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Items: 45


Widespread enhancer activation via ERα mediates estrogen response in vivo during uterine development.

Jefferson WN, Kinyamu HK, Wang T, Miranda AX, Padilla-Banks E, Suen AA, Williams CJ.

Nucleic Acids Res. 2018 Jun 20;46(11):5487-5503. doi: 10.1093/nar/gky260.


Mediator complex component MED13 regulates zygotic genome activation and is required for postimplantation development in the mouse.

Miao YL, Gambini A, Zhang Y, Padilla-Banks E, Jefferson WN, Bernhardt ML, Huang W, Li L, Williams CJ.

Biol Reprod. 2018 Apr 1;98(4):449-464. doi: 10.1093/biolre/ioy004.


Methionine metabolism is essential for SIRT1-regulated mouse embryonic stem cell maintenance and embryonic development.

Tang S, Fang Y, Huang G, Xu X, Padilla-Banks E, Fan W, Xu Q, Sanderson SM, Foley JF, Dowdy S, McBurney MW, Fargo DC, Williams CJ, Locasale JW, Guan Z, Li X.

EMBO J. 2017 Nov 2;36(21):3175-3193. doi: 10.15252/embj.201796708. Epub 2017 Oct 11.


Epithelial membrane protein 2 (EMP2) deficiency alters placental angiogenesis, mimicking features of human placental insufficiency.

Williams CJ, Chu A, Jefferson WN, Casero D, Sudhakar D, Khurana N, Hogue CP, Aryasomayajula C, Patel P, Sullivan P, Padilla-Banks E, Mohandessi S, Janzen C, Wadehra M.

J Pathol. 2017 Jun;242(2):246-259. doi: 10.1002/path.4893. Epub 2017 May 3.


Store-operated Ca2+ entry is not required for fertilization-induced Ca2+ signaling in mouse eggs.

Bernhardt ML, Padilla-Banks E, Stein P, Zhang Y, Williams CJ.

Cell Calcium. 2017 Jul;65:63-72. doi: 10.1016/j.ceca.2017.02.004. Epub 2017 Feb 11.


SIX1 Oncoprotein as a Biomarker in a Model of Hormonal Carcinogenesis and in Human Endometrial Cancer.

Suen AA, Jefferson WN, Wood CE, Padilla-Banks E, Bae-Jump VL, Williams CJ.

Mol Cancer Res. 2016 Sep;14(9):849-58. doi: 10.1158/1541-7786.MCR-16-0084. Epub 2016 Jun 3.


Oviductal estrogen receptor α signaling prevents protease-mediated embryo death.

Winuthayanon W, Bernhardt ML, Padilla-Banks E, Myers PH, Edin ML, Lih FB, Hewitt SC, Korach KS, Williams CJ.

Elife. 2015 Dec 1;4:e10453. doi: 10.7554/eLife.10453.


CaV3.2 T-type channels mediate Ca²⁺ entry during oocyte maturation and following fertilization.

Bernhardt ML, Zhang Y, Erxleben CF, Padilla-Banks E, McDonough CE, Miao YL, Armstrong DL, Williams CJ.

J Cell Sci. 2015 Dec 1;128(23):4442-52. doi: 10.1242/jcs.180026. Epub 2015 Oct 19.


Regulator of G-protein signaling 2 (RGS2) suppresses premature calcium release in mouse eggs.

Bernhardt ML, Lowther KM, Padilla-Banks E, McDonough CE, Lee KN, Evsikov AV, Uliasz TF, Chidiac P, Williams CJ, Mehlmann LM.

Development. 2015 Aug 1;142(15):2633-40. doi: 10.1242/dev.121707. Epub 2015 Jul 9.


Transducin-like enhancer of split-6 (TLE6) is a substrate of protein kinase A activity during mouse oocyte maturation.

Duncan FE, Padilla-Banks E, Bernhardt ML, Ord TS, Jefferson WN, Moss SB, Williams CJ.

Biol Reprod. 2014 Mar 20;90(3):63. doi: 10.1095/biolreprod.113.112565. Print 2014 Mar.


Bisphenol A exposure alters developmental gene expression in the fetal rhesus macaque uterus.

Calhoun KC, Padilla-Banks E, Jefferson WN, Liu L, Gerrish KE, Young SL, Wood CE, Hunt PA, Vandevoort CA, Williams CJ.

PLoS One. 2014 Jan 23;9(1):e85894. doi: 10.1371/journal.pone.0085894. eCollection 2014.


Persistently altered epigenetic marks in the mouse uterus after neonatal estrogen exposure.

Jefferson WN, Chevalier DM, Phelps JY, Cantor AM, Padilla-Banks E, Newbold RR, Archer TK, Kinyamu HK, Williams CJ.

Mol Endocrinol. 2013 Oct;27(10):1666-77. doi: 10.1210/me.2013-1211. Epub 2013 Sep 3.


The estrogenic content of rodent diets, bedding, cages, and water bottles and its effect on bisphenol A studies.

Thigpen JE, Setchell KD, Kissling GE, Locklear J, Caviness GF, Whiteside T, Belcher SM, Brown NM, Collins BJ, Lih FB, Tomer KB, Padilla-Banks E, Camacho L, Adsit FG, Grant M.

J Am Assoc Lab Anim Sci. 2013 Mar;52(2):130-41. Review.


Neonatal phytoestrogen exposure alters oviduct mucosal immune response to pregnancy and affects preimplantation embryo development in the mouse.

Jefferson WN, Padilla-Banks E, Phelps JY, Cantor AM, Williams CJ.

Biol Reprod. 2012 Jul 1;87(1):10, 1-10. doi: 10.1095/biolreprod.112.099846. Print 2012 Jul.


Calcium influx-mediated signaling is required for complete mouse egg activation.

Miao YL, Stein P, Jefferson WN, Padilla-Banks E, Williams CJ.

Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4169-74. doi: 10.1073/pnas.1112333109. Epub 2012 Feb 27.


Metastasis-associated protein 3 (MTA3) regulates G2/M progression in proliferating mouse granulosa cells.

Kwintkiewicz J, Padilla-Banks E, Jefferson WN, Jacobs IM, Wade PA, Williams CJ.

Biol Reprod. 2012 Mar 8;86(3):1-8. doi: 10.1095/biolreprod.111.096032. Print 2012 Mar.


Neonatal phytoestrogen exposure causes hypospadias in female mice.

Padilla-Banks E, Jefferson WN, Myers PH, Goulding DR, Williams CJ.

Mol Reprod Dev. 2012 Jan;79(1):3. doi: 10.1002/mrd.21395. Epub 2011 Oct 11. No abstract available.


Permanent oviduct posteriorization after neonatal exposure to the phytoestrogen genistein.

Jefferson WN, Padilla-Banks E, Phelps JY, Gerrish KE, Williams CJ.

Environ Health Perspect. 2011 Nov;119(11):1575-82. doi: 10.1289/ehp.1104018. Epub 2011 Aug 2.


Oral exposure to genistin, the glycosylated form of genistein, during neonatal life adversely affects the female reproductive system.

Jefferson WN, Doerge D, Padilla-Banks E, Woodling KA, Kissling GE, Newbold R.

Environ Health Perspect. 2009 Dec;117(12):1883-9. doi: 10.1289/ehp.0900923. Epub 2009 Jul 27.


Prenatal exposure to bisphenol a at environmentally relevant doses adversely affects the murine female reproductive tract later in life.

Newbold RR, Jefferson WN, Padilla-Banks E.

Environ Health Perspect. 2009 Jun;117(6):879-85. doi: 10.1289/ehp.0800045. Epub 2009 Jan 15.


Environmental estrogens and obesity.

Newbold RR, Padilla-Banks E, Jefferson WN.

Mol Cell Endocrinol. 2009 May 25;304(1-2):84-9. doi: 10.1016/j.mce.2009.02.024. Epub 2009 Mar 9. Review.


Neonatal exposure to genistein disrupts ability of female mouse reproductive tract to support preimplantation embryo development and implantation.

Jefferson WN, Padilla-Banks E, Goulding EH, Lao SP, Newbold RR, Williams CJ.

Biol Reprod. 2009 Mar;80(3):425-31. doi: 10.1095/biolreprod.108.073171. Epub 2008 Nov 12.


Effects of endocrine disruptors on obesity.

Newbold RR, Padilla-Banks E, Jefferson WN, Heindel JJ.

Int J Androl. 2008 Apr;31(2):201-8. doi: 10.1111/j.1365-2605.2007.00858.x. Review.


Variations in phytoestrogen content between different mill dates of the same diet produces significant differences in the time of vaginal opening in CD-1 mice and F344 rats but not in CD Sprague-Dawley rats.

Thigpen JE, Setchell KD, Padilla-Banks E, Haseman JK, Saunders HE, Caviness GF, Kissling GE, Grant MG, Forsythe DB.

Environ Health Perspect. 2007 Dec;115(12):1717-26.


Long-term adverse effects of neonatal exposure to bisphenol A on the murine female reproductive tract.

Newbold RR, Jefferson WN, Padilla-Banks E.

Reprod Toxicol. 2007 Aug-Sep;24(2):253-8. Epub 2007 Jul 27.


Perinatal exposure to environmental estrogens and the development of obesity.

Newbold RR, Padilla-Banks E, Snyder RJ, Jefferson WN.

Mol Nutr Food Res. 2007 Jul;51(7):912-7. Review.


Disruption of the developing female reproductive system by phytoestrogens: genistein as an example.

Jefferson WN, Padilla-Banks E, Newbold RR.

Mol Nutr Food Res. 2007 Jul;51(7):832-44. Review.


Estradiol, progesterone, and genistein inhibit oocyte nest breakdown and primordial follicle assembly in the neonatal mouse ovary in vitro and in vivo.

Chen Y, Jefferson WN, Newbold RR, Padilla-Banks E, Pepling ME.

Endocrinology. 2007 Aug;148(8):3580-90. Epub 2007 Apr 19.


Developmental exposure to diethylstilbestrol alters uterine gene expression that may be associated with uterine neoplasia later in life.

Newbold RR, Jefferson WN, Grissom SF, Padilla-Banks E, Snyder RJ, Lobenhofer EK.

Mol Carcinog. 2007 Sep;46(9):783-96.


Developmental exposure to endocrine disruptors and the obesity epidemic.

Newbold RR, Padilla-Banks E, Snyder RJ, Phillips TM, Jefferson WN.

Reprod Toxicol. 2007 Apr-May;23(3):290-6. Epub 2007 Jan 17. Review.


Disruption of the female reproductive system by the phytoestrogen genistein.

Jefferson WN, Padilla-Banks E, Newbold RR.

Reprod Toxicol. 2007 Apr-May;23(3):308-16. Epub 2006 Dec 9. Review.


Studies of the effects of neonatal exposure to genistein on the developing female reproductive system.

Jefferson WN, Padilla-Banks E, Newbold RR.

J AOAC Int. 2006 Jul-Aug;89(4):1189-96. Review.


Neonatal exposure to the phytoestrogen genistein alters mammary gland growth and developmental programming of hormone receptor levels.

Padilla-Banks E, Jefferson WN, Newbold RR.

Endocrinology. 2006 Oct;147(10):4871-82. Epub 2006 Jul 20.


Adverse effects of the model environmental estrogen diethylstilbestrol are transmitted to subsequent generations.

Newbold RR, Padilla-Banks E, Jefferson WN.

Endocrinology. 2006 Jun;147(6 Suppl):S11-7. Epub 2006 May 11. Review.


Neonatal genistein treatment alters ovarian differentiation in the mouse: inhibition of oocyte nest breakdown and increased oocyte survival.

Jefferson W, Newbold R, Padilla-Banks E, Pepling M.

Biol Reprod. 2006 Jan;74(1):161-8. Epub 2005 Sep 28.


Developmental exposure to estrogenic compounds and obesity.

Newbold RR, Padilla-Banks E, Snyder RJ, Jefferson WN.

Birth Defects Res A Clin Mol Teratol. 2005 Jul;73(7):478-80. No abstract available.


Developmental exposure to diethylstilbestrol (DES) alters uterine response to estrogens in prepubescent mice: low versus high dose effects.

Newbold RR, Jefferson WN, Padilla-Banks E, Haseman J.

Reprod Toxicol. 2004 May;18(3):399-406.


A natural antioxidant mixture from spinach does not have estrogenic or antiestrogenic activity in immature CD-1 mice.

Lomnitski L, Padilla-Banks E, Jefferson WN, Nyska A, Grossman S, Newbold RR.

J Nutr. 2003 Nov;133(11):3584-7.


Assessing estrogenic activity of phytochemicals using transcriptional activation and immature mouse uterotrophic responses.

Jefferson WN, Padilla-Banks E, Clark G, Newbold RR.

J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Sep 25;777(1-2):179-89.


The mouse uterotrophic assay: other end points.

Newbold RR, Jefferson WN, Padilla-Banks E.

Environ Health Perspect. 2001 Dec;109(12):A569-70. No abstract available.


The immature mouse is a suitable model for detection of estrogenicity in the uterotropic bioassay.

Padilla-Banks E, Jefferson WN, Newbold RR.

Environ Health Perspect. 2001 Aug;109(8):821-6.


Cell response endpoints enhance sensitivity of the immature mouse uterotropic assay.

Newbold RR, Jefferson WN, Padilla-Banks E, Walker VR, Pena DS; Developmental Endocrinology Studies Group.

Reprod Toxicol. 2001 May-Jun;15(3):245-52. Erratum in: Reprod Toxicol 2001 Jul-Aug;15(4):465-6.


Lactoferrin is an estrogen responsive protein in the uterus of mice and rats.

Jefferson WN, Padilla-Banks E, Newbold RR.

Reprod Toxicol. 2000 Mar-Apr;14(2):103-10.


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