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Summary Expression Phenotypes Gene Literature (54) GO Terms (11) Nucleotides (63) Proteins (242) Interactants (362) Wiki
XB--479428

Papers associated with ar



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Evaluation of a multiplexed, multispecies nuclear receptor assay for chemical hazard assessment., Houck KA, Simha A, Bone A, Doering JA, Vliet SMF, LaLone C, Medvedev A, Makarov S., Toxicol In Vitro. April 1, 2021; 72 105016.

Thyroid hormones and androgens differentially regulate gene expression in testes and ovaries of sexually mature Silurana tropicalis., Campbell DEK, Langlois VS., Gen Comp Endocrinol. October 1, 2018; 267 172-182.            

Developmental profiles of progesterone receptor transcripts and molecular responses to gestagen exposure during Silurana tropicalis early development., Thomson P, Langlois VS., Gen Comp Endocrinol. September 1, 2018; 265 4-14.          

Exposure to an anti-androgenic herbicide negatively impacts reproductive physiology and fertility in Xenopus tropicalis., Orton F, Säfholm M, Jansson E, Carlsson Y, Eriksson A, Fick J, Uren Webster T, McMillan T, Leishman M, Verbruggen B, Economou T, Tyler CR, Berg C., Sci Rep. June 14, 2018; 8 (1): 9124.          

Inhibition of germinal vesicle breakdown in Xenopus oocytes in vitro by a series of substituted glycol ethers., Fort DJ, Mathis MB, Guiney PD, Weeks JA., J Appl Toxicol. May 1, 2018; 38 (5): 628-637.      

Insight into the neuroendocrine basis of signal evolution: a case study in foot-flagging frogs., Mangiamele LA, Fuxjager MJ., J Comp Physiol A Neuroethol Sens Neural Behav Physiol. January 1, 2018; 204 (1): 61-70.

Transcriptome analysis identifies genes involved in sex determination and development of Xenopus laevis gonads., Piprek RP, Damulewicz M, Kloc M, Kubiak JZ., Differentiation. January 1, 2018; 100 46-56.                          

An evaluation of the endocrine disruptive potential of crude oil water accommodated fractions and crude oil contaminated surface water to freshwater organisms using in vitro and in vivo approaches., Truter JC, van Wyk JH, Oberholster PJ, Botha AM, Mokwena LM., Environ Toxicol Chem. May 1, 2017; 36 (5): 1330-1342.

Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors., Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Müller AL, Pichler R, Grahammer F, Kretz O, Huber TB, Walz G, Arnold SJ, Lienkamp SS., Nat Cell Biol. December 1, 2016; 18 (12): 1269-1280.                  

Lethal and sublethal effects of phthalate diesters in Silurana tropicalis larvae., Mathieu-Denoncourt J, Martyniuk CJ, Loughery JR, Yargeau V, de Solla SR, Langlois VS., 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, Koch I, Reimer KJ, Cullen WR, Langlois VS., Gen Comp Endocrinol. August 1, 2016; 234 133-41.        

Quantification of transcription factor-DNA binding affinity in a living cell., Belikov S, Berg OG, Wrange Ö., Nucleic Acids Res. April 20, 2016; 44 (7): 3045-58.            

Screening breeding sites of the common toad (Bufo bufo) in England and Wales for evidence of endocrine disrupting activity., Pickford DB, Jones A, Velez-Pelez A, Orton F, Iguchi T, Mitsui N, Tooi O., Ecotoxicol Environ Saf. July 1, 2015; 117 7-19.

Transcriptomic profiling in Silurana tropicalis testes exposed to finasteride., Bissegger S, Martyniuk CJ, Langlois VS., Gen Comp Endocrinol. July 1, 2014; 203 137-45.

Toxicity of the azo dyes Acid Red 97 and Bismarck Brown Y to Western clawed frog (Silurana tropicalis)., Soriano JJ, Mathieu-Denoncourt J, Norman G, de Solla SR, Langlois VS., Environ Sci Pollut Res Int. March 1, 2014; 21 (5): 3582-91.

Effects of perfluorooctanesulfonate and perfluorobutanesulfonate on the growth and sexual development of Xenopus laevis., Lou QQ, Zhang YF, Zhang YF, Zhou Z, Shi YL, Ge YN, Ren DK, Xu HM, Zhao YX, Wei WJ, Qin ZF., Ecotoxicology. September 1, 2013; 22 (7): 1133-44.

Identification of androgen receptor variants in testis from humans and other vertebrates., Laurentino SS, Pinto PI, Tomás J, Cavaco JE, Sousa M, Barros A, Power DM, Canário AV, Socorro S., Andrologia. June 1, 2013; 45 (3): 187-94.

Thyroid hormone-dependent development in Xenopus laevis: a sensitive screen of thyroid hormone signaling disruption by municipal wastewater treatment plant effluent., Searcy BT, Beckstrom-Sternberg SM, Beckstrom-Sternberg JS, Stafford P, Schwendiman AL, Soto-Pena J, Owen MC, Ramirez C, Phillips J, Veldhoen N, Helbing CC, Propper CR., Gen Comp Endocrinol. May 1, 2012; 176 (3): 481-92.

The Rift Valley is a major barrier to dispersal of African clawed frogs (Xenopus) in Ethiopia., Evans BJ, Bliss SM, Mendel SA, Tinsley RC., Mol Ecol. October 1, 2011; 20 (20): 4216-30.

Isolation and characterization of the CYP17A1 gene and its processed pseudogene in Rana rugosa., Suda M, Uno Y, Fujii J, Matsuda Y, Nakamura M., Comp Biochem Physiol B Biochem Mol Biol. September 1, 2011; 160 (1): 54-61.

Expression profiles of reproduction- and thyroid hormone-related transcripts in the brains of chemically-induced intersex frogs., Langlois VS, Duarte-Guterman P, Trudeau VL., Sex Dev. January 1, 2011; 5 (1): 26-32.

Paxillin regulates androgen- and epidermal growth factor-induced MAPK signaling and cell proliferation in prostate cancer cells., Sen A, O'Malley K, Wang Z, Raj GV, Defranco DB, Hammes SR., J Biol Chem. September 10, 2010; 285 (37): 28787-95.

Aqueous leaf extracts display endocrine activities in vitro and disrupt sexual differentiation of male Xenopus laevis tadpoles in vivo., Hermelink B, Urbatzka R, Wiegand C, Pflugmacher S, Lutz I, Kloas W., Gen Comp Endocrinol. September 1, 2010; 168 (2): 245-55.

Regulation of thyroid hormone-, oestrogen- and androgen-related genes by triiodothyronine in the brain of Silurana tropicalis., Duarte-Guterman P, Trudeau VL., J Neuroendocrinol. September 1, 2010; 22 (9): 1023-31.        

Expression and T3 regulation of thyroid hormone- and sex steroid-related genes during Silurana (Xenopus) tropicalis early development., Duarte-Guterman P, Langlois VS, Pauli BD, Trudeau VL., Gen Comp Endocrinol. April 1, 2010; 166 (2): 428-35.          

A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation., Hageman J, Rujano MA, van Waarde MA, Kakkar V, Dirks RP, Govorukhina N, Oosterveld-Hut HM, Lubsen NH, Kampinga HH., Mol Cell. February 12, 2010; 37 (3): 355-69.              

Androgen receptor of the frog Rana rugosa: molecular cloning and its characterization., Yokoyama S, Oshima Y, Tokita J, Suda M, Shinozuka T, Nakamura M., J Exp Zool A Ecol Genet Physiol. December 1, 2009; 311 (10): 796-812.

Deleted in breast cancer 1, a novel androgen receptor (AR) coactivator that promotes AR DNA-binding activity., Fu J, Jiang J, Li J, Wang S, Shi G, Feng Q, White E, Qin J, Wong J., J Biol Chem. March 13, 2009; 284 (11): 6832-40.

Split Gaussia luciferase-based bioluminescence template for tracing protein dynamics in living cells., Kim SB, Sato M, Tao H., Anal Chem. January 1, 2009; 81 (1): 67-74.

MCM7 interacts with androgen receptor., Shi YK, Yu YP, Zhu ZH, Han YC, Ren B, Nelson JB, Luo JH., Am J Pathol. December 1, 2008; 173 (6): 1758-67.

Steroidal androgens and nonsteroidal, tissue-selective androgen receptor modulator, S-22, regulate androgen receptor function through distinct genomic and nongenomic signaling pathways., Narayanan R, Coss CC, Yepuru M, Kearbey JD, Miller DD, Dalton JT., Mol Endocrinol. November 1, 2008; 22 (11): 2448-65.

A role of the amino-terminal (N) and carboxyl-terminal (C) interaction in binding of androgen receptor to chromatin., Li J, Fu J, Toumazou C, Yoon HG, Wong J., Mol Endocrinol. April 1, 2006; 20 (4): 776-85.

HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM, van Venrooy S, Ritthaler M, Wedlich D, Gradl D., J Biol Chem. January 20, 2006; 281 (3): 1755-64.            

The modulator of nongenomic actions of the estrogen receptor (MNAR) regulates transcription-independent androgen receptor-mediated signaling: evidence that MNAR participates in G protein-regulated meiosis in Xenopus laevis oocytes., Haas D, White SN, Lutz LB, Rasar M, Hammes SR., Mol Endocrinol. August 1, 2005; 19 (8): 2035-46.

Selective modulation of genomic and nongenomic androgen responses by androgen receptor ligands., Lutz LB, Jamnongjit M, Yang WH, Jahani D, Gill A, Hammes SR., Mol Endocrinol. June 1, 2003; 17 (6): 1106-16.

A role for cofactor-cofactor and cofactor-histone interactions in targeting p300, SWI/SNF and Mediator for transcription., Huang ZQ, Li J, Sachs LM, Cole PA, Wong J., EMBO J. May 1, 2003; 22 (9): 2146-55.

Functional genomics and sexual differentiation in amphibians., Bögi C, Levy G, Lutz I, Kloas W., Comp Biochem Physiol B Biochem Mol Biol. December 1, 2002; 133 (4): 559-70.

Complete androgen insensitivity syndrome caused by a novel mutation in the ligand-binding domain of the androgen receptor: functional characterization., Rosa S, Biason-Lauber A, Mongan NP, Navratil F, Schoenle EJ., J Clin Endocrinol Metab. September 1, 2002; 87 (9): 4378-82.

Evidence that androgens are the primary steroids produced by Xenopus laevis ovaries and may signal through the classical androgen receptor to promote oocyte maturation., Lutz LB, Cole LM, Gupta MK, Kwist KW, Auchus RJ, Hammes SR., Proc Natl Acad Sci U S A. November 20, 2001; 98 (24): 13728-33.

Rho GTPases as modulators of the estrogen receptor transcriptional response., Su LF, Knoblauch R, Garabedian MJ., J Biol Chem. February 2, 2001; 276 (5): 3231-7.

Sequence and expression of a cDNA encoding the red seabream androgen receptor., Touhata K, Kinoshita M, Tokuda Y, Toyohara H, Sakaguchi M, Yokoyama Y, Yamashita S., Biochim Biophys Acta. July 8, 1999; 1450 (3): 481-5.

Sequence and expression of a cDNA encoding the red sea bream androgen receptor., Touhata K, Kinoshita M, Tokuda Y, Toyohara H, Sakaguchi M, Yokoyama Y, Yamashita S., Biochim Biophys Acta. March 8, 1999; 1449 (2): 199-202.

Evolution of the androgen receptor: structure-function implications., Thornton JW, Kelley DB., Bioessays. October 1, 1998; 20 (10): 860-9.

Trophic effects of androgen: receptor expression and the survival of laryngeal motor neurons after axotomy., Pérez J, Kelley DB., J Neurosci. November 1, 1996; 16 (21): 6625-33.              

Androgen receptor mRNA expression in Xenopus laevis CNS: sexual dimorphism and regulation in laryngeal motor nucleus., Pérez J, Cohen MA, Kelley DB., J Neurobiol. August 1, 1996; 30 (4): 556-68.                

Occurrence of androgen and estrogen receptor mRNAs in the harderian gland: a comparative survey., Varriale B., Microsc Res Tech. June 1, 1996; 34 (2): 97-103.

Androgen-directed development of the Xenopus laevis larynx: control of androgen receptor expression and tissue differentiation., Fischer LM, Catz D, Kelley DB., Dev Biol. July 1, 1995; 170 (1): 115-26.            

Androgen regulation of neuromuscular junction structure and function in a sexually dimorphic muscle of the frog Xenopus laevis., Brennan C, Henderson LP., J Neurobiol. June 1, 1995; 27 (2): 172-88.

The androgen receptor mRNA is up-regulated by testosterone in both the Harderian gland and thumb pad of the frog, Rana esculenta., Varriale B, Serino I., J Steroid Biochem Mol Biol. December 1, 1994; 51 (5-6): 259-65.

Effects of testosterone on a sexually dimorphic frog muscle: repeated in vivo observations and androgen receptor distribution., Dorlöchter M, Astrow SH, Herrera AA., J Neurobiol. August 1, 1994; 25 (8): 897-916.

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