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cyp21a2 Knockout Tadpoles Survive Metamorphosis Despite Low Corticosterone. , Paul B ., Endocrinology. November 14, 2022; 164 (1):
Some aspects of the hypothalamic and pituitary development, metamorphosis, and reproductive behavior as studied in amphibians. , Kikuyama S., Gen Comp Endocrinol. December 1, 2019; 284 113212.
Distribution and neuronal circuit of spexin 1/2 neurons in the zebrafish CNS. , Kim E ., Sci Rep. March 22, 2019; 9 (1): 5025.
Melanocortin Receptor 4 Signaling Regulates Vertebrate Limb Regeneration. , Zhang M., Dev Cell. August 20, 2018; 46 (4): 397-409.e5.
Spatial and temporal expression profiles of urocortin 3 mRNA in the brain of the chicken (Gallus gallus). , Grommen SVH., J Comp Neurol. August 1, 2017; 525 (11): 2583-2591.
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.
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.
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.
Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent. , Searcy BT., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.
Expression of orexin receptors in the pituitary. , Kaminski T., Vitam Horm. January 1, 2012; 89 61-73.
Plasticity of melanotrope cell regulations in Xenopus laevis. , Roubos EW ., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.
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.
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.
Polychlorinated biphenyl exposure delays metamorphosis and alters thyroid hormone system gene expression in developing Xenopus laevis. , Lehigh Shirey EA., Environ Res. October 1, 2006; 102 (2): 205-14.
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.
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.
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.
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.
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.
Timing of metamorphosis and the onset of the negative feedback loop between the thyroid gland and the pituitary is controlled by type II iodothyronine deiodinase in Xenopus laevis. , Huang H., Proc Natl Acad Sci U S A. June 19, 2001; 98 (13): 7348-53.
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.
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.
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.
Processing of the precursors to neurotensin and other bioactive peptides by cathepsin E. , Kageyama T., J Biol Chem. August 11, 1995; 270 (32): 19135-40.
The TRH neuronal phenotype forms embryonic cell clusters that go on to establish a regionalized cell fate in forebrain. , Hayes WP., J Neurobiol. September 1, 1994; 25 (9): 1095-112.
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.
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 analysis of proenkephalin-derived peptides in the amphibian hypothalamus and optic tectum. , Merchenthaler I., Dev Biol. July 28, 1987; 416 (2): 219-27.
An NPY-like peptide may function as MSH-release inhibiting factor in Xenopus laevis. , Verburg-van Kemenade BM., Peptides. January 1, 1987; 8 (1): 61-7.
The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis. , Eagleson GW ., J Embryol Exp Morphol. June 1, 1986; 95 1-14.