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Summary Anatomy Item Literature (327) Expression Attributions Wiki
XB-ANAT-452

Papers associated with melanophore (and pomc)

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Pharmacological Modulation of Melanocortin 1 Receptor Signaling by Mrap Proteins in Xenopus tropicalis., Tai X., Front Endocrinol (Lausanne). January 1, 2022; 13 892407.              


Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS., Kim E., Sci Rep. March 22, 2019; 9 (1): 5025.              


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.


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.        


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.      


Extracellular-signal regulated kinase regulates production of pro-opiomelanocortin in pituitary melanotroph cells., Kuribara M., J Neuroendocrinol. March 1, 2011; 23 (3): 261-8.


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.        


V-ATPase-mediated granular acidification is regulated by the V-ATPase accessory subunit Ac45 in POMC-producing cells., Jansen EJ., Mol Biol Cell. October 1, 2010; 21 (19): 3330-9.                


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.        


A developmental analysis of periodic albinism in the amphibian Xenopus laevis., Eagleson GW., Gen Comp Endocrinol. September 1, 2010; 168 (2): 302-6.        


Light modulates the melanophore response to alpha-MSH in Xenopus laevis: an analysis of the signal transduction crosstalk mechanisms involved., Isoldi MC., Gen Comp Endocrinol. January 1, 2010; 165 (1): 104-10.          


The dynamic properties of intermediate filaments during organelle transport., Chang L., J Cell Sci. August 15, 2009; 122 (Pt 16): 2914-23.                


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.                  


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.      


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.


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.


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.


Frog melanophores cultured on fluorescent microbeads: biomimic-based biosensing., Andersson TP., Biosens Bioelectron. July 15, 2005; 21 (1): 111-20.


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.


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.


Mutational analysis of evolutionarily conserved ACTH residues., Costa JL., Gen Comp Endocrinol. March 1, 2004; 136 (1): 12-6.


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.


Regulation of TNF-alpha secretion by a specific melanocortin-1 receptor peptide agonist., Ignar DM., Peptides. May 1, 2003; 24 (5): 709-16.


Ca2+ oscillations in melanotropes of Xenopus laevis: their generation, propagation, and function., Jenks BG., Gen Comp Endocrinol. May 1, 2003; 131 (3): 209-19.


Differential distribution of melatonin receptors in the pituitary gland of Xenopus laevis., Wiechmann AF., Anat Embryol (Berl). March 1, 2003; 206 (4): 291-9.


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 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.


Molecular cloning and characterization of the chicken pro-opiomelanocortin (POMC) gene., Takeuchi S., Biochim Biophys Acta. July 8, 1999; 1450 (3): 452-9.


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.


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.


Deciphering posttranslational processing events in the pituitary of a neopterygian fish: cloning of a gar proopiomelanocortin cDNA., Dores RM., Gen Comp Endocrinol. September 1, 1997; 107 (3): 401-13.


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.


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.


Molecular probing of the secretory pathway in peptide hormone-producing cells., Holthuis JC., J Cell Sci. October 1, 1995; 108 ( Pt 10) 3295-305.


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.


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.


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.


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.


Structure and expression of Xenopus prohormone convertase PC2., Braks JA., FEBS Lett. June 22, 1992; 305 (1): 45-50.

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