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Page 1
Towards consensus practices to qualify safety biomarkers for use in early drug development.
Sistare FD, Dieterle F, Troth S, Holder DJ, Gerhold D, Andrews-Cleavenger D, Baer W, Betton G, Bounous D, Carl K, Collins N, Goering P, Goodsaid F, Gu YZ, Guilpin V, Harpur E, Hassan A, Jacobson-Kram D, Kasper P, Laurie D, Lima BS, Maciulaitis R, Mattes W, Maurer G, Obert LA, Ozer J, Papaluca-Amati M, Phillips JA, Pinches M, Schipper MJ, Thompson KL, Vamvakas S, Vidal JM, Vonderscher J, Walker E, Webb C, Yu Y. Sistare FD, et al. Among authors: guilpin v. Nat Biotechnol. 2010 May;28(5):446-54. doi: 10.1038/nbt.1634. Epub 2010 May 10. Nat Biotechnol. 2010. PMID: 20458314
Response letter from Clinical Pathology Interest Group of the Society of Toxicologic Pathology (STP) for manuscript entitled International recommendations for training future toxicologic pathologists participating in regulatory-type, nonclinical toxicity studies by Bolon et al.
Tripathi NK, Schultze AE, Pearson RC, Everds NE, Elliott GS, Ramaiah L, Wells MY, Latimer KS, Walter GL, Katavolos P, Collins ND, Tarrant J, Walker DB, Topper MJ, Jordan HL, O'Rourke LG, Guilpin VB, Brockus CW, Wilcox AL, Clemo FA, Smith GS, Reagan WJ, McCartney JE. Tripathi NK, et al. Among authors: guilpin vb. Exp Toxicol Pathol. 2013 Jan;65(1-2):39. doi: 10.1016/j.etp.2011.05.007. Epub 2011 Jun 15. Exp Toxicol Pathol. 2013. PMID: 21676604 No abstract available.