Franc M - Search Results

1

PhRMA white paper on ADME pharmacogenomics.

Williams JA, Andersson T, Andersson TB, Blanchard R, Behm MO, Cohen N, Edeki T, Franc M, Hillgren KM, Johnson KJ, Katz DA, Milton MN, Murray BP, Polli JW, Ricci D, Shipley LA, Vangala S, Wrighton SA. Williams JA, et al. Among authors: franc m. J Clin Pharmacol. 2008 Jul;48(7):849-89. doi: 10.1177/0091270008319329. Epub 2008 Jun 4. J Clin Pharmacol. 2008. PMID: 18524998 Review.

2

Current practices for DNA sample collection and storage in the pharmaceutical industry, and potential areas for harmonization: perspective of the I-PWG.

Franc MA, Warner AW, Cohen N, Shaw PM, Groenen P, Snapir A. Franc MA, et al. Clin Pharmacol Ther. 2011 Apr;89(4):546-53. doi: 10.1038/clpt.2010.338. Epub 2011 Mar 2. Clin Pharmacol Ther. 2011. PMID: 21368755

3

Coding of DNA samples and data in the pharmaceutical industry: current practices and future directions--perspective of the I-PWG.

Franc MA, Cohen N, Warner AW, Shaw PM, Groenen P, Snapir A; Industry Pharmacogenomics Working Group. Franc MA, et al. Clin Pharmacol Ther. 2011 Apr;89(4):537-45. doi: 10.1038/clpt.2010.306. Epub 2011 Feb 23. Clin Pharmacol Ther. 2011. PMID: 21346752

4

PhRMA survey of pharmacogenomic and pharmacodynamic evaluations: what next?

Grecco N, Cohen N, Warner AW, Lopez-Correa C, Truter SL, Snapir A, Piccoli SP, Wang D, Westelinck A, Hinman L, Franc MA; Industry Pharmacogenomics Working Group. Grecco N, et al. Among authors: franc ma. Clin Pharmacol Ther. 2012 Jun;91(6):1035-43. doi: 10.1038/clpt.2011.334. Clin Pharmacol Ther. 2012. PMID: 22534869

5

Prospective-retrospective biomarker analysis for regulatory consideration: white paper from the industry pharmacogenomics working group.

Patterson SD, Cohen N, Karnoub M, Truter SL, Emison E, Khambata-Ford S, Spear B, Ibia E, Sproule R, Barnes D, Bhathena A, Bristow MR, Russell C, Wang D, Warner A, Westelinck A, Brian W, Snapir A, Franc MA, Wong P, Shaw PM. Patterson SD, et al. Among authors: franc ma. Pharmacogenomics. 2011 Jul;12(7):939-51. doi: 10.2217/pgs.11.52. Pharmacogenomics. 2011. PMID: 21787188

6

Challenges in obtaining adequate genetic sample sets in clinical trials: the perspective of the industry pharmacogenomics working group.

Warner AW, Bhathena A, Gilardi S, Mohr D, Leong D, Bienfait KL, Sarang J, Duprey S, Franc MA, Nelsen A, Snapir A. Warner AW, et al. Among authors: franc ma. Clin Pharmacol Ther. 2011 Apr;89(4):529-36. doi: 10.1038/clpt.2010.305. Epub 2011 Feb 23. Clin Pharmacol Ther. 2011. PMID: 21346757

7

The effect of UGT2B7*2 polymorphism on the pharmacokinetics of OROS® hydromorphone in Taiwanese subjects.

Vandenbossche J, Richards H, Francke S, Van Den Bergh A, Lu CC, Franc MA. Vandenbossche J, et al. J Clin Pharmacol. 2014 Oct;54(10):1170-9. doi: 10.1002/jcph.305. Epub 2014 Apr 15. J Clin Pharmacol. 2014. PMID: 24706503 Clinical Trial.

8

Effect of CYP2D6 genetic polymorphism on the population pharmacokinetics of tipifarnib.

Perez-Ruixo JJ, Zannikos P, Ozdemir V, Franc MA, Francke S, Piotrovsky V. Perez-Ruixo JJ, et al. Cancer Chemother Pharmacol. 2006 Nov;58(5):681-91. doi: 10.1007/s00280-006-0215-8. Epub 2006 Mar 17. Cancer Chemother Pharmacol. 2006. PMID: 16544144 Clinical Trial.

9

Pharmacokinetics of carisbamate (RWJ-333369) in healthy Japanese and Western subjects.

Zannikos P, Novak G, Yao C, Verhaeghe T, Franc MA, Solanki B, Bialer M. Zannikos P, et al. Among authors: franc ma. Epilepsia. 2009 Aug;50(8):1850-9. doi: 10.1111/j.1528-1167.2009.02081.x. Epub 2009 May 11. Epilepsia. 2009. PMID: 19453703 Free article.

10

Toxicological implications of polymorphisms in receptors for xenobiotic chemicals: the case of the aryl hydrocarbon receptor.

Okey AB, Franc MA, Moffat ID, Tijet N, Boutros PC, Korkalainen M, Tuomisto J, Pohjanvirta R. Okey AB, et al. Among authors: franc ma. Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):43-51. doi: 10.1016/j.taap.2004.12.028. Toxicol Appl Pharmacol. 2005. PMID: 15993909 Review.

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