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  1. Identification and Characterization of Efflux Transporters That Modulate the Subtoxic Disposition of Diclofenac and Its Metabolites
  2. Modulation of Hepatic MRP3/ABCC3 by Xenobiotics and Pathophysiological Conditions: Role in Drug Pharmacokinetics
  3. The Role of Cyclic Nucleotides in Compensatory Hepatocyte Proliferation
  4. The trypanocidal benznidazole promotes adaptive response to oxidative injury: Involvement of the nuclear factor-erythroid 2-related factor-2 (Nrf2) and multidrug resistance associated protein 2 (MRP2)
  5. From hepatoprotection models to new therapeutic modalities for treating liver diseases: a personal perspective
  6. Preventing Liver Toxicity
  7. Acetaminophen Attenuates House Dust Mite-Induced Allergic Airway Disease in Mice
  8. Acetaminophen from liver to brain: New insights into drug pharmacological action and toxicity
  9. Reduced in vivo toxicity of doxorubicin by encapsulation in cholesterol-containing self-assembled nanoparticles
  10. Enhanced hepatotoxicity by acetaminophen in Vanin-1 knockout mice is associated with deficient proliferative and immune responses
  11. Oxidative stress-responsive transcription factor NRF2 is not indispensable for the human hepatic Flavin-containing monooxygenase-3 (FMO3) gene expression in HepG2 cells
  12. Green tea extract provides extensive Nrf2-independent protection against lipid accumulation and NFκB pro- inflammatory responses during nonalcoholic steatohepatitis in mice fed a high-fat diet
  13. Elucidation of the Mechanisms through Which the Reactive Metabolite Diclofenac Acyl Glucuronide Can Mediate Toxicity
  14. Effects of Acetaminophen on Oxidant and Irritant Respiratory Tract Responses to Environmental Tobacco Smoke in Female Mice
  15. Identifying and prioritising emerging issues in human & environmental sciences
  16. Antioxidant fractions of Khaya grandifoliola C.DC. and Entada africana Guill. et Perr. induce nuclear translocation of Nrf2 in HC-04 cells
  17. Influence of Vanin-1 and Catalytic Products in Liver During Normal and Oxidative Stress Conditions
  18. Multidrug Resistance-Associated Protein 3 Plays an Important Role in Protection against Acute Toxicity of Diclofenac
  19. Role of nuclear factor-erythroid 2-related factor 2 (Nrf2) in the transcriptional regulation of brain ABC transporters during acute acetaminophen (APAP) intoxication in mice
  20. Altered Regulation of Hepatic Efflux Transporters Disrupts Acetaminophen Disposition in Pediatric Nonalcoholic Steatohepatitis
  21. Differential Fmo3 gene expression in various liver injury models involving hepatic oxidative stress in mice
  22. Is Nuclear Factor Erythroid 2–Related Factor 2 Responsible for Sex Differences in Susceptibility to Acetaminophen-Induced Hepatotoxicity in Mice?
  23. Tolerance to Acetaminophen Hepatotoxicity in the Mouse Model of Autoprotection Is Associated with Induction of Flavin-Containing Monooxygenase-3 (FMO3) in Hepatocytes
  24. Transgenic Expression of the Human MRP2 Transporter Reduces Cisplatin Accumulation and Nephrotoxicity in Mrp2-Null Mice
  25. ChemInform Abstract: Rubescins A (I), B (II) and C (III): New Havanensin Type Limonoids from Root Bark of Trichilia rubescens (Meliaceae).
  26. Analysis of changes in hepatic gene expression in a murine model of tolerance to acetaminophen hepatotoxicity (autoprotection)
  27. CYP2E1-dependent and leptin-mediated hepatic CD57 expression on CD8+ T cells aid progression of environment-linked nonalcoholic steatohepatitis
  28. Cholesterol-Secreting and Statin-Responsive Hepatocytes from Human ES and iPS Cells to Model Hepatic Involvement in Cardiovascular Health
  29. Acute glutathione depletion induces hepatic methylglyoxal accumulation by impairing its detoxification to d-lactate
  30. Rubescins A, B and C: New Havanensin Type Limonoids from Root Bark of Trichilia rubescens (Meliaceae)
  31. Altered UDP-Glucuronosyltransferase and Sulfotransferase Expression and Function during Progressive Stages of Human Nonalcoholic Fatty Liver Disease
  32. Nrf2: A Potential Target for New Therapeutics in Liver Disease
  33. Drug Transporters
  34. Molecular mechanisms underlying chemical liver injury
  35. Constitutive activation of nuclear factor-E2-related factor 2 induces biotransformation enzyme and transporter expression in livers of mice with hepatocyte-specific deletion of Kelch-like ECH-associated protein 1
  36. Green tea extract attenuates hepatic steatosis by decreasing adipose lipogenesis and enhancing hepatic antioxidant defenses in ob/ob mice
  37. Transcriptional Regulation of Renal Cytoprotective Genes by Nrf2 and Its Potential Use as a Therapeutic Target to Mitigate Cisplatin-Induced Nephrotoxicity
  38. Vanin-1 deficient mice have enhanced susceptibility to acetaminophen hepatotoxicity
  39. Regulation of hepatic ABCC transporters by xenobiotics and in disease states
  40. Regulation of Hepatobiliary Transporters during Liver Injury
  41. Effect of allyl alcohol on hepatic transporter expression: Zonal patterns of expression and role of Kupffer cell function
  42. Coordinated induction of Nrf2 target genes protects against iron nitrilotriacetate (FeNTA)-induced nephrotoxicity
  43. Renal xenobiotic transporters are differentially expressed in mice following cisplatin treatment
  44. Nrf2- and PPAR -Mediated Regulation of Hepatic Mrp Transporters after Exposure to Perfluorooctanoic Acid and Perfluorodecanoic Acid
  45. Hepatic Mrp4 induction following acetaminophen exposure is dependent on Kupffer cell function
  46. Drug-Metabolizing Enzyme and Transporter Expression in a Mouse Model of Diabetes and Obesity
  47. Renal and Hepatic Transporter Expression in Type 2 Diabetic Rats
  48. Induction of Mrp3 and Mrp4 transporters during acetaminophen hepatotoxicity is dependent on Nrf2
  49. Acquired Resistance to Acetaminophen Hepatotoxicity is Associated with Induction of Multidrug Resistance-Associated Protein 4 (Mrp4) in Proliferating Hepatocytes
  50. Influence of Acetaminophen Vehicle on Regulation of Transporter Gene Expression During Hepatotoxicity
  51. Oxidative and electrophilic stress induces multidrug resistance-associated protein transporters via the nuclear factor-E2-related factor-2 transcriptional pathway
  52. Efflux Transporter Expression and Acetaminophen Metabolite Excretion Are Altered in Rodent Models of Nonalcoholic Fatty Liver Disease
  53. Differential gene expression in mouse liver associated with the hepatoprotective effect of clofibrate☆
  54. Induction of Hepatobiliary Efflux Transporters in Acetaminophen-Induced Acute Liver Failure Cases
  55. Emerging Role of Nrf2 in Protecting Against Hepatic and Gastrointestinal Disease
  56. Regulation of transporter expression in mouse liver, kidney, and intestine during extrahepatic cholestasis
  57. Role of NAD(P)H:quinone oxidoreductase 1 in clofibrate-mediated hepatoprotection from acetaminophen
  58. Cholestasis induced by model organic anions protects from acetaminophen hepatotoxicity in male CD-1 mice
  59. Nuclear factor-E2-related factor 2 expression in liver is critical for induction of NAD(P)H:quinone oxidoreductase 1 during cholestasis
  60. Transport deficient (TR−) hyperbilirubinemic rats are resistant to acetaminophen hepatotoxicity
  61. Altered disposition of acetaminophen in mice with a disruption of theMrp3 gene
  62. The shark bile salt 5 beta-scymnol abates acetaminophen toxicity, but not covalent binding
  63. Collection of Bile and Urine Samples for Determining the Urinary and Hepatobiliary Disposition of Xenobiotics in Mice
  64. CAR inhibitors: new line of treatment for APAP poisoning?
  65. Protection against acetaminophen hepatotoxicity by clofibrate pretreatment: Role of catalase induction
  66. Changes in susceptibility to acetaminophen-induced liver injury by the organic anion indocyanine green
  67. Effects of clofibrate and indocyanine green on the hepatobiliary disposition of acetaminophen and its metabolites in male CD-1 mice
  68. In vivo covalent binding of acetaminophen to canalicular and basolateral membrane proteins in mouse liver
  69. Repeated dosing with the peroxisome proliferator clofibrate decreases the toxicity of model hepatotoxic agents in male mice1Presented in part at the at the 35th Annual Meeting of the Society of Toxicology, Anaheim, CA, 1996.1
  70. Protection by Clofibrate against Acetaminophen Hepatotoxicity in Male CD-1 Mice Is Associated with an Early Increase in Biliary Concentration of Acetaminophen–Glutathione Adducts
  71. Protection against Acetaminophen Hepatotoxicity by a Single Dose of Clofibrate: Effects on Selective Protein Arylation and Glutathione Depletion
  72. Protection against Acetaminophen Hepatotoxicity by a Single Dose of Clofibrate: Effects on Selective Protein Arylation and Glutathione Depletion
  73. Evidence Suggesting the 58-kDa Acetaminophen Binding Protein Is a Preferential Target for Acetaminophen Electrophile
  74. Evidence for common binding of acetaminophen and bromobenzene to the 58‐kda acetaminophen‐binding protein
  75. Clofibrate Pretreatment Diminishes Acetaminophen′s Selective Covalent Binding and Hepatotoxicity
  76. Oxidative and non-oxidative metabolism of ethanol by the rabbit lung
  77. Comparison of rat pulmonary and hepatic cytosolic alcohol dehydrogenase activities
  78. Comparison of pulmonary and hepatic glucuronidation and sulphation of ethanol in rat and rabbit in vitro
  79. Ethanol-induced fatty acid ethyl ester formation in vivo and in vitro in rat lung
  80. Effect of the intrauterine contraceptive device upon the biochemical composition of human endometrium