Papers associated with viscus (and thrb)

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	Stem cell development involves divergent thyroid hormone receptor subtype expression and epigenetic modifications in the amphibian intestine during metamorphosis., Hasebe T., Vitam Horm. January 1, 2023; 122 1-22.
	Glucocorticoid receptor mediates corticosterone-thyroid hormone synergy essential for metamorphosis in Xenopus tropicalis tadpoles., Sterner ZR., Gen Comp Endocrinol. January 1, 2022; 315 113942.
	Analysis of Thyroid Hormone Receptor α-Knockout Tadpoles Reveals That the Activation of Cell Cycle Program Is Involved in Thyroid Hormone-Induced Larval Epithelial Cell Death and Adult Intestinal Stem Cell Development During Xenopus tropicalis Metamorphosis., Tanizaki Y., Thyroid. January 1, 2021; 31 (1): 128-142.
	The development of adult intestinal stem cells: Insights from studies on thyroid hormone-dependent anuran metamorphosis., Shi YB, Shi YB., Vitam Horm. January 1, 2021; 116 269-293.
	Amiodarone bioconcentration and suppression of metamorphosis in Xenopus., Sanoh S., Aquat Toxicol. November 1, 2020; 228 105623.
	Stem cell development involves divergent thyroid hormone receptor subtype expression and epigenetic modifications in the Xenopus metamorphosing intestine., Hasebe T., Gen Comp Endocrinol. June 1, 2020; 292 113441.
	Glucocorticoid receptor is required for survival through metamorphosis in the frog Xenopus tropicalis., Sterner ZR., Gen Comp Endocrinol. May 15, 2020; 291 113419.
	Developmental gene expression patterns in the brain and liver of Xenopus tropicalis during metamorphosis climax., Yaoita Y., Genes Cells. December 1, 2018; 23 (12): 998-1008.
	Expression of hyaluronan synthases upregulated by thyroid hormone is involved in intestinal stem cell development during Xenopus laevis metamorphosis., Fujimoto K., Dev Genes Evol. December 1, 2018; 228 (6): 267-273.
	Dual function model revised by thyroid hormone receptor alpha knockout frogs., Buchholz DR., Gen Comp Endocrinol. September 1, 2018; 265 214-218.
	The balance of two opposing factors Mad and Myc regulates cell fate during tissue remodeling., Okada M., Cell Biosci. April 19, 2018; 8 51.
	Thyroid Hormone Receptor α- and β-Knockout Xenopus tropicalis Tadpoles Reveal Subtype-Specific Roles During Development., Nakajima K., Endocrinology. February 1, 2018; 159 (2): 733-743.
	Genome-wide identification of thyroid hormone receptor targets in the remodeling intestine during Xenopus tropicalis metamorphosis., Fu L., Sci Rep. July 25, 2017; 7 (1): 6414.
	Thyroid Hormone Receptor α Controls Developmental Timing and Regulates the Rate and Coordination of Tissue-Specific Metamorphosis in Xenopus tropicalis., Wen L., Endocrinology. June 1, 2017; 158 (6): 1985-1998.
	The heterochronic gene Lin28 regulates amphibian metamorphosis through disturbance of thyroid hormone function., Faunes F., Dev Biol. May 15, 2017; 425 (2): 142-151.
	Direct Regulation of Histidine Ammonia-Lyase 2 Gene by Thyroid Hormone in the Developing Adult Intestinal Stem Cells., Luu N., Endocrinology. April 1, 2017; 158 (4): 1022-1033.
	Lethal and sublethal effects of phthalate diesters in Silurana tropicalis larvae., Mathieu-Denoncourt J., Environ Toxicol Chem. October 1, 2016; 35 (10): 2511-2522.
	Life cycle exposure of the frog Silurana tropicalis to arsenate: Steroid- and thyroid hormone-related genes are differently altered throughout development., Gibson LA., Gen Comp Endocrinol. August 1, 2016; 234 133-41.
	Direct Activation of Amidohydrolase Domain-Containing 1 Gene by Thyroid Hormone Implicates a Role in the Formation of Adult Intestinal Stem Cells During Xenopus Metamorphosis., Okada M., Endocrinology. September 1, 2015; 156 (9): 3381-93.
	Enabling comparative gene expression studies of thyroid hormone action through the development of a flexible real-time quantitative PCR assay for use across multiple anuran indicator and sentinel species., Veldhoen N., Aquat Toxicol. March 1, 2014; 148 162-73.
	Metamorphosis in a frog that does not have a tadpole., Elinson RP., Curr Top Dev Biol. January 1, 2013; 103 259-76.
	The origins and evolution of vertebrate metamorphosis., Laudet V., Curr Biol. September 27, 2011; 21 (18): R726-37.
	Amphibian metamorphosis., Brown DD., Dev Biol. June 1, 2007; 306 (1): 20-33.
	Development of biomarkers of endocrine disrupting activity in emerging amphibian model, Silurana (Xenopus) tropicalis., Takase M., Environ Sci. January 1, 2007; 14 (6): 285-96.
	Thyroid hormone receptor expression in the obligatory paedomorphic salamander Necturus maculosus., Vlaeminck-Guillem V., Int J Dev Biol. January 1, 2006; 50 (6): 553-60.
	Early expression of thyroid hormone receptor beta and retinoid X receptor gamma in the Xenopus embryo., Cossette SM., Differentiation. June 1, 2004; 72 (5): 239-49.
	Developmental expression and hormonal regulation of glucocorticoid and thyroid hormone receptors during metamorphosis in Xenopus laevis., Krain LP., J Endocrinol. April 1, 2004; 181 (1): 91-104.
	Basic transcription element binding protein is a thyroid hormone-regulated transcription factor expressed during metamorphosis in Xenopus laevis., Hoopfer ED., Dev Growth Differ. October 1, 2002; 44 (5): 365-81.
	Expression of thyroid hormone receptor betaA gene assayed by transgenic Xenopus laevis carrying its promoter sequences., Oofusa K., Mol Cell Endocrinol. July 5, 2001; 181 (1-2): 97-110.
	Role of type III iodothyronine 5-deiodinase gene expression in temporal regulation of Xenopus metamorphosis., Kawahara A., Dev Growth Differ. June 1, 1999; 41 (3): 365-73.
	An immunocytochemical analysis of the expression of thyroid hormone receptor alpha and beta proteins during natural and thyroid hormone-induced metamorphosis in Xenopus., Fairclough L., Dev Growth Differ. June 1, 1997; 39 (3): 273-83.
	Characterization and expression of C/EPB-like genes in the liver of Rana catesbeiana tadpoles during spontaneous and thyroid hormone-induced metamorphosis., Chen Y., Dev Genet. January 1, 1994; 15 (4): 366-77.
	Developmental and regional expression of thyroid hormone receptor genes during Xenopus metamorphosis., Kawahara A., Development. August 1, 1991; 112 (4): 933-43.

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