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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 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.
Mutagenesis studies in transgenic Xenopus intermediate pituitary cells reveal structural elements necessary for correct prion protein biosynthesis. , van Rosmalen JW., Dev Neurobiol. May 1, 2007; 67 (6): 715-27.
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.
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.
Ion transport across Xenopus alveolar epithelium is regulated by extracellular ATP, UTP and adenosine. , Fronius M., Respir Physiol Neurobiol. January 15, 2004; 139 (2): 133-44.
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.
Expression of LIM class homeobox gene Xlim-3 in Xenopus development is limited to neural and neuroendocrine tissues. , Taira M ., Dev Biol. September 1, 1993; 159 (1): 245-56.
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.
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.