Papers associated with surface structure (and pomc)

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	Impaired negative feedback and death following acute stress in glucocorticoid receptor knockout Xenopus tropicalis tadpoles., Paul B., Gen Comp Endocrinol. September 15, 2022; 326 114072.
	Pharmacological Modulation of Melanocortin 1 Receptor Signaling by Mrap Proteins in Xenopus tropicalis., Tai X., Front Endocrinol (Lausanne). January 1, 2022; 13 892407.
	Pituitary cell translation and secretory capacities are enhanced cell autonomously by the transcription factor Creb3l2., Khetchoumian K., Nat Commun. September 3, 2019; 10 (1): 3960.
	Plasticity for colour adaptation in vertebrates explained by the evolution of the genes pomc, pmch and pmchl., Bertolesi GE., Pigment Cell Melanoma Res. July 1, 2019; 32 (4): 510-527.
	Interaction and developmental activation of two neuroendocrine systems that regulate light-mediated skin pigmentation., Bertolesi GE., Pigment Cell Melanoma Res. July 1, 2017; 30 (4): 413-423.
	The melanocyte photosensory system in the human skin., Iyengar B., Springerplus. April 12, 2013; 2 (1): 158.
	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.
	BDNF stimulates Ca2+ oscillation frequency in melanotrope cells of Xenopus laevis: contribution of IP3-receptor-mediated release of intracellular Ca2+ to gene expression., Kuribara M., Gen Comp Endocrinol. November 1, 2010; 169 (2): 123-9.
	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.
	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.
	Actions of PACAP and VIP on melanotrope cells of Xenopus laevis., Kidane AH., Peptides. September 1, 2007; 28 (9): 1790-6.
	Plasticity in the melanotrope neuroendocrine interface of Xenopus laevis., Jenks BG., Neuroendocrinology. January 1, 2007; 85 (3): 177-85.
	Studies of pigment transfer between Xenopus laevis melanophores and fibroblasts in vitro and in vivo., Aspengren S., Pigment Cell Res. April 1, 2006; 19 (2): 136-45.
	Widespread tissue distribution and diverse functions of corticotropin-releasing factor and related peptides., Boorse GC., Gen Comp Endocrinol. March 1, 2006; 146 (1): 9-18.
	Urocortins of the South African clawed frog, Xenopus laevis: conservation of structure and function in tetrapod evolution., Boorse GC., Endocrinology. November 1, 2005; 146 (11): 4851-60.
	Frog melanophores cultured on fluorescent microbeads: biomimic-based biosensing., Andersson TP., Biosens Bioelectron. July 15, 2005; 21 (1): 111-20.
	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.
	Expression of type II iodothyronine deiodinase marks the time that a tissue responds to thyroid hormone-induced metamorphosis in Xenopus laevis., Cai L., Dev Biol. February 1, 2004; 266 (1): 87-95.
	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.
	Characterization and functional expression of cDNAs encoding thyrotropin-releasing hormone receptor from Xenopus laevis., Bidaud I., Eur J Biochem. September 1, 2002; 269 (18): 4566-76.
	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.
	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.
	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.
	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.
	The thyroid hormone-induced tail resorption program during Xenopus laevis metamorphosis., Brown DD., Proc Natl Acad Sci U S A. March 5, 1996; 93 (5): 1924-9.
	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.
	Structure and expression of Xenopus prohormone convertase PC2., Braks JA., FEBS Lett. June 22, 1992; 305 (1): 45-50.
	Comparative structural analysis of the transcriptionally active proopiomelanocortin genes A and B of Xenopus laevis., Deen PM., Mol Biol Evol. May 1, 1992; 9 (3): 483-94.
	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.
	Control of melanoblast differentiation in amphibia by alpha-melanocyte stimulating hormone, a serum melanization factor, and a melanization inhibiting factor., Fukuzawa T., Pigment Cell Res. January 1, 1989; 2 (3): 171-81.
	The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis., Eagleson GW., J Embryol Exp Morphol. June 1, 1986; 95 1-14.
	Further studies on the melanophores of periodic albino mutant of Xenopus laevis., Fukuzawa T., J Embryol Exp Morphol. February 1, 1986; 91 65-78.
	Characterization of alpha-MSH-induced changes in the phosphorylation of a 53 kDa protein in Xenopus melanophores., de Graan PN., Mol Cell Endocrinol. September 1, 1985; 42 (2): 127-33.
	[Nle4, D-Phe7]-alpha-MSH: a superpotent melanotropin with prolonged action on vertebrate chromatophores., Hadley ME., Comp Biochem Physiol A Comp Physiol. January 1, 1985; 81 (1): 1-6.
	Calcium sites in MSH stimulation of xenopus melanophores: studies with photoreactive alpha-MSH., de Graan PN., Mol Cell Endocrinol. May 1, 1982; 26 (3): 327-9.
	Calcium requirement for alpha-MSH action on tail-fin melanophores of xenopus tadpoles., de Graan PN., Mol Cell Endocrinol. May 1, 1982; 26 (3): 315-26.
	Biosynthesis, processing, and control of release of melanotropic peptides in the neurointermediate lobe of Xenopus laevis., Loh YP., J Gen Physiol. July 1, 1977; 70 (1): 37-58.

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