Papers associated with brain (and crh)

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	cyp21a2 Knockout Tadpoles Survive Metamorphosis Despite Low Corticosterone., Paul B., Endocrinology. November 14, 2022; 164 (1):
	Thyroid Disrupting Chemicals in Mixture Perturb Thymocyte Differentiation in Xenopus laevis Tadpoles., McGuire CC., Toxicol Sci. May 27, 2021; 181 (2): 262-272.
	Tectal CRFR1 receptor involvement in avoidance and approach behaviors in the South African clawed frog, Xenopus laevis., Prater CM., Horm Behav. April 1, 2020; 120 104707.
	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.
	Leukemia inhibitory factor signaling in Xenopus embryo: Insights from gain of function analysis and dominant negative mutant of the receptor., Jalvy S., Dev Biol. March 15, 2019; 447 (2): 200-213.
	Tectal CRFR1 receptors modulate food intake and feeding behavior in the South African clawed frog Xenopus laevis., Prater CM., Horm Behav. September 1, 2018; 105 86-94.
	Tectal corticotropin-releasing factor (CRF) neurons respond to fasting and a reactive stressor in the African Clawed Frog, Xenopus laevis., Prater CM., Gen Comp Endocrinol. March 1, 2018; 258 91-98.
	Digital dissection of the model organism Xenopus laevis using contrast-enhanced computed tomography., Porro LB., J Anat. August 1, 2017; 231 (2): 169-191.
	An intrinsic CRF signaling system within the optic tectum., Carr JA., Gen Comp Endocrinol. July 1, 2013; 188 204-11.
	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.
	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.
	Teratogenic effects of chronic treatment with corticosterone on tadpoles of Xenopus laevis., Lorenz C., Ann N Y Acad Sci. April 1, 2009; 1163 454-6.
	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.
	Structural and functional conservation of vertebrate corticotropin-releasing factor genes: evidence for a critical role for a conserved cyclic AMP response element., Yao M., Endocrinology. May 1, 2007; 148 (5): 2518-31.
	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.
	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.
	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.
	Opioid peptides, CRF, and urocortin in cerebrospinal fluid-contacting neurons in Xenopus laevis., Calle M., Ann N Y Acad Sci. April 1, 2005; 1040 249-52.
	Distribution and acute stressor-induced activation of corticotrophin-releasing hormone neurones in the central nervous system of Xenopus laevis., Yao M., J Neuroendocrinol. November 1, 2004; 16 (11): 880-93.
	Regulation of pituitary thyrotropin gene expression during Xenopus metamorphosis: negative feedback is functional throughout metamorphosis., Manzon RG., J Endocrinol. August 1, 2004; 182 (2): 273-85.
	Cloning and tissue distribution of the chicken type 2 corticotropin-releasing hormone receptor., de Groef B., Gen Comp Endocrinol. August 1, 2004; 138 (1): 89-95.
	Expression and hypophysiotropic actions of corticotropin-releasing factor in Xenopus laevis., Boorse GC., Gen Comp Endocrinol. July 1, 2004; 137 (3): 272-82.
	Roles of corticotropin-releasing factor, neuropeptide Y and corticosterone in the regulation of food intake in Xenopus laevis., Crespi EJ., J Neuroendocrinol. March 1, 2004; 16 (3): 279-88.
	Corticotropin-releasing hormone-binding protein: biochemistry and function from fishes to mammals., Seasholtz AF., J Endocrinol. October 1, 2002; 175 (1): 89-97.
	Biochemical characterization and expression analysis of the Xenopus laevis corticotropin-releasing hormone binding protein., Valverde RA., Mol Cell Endocrinol. February 28, 2001; 173 (1-2): 29-40.
	Characterization of three corticotropin-releasing factor receptors in catfish: a novel third receptor is predominantly expressed in pituitary and urophysis., Arai M., Endocrinology. January 1, 2001; 142 (1): 446-54.
	125I-Antisauvagine-30: a novel and specific high-affinity radioligand for the characterization of corticotropin-releasing factor type 2 receptors., Higelin J., Neuropharmacology. January 1, 2001; 40 (1): 114-22.
	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.
	Structure and function of the ovine type 1 corticotropin releasing factor receptor (CRF1) and a carboxyl-terminal variant., Myers DA., Mol Cell Endocrinol. September 25, 1998; 144 (1-2): 21-35.
	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.
	Identification of two corticotropin-releasing factor receptors from Xenopus laevis with high ligand selectivity: unusual pharmacology of the type 1 receptor., Dautzenberg FM., J Neurochem. October 1, 1997; 69 (4): 1640-9.
	Immunohistochemical studies on the development of the hypothalamo-hypophysial system in Xenopus laevis., Ogawa K., Anat Rec. February 1, 1995; 241 (2): 244-54.
	Spontaneous cytosolic calcium pulsing detected in Xenopus melanotrophs: modulation by secreto-inhibitory and stimulant ligands., Shibuya I., Endocrinology. May 1, 1993; 132 (5): 2166-75.
	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.
	Functional expression of brain cholecystokinin and bombesin receptors in Xenopus oocytes., Moriarty TM., Dev Biol. August 1, 1988; 464 (1): 75-9.
	Immunocytochemical analysis of proenkephalin-derived peptides in the amphibian hypothalamus and optic tectum., Merchenthaler I., Dev Biol. July 28, 1987; 416 (2): 219-27.
	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.
	Regulation of MSH release from the neurointermediate lobe of Xenopus laevis by CRF-like peptides., Verburg-Van Kemenade BM., Peptides. January 1, 1987; 8 (6): 1093-100.
	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.

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