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Journal of Proteome Research|June 17, 2020
A Two-Way Interaction between Methotrexate and the Gut Microbiota of Male Sprague-Dawley RatsMarine P M Letertre, Nyasha Munjoma, Kate Wolfer, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 20, 2015
Altered regulation of hepatic efflux transporters disrupts acetaminophen disposition in pediatric nonalcoholic steatohepatitisMark J Canet, Matthew D Merrell, Rhiannon N Hardwick, et al.Journal of the National Cancer Institute|October 18, 2015
Suppression of TGFβ and Angiogenesis by Type VII Collagen in Cutaneous SCCV L Martins, M P Caley, K Moore, et al.Cell Death & Disease|July 6, 2012
Promoter methylation of argininosuccinate synthetase-1 sensitises lymphomas to arginine deiminase treatment, autophagy and caspase-dependent apoptosisB Delage, P Luong, L Maharaj, et al.Toxicological Sciences : an Official Journal of the Society of Toxicology|June 11, 2022
Microphysiological Systems Evaluation: Experience of TEX-VAL Tissue Chip Testing ConsortiumIvan Rusyn, Courtney Sakolish, Yuki Kato, et al.The British Journal of Dermatology|January 15, 2013
Comparison of three screening tools to detect psoriatic arthritis in patients with psoriasis (CONTEST study)L C Coates, T Aslam, F Al Balushi, et al.ALTEX|January 22, 2022
Perspectives on the evaluation and adoption of complex in vitro models in drug development: Workshop with the FDA and the pharmaceutical industry (IQ MPS Affiliate)Szczepan W Baran, Paul C Brown, Andreas R Baudy, et al.Advanced Biology|October 9, 2023
Considerations from an International Regulatory and Pharmaceutical Industry (IQ MPS Affiliate) Workshop on the Standardization of Complex In Vitro Models in Drug DevelopmentLindsay Tomlinson, Diane Ramsden, Sofia Batista Leite, et al.ALTEX|April 12, 2025
Considerations from the pharmaceutical industry (IQ MPS affiliate) workshop on animal microphysiological systems and 3Rs in drug developmentPatrick J Devine, Manti Guha, Jason E Ekert, et al.Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.Pageof 12