Papers associated with neurohypophysis

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	FERM domain-containing protein 6 identifies a subpopulation of varicose nerve fibers in different vertebrate species., Beck J., Cell Tissue Res. July 1, 2020; 381 (1): 13-24.
	The medio-basal hypothalamus as a dynamic and plastic reproduction-related kisspeptin-gnrh-pituitary center in fish., Zmora N., Endocrinology. May 1, 2014; 155 (5): 1874-86.
	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.
	Ciliogenesis and cerebrospinal fluid flow in the developing Xenopus brain are regulated by foxj1., Hagenlocher C., Cilia. April 29, 2013; 2 (1): 12.
	Expression of orexin receptors in the pituitary., Kaminski T., Vitam Horm. January 1, 2012; 89 61-73.
	Alterations along the Hypothalamic-Pituitary-Thyroid Axis of the Zebrafish (Danio rerio) after Exposure to Propylthiouracil., Schmidt F., J Thyroid Res. January 1, 2011; 2011 376243.
	Plasticity of melanotrope cell regulations in Xenopus laevis., Roubos EW., Eur J Neurosci. December 1, 2010; 32 (12): 2082-6.
	A novel cyclic nucleotide-gated ion channel enriched in synaptic terminals of isotocin neurons in zebrafish brain and pituitary., Khan S., Neuroscience. January 13, 2010; 165 (1): 79-89.
	About a snail, a toad, and rodents: animal models for adaptation research., Roubos EW., Front Endocrinol (Lausanne). January 1, 2010; 1 4.
	Protein expression of the transcriptional regulator MI-ER1 alpha in adult mouse tissues., Thorne LB., J Mol Histol. February 1, 2008; 39 (1): 15-24.
	Actions of PACAP and VIP on melanotrope cells of Xenopus laevis., Kidane AH., Peptides. September 1, 2007; 28 (9): 1790-6.
	Positioning the extreme anterior in Xenopus: cement gland, primary mouth and anterior pituitary., Dickinson A., Semin Cell Dev Biol. August 1, 2007; 18 (4): 525-33.
	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.
	Differential distribution of melatonin receptors in the pituitary gland of Xenopus laevis., Wiechmann AF., Anat Embryol (Berl). March 1, 2003; 206 (4): 291-9.
	Cell type specific expression of secretory TFF peptides: colocalization with mucins and synthesis in the brain., Hoffmann W., Int Rev Cytol. January 1, 2002; 213 147-81.
	Relationships between CB1 cannabinoid receptors and pituitary endocrine cells in Xenopus laevis: an immunohistochemical study., Cesa R., Gen Comp Endocrinol. January 1, 2002; 125 (1): 17-24.
	Expression of the medaka (Oryzias latipes) Ol-Rx3 paired-like gene in two diencephalic derivatives, the eye and the hypothalamus., Deschet K., Mech Dev. May 1, 1999; 83 (1-2): 179-82.
	Identification of suprachiasmatic melanotrope-inhibiting neurons in Xenopus laevis: a confocal laser-scanning microscopy study., Ubink R., J Comp Neurol. July 20, 1998; 397 (1): 60-8.
	Micromolar 4-aminopyridine enhances invasion of a vertebrate neurosecretory terminal arborization: optical recording of action potential propagation using an ultrafast photodiode-MOSFET camera and a photodiode array., Obaid AL., J Gen Physiol. March 1, 1996; 107 (3): 353-68.
	Immunohistochemical studies on the development of TSH cells in the pituitary of Xenopus laevis larvae., Ogawa K., J Vet Med Sci. June 1, 1995; 57 (3): 539-42.
	Presynaptic excitability., Jackson MB., Int Rev Neurobiol. January 1, 1995; 38 201-51.
	An additional arginine-vasotocin-related peptide, vasotocinyl-Gly-Lys, in Xenopus neurohypophysis., Iwamuro S., Biochim Biophys Acta. March 10, 1993; 1176 (1-2): 143-7.
	Distribution of proneuropeptide Y-derived peptides in the brain of Rana esculenta and Xenopus laevis., Lázár G., J Comp Neurol. January 22, 1993; 327 (4): 551-71.
	Immunocytochemical localization of a galanin-like peptidergic system in the brain of two urodele and two anuran species (Amphibia)., Olivereau M., Histochemistry. August 1, 1992; 98 (1): 51-66.
	Localization of binding sites for atrial natriuretic factor and angiotensin II in the central nervous system of the clawed toad Xenopus laevis., Kloas W., Cell Tissue Res. February 1, 1992; 267 (2): 365-73.
	Calcium channels that are required for secretion from intact nerve terminals of vertebrates are sensitive to omega-conotoxin and relatively insensitive to dihydropyridines. Optical studies with and without voltage-sensitive dyes., Obaid AL., J Gen Physiol. April 1, 1989; 93 (4): 715-29.
	Visualization of secretory activities in the Xenopus neurohypophysis by a high S/N video camera., Terakawa S., Dev Biol. December 1, 1987; 435 (1-2): 380-6.
	Isolation of immunoreactive beta-endorphin-related and Met-enkephalin-related peptides from the posterior pituitary of the amphibian, Xenopus laevis., Dores RM., Peptides. January 1, 1987; 8 (6): 1119-25.
	Active calcium responses recorded optically from nerve terminals of the frog neurohypophysis., Obaid AL., J Gen Physiol. April 1, 1985; 85 (4): 481-9.
	Phylogenetic cross-reactivities of monoclonal antibodies produced against rat neurophysin., Ben-Barak Y., Cell Mol Neurobiol. December 1, 1984; 4 (4): 339-49.
	Optical recording of action potentials from vertebrate nerve terminals using potentiometric probes provides evidence for sodium and calcium components., Salzberg BM., Nature. November 3, 1983; 306 (5938): 36-40.
	The relation between the caudo-dorsal region of the preoptic nucleus and the pars nervosa of the pituitary gland in Xenopus lavis tadpoles. An investigation based on hypothalamic lesions., Notenboom CD., Cell Tissue Res. June 24, 1974; 149 (4): 457-71.

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