoubi TA., Endocrinology. June 1, 1992; 130 (6): 3560-6.
	Structure and expression of Xenopus prohormone convertase PC2., Braks JA., FEBS Lett. June 22, 1992; 305 (1): 45-50.
	Analysis of autofeedback mechanisms in the secretion of pro-opiomelanocortin-derived peptides by melanotrope cells of Xenopus laevis., de Koning HP., Gen Comp Endocrinol. September 1, 1992; 87 (3): 394-401.
	Differential effects of coexisting dopamine, GABA and NPY on alpha-MSH secretion from melanotrope cells of Xenopus laevis., Leenders HJ., Life Sci. January 1, 1993; 52 (24): 1969-75.
	Alpha,N-acetyl beta-endorphin [1-8] is the terminal product of processing of endorphins in the melanotrope cells of Xenopus laevis, as demonstrated by FAB tandem mass spectrometry., van Strien FJ., Biochem Biophys Res Commun. February 26, 1993; 191 (1): 262-8.
	Analysis of inositol phosphate metabolism in melanotrope cells of Xenopus laevis in relation to background adaptation., Jenks BG., Ann N Y Acad Sci. May 31, 1993; 680 188-98.
	Effects of background adaptation on alpha-MSH and beta-endorphin in secretory granule types of melanotrope cells of Xenopus laevis., Roubos EW., Cell Tissue Res. December 1, 1993; 274 (3): 587-96.
	Action of stimulatory and inhibitory alpha-MSH secretagogues on spontaneous calcium oscillations in melanotrope cells of Xenopus laevis., Scheenen WJ., Pflugers Arch. June 1, 1994; 427 (3-4): 244-51.
	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.
	The secretion of alpha-MSH from xenopus melanotropes involves calcium influx through omega-conotoxin-sensitive voltage-operated calcium channels., Scheenen WJ., J Neuroendocrinol. August 1, 1994; 6 (4): 457-64.
	Central control of melanotrope cells of Xenopus laevis., Tuinhof R., Eur J Morphol. August 1, 1994; 32 (2-4): 307-10.
	Biosynthesis and processing of the N-terminal part of proopiomelanocortin in Xenopus laevis: characterization of gamma-MSH peptides., van Strien FJ., J Neuroendocrinol. October 1, 1995; 7 (10): 807-15.
	Molecular probing of the secretory pathway in peptide hormone-producing cells., Holthuis JC., J Cell Sci. October 1, 1995; 108 ( Pt 10) 3295-305.
	Inhibition of alpha-MSH secretion is associated with increased cyclic-AMP egress from the neurointermediate lobe of Xenopus laevis., Leenders HJ., Life Sci. November 17, 1995; 57 (26): 2447-53.
	Identification of POMC processing products in single melanotrope cells by matrix-assisted laser desorption/ionization mass spectrometry., van Strien FJ., FEBS Lett. January 29, 1996; 379 (2): 165-70.
	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.
	Physiologically induced Fos expression in the hypothalamo-hypophyseal system of Xenopus laevis., Ubink R., Neuroendocrinology. June 1, 1997; 65 (6): 413-22.
	Immunocytochemical localization of prohormone convertases PC1 and PC2 in the anuran pituitary gland: subcellular localization in corticotrope and melanotrope cells., Kurabuchi S., Cell Tissue Res. June 1, 1997; 288 (3): 485-96.
	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.
	The secretory granule and pro-opiomelanocortin processing in Xenopus melanotrope cells during background adaptation., Berghs CA., J Histochem Cytochem. December 1, 1997; 45 (12): 1673-82.
	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.
	Cholinergic regulation of the pituitary: autoexcitatory control by acetylcholine of melanotrope cell activity in Xenopus laevis., van Strien FJ., Ann N Y Acad Sci. May 15, 1998; 839 66-73.
	Dynamics of proopiomelanocortin and prohormone convertase 2 gene expression in Xenopus melanotrope cells during long-term background adaptation., Dotman CH., J Endocrinol. November 1, 1998; 159 (2): 281-6.
	Biosynthesis of the vacuolar H+-ATPase accessory subunit Ac45 in Xenopus pituitary., Holthuis JC., Eur J Biochem. June 1, 1999; 262 (2): 484-91.
	Differential induction of two p24delta putative cargo receptors upon activation of a prohormone-producing cell., Kuiper RP., Mol Biol Cell. January 1, 2000; 11 (1): 131-40.
	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.
	Cell-type-specific and selectively induced expression of members of the p24 family of putative cargo receptors., Rötter J., J Cell Sci. March 1, 2002; 115 (Pt 5): 1049-58.
	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.
	Transgene-driven protein expression specific to the intermediate pituitary melanotrope cells of Xenopus laevis., Jansen EJ., FEBS Lett. April 10, 2002; 516 (1-3): 201-7.
	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.
	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.
	Ca2+ oscillations in melanotropes of Xenopus laevis: their generation, propagation, and function., Jenks BG., Gen Comp Endocrinol. May 1, 2003; 131 (3): 209-19.
	Expression and characterization of the extracellular Ca(2+)-sensing receptor in melanotrope cells of Xenopus laevis., van den Hurk MJ., Endocrinology. June 1, 2003; 144 (6): 2524-33.
	Activity-dependent dynamics of coexisting brain-derived neurotrophic factor, pro-opiomelanocortin and alpha-melanophore-stimulating hormone in melanotrope cells of Xenopus laevis., Wang LC., J Neuroendocrinol. January 1, 2004; 16 (1): 19-25.
	A cell-specific transgenic approach in Xenopus reveals the importance of a functional p24 system for a secretory cell., Bouw G., Mol Biol Cell. March 1, 2004; 15 (3): 1244-53.
	The extracellular calcium-sensing receptor increases the number of calcium steps and action currents in pituitary melanotrope cells., van den Hurk MJ., Neurosci Lett. March 29, 2005; 377 (2): 125-9.
	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.
	Analysis of Xenopus melanotrope cell size and POMC-gene expression., Corstens GJ., Ann N Y Acad Sci. April 1, 2005; 1040 269-72.
	Neuronal, neurohormonal, and autocrine control of Xenopus melanotrope cell activity., Roubos EW., Ann N Y Acad Sci. April 1, 2005; 1040 172-83.
	In situ hybridization localization of TRH precursor and TRH receptor mRNAs in the brain and pituitary of Xenopus laevis., Galas L., Ann N Y Acad Sci. April 1, 2005; 1040 95-105.
	A fast method to study the secretory activity of neuroendocrine cells at the ultrastructural level., Van Herp F., J Microsc. April 1, 2005; 218 (Pt 1): 79-83.
	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.
	High-pressure freezing followed by cryosubstitution as a tool for preserving high-quality ultrastructure and immunoreactivity in the Xenopus laevis pituitary gland., Wang L., Brain Res Brain Res Protoc. September 1, 2005; 15 (3): 155-63.
	Expression of neuroserpin is linked to neuroendocrine cell activation., de Groot DM., Endocrinology. September 1, 2005; 146 (9): 3791-9.
	Cell type-specific transgene expression of the prion protein in Xenopus intermediate pituitary cells., van Rosmalen JW., FEBS J. February 1, 2006; 273 (4): 847-62.
	Prion protein mRNA expression in Xenopus laevis: no induction during melanotrope cell activation., van Rosmalen JW., Dev Biol. February 23, 2006; 1075 (1): 20-5.

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