Skip to search formSkip to main contentSkip to account menu

Carnitine Palmitoyltransferase II

Known as: CPT II, II, Carnitine Palmitoyltransferase, Palmitoyltransferase II, Carnitine 
National Institutes of Health

Related topics

Related topics

3 relations
CPT2 geneCarnitine palmitoyl transferase 2 deficiency

Broader (1)

Carnitine O-Palmitoyltransferase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza‐associated encephalopathy
Influenza‐associated encephalopathy (IAE) is characterized by persistent high fever, febrile convulsions, severe brain edema, and… 
2000
2000
A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene.
Adult-onset carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive disease characterized by muscle pain… 
Highly Cited
1998
Highly Cited
1998
Carnitine palmitoyltransferase I, carnitine palmitoyltransferase II, and Acyl-CoA oxidase activities in atlantic salmon (Salmo salar)
Salmon farmers are currently using high-energy feeds containing up to 35% fat; the fish's capability of fully utilizing these… 
1998
1998
Carnitine palmitoyltransferase II specificity towards beta-oxidation intermediates--evidence for a reverse carnitine cycle in mitochondria.
Using isolated rat liver mitochondria, in the absence or presence of malonyl-CoA (an inhibitor of carnitine palmitoyltransferase… 
1998
1998
A novel mutation identified in carnitine palmitoyltransferase II deficiency.
Carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive disorder of mitochondrial fatty-acid oxidation… 
Highly Cited
1996
Highly Cited
1996
Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression.
Carnitine palmitoyltransferase (CPT) II deficiency, an inherited disorder of mitochondrial long-chain fatty-acid (LCFA) oxidation… 
Highly Cited
1994
Highly Cited
1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32.
In the study reported here, a new set of FISH experiments was carried out with the two positively identified CPT1-specific probes… 
Highly Cited
1991
Highly Cited
1991
Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II.
IN adults, deficiency of carnitine palmitoyltransferase (CPT) II is a genetic disorder characterized by exercise intolerance and… 
Highly Cited
1991
Highly Cited
1991
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
Reported cases of carnitine palmitoyltransferase II (CPT II) deficiency are characterized only by a muscular symptomatology in… 
Highly Cited
1987
Highly Cited
1987
Characterization of the mitochondrial carnitine palmitoyltransferase enzyme system. I. Use of inhibitors.
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)