3,7,12-trihydroxycoprostanic acid has been researched along with Liver Diseases in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Witzleben, CL | 1 |
| Casteels, M; Mannaerts, GP; Przyrembel, H; Schutgens, RB; van Roermund, CW; Wanders, RJ | 1 |
| Hoshita, T; Tada, K; Tazawa, Y; Une, M | 1 |
| Björkhem, I; Hågå, P; Kase, BF; Pedersen, JI | 1 |
| Björkhem, I; Kase, BF; Pedersen, JI; Strandvik, B | 1 |
5 other study(ies) available for 3,7,12-trihydroxycoprostanic acid and Liver Diseases
| Article | Year |
|---|---|
Bile duct paucity ("intrahepatic atresia").
Topics: alpha 1-Antitrypsin Deficiency; Bile Ducts; Bile Ducts, Intrahepatic; Child; Child, Preschool; Cholestasis; Cholic Acids; Chromosome Aberrations; Chromosome Disorders; Diagnosis, Differential; Graft vs Host Reaction; Humans; Infant; Infant, Newborn; Liver; Liver Diseases; Syndrome; Virus Diseases | 1982 |
Di- and trihydroxycholestanoic acidaemia with hepatic failure.
Topics: Acatalasia; Bile Acids and Salts; Cholestanols; Cholic Acids; Fatty Acids; Humans; Infant; Liver Diseases; Male; Oxidoreductases | 1990 |
Occurrence of both (25R)- and (25S)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acids in urine from an infant with Zellweger's syndrome.
Topics: Bile Acids and Salts; Brain Diseases; Cholic Acids; Chromatography, Gas; Gas Chromatography-Mass Spectrometry; Humans; Infant; Kidney Diseases; Liver Diseases; Male; Mass Spectrometry; Stereoisomerism; Syndrome | 1987 |
Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger.
Topics: Bile; Bile Acids and Salts; Cholic Acid; Cholic Acids; Female; Humans; Infant, Newborn; Kidney Diseases; Liver; Liver Diseases; Microbodies; Syndrome | 1985 |
In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid.
Topics: Bile Acids and Salts; Chenodeoxycholic Acid; Cholestenones; Cholic Acid; Cholic Acids; Humans; Kinetics; Liver Diseases; Metabolic Clearance Rate; Microbodies; Subcellular Fractions; Syndrome | 1985 |