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Items: 1 to 20 of 28

1.

Cytosolic sulfotransferase 1A1 regulates HIV-1 minus-strand DNA elongation in primary human monocyte-derived macrophages.

Swann J, Murry J, Young JA.

Virol J. 2016 Feb 24;13:30. doi: 10.1186/s12985-016-0491-9.

2.

The Regulation of Steroid Action by Sulfation and Desulfation.

Mueller JW, Gilligan LC, Idkowiak J, Arlt W, Foster PA.

Endocr Rev. 2015 Oct;36(5):526-63. doi: 10.1210/er.2015-1036. Epub 2015 Jul 27. Review.

3.

Genetics of cardiovascular disease: Importance of sex and ethnicity.

Winham SJ, de Andrade M, Miller VM.

Atherosclerosis. 2015 Jul;241(1):219-28. doi: 10.1016/j.atherosclerosis.2015.03.021. Epub 2015 Mar 16. Review.

4.

Congress on women's health Trudy Bush lecture 2014: new insights into sex Hormones and Cardiovascular disease.

Miller VM.

J Womens Health (Larchmt). 2014 Dec;23(12):997-1004. doi: 10.1089/jwh.2014.4995.

5.

Pharmacogenetics of SULT1A1.

Daniels J, Kadlubar S.

Pharmacogenomics. 2014 Nov;15(14):1823-1838.

6.

Diversity Outbred Mice Identify Population-Based Exposure Thresholds and Genetic Factors that Influence Benzene-Induced Genotoxicity.

French JE, Gatti DM, Morgan DL, Kissling GE, Shockley KR, Knudsen GA, Shepard KG, Price HC, King D, Witt KL, Pedersen LC, Munger SC, Svenson KL, Churchill GA.

Environ Health Perspect. 2015 Mar;123(3):237-45. doi: 10.1289/ehp.1408202. Epub 2014 Nov 6.

7.

Pharmacogenomics of acetaminophen in pediatric populations: a moving target.

Krasniak AE, Knipp GT, Svensson CK, Liu W.

Front Genet. 2014 Oct 14;5:314. doi: 10.3389/fgene.2014.00314. eCollection 2014. Review.

8.

Parallel selection on gene copy number variations through evolution of three-spined stickleback genomes.

Hirase S, Ozaki H, Iwasaki W.

BMC Genomics. 2014 Aug 29;15:735. doi: 10.1186/1471-2164-15-735.

9.

Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats.

Brahmachary M, Guilmatre A, Quilez J, Hasson D, Borel C, Warburton P, Sharp AJ.

PLoS Genet. 2014 Jun 19;10(6):e1004418. doi: 10.1371/journal.pgen.1004418. eCollection 2014 Jun.

10.

Integrative analyses of hepatic differentially expressed genes and blood biomarkers during the peripartal period between dairy cows overfed or restricted-fed energy prepartum.

Shahzad K, Bionaz M, Trevisi E, Bertoni G, Rodriguez-Zas SL, Loor JJ.

PLoS One. 2014 Jun 10;9(6):e99757. doi: 10.1371/journal.pone.0099757. eCollection 2014.

11.

Sulfotransferase 1A1 (SULT1A1) gene expression is regulated by members of the NFI transcription factors in human breast cancer cells.

Yao-Borengasser A, Rogers LJ, Edavana VK, Penney RB, Yu X, Dhakal IB, Williams S, Kadlubar SA.

BMC Clin Pathol. 2014 Jan 6;14(1):1. doi: 10.1186/1472-6890-14-1.

12.

Sulfotransferase genetic variation: from cancer risk to treatment response.

Daniels J, Kadlubar S.

Drug Metab Rev. 2013 Nov;45(4):415-22. doi: 10.3109/03602532.2013.835621. Epub 2013 Sep 6. Review.

13.

SULT2A1 Gene Copy Number Variation is Associated with Urinary Excretion Rate of Steroid Sulfates.

Schulze J, Johansson M, Thörngren JO, Garle M, Rane A, Ekström L.

Front Endocrinol (Lausanne). 2013 Jul 12;4:88. doi: 10.3389/fendo.2013.00088. eCollection 2013.

14.

SULT1A1 gene deletion in BRCA2-associated male breast cancer: a link between genes and environmental exposures?

Palli D, Rizzolo P, Zanna I, Silvestri V, Saieva C, Falchetti M, Navazio AS, Graziano V, Masala G, Bianchi S, Russo A, Tommasi S, Ottini L.

J Cell Mol Med. 2013 May;17(5):605-7. doi: 10.1111/jcmm.12043.

15.

Copy number variation in sulfotransferase isoform 1A1 (SULT1A1) is significantly associated with enzymatic activity in Japanese subjects.

Yu X, Kubota T, Dhakal I, Hasegawa S, Williams S, Ozawa S, Kadlubar S.

Pharmgenomics Pers Med. 2013;6:19-24. doi: 10.2147/PGPM.S36579. Epub 2013 Mar 6.

16.

Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management.

Rofaiel S, Muo EN, Mousa SA.

Pharmgenomics Pers Med. 2010;3:129-43. doi: 10.2147/PGPM.S10789. Epub 2010 Sep 17.

17.

Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation.

Martis S, Mei H, Vijzelaar R, Edelmann L, Desnick RJ, Scott SA.

Pharmacogenomics J. 2013 Dec;13(6):558-66. doi: 10.1038/tpj.2012.48. Epub 2012 Nov 20.

18.

Sulfation of fulvestrant by human liver cytosols and recombinant SULT1A1 and SULT1E1.

Edavana VK, Yu X, Dhakal IB, Williams S, Ning B, Cook IT, Caldwell D, Falany CN, Kadlubar S.

Pharmgenomics Pers Med. 2011 Nov 16;4:137-145.

19.

Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterization.

Hebbring SJ, Chai Y, Ji Y, Abo RP, Jenkins GD, Fridley B, Zhang J, Eckloff BW, Wieben ED, Weinshilboum RM.

J Neurochem. 2012 Mar;120(6):881-90. doi: 10.1111/j.1471-4159.2012.07646.x. Epub 2012 Feb 6.

20.

Copy number variation and warfarin dosing: evaluation of CYP2C9, VKORC1, CYP4F2, GGCX and CALU.

Scott SA, Patel M, Martis S, Lubitz SA, van der Zee S, Yoo C, Edelmann L, Halperin JL, Desnick RJ.

Pharmacogenomics. 2012 Feb;13(3):297-307. doi: 10.2217/pgs.11.156. Epub 2011 Dec 21.

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