PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 3955844-4 1986 This effect of cycloheximide lends support to the hypothesis that the liver enzyme increases after CCl4 are probably due to increased synthesis, in addition to the classically held mechanisms of leakage from necrotic or damaged hepatocytes. Cycloheximide 15-28 C-C motif chemokine ligand 4 Rattus norvegicus 99-103 131362-4 1976 Aminotriazole or cycloheximide pretreatment but not pyrazole administration decrease the intensity of polysome rupture caused by CCl4. Cycloheximide 17-30 C-C motif chemokine ligand 4 Rattus norvegicus 129-133 6301476-2 1983 The administration of either cycloheximide or actinomycin D completely blocked the CCl4-mediated induction of choline kinase activity, indicating that the elevated activity could be due to the change in the enzyme level. Cycloheximide 29-42 C-C motif chemokine ligand 4 Rattus norvegicus 83-87 6696388-1 1984 The previously reported increases in liver and serum aspartate aminotransferase (ASAT) activities and liver protein content 24 hours after the administration of carbon tetrachloride (CCl4) were reduced by administering multiple doses of the protein synthesis inhibitor cycloheximide (CH). Cycloheximide 269-282 C-C motif chemokine ligand 4 Rattus norvegicus 183-187 6696388-1 1984 The previously reported increases in liver and serum aspartate aminotransferase (ASAT) activities and liver protein content 24 hours after the administration of carbon tetrachloride (CCl4) were reduced by administering multiple doses of the protein synthesis inhibitor cycloheximide (CH). Cycloheximide 284-286 C-C motif chemokine ligand 4 Rattus norvegicus 183-187