Integration of clinical and gene expression endpoints to explore furan-mediated hepatotoxicity.
暂无分享,去创建一个
Kerry Blanchard | Supriya Jayadev | Cynthia A Afshari | Jeff Chou | Qihong Huang | P. Bushel | J. Chou | J. Collins | C. J. Tucker | C. Afshari | H. Hamadeh | S. Jayadev | Qihong Huang | Hisham K Hamadeh | Raymond Stoll | Elias T Gaillard | Charles J Tucker | Jennifer Collins | Robert Maronpot | Pierre Bushel | R. Stoll | K. Blanchard | E. Gaillard | R. Maronpot
[1] Lee Bennett,et al. Gene expression analysis reveals chemical-specific profiles. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.
[2] Kerry Blanchard,et al. Methapyrilene Toxicity: Anchorage of Pathologic Observations to Gene Expression Alterations , 2002, Toxicologic pathology.
[3] D. Brenner,et al. Hepatic Stellate Cells as a Target for the Treatment of Liver Fibrosis , 2001, Seminars in liver disease.
[4] R G Ulrich,et al. Clustering of hepatotoxins based on mechanism of toxicity using gene expression profiles. , 2001, Toxicology and applied pharmacology.
[5] D. Schuppan,et al. The serum concentrations of the aminoterminal propeptide of procollagen type III and the hepatic content of mRNA for the alpha 1 chain of procollagen type III in carbon tetrachloride-induced rat liver fibrogenesis. , 1991, Journal of hepatology.
[6] I. Jolliffe. Principal Component Analysis , 2002 .
[7] L. Elmore,et al. Sequential appearance of intestinal mucosal cell types in the right and caudate liver lobes of furan‐treated rats , 1992, Hepatology.
[8] Developing toxicologically predictive gene sets using cDNA microarrays and Bayesian classification. , 2002, Methods in enzymology.
[9] Y. N. Park,et al. Increased expression of O-acetyl disialoganglioside synthase during rat liver fibrogenesis relates to stellate cell activation. , 2003, Biochemical and biophysical research communications.
[10] L. Elmore,et al. Phenotypic characterization of metaplastic intestinal glands and ductular hepatocytes in cholangiofibrotic lesions rapidly induced in the caudate liver lobe of rats treated with furan. , 1991, Cancer research.
[11] D. Schuppan,et al. Elevated serum aminoterminal procollagen type-III-peptide parallels collagen accumulation in rats with secondary biliary fibrosis. , 1996, Journal of hepatology.
[12] D. B. Kristensen,et al. Characterization of a Stellate Cell Activation-associated Protein (STAP) with Peroxidase Activity Found in Rat Hepatic Stellate Cells* , 2001, The Journal of Biological Chemistry.
[13] S. Thorgeirsson,et al. Tissue inhibitor of metalloproteinases‐1 promotes liver fibrosis development in a transgenic mouse model , 2000, Hepatology.
[14] Wen-bin Liu,et al. Inhibition on the production of collagen type I, III of activated hepatic stellate cells by antisense TIMP-1 recombinant plasmid. , 2003, World journal of gastroenterology.
[15] Lee Bennett,et al. Prediction of compound signature using high density gene expression profiling. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.
[16] J. Iredale,et al. Mechanisms of spontaneous resolution of rat liver fibrosis. Hepatic stellate cell apoptosis and reduced hepatic expression of metalloproteinase inhibitors. , 1998, The Journal of clinical investigation.
[17] L. Elmore,et al. "Intestinal-type" of adenocarcinoma preferentially induced in right/caudate liver lobes of rats treated with furan. , 1993, Cancer research.
[18] Kate Johnson,et al. MAPS: a microarray project system for gene expression experiment information and data validation , 2001, Bioinform..
[19] J. Iredale,et al. Expression of tissue inhibitor of metalloproteinases 1 and 2 is increased in fibrotic human liver. , 1996, Gastroenterology.