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Renal biomarker qualification submission: a dialog between the FDA-EMEA and Predictive Safety Testing Consortium.
Nat Biotechnol. 2010 May;28(5):455-62. doi: 10.1038/nbt.1625. Epub 2010 May 10.
Nat Biotechnol. 2010.
PMID: 20458315
STP Best Practices for Evaluating Clinical Pathology in Pharmaceutical Recovery Studies.
Tomlinson L, Ramaiah L, Tripathi NK, Barlow VG, Vitsky A, Poitout-Belissent FM, Bounous DI, Ennulat D.
Tomlinson L, et al. Among authors: barlow vg.
Toxicol Pathol. 2016 Feb;44(2):163-72. doi: 10.1177/0192623315624165. Epub 2016 Feb 14.
Toxicol Pathol. 2016.
PMID: 26879687
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Principles for Assessing Adversity in Toxicologic Clinical Pathology.
Ramaiah L, Tomlinson L, Tripathi NK, Cregar LC, Vitsky A, Beust BV, Barlow VG, Reagan WJ, Ennulat D.
Ramaiah L, et al. Among authors: barlow vg.
Toxicol Pathol. 2017 Feb;45(2):260-266. doi: 10.1177/0192623316681646. Epub 2017 Jan 5.
Toxicol Pathol. 2017.
PMID: 28056663
Review.
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Analytic evaluation of a human ELISA kit for measurement of inhibin B in rat samples.
Coulson M, Bickerton S, Betts CJ, Jacobsen M, Stewart J, Chapin RE, Reagan WJ, Alvey J, Erdos Z, Saldutti LP, Sonee M, Bogdan N, Singer M, Vinken P, Barlow V, Czajkowski K, Kim JH.
Coulson M, et al.
Birth Defects Res B Dev Reprod Toxicol. 2013 Feb;98(1):4-16. doi: 10.1002/bdrb.21047. Epub 2013 Jan 24.
Birth Defects Res B Dev Reprod Toxicol. 2013.
PMID: 23349040
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