Skip to search formSkip to main contentSkip to account menu

isoleucine catabolic process

Known as: isoleucine breakdown, isoleucine catabolism, isoleucine degradation 
The chemical reactions and pathways resulting in the breakdown of isoleucine, (2R*,3R*)-2-amino-3-methylpentanoic acid. [GOC:ai]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A five‐miRNA expression signature predicts survival in hepatocellular carcinoma
The aim of this study was to identify a microRNA (miRNA) expression signature for predicting HCC (hepatocellular carcinoma… 
2011
2011
Transcriptional profiling analysis of HMP-treated rats with experimentally induced myocardial infarction.
1997
1997
[Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in Argentina].
From the description of two pairs of siblings belonging to unrelated families, one Argentine family with a history of… 
1992
1992
A new case of succinyl-CoA: Acetoacetate transferase deficiency
Succinyl-CoA transferase deficiency (McKusick 245050) is a rare inherited metabolic disease affecting ketone body utilization in… 
1992
1992
A coupled assay detecting defects in fibroblast isoleucine degradation distal to enoyl-CoA hydratase: application to 3-oxothiolase deficiency.
1987
1987
β-Ketothiolase deficiency: Two siblings with different clinical conditions
[3-Ketothiolase deficiency .(McKusick 20375) is an uncommon inborn error of isoleucine catabolism, characterized by the excretion… 
1979
1979
Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels
An 11-year old girl with spastic paraplegia and mental retardation has suffered from attacks of metabolic acidosis since the age… 
1978
1978
Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia
Two patients with methylmalonic acidaemia due to methylmalonyl-CoA mutase deficiency were studied for several years. Both… 
1974
1974
Possibility of inborn defect in isovalericacidaemia involving altered enzyme specificity rather than total inactivity
TANAKA, Isselbacher and colleagues1 have described an inherited metabolic defect, isovalericacidaemia, which, though not fatal in… 
1973
1973
Inhibition of Glycine Oxidation in Cultured Fibroblasts by Isoleucine
Extract: Cultured fibroblasts were shown to oxidize glycine to CO2-Isoleucine (10 mM) inhibited glycine oxidation to CO2 by about… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)