bromodichloromethane has been researched along with Kidney Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alhasson, F; Chandrashekaran, V; Chatterjee, S; Das, S; Dattaroy, D; Schnellmann, RG; Seth, RK | 1 |
| Brown, EM; Hewitt, WR; Plaa, GL | 1 |
| Lilly, PD; Pegram, RA; Ross, TM | 1 |
| Boorman, GA; Butterworth, BE; Cobb, AJ; Everitt, JI; Marshall, MW; Torti, VR | 1 |
4 other study(ies) available for bromodichloromethane and Kidney Diseases
| Article | Year |
|---|---|
NKT cell modulates NAFLD potentiation of metabolic oxidative stress-induced mesangial cell activation and proximal tubular toxicity.
Topics: Animals; Antigens, CD1d; Cell Death; Cell Line; Cell Proliferation; Cellular Microenvironment; Cytochrome P-450 CYP2E1; Diet, High-Fat; Disease Models, Animal; Fibrosis; HMGB1 Protein; Inflammation Mediators; Kidney Diseases; Kidney Tubules, Proximal; Lipid Peroxidation; Liver; Male; Mesangial Cells; Mice, Inbred C57BL; Mice, Knockout; Natural Killer T-Cells; Non-alcoholic Fatty Liver Disease; Oxidative Stress; Toll-Like Receptor 4; Transforming Growth Factor beta; Trihalomethanes | 2016 |
Acetone-induced potentiation of trihalomethane toxicity in male rats.
Topics: Acetone; Alanine Transaminase; Animals; Chemical and Drug Induced Liver Injury; Dose-Response Relationship, Drug; Drug Synergism; Hydrocarbons, Halogenated; Kidney Diseases; Male; Organ Size; Ornithine Carbamoyltransferase; Rats; Rats, Inbred Strains; Trihalomethanes | 1983 |
Trihalomethane comparative toxicity: acute renal and hepatic toxicity of chloroform and bromodichloromethane following aqueous gavage.
Topics: Animals; Body Weight; Chemical and Drug Induced Liver Injury; Chloroform; Hydrocarbons, Halogenated; Kidney Diseases; Male; Organ Size; Rats; Rats, Inbred F344; Solvents; Trihalomethanes | 1997 |
Nephrotoxicity and hepatotoxicity induced by inhaled bromodichloromethane in wild-type and p53-heterozygous mice.
Topics: Animals; Body Weight; Carcinogens; Chemical and Drug Induced Liver Injury; Genotype; Heterozygote; Inhalation Exposure; Kidney; Kidney Diseases; Liver; Liver Diseases; Mice; Mice, Inbred C57BL; Mice, Inbred Strains; Organ Size; Species Specificity; Time Factors; Trihalomethanes; Tumor Suppressor Protein p53 | 2001 |