Perkins RG - Search Results

1

Kennedy GL Jr, Butenhoff JL, Olsen GW, O'Connor JC, Seacat AM, Perkins RG, Biegel LB, Murphy SR, Farrar DG. Kennedy GL Jr, et al. Among authors: perkins rg. Crit Rev Toxicol. 2004 Jul-Aug;34(4):351-84. doi: 10.1080/10408440490464705. Crit Rev Toxicol. 2004. PMID: 15328768 Review.

2

13-week dietary toxicity study of ammonium perfluorooctanoate (APFO) in male rats.

Perkins RG, Butenhoff JL, Kennedy GL Jr, Palazzolo MJ. Perkins RG, et al. Drug Chem Toxicol. 2004 Nov;27(4):361-78. doi: 10.1081/dct-200039773. Drug Chem Toxicol. 2004. PMID: 15573472

3

Rat α-Fetoprotein binding affinities of a large set of structurally diverse chemicals elucidated the relationships between structures and binding affinities.

Hong H, Branham WS, Dial SL, Moland CL, Fang H, Shen J, Perkins R, Sheehan D, Tong W. Hong H, et al. Chem Res Toxicol. 2012 Nov 19;25(11):2553-66. doi: 10.1021/tx3003406. Epub 2012 Oct 12. Chem Res Toxicol. 2012. PMID: 23013281

4

Phytoestrogens and mycoestrogens bind to the rat uterine estrogen receptor.

Branham WS, Dial SL, Moland CL, Hass BS, Blair RM, Fang H, Shi L, Tong W, Perkins RG, Sheehan DM. Branham WS, et al. Among authors: perkins rg. J Nutr. 2002 Apr;132(4):658-64. doi: 10.1093/jn/132.4.658. J Nutr. 2002. PMID: 11925457

5

Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.

Fang H, Tong W, Branham WS, Moland CL, Dial SL, Hong H, Xie Q, Perkins R, Owens W, Sheehan DM. Fang H, et al. Chem Res Toxicol. 2003 Oct;16(10):1338-58. doi: 10.1021/tx030011g. Chem Res Toxicol. 2003. PMID: 14565775

6

Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein.

Hong H, Branham WS, Ng HW, Moland CL, Dial SL, Fang H, Perkins R, Sheehan D, Tong W. Hong H, et al. Toxicol Sci. 2015 Feb;143(2):333-48. doi: 10.1093/toxsci/kfu231. Epub 2014 Oct 27. Toxicol Sci. 2015. PMID: 25349334

7

Estrogenic activity data extraction and in silico prediction show the endocrine disruption potential of bisphenol A replacement compounds.

Ng HW, Shu M, Luo H, Ye H, Ge W, Perkins R, Tong W, Hong H. Ng HW, et al. Chem Res Toxicol. 2015 Sep 21;28(9):1784-95. doi: 10.1021/acs.chemrestox.5b00243. Epub 2015 Sep 2. Chem Res Toxicol. 2015. PMID: 26308263

8

The estrogen receptor relative binding affinities of 188 natural and xenochemicals: structural diversity of ligands.

Blair RM, Fang H, Branham WS, Hass BS, Dial SL, Moland CL, Tong W, Shi L, Perkins R, Sheehan DM. Blair RM, et al. Toxicol Sci. 2000 Mar;54(1):138-53. doi: 10.1093/toxsci/54.1.138. Toxicol Sci. 2000. PMID: 10746941

9

QSAR models using a large diverse set of estrogens.

Shi LM, Fang H, Tong W, Wu J, Perkins R, Blair RM, Branham WS, Dial SL, Moland CL, Sheehan DM. Shi LM, et al. J Chem Inf Comput Sci. 2001 Jan-Feb;41(1):186-95. doi: 10.1021/ci000066d. J Chem Inf Comput Sci. 2001. PMID: 11206373

10

Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.

Fang H, Tong W, Shi LM, Blair R, Perkins R, Branham W, Hass BS, Xie Q, Dial SL, Moland CL, Sheehan DM. Fang H, et al. Chem Res Toxicol. 2001 Mar;14(3):280-94. doi: 10.1021/tx000208y. Chem Res Toxicol. 2001. PMID: 11258977

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