Papers associated with nervous system (and prl.2)

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	The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus., Beckers A., Sci Rep. June 25, 2021; 11 (1): 13333.
	Characterization of a novel thyrotropin-releasing hormone receptor, TRHR3, in chickens., Li X., Poult Sci. March 1, 2020; 99 (3): 1643-1654.
	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.
	Adaptive correction of craniofacial defects in pre-metamorphic Xenopus laevis tadpoles involves thyroid hormone-independent tissue remodeling., Pinet K., Development. July 22, 2019; 146 (14):
	The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice., Beckers A., Sci Rep. October 2, 2018; 8 (1): 14678.
	Opn5L1 is a retinal receptor that behaves as a reverse and self-regenerating photoreceptor., Sato K., Nat Commun. March 28, 2018; 9 (1): 1255.
	miR-182 Regulates Slit2-Mediated Axon Guidance by Modulating the Local Translation of a Specific mRNA., Bellon A., Cell Rep. January 31, 2017; 18 (5): 1171-1186.
	Protein tyrosine phosphatase 4A3 (PTP4A3) is required for Xenopus laevis cranial neural crest migration in vivo., Maacha S., PLoS One. December 9, 2013; 8 (12): e84717.
	A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome., Rienhoff HY., Am J Med Genet A. August 1, 2013; 161A (8): 2040-6.
	The melanocyte photosensory system in the human skin., Iyengar B., Springerplus. April 12, 2013; 2 (1): 158.
	Dishevelled limits Notch signalling through inhibition of CSL., Collu GM., Development. December 1, 2012; 139 (23): 4405-15.
	Comparative expression analysis of the H3K27 demethylases, JMJD3 and UTX, with the H3K27 methylase, EZH2, in Xenopus., Kawaguchi A., Int J Dev Biol. January 1, 2012; 56 (4): 295-300.
	The synthetic gestagen levonorgestrel impairs metamorphosis in Xenopus laevis by disruption of the thyroid system., Lorenz C., Toxicol Sci. September 1, 2011; 123 (1): 94-102.
	Xenopus Dbx2 is involved in primary neurogenesis and early neural plate patterning., Ma P., Biochem Biophys Res Commun. August 19, 2011; 412 (1): 170-4.
	Expression patterns of genes encoding small GTPases Ras-dva-1 and Ras-dva-2 in the Xenopus laevis tadpoles., Tereshina MB., Gene Expr Patterns. January 1, 2011; 11 (1-2): 156-61.
	Isolation and characterisation of prolactin-releasing peptide in chicks and its effect on prolactin release and feeding behaviour., Tachibana T., J Neuroendocrinol. January 1, 2011; 23 (1): 74-81.
	Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.
	Xenopus RCOR2 (REST corepressor 2) interacts with ZMYND8, which is involved in neural differentiation., Zeng W., Biochem Biophys Res Commun. April 16, 2010; 394 (4): 1024-9.
	A novel prolactin-like protein (PRL-L) gene in chickens and zebrafish: cloning and characterization of its tissue expression., Wanga Y., Gen Comp Endocrinol. March 1, 2010; 166 (1): 200-10.
	Secreted factor FAM3C (ILEI) is involved in retinal laminar formation., Katahira T., Biochem Biophys Res Commun. February 12, 2010; 392 (3): 301-6.
	Corticosteroids disrupt amphibian metamorphosis by complex modes of action including increased prolactin expression., Lorenz C., Comp Biochem Physiol C Toxicol Pharmacol. August 1, 2009; 150 (2): 314-21.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	Molecular cloning and functional characterization of a prolactin-releasing peptide homolog from Xenopus laevis., Sakamoto T., Peptides. December 1, 2006; 27 (12): 3347-51.
	One of the duplicated matrix metalloproteinase-9 genes is expressed in regressing tail during anuran metamorphosis., Fujimoto K., Dev Growth Differ. May 1, 2006; 48 (4): 223-41.
	Temporal and spatial expression patterns of FoxN genes in Xenopus laevis embryos., Schuff M., Int J Dev Biol. January 1, 2006; 50 (4): 429-34.
	RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J., J Cell Biol. December 5, 2005; 171 (5): 785-97.
	Functional role of a novel ternary complex comprising SRF and CREB in expression of Krox-20 in early embryos of Xenopus laevis., Watanabe T., Dev Biol. January 15, 2005; 277 (2): 508-21.
	Integration of multiple signal transducing pathways on Fgf response elements of the Xenopus caudal homologue Xcad3., Haremaki T., Development. October 1, 2003; 130 (20): 4907-17.
	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 and function of Xenopus laevis p75(NTR) suggest evolution of developmental regulatory mechanisms., Hutson LD., J Neurobiol. November 5, 2001; 49 (2): 79-98.
	Xebf3 is a regulator of neuronal differentiation during primary neurogenesis in Xenopus., Pozzoli O., Dev Biol. May 15, 2001; 233 (2): 495-512.
	Xenopus frizzled-5: a frizzled family member expressed exclusively in the neural retina of the developing eye., Sumanas S., Mech Dev. May 1, 2001; 103 (1-2): 133-6.
	Cloning of a cDNA for Xenopus prolactin receptor and its metamorphic expression profile., Yamamoto T., Dev Growth Differ. April 1, 2000; 42 (2): 167-74.
	Metamorphosis: an exquisite model for hormonal regulation of post-embryonic development., Tata JR., Biochem Soc Symp. January 1, 1996; 62 123-36.
	Immunocytochemical identification of growth hormone (GH) cells in the pituitary of three anuran species using an antiserum against purified bullfrog GH., Olivereau M., Cell Tissue Res. December 1, 1993; 274 (3): 627-30.

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