The Role of Covalent Binding to Microsomal Proteins in the Hepatotoxicity of Acetaminophen

This publication has 37 references indexed in Scilit:

• Paracetamol toxicity in hamster isolated hepatocytes: The increase in cytosolic calcium accompanies, rather than precedes, loss of viability
  Archives of Toxicology, 1992
• A metabolite of acetaminophen covalently binds to the 56 kDa selenium binding protein
  Biochemical and Biophysical Research Communications, 1992
• A metabolite of halothane covalently binds to an endoplasmic reticulum protein that is highly homologous to phosphatidylinositol-specific phospholipase C-α but has no activity
  Biochemical and Biophysical Research Communications, 1991
• The role of calcium in lethal cell injury
  Chemical Research in Toxicology, 1990
• The high-affinity calcium binding protein of sarcoplasmic reticulum. Tissue distribution, and homology with calregulin
  Biochimica et Biophysica Acta (BBA) - Biomembranes, 1989
• Immediate rise in intracellular calcium and glycogen phosphorylase a activities upon acetaminophen covalent binding leading to hepatotoxicity in mice
  Toxicology, 1988
• Covalent binding of [14C]methoxychlor metabolite(s) to rat liver microsomal components
  Toxicology and Applied Pharmacology, 1983
• Bromobenzene and p-bromophenol toxicity and covalent binding
  Life Sciences, 1982
• N-hydroxyacetaminophen: A microsomal metabolite of N-hydroxyphenacetin but apparently not of acetaminophen
  Life Sciences, 1979
• Metabolic products of naphthalene in mammalian systems
  Journal of the American Chemical Society, 1967