dicarbethoxydihydrocollidine has been researched along with bromochloroacetic acid in 18 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (5.56) | 18.7374 |
1990's | 3 (16.67) | 18.2507 |
2000's | 10 (55.56) | 29.6817 |
2010's | 4 (22.22) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Arak, S; Harwood, TR; Tsunoo, C; Yokoo, H | 1 |
Bergeron, C; Goh, MC; Markiewicz, P; Pollanen, MS; Weyer, L | 1 |
French, BA; French, SW; Fu, P; Marceau, N; Yuan, QX | 1 |
French, SW; Gaal, K; Hu, B; Nagao, Y; Yuan, QX | 1 |
Denk, H; Fickert, P; Omary, MB; Stumptner, C; Zatloukal, K | 1 |
Baribault, H; Denk, H; Eshkind, LG; Franke, WW; Lehner, M; Stumptner, C; Zatloukal, K | 1 |
French, BA; French, SW; Nagao, Y; Wan, YJ; Yuan, QX | 1 |
Denk, H; Fuchsbichler, A; Lehner, M; Stumptner, C; Zatloukal, K | 1 |
Denk, H; Fuchsbichler, A; Heid, H; Stumptner, C; Zatloukal, K | 1 |
Bardag-Gorce, F; French, BA; French, SW; Li, J; Lue, YH; McPhaul, LW; Nguyen, V; Riley, N; van Leeuwen, FW | 1 |
Denk, H; Fickert, P; Fuchsbichler, A; Stumptner, C; Trauner, M; Zatloukal, K | 1 |
Bardag-Gorce, F; French, BA; French, SW; Li, J; Lue, YH; Montgomery, RO; Nan, L; Riley, NE | 1 |
Bardag-Gorce, F; Dedes, J; French, BA; French, SW; Li, J; Nan, L; Wu, Y | 1 |
Choi, K; Khosla, C; Kosek, JC; Omary, MB; Siegel, M; Strnad, P; Toivola, DM | 1 |
Bardag-Gorce, F; French, BA; French, SW; Li, J; Oliva, J | 1 |
Abuja, PM; Kratky, D; Lackner, C; Nikam, A; Patankar, JV; Schöck, E; Zatloukal, K | 1 |
Haybaeck, J; Kufferath, I; Landegren, U; Thueringer, A; Zatloukal, B; Zatloukal, K | 1 |
Boor, P; Couchy, G; Guldiken, N; Kobazi Ensari, G; Lahiri, P; Liedtke, C; Preisinger, C; Strnad, P; Trautwein, C; Zimmermann, HW; Ziol, M; Zucman-Rossi, J | 1 |
18 other study(ies) available for dicarbethoxydihydrocollidine and bromochloroacetic acid
Article | Year |
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Cytoskeletal alterations leading to Mallory body formation in livers of mice fed 3,5-diethoxycarbonyl-1,4-dihydrocollidine.
Topics: Animals; Cytoskeleton; Dicarbethoxydihydrocollidine; Dihydropyridines; Fluorescent Antibody Technique; Intermediate Filaments; Keratins; Liver; Male; Mice; Microscopy, Electron | 1987 |
Mallory body filaments become insoluble after normal assembly into intermediate filaments.
Topics: Animals; Dicarbethoxydihydrocollidine; Electrophoresis, Polyacrylamide Gel; Inclusion Bodies; Intermediate Filaments; Keratins; Liver; Male; Mice | 1994 |
Mallory body induction in drug-primed mouse liver.
Topics: Animals; Blotting, Western; Dihydropyridines; Griseofulvin; Inclusion Bodies; Keratins; Liver; Male; Mice; Mice, Inbred C3H; Microscopy, Electron; Proteins | 1996 |
Mechanisms of mallory body formation induced by okadaic acid in drug-primed mice.
Topics: Animals; Blotting, Western; Dicarbethoxydihydrocollidine; Electrophoresis, Polyacrylamide Gel; Enzyme Inhibitors; Immunoenzyme Techniques; Inclusion Bodies; Keratins; Liver; Male; Mice; Mice, Inbred C3H; NF-kappa B; Okadaic Acid; Phosphothreonine | 1998 |
Hepatocyte cytokeratins are hyperphosphorylated at multiple sites in human alcoholic hepatitis and in a mallory body mouse model.
Topics: Animals; Dicarbethoxydihydrocollidine; Hepatitis, Alcoholic; Humans; Inclusion Bodies; Keratins; Liver; Male; Mice; Phosphorylation | 2000 |
Cytokeratin 8 protects from hepatotoxicity, and its ratio to cytokeratin 18 determines the ability of hepatocytes to form Mallory bodies.
Topics: Animals; Bile Ducts; Chemical and Drug Induced Liver Injury; Cytoplasm; Cytoskeleton; Dicarbethoxydihydrocollidine; Epithelium; Keratin-7; Keratins; Liver; Liver Diseases; Mice; Mice, Inbred Strains; Mice, Knockout | 2000 |
Dexamethasone enhances mallory body formation in drug-primed mouse liver.
Topics: Animals; Blotting, Western; Dexamethasone; Dihydropyridines; Electrophoresis, Polyacrylamide Gel; Glucocorticoids; Inclusion Bodies; Keratins; Liver; Male; Mice; Mice, Inbred C3H; Microscopy, Electron; NF-kappa B; Proto-Oncogene Proteins c-myc | 2000 |
Sequence of events in the assembly of Mallory body components in mouse liver: clues to the pathogenesis and significance of Mallory body formation.
Topics: Animals; Antigens, Surface; Colchicine; Dicarbethoxydihydrocollidine; Griseofulvin; Immunohistochemistry; Inclusion Bodies; Keratin-8; Keratins; Liver; Lumicolchicines; Male; Mice; Phosphorylation; RNA, Messenger; Time Factors; Ubiquitin | 2001 |
Mallory body--a disease-associated type of sequestosome.
Topics: Adaptor Proteins, Signal Transducing; Animals; Antibodies; Biopsy; Blotting, Northern; Blotting, Western; Carrier Proteins; Chemical and Drug Induced Liver Injury; Dicarbethoxydihydrocollidine; Humans; Immediate-Early Proteins; Inclusion Bodies; Keratins; Liver; Liver Diseases; Male; Mice; Microscopy, Immunoelectron; Proteins; RNA, Messenger; Sequestosome-1 Protein; Transcription Factor TFIIH; Transcription Factors; Ubiquitin | 2002 |
The role of the ubiquitin-proteasome pathway in the formation of mallory bodies.
Topics: Adenosine Triphosphatases; Administration, Oral; Animals; Blotting, Western; Cell-Free System; Chlormethiazole; Cysteine Endopeptidases; Cytochrome P-450 CYP2E1 Inhibitors; Dihydropyridines; Enzyme Inhibitors; Hepatocytes; Inclusion Bodies; Keratins; Liver; Male; Mice; Mice, Inbred C3H; Mice, Inbred Strains; Multienzyme Complexes; Peptide Hydrolases; Proteasome Endopeptidase Complex; Protein Biosynthesis; Proteins; Ubiquitins | 2002 |
Bile acid-induced Mallory body formation in drug-primed mouse liver.
Topics: Animals; Bile Acids and Salts; Bile Ducts; Cholestasis; Cholic Acid; Dicarbethoxydihydrocollidine; Diet; Hepatocytes; Humans; Inclusion Bodies; Keratins; Ligation; Liver; Male; Mice; Phosphorylation; Ubiquitin | 2002 |
The proteasome inhibitor, PS-341, causes cytokeratin aggresome formation.
Topics: Actins; Animals; Boronic Acids; Bortezomib; Cell Membrane; Cells, Cultured; Chlormethiazole; Dicarbethoxydihydrocollidine; Disease Models, Animal; Dose-Response Relationship, Drug; Fluorescent Antibody Technique; Fluorescent Antibody Technique, Indirect; Hepatocytes; Inclusion Bodies; Keratins; Male; Membrane Proteins; Mice; Mice, Inbred C3H; Microscopy, Confocal; Phosphoproteins; Protease Inhibitors; Pyrazines; Zonula Occludens-1 Protein | 2004 |
Mallory body (cytokeratin aggresomes) formation is prevented in vitro by p38 inhibitor.
Topics: Animals; Blotting, Western; Cell Adhesion Molecules; Dihydropyridines; Fluorescent Antibody Technique; Hepatocytes; In Vitro Techniques; Inclusion Bodies; Keratins; Male; Mice; Mice, Inbred C3H; Oligonucleotide Array Sequence Analysis; p38 Mitogen-Activated Protein Kinases; Phosphorylation; Protein Kinase Inhibitors; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2006 |
Pharmacologic transglutaminase inhibition attenuates drug-primed liver hypertrophy but not Mallory body formation.
Topics: Animals; Cell Size; Chemical and Drug Induced Liver Injury; Dicarbethoxydihydrocollidine; Enzyme Inhibitors; GTP-Binding Proteins; Hepatomegaly; Humans; Inclusion Bodies; Isoxazoles; Keratins; Liver Diseases; Mice; Mice, Inbred C3H; Protein Glutamine gamma Glutamyltransferase 2; Proteins; Transglutaminases | 2006 |
SAMe prevents the induction of the immunoproteasome and preserves the 26S proteasome in the DDC-induced MDB mouse model.
Topics: Animals; Base Sequence; Cysteine Endopeptidases; Dihydropyridines; Disease Models, Animal; DNA Primers; Gene Expression; Inclusion Bodies; Keratins; Liver; Liver Diseases, Alcoholic; Male; Mice; Mice, Inbred C3H; Multienzyme Complexes; Proteasome Endopeptidase Complex; S-Adenosylmethionine; Ubiquitin; Ubiquitins | 2010 |
Transition between acute and chronic hepatotoxicity in mice is associated with impaired energy metabolism and induction of mitochondrial heme oxygenase-1.
Topics: Acute Disease; Adaptor Proteins, Signal Transducing; Adenosine Triphosphate; Animals; Body Weight; Chemical and Drug Induced Liver Injury; Chemical and Drug Induced Liver Injury, Chronic; Energy Metabolism; Enzyme Induction; Gene Expression; Heat-Shock Proteins; Heme Oxygenase-1; Hepatocytes; Keratins; Liver; Male; Mallory Bodies; Mice; Mitochondria; Oxidative Stress; Protein Folding; Pyridines; Sequestosome-1 Protein; Time Factors | 2013 |
Sensitivity and specificity of in situ proximity ligation for protein interaction analysis in a model of steatohepatitis with Mallory-Denk bodies.
Topics: Animals; Cytoplasm; Disease Models, Animal; Fatty Liver; Genetic Techniques; Hepatocytes; Keratins; Liver; Male; Mallory Bodies; Mice; Mice, Transgenic; Microscopy, Fluorescence; Protein Interaction Mapping; Protein Processing, Post-Translational; Pyridines; Reproducibility of Results; Transcription Factor TFIIH; Transcription Factors | 2014 |
Keratin 23 is a stress-inducible marker of mouse and human ductular reaction in liver disease.
Topics: Animals; Humans; Keratins; Keratins, Type I; Liver; Liver Diseases; Mice; Pyridines | 2016 |