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Carnitine palmitoyl transferase 1A deficiency

Known as: CPT 1A Deficiency, CPT Deficiency, Hepatic, Type I, Carnitine palmitoyltransferase 1 deficiency 
A rare autosomal recessive inherited disorder caused by mutations in the CPT1A gene. It is characterized by the presence of defective carnitine… 
National Institutes of Health

Papers overview

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Highly Cited
2018
Highly Cited
2018
Background Post-traumatic stress disorder (PTSD) is a debilitating disorder, and current treatments leave the majority of… 
Highly Cited
2014
Highly Cited
2014
Lycium barbarum polysaccharide (LBP) is well known in traditional Chinese herbal medicine that, has beneficial effects. Previous… 
Highly Cited
2010
Highly Cited
2010
OBJECTIVE We examined in insulin-resistant muscle if, in contrast to long-standing dogma, mitochondrial fatty acid oxidation is… 
Highly Cited
2008
Highly Cited
2008
Peroxisome proliferator‐activated receptors (PPARs) alter the expression of genes involved in regulating lipid metabolism… 
Highly Cited
2005
Highly Cited
2005
PurposeThe multidrug resistance associated protein (MRP) 4 is a member of the adenosine triphosphate (ATP)-binding cassette… 
Highly Cited
2005
Highly Cited
2005
The rate of cardiac fatty acid oxidation is regulated by the activity of carnitine palmitoyltransferase-I (CPT-I), which is… 
Highly Cited
2004
Highly Cited
2004
Obesity and its attendant disorders, such as type 2 diabetes, are global health problems. We previously reported that C75, an… 
1985
1985
Abstract The oral hypoglycemic agent, methyl 2-tetradecylglycidate (Me-TDGA), which inhibits in vitro mitochondrial carnitine…