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Page 1
The use of mass spectrometry in genomics.
Biomol Eng. 2004 Jan;21(1):1-13. doi: 10.1016/j.bioeng.2003.08.001.
Biomol Eng. 2004.
PMID: 14715314
Review.
Accelerated urinary excretion of methylmercury following administration of its antidote N-acetylcysteine requires Mrp2/Abcc2, the apical multidrug resistance-associated protein.
Madejczyk MS, Aremu DA, Simmons-Willis TA, Clarkson TW, Ballatori N.
Madejczyk MS, et al. Among authors: simmons willis ta.
J Pharmacol Exp Ther. 2007 Jul;322(1):378-84. doi: 10.1124/jpet.107.122812. Epub 2007 Apr 11.
J Pharmacol Exp Ther. 2007.
PMID: 17429056
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Identification of a mechanism by which the methylmercury antidotes N-acetylcysteine and dimercaptopropanesulfonate enhance urinary metal excretion: transport by the renal organic anion transporter-1.
Koh AS, Simmons-Willis TA, Pritchard JB, Grassl SM, Ballatori N.
Koh AS, et al. Among authors: simmons willis ta.
Mol Pharmacol. 2002 Oct;62(4):921-6. doi: 10.1124/mol.62.4.921.
Mol Pharmacol. 2002.
PMID: 12237339
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Transport of a neurotoxicant by molecular mimicry: the methylmercury-L-cysteine complex is a substrate for human L-type large neutral amino acid transporter (LAT) 1 and LAT2.
Simmons-Willis TA, Koh AS, Clarkson TW, Ballatori N.
Simmons-Willis TA, et al.
Biochem J. 2002 Oct 1;367(Pt 1):239-46. doi: 10.1042/BJ20020841.
Biochem J. 2002.
PMID: 12117417
Free PMC article.
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