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Carnitine palmitoyltransferases 1 and 2: biochemical, molecular and medical aspects

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inferredcites →https://doi.org/10.1001/archneur.1989.00520410111034openalex-snapshot
Chronic Myopathy With a Partial Deficiency of the Carnitine Palmityltransferase Enzyme
inferredcites →https://doi.org/10.1001/archneur.1989.00520430115027openalex-snapshot
An Unusual Case of Carnitine Palmitoyl Transferase Deficiency
inferredcites →https://doi.org/10.1002/(sici)1097-4598(199907)22:7<941::aid-mus20>3.0.co;2-zopenalex-snapshot
Molecular analysis in spanish patients with muscle carnitine palmitoyltransferase deficiency
inferredcites →https://doi.org/10.1002/(sici)1098-1004(1998)11:5<377::aid-humu5>3.0.co;2-eopenalex-snapshot
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: Functional analysis and association with polymorphic haplotypes and two clinical phenotypes
inferredcites →https://doi.org/10.1002/(sici)1098-1004(1999)13:3<210::aid-humu5>3.0.co;2-0openalex-snapshot
Novel mutations associated with carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1002/1098-1004(200006)15:6<579::aid-humu14>3.0.co;2-hopenalex-snapshot
Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1002/ajmg.1457openalex-snapshot
Antenatal presentation of carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1002/humu.10201openalex-snapshot
Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency
inferredcites →https://doi.org/10.1002/mus.10217openalex-snapshot
Phenotypic variability among first‐degree relatives with carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1002/mus.880160509openalex-snapshot
Carnitine palmitoyl transferase deficiency in malignant hyperthermia
inferredcites →https://doi.org/10.1002/pd.713openalex-snapshot
Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach
inferredcites →https://doi.org/10.1006/abio.2001.5554openalex-snapshot
Tandem Mass Spectrometric Assay for the Determination of Carnitine Palmitoyltransferase II Activity in Muscle Tissue
inferredcites →https://doi.org/10.1006/bbrc.2001.5201openalex-snapshot
Carnitine Palmitoyl Transferase I and the Control of β-Oxidation in Heart Mitochondria
inferredcites →https://doi.org/10.1006/geno.1994.1605openalex-snapshot
Assignment of the Human Carnitine Palmitoyltransferase II Gene (CPT1) to Chromosome 1p32
inferredcites →https://doi.org/10.1006/geno.1996.4539openalex-snapshot
Fine Chromosome Mapping of the Genes for Human Liver and Muscle Carnitine Palmitoyltransferase I (CPT1A and CPT1B)
inferredcites →https://doi.org/10.1006/geno.2002.6845openalex-snapshot
A Novel Brain-Expressed Protein Related to Carnitine Palmitoyltransferase I
inferredcites →https://doi.org/10.1006/jmcc.2000.1304openalex-snapshot
Differential Regulation of Carnitine Palmitoyltransferase-I Gene Isoforms (CPT-I and CPT-I ) in the Rat Heart
inferredcites →https://doi.org/10.1006/mgme.1997.2656openalex-snapshot
A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency
inferredcites →https://doi.org/10.1006/mgme.1998.2711openalex-snapshot
Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency
inferredcites →https://doi.org/10.1006/mgme.1999.2938openalex-snapshot
Carnitine Palmitoyltransferase Deficiencies
inferredcites →https://doi.org/10.1006/mgme.2000.3009openalex-snapshot
A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene
inferredcites →https://doi.org/10.1006/mgme.2001.3149openalex-snapshot
Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a DNA-Based Newborn Screening Program
inferredcites →https://doi.org/10.1006/mgme.2001.3176openalex-snapshot
Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community
inferredcites →https://doi.org/10.1006/mgme.2001.3281openalex-snapshot
A Novel Nonsense Mutation (515del4) in Muscle Carnitine Palmitoyltransferase II Deficiency
inferredcites →https://doi.org/10.1007/0-306-46818-2_9openalex-snapshot
Kinetic Investigation of Carnitine Palmitoyltransferases in Homogenates of Human Skeletal Muscle Using L-amino-Carnitine and Malonyl-CoA
inferredcites →https://doi.org/10.1007/bf00710434openalex-snapshot
Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onset
inferredcites →https://doi.org/10.1007/bf01800021openalex-snapshot
Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase‐1 deficiency
inferredcites →https://doi.org/10.1007/bf01956748openalex-snapshot
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia
inferredcites →https://doi.org/10.1007/bf02185756openalex-snapshot
Inheritance of the S113L mutation within an inbred family with carnitine palmitoyltransferase enzyme deficiency
inferredcites →https://doi.org/10.1007/s001340100985openalex-snapshot
Recurrent rhabdomyolysis and acute respiratory failure due to carnitine palmityltransferase deficiency
inferredcites →https://doi.org/10.1007/s004310100802openalex-snapshot
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old child
inferredcites →https://doi.org/10.1007/s00439-002-0752-0openalex-snapshot
Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia
inferredcites →https://doi.org/10.1007/s004390050170openalex-snapshot
Two novel gene mutations (Glu174→Lys, Phe383→Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1007/s100380200047openalex-snapshot
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
inferredcites →https://doi.org/10.1007/s100380300001openalex-snapshot
A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiency
inferredcites →https://doi.org/10.1016/0003-2697(72)90061-9openalex-snapshot
A rapid spectrophotometric assay for carnitine palmitoyltransferase
inferredcites →https://doi.org/10.1016/0014-5793(93)81007-mopenalex-snapshot
Mature carnitine palmitoyltransferase I retains the N‐terminus of the nascent protein in rat liver
inferredcites →https://doi.org/10.1016/0014-5793(95)00277-gopenalex-snapshot
High expression of a novel carnitine palmitoyltransferase I like protein in rat brown adipose tissue and heart: isolation and characterization of its cDNA clone
inferredcites →https://doi.org/10.1016/0022-510x(89)90139-1openalex-snapshot
Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts
inferredcites →https://doi.org/10.1016/0022-510x(94)00223-bopenalex-snapshot
Atypical presentation of carnitine palmitoyltransferase (CPT) deficiency as status epilepticus
inferredcites →https://doi.org/10.1016/0167-4781(96)00069-3openalex-snapshot
Isolation and characterization of cDNA and genomic clones encoding human muscle type carnitine palmitoyltransferase I
inferredcites →https://doi.org/10.1016/0387-7604(94)90051-5openalex-snapshot
Central nervous system disorders and possible brain type carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1016/0887-8994(87)90056-7openalex-snapshot
Carnitine palmityltransferase deficiency with permanent weakness
inferredcites →https://doi.org/10.1016/0926-6569(64)90103-8openalex-snapshot
Palmityl-coa:carnitine palmityltransferase
inferredcites →https://doi.org/10.1016/j.ymgme.2004.02.004openalex-snapshot
Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency
inferredcites →https://doi.org/10.1016/s0009-8981(98)00041-2openalex-snapshot
Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiency
inferredcites →https://doi.org/10.1016/s0014-5793(97)00561-9openalex-snapshot
Structural features of the gene encoding human muscle type carnitine palmitoyltransferase I1
inferredcites →https://doi.org/10.1016/s0021-9258(17)32300-1openalex-snapshot
Malonyl-CoA-sensitive and -insensitive carnitine palmitoyltransferase activities of microsomes are due to different proteins
inferredcites →https://doi.org/10.1016/s0021-9258(17)34693-8openalex-snapshot
Carnitine palmitoyltransferase I. The site of inhibition of hepatic fatty acid oxidation by malonyl-CoA.
inferredcites →https://doi.org/10.1016/s0021-9258(18)48007-6openalex-snapshot
Characterization of the mitochondrial carnitine palmitoyltransferase enzyme system. II. Use of detergents and antibodies.
inferredcites →https://doi.org/10.1016/s0021-9258(18)53392-5openalex-snapshot
Cloning, sequencing, and expression of a cDNA encoding rat liver carnitine palmitoyltransferase I. Direct evidence that a single polypeptide is involved in inhibitor interaction and catalytic function.
inferredcites →https://doi.org/10.1016/s0021-9258(18)67896-2openalex-snapshot
Carnitine in Intermediary Metabolism
inferredcites →https://doi.org/10.1016/s0021-9258(18)87005-3openalex-snapshot
Inter-tissue and inter-species characteristics of the mitochondrial carnitine palmitoyltransferase enzyme system.
inferredcites →https://doi.org/10.1016/s0021-9258(18)87006-5openalex-snapshot
Cloning, sequencing, and expression of a cDNA encoding rat liver mitochondrial carnitine palmitoyltransferase II.
inferredcites →https://doi.org/10.1016/s0021-9258(19)68001-4openalex-snapshot
Properties of Partially Purified Carnitine Acetyltransferase
inferredcites →https://doi.org/10.1016/s0022-2275(20)31604-7openalex-snapshot
Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme
inferredcites →https://doi.org/10.1016/s0022-3476(05)83187-7openalex-snapshot
Carnitine palmitoyltransferase II deficiency: A new cause of recurrent pancreatitis
inferredcites →https://doi.org/10.1016/s0022-3476(09)90019-1openalex-snapshot
Recurrent metabolic decompensation in profound carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1016/s0022-3476(81)80834-7openalex-snapshot
Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency
inferredcites →https://doi.org/10.1016/s0167-4838(01)00147-9openalex-snapshot
Molecular enzymology of carnitine transfer and transport
inferredcites →https://doi.org/10.1016/s0887-8994(99)00125-3openalex-snapshot
Muscular carnitine palmitoyltransferase II deficiency in infancy
inferredcites →https://doi.org/10.1016/s0960-8966(01)00228-0openalex-snapshot
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency
inferredcites →https://doi.org/10.1016/s0960-8966(99)00096-6openalex-snapshot
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient
inferredcites →https://doi.org/10.1016/s1096-7192(03)00067-2openalex-snapshot
A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1021/jm010889+openalex-snapshot
Reversible Carnitine Palmitoyltransferase Inhibitors with Broad Chemical Diversity as Potential Antidiabetic Agents
inferredcites →https://doi.org/10.1023/a:1005552106301openalex-snapshot
Defects in activation and transport of fatty acids
inferredcites →https://doi.org/10.1023/a:1005556207210openalex-snapshot
Recognition and management of fatty acid oxidation defects: A series of 107 patients
inferredcites →https://doi.org/10.1023/a:1005606805951openalex-snapshot
Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile
inferredcites →https://doi.org/10.1023/a:1005694320063openalex-snapshot
Features of carnitine palmitoyltransferase type I deficiency
inferredcites →https://doi.org/10.1023/a:1007221708765openalex-snapshot
Participation of carnitine palmitoyltransferase in the synthesis of dipalmitoylphosphatidylcholine in rat alveolar type II cells
inferredcites →https://doi.org/10.1023/a:1012476029536openalex-snapshot
Lethal neonatal presentation of carnitine palmitoyltransferase I deficiency
inferredcites →https://doi.org/10.1023/a:1015109127986openalex-snapshot
Screening for Carnitine Palmitoyltransferase II Deficiency by Tandem Mass Spectrometry
inferredcites →https://doi.org/10.1023/a:1025947930752openalex-snapshot
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency
inferredcites →https://doi.org/10.1038/ng0793-314openalex-snapshot
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
inferredcites →https://doi.org/10.1038/nm873openalex-snapshot
Inhibition of hypothalamic carnitine palmitoyltransferase-1 decreases food intake and glucose production
inferredcites →https://doi.org/10.1042/0300-5127:0290287openalex-snapshot
Structure-function relationships of the liver and muscle isoforms of carnitine palmitoyltransferase I
inferredcites →https://doi.org/10.1042/0300-5127:0290310openalex-snapshot
Regulation of liver carnitine palmitoyltransferase I gene expression by hormones and fatty acids
inferredcites →https://doi.org/10.1042/bj1190547openalex-snapshot
Carnitine palmitoyltransferase activities (EC 2.3.1.–) of rat liver mitochondria
inferredcites →https://doi.org/10.1042/bj1300697openalex-snapshot
The activities of lipases and carnitine palmitoyl-transferase in muscles from vertebrates and invertebrates
inferredcites →https://doi.org/10.1042/bj20020851openalex-snapshot
Control of human carnitine palmitoyltransferase II gene transcription by peroxisome proliferator-activated receptor through a partially conserved peroxisome proliferator-responsive element
inferredcites →https://doi.org/10.1042/bj20031373openalex-snapshot
Structural model of carnitine palmitoyltransferase I based on the carnitine acetyltransferase crystal
inferredcites →https://doi.org/10.1042/bj2940645openalex-snapshot
Comparison of the active sites of the purified carnitine acyltransferases from peroxisomes and mitochondria by using a reaction-intermediate analogue
inferredcites →https://doi.org/10.1042/bj3000583openalex-snapshot
Expression of liver carnitine palmitoyltransferase I and II genes during development in the rat
inferredcites →https://doi.org/10.1042/bj3270225openalex-snapshot
Mouse white adipocytes and 3T3-L1 cells display an anomalous pattern of carnitine palmitoyltransferase (CPT) I isoform expression during differentiation: Inter-tissue and inter-species expression of CPT I and CPT II enzymes
inferredcites →https://doi.org/10.1042/bj3340225openalex-snapshot
Expression of novel isoforms of carnitine palmitoyltransferase I (CPT-1) generated by alternative splicing of the CPT-Iβ gene
inferredcites →https://doi.org/10.1046/j.1526-4610.2003.03095.xopenalex-snapshot
Carnitine Palmityltransferase II (CPT2) Deficiency and Migraine Headache: Two Case Reports
inferredcites →https://doi.org/10.1055/s-2003-37952openalex-snapshot
Lethal Neonatal Carnitine Palmitoyltransferase II Deficiency: An Unusual Presentation of a Rare Disorder
inferredcites →https://doi.org/10.1055/s-2008-1065012openalex-snapshot
Abnorme Regulation der Carnitin-Palmitoyltransferase bei eineiigen Zwillingen als Ursache einer Rhabdomyolyse
inferredcites →https://doi.org/10.1056/nejm199112263252607openalex-snapshot
Lethal Neonatal Multiorgan Deficiency of Carnitine Palmitoyltransferase II
inferredcites →https://doi.org/10.1056/nejm199207023270105openalex-snapshot
Renal Tubular Acidosis in Carnitine Palmitoyltransferase Type 1 Deficiency
inferredcites →https://doi.org/10.1067/mpd.2002.128545openalex-snapshot
Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutations
inferredcites →https://doi.org/10.1073/pnas.54.4.1226openalex-snapshot
The role of acylcarnitine esters and carnitine palmityltransferase in the transport of fatty acyl groups across mitochondrial membranes.
inferredcites →https://doi.org/10.1073/pnas.72.3.883openalex-snapshot
A mitochondrial carnitine acylcarnitine translocase system.
inferredcites →https://doi.org/10.1073/pnas.84.2.378openalex-snapshot
Malonyl-CoA binding site and the overt carnitine palmitoyltransferase activity reside on the opposite sides of the outer mitochondrial membrane.
inferredcites →https://doi.org/10.1073/pnas.89.18.8429openalex-snapshot
Molecular characterization of inherited carnitine palmitoyltransferase II deficiency.
inferredcites →https://doi.org/10.1073/pnas.92.6.1984openalex-snapshot
Human liver mitochondrial carnitine palmitoyltransferase I: characterization of its cDNA and chromosomal localization and partial analysis of the gene.
inferredcites →https://doi.org/10.1074/jbc.270.15.8952openalex-snapshot
Mitochondrial Carnitine Palmitoyltransferase I Isoform Switching in the Developing Rat Heart
inferredcites →https://doi.org/10.1074/jbc.270.2.530openalex-snapshot
Evidence for Intermediate Channeling in Mitochondrial β -Oxidation
inferredcites →https://doi.org/10.1074/jbc.271.12.6972openalex-snapshot
Expression of a cDNA Isolated from Rat Brown Adipose Tissue and Heart Identifies the Product as the Muscle Isoform of Carnitine Palmitoyltransferase I (M-CPT I)
inferredcites →https://doi.org/10.1074/jbc.273.45.29896openalex-snapshot
The N-terminal Domain of Rat Liver Carnitine Palmitoyltransferase 1 Mediates Import into the Outer Mitochondrial Membrane and Is Essential for Activity and Malonyl-CoA Sensitivity
inferredcites →https://doi.org/10.1074/jbc.273.49.32901openalex-snapshot
Co-regulation of Tissue-specific Alternative Human Carnitine Palmitoyltransferase Iβ Gene Promoters by Fatty Acid Enzyme Substrate
inferredcites →https://doi.org/10.1074/jbc.m106920200openalex-snapshot
Structural Model of the Catalytic Core of Carnitine Palmitoyltransferase I and Carnitine Octanoyltransferase (COT)
inferredcites →https://doi.org/10.1074/jbc.m203189200openalex-snapshot
Structural and Functional Genomics of the CPT1B Gene for Muscle-type Carnitine Palmitoyltransferase I in Mammals
inferredcites →https://doi.org/10.1074/jbc.m310130200openalex-snapshot
Functional and Structural Basis of Carnitine Palmitoyltransferase 1A Deficiency
inferredcites →https://doi.org/10.1093/clinchem/47.10.1763openalex-snapshot
Hepatic Carnitine Palmitoyltransferase I Deficiency: Acylcarnitine Profiles in Blood Spots Are Highly Specific
inferredcites →https://doi.org/10.1093/hmg/2.3.334openalex-snapshot
Two novel sequence polymorphisms of the human carnitine palmitoyltransferase II (CPT1) gene
inferredcites →https://doi.org/10.1093/hmg/4.1.19openalex-snapshot
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations
inferredcites →https://doi.org/10.1097/01.lab.0000098428.51765.83openalex-snapshot
Carnitine Palmitoyltransferase II Deficiency: A Clinical, Biochemical, and Molecular Review
inferredcites →https://doi.org/10.1111/j.1432-1033.1997.00001.xopenalex-snapshot
The Mitochondrial Carnitine Palmitoyltransferase System — From Concept to Molecular Analysis
inferredcites →https://doi.org/10.1126/science.182.4115.929openalex-snapshot
Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria
inferredcites →https://doi.org/10.1126/science.288.5475.2379openalex-snapshot
Reduced Food Intake and Body Weight in Mice Treated with Fatty Acid Synthase Inhibitors
inferredcites →https://doi.org/10.1136/jnnp.50.8.1060openalex-snapshot
Carnitine palmitoyl transferase deficiency with an atypical presentation and ultrastructural mitochondrial abnormalities.
inferredcites →https://doi.org/10.1136/jnnp.62.2.169openalex-snapshot
Characterisation of carnitine palmitoyltransferases in patients with a carnitine palmitoyltransferase deficiency: implications for diagnosis and therapy.
inferredcites →https://doi.org/10.1139/o71-136openalex-snapshot
Properties of a Purified Carnitine Palmitoyltransferase, and Evidence for the Existence of Other Carnitine Acyltransferases
inferredcites →https://doi.org/10.1152/ajpendo.2001.280.2.e270openalex-snapshot
A potent PPARα agonist stimulates mitochondrial fatty acid β-oxidation in liver and skeletal muscle
inferredcites →https://doi.org/10.1161/01.res.0000060700.55247.7copenalex-snapshot
Peroxisome Proliferator-Activated Receptor (PPAR) α and PPARβ/δ, but not PPARγ, Modulate the Expression of Genes Involved in Cardiac Lipid Metabolism
inferredcites →https://doi.org/10.1172/jci113863openalex-snapshot
Cytoplasmic pH regulation and chloride/bicarbonate exchange in avian osteoclasts.
inferredcites →https://doi.org/10.1172/jci113978openalex-snapshot
Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation.
inferredcites →https://doi.org/10.1172/jci115090openalex-snapshot
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
inferredcites →https://doi.org/10.1172/jci15311openalex-snapshot
Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride
inferredcites →https://doi.org/10.1172/jci15715openalex-snapshot
Malonyl coenzyme A and the regulation of functional carnitine palmitoyltransferase-1 activity and fat oxidation in human skeletal muscle
inferredcites →https://doi.org/10.1172/jci2927openalex-snapshot
Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.
inferredcites →https://doi.org/10.1177/088307380001500607openalex-snapshot
Novel Mutation in the CPT II Gene in a Child With Periodic Febrile Myalgia and Myoglobinuria
inferredcites →https://doi.org/10.1177/088307388900400310openalex-snapshot
Deficiency of Carnitine Palmitoyltransferase I
inferredcites →https://doi.org/10.1201/b13565-47openalex-snapshot
Carnitine palmitoyl transferase I deficiency
inferredcites →https://doi.org/10.1203/00006450-198809000-00006openalex-snapshot
Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities
inferredcites →https://doi.org/10.1203/00006450-199005000-00016openalex-snapshot
Immunoquantitative Analysis of Human Carnitine Palmitoyltransferase I and II Defects
inferredcites →https://doi.org/10.1203/00006450-199411000-00007openalex-snapshot
Rate-Dependent Distal Renal Tubular Acidosis and Carnitine Palmitoyltransferase I Deficiency
inferredcites →https://doi.org/10.1203/00006450-199610000-00005openalex-snapshot
Complementation Analysis of Carnitine Palmitoyltransferase I and II Defects
inferredcites →https://doi.org/10.1203/00006450-200001000-00005openalex-snapshot
Metabolic Disease in the Fetus Predisposes to Maternal Hepatic Complications of Pregnancy
inferredcites →https://doi.org/10.1203/00006450-200001000-00010openalex-snapshot
Hepatic Carnitine Palmitoyltransferase I Deficiency Presenting as Maternal Illness in Pregnancy
inferredcites →https://doi.org/10.1203/01.pdr.0000083001.91588.bbopenalex-snapshot
Correction of Fatty Acid Oxidation in Carnitine Palmitoyl Transferase 2–Deficient Cultured Skin Fibroblasts by Bezafibrate
inferredcites →https://doi.org/10.1212/01.wnl.0000055901.58642.48openalex-snapshot
Carnitine palmitoyltransferase II deficiency
inferredcites →https://doi.org/10.1542/peds.107.6.e103openalex-snapshot
Detection of Neonatal Carnitine Palmitoyltransferase II Deficiency by Expanded Newborn Screening With Tandem Mass Spectrometry
inferredcites →https://doi.org/10.1542/peds.84.2.312openalex-snapshot
Fatal Rhabdomyolysis Following Influenza Infection in a Girl With Familial Carnitine Palmityl Transferase Deficiency
inferredcites →https://doi.org/10.2337/diab.43.7.878openalex-snapshot
More Direct Evidence for a Malonyl-CoA–Carnitine Palmitoyltransferase I Interaction as a Key Event in Pancreatic β-Cell Signaling

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Heterogeneity of fatty acid metabolism in breast cancer cells underlies differential sensitivity to palmitate‐induced apoptosis
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The FABP12/PPARγ pathway promotes metastatic transformation by inducing epithelial‐to‐mesenchymal transition and lipid‐derived energy production in prostate cancer cells
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Fatty Acid Oxidation Disorders
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Genetics and Liver Diseases
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Oxidative Stress and Protein Oxidation
inferred← citeshttps://doi.org/10.1002/advs.202411559openalex-snapshot
Mechanical Activation of cPLA2 Impedes Fatty Acid β‐Oxidation in Vein Grafts
inferred← citeshttps://doi.org/10.1002/ajmg.c.30087openalex-snapshot
Disorders of carnitine transport and the carnitine cycle
inferred← citeshttps://doi.org/10.1002/ajmg.c.30290openalex-snapshot
Newborn screening and inborn errors of metabolism
inferred← citeshttps://doi.org/10.1002/ddr.21770openalex-snapshot
Marein ameliorates Ang II /hypoxia‐induced abnormal glucolipid metabolism by modulating the HIF ‐1α/ PPARα /γ pathway in H9c2 cells
inferred← citeshttps://doi.org/10.1002/ddr.70014openalex-snapshot
The Role of Fatty Acid Metabolism, the Related Potential Biomarkers, and Targeted Therapeutic Strategies in Gastrointestinal Cancers
inferred← citeshttps://doi.org/10.1002/hep.25543openalex-snapshot
Argininosuccinate synthase conditions the response to acute and chronic ethanol-induced liver injury in mice
inferred← citeshttps://doi.org/10.1002/humu.20717openalex-snapshot
Thermal instability of compound variants of carnitine palmitoyltransferase II and impaired mitochondrial fuel utilization in influenza-associated encephalopathy
inferred← citeshttps://doi.org/10.1002/jbmr.2150openalex-snapshot
Palmitic Acid and DGAT1 Deficiency Enhance Osteoclastogenesis, while Oleic Acid-Induced Triglyceride Formation Prevents It
inferred← citeshttps://doi.org/10.1002/jcp.27042openalex-snapshot
Effects of carnitine palmitoyltransferases on cancer cellular senescence
inferred← citeshttps://doi.org/10.1002/jcp.29906openalex-snapshot
Carnitine palmitoyltransferase 1C reverses cellular senescence of MRC‐5 fibroblasts via regulating lipid accumulation and mitochondrial function
inferred← citeshttps://doi.org/10.1002/jcsm.12654openalex-snapshot
Effects of statins on mitochondrial pathways
inferred← citeshttps://doi.org/10.1002/jcsm.13065openalex-snapshot
Cathelicidin‐related antimicrobial peptide mediates skeletal muscle degeneration caused by injury and Duchenne muscular dystrophy in mice
inferred← citeshttps://doi.org/10.1002/jimd.12098openalex-snapshot
Implementation of a fast method for the measurement of carnitine palmitoyltransferase 2 activity in lymphocytes by tandem mass spectrometry as confirmation for newborn screening
inferred← citeshttps://doi.org/10.1002/jimd.12644openalex-snapshot
Exercise testing and prescription in patients with inborn errors of muscle energy metabolism
inferred← citeshttps://doi.org/10.1002/jimd.70057openalex-snapshot
Screening for Life: Perspectives From Adult Metabolic Specialists on Newborn Screening for Inherited Metabolic Diseases
inferred← citeshttps://doi.org/10.1002/jmd2.12243openalex-snapshot
Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development
inferred← citeshttps://doi.org/10.1002/mnfr.70342openalex-snapshot
Monascus pilosus SWM‐008–Fermented Red Mold Rice and Its Monascinol Ameliorate Non‐Alcoholic Fatty Liver Disease via Activation of the AMPK–ATGL Pathway and Enrichment of Butyrate‐Producing Bacteria
inferred← citeshttps://doi.org/10.1002/mrd.22505openalex-snapshot
Acetyl CoA carboxylase inactivation and meiotic maturation in mouse oocytes
inferred← citeshttps://doi.org/10.1002/mrm.25485openalex-snapshot
Metabolic imaging of hyperpolarized [1‐13C]acetate and [1‐13C]acetylcarnitine ‐ investigation of the influence of dobutamine induced stress
inferred← citeshttps://doi.org/10.1002/prot.21611openalex-snapshot
Crystal structure of the biotin carboxylase domain of human acetyl‐CoA carboxylase 2
inferred← citeshttps://doi.org/10.1007/8904_2011_35openalex-snapshot
Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark
inferred← citeshttps://doi.org/10.1007/8904_2011_94openalex-snapshot
A Novel Mutation in CPT1A Resulting in Hepatic CPT Deficiency
inferred← citeshttps://doi.org/10.1007/8904_2016_528openalex-snapshot
Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency
inferred← citeshttps://doi.org/10.1007/8904_2016_564openalex-snapshot
Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcarnitine Profiles
inferred← citeshttps://doi.org/10.1007/8904_2017_74openalex-snapshot
Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous Mutation
inferred← citeshttps://doi.org/10.1007/978-1-4614-5203-4_5openalex-snapshot
Cardiac Metabolic Adaptation During Postnatal Development
inferred← citeshttps://doi.org/10.1007/978-3-030-68844-8_4openalex-snapshot
Non-coding RNAs Related to Lipid Metabolism and Non-alcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-87227-4_12openalex-snapshot
Nonprotein Amino Acids—‘Fuel at All?’
inferred← citeshttps://doi.org/10.1007/978-3-030-94305-9_8openalex-snapshot
Regulation of Fatty Acid Oxidation in Skeletal Muscle During Exercise: Effect of Obesity
inferred← citeshttps://doi.org/10.1007/978-3-319-14621-8_23openalex-snapshot
Nutrition Studies in Long-Chain Fatty Acid Oxidation Disorders: Diet Composition and Monitoring
inferred← citeshttps://doi.org/10.1007/978-3-319-31143-2_108-1openalex-snapshot
Methylation in CPT1A, Lipoproteins, and Epigenetics
inferred← citeshttps://doi.org/10.1007/978-3-319-31251-4_4openalex-snapshot
Cardiac Metabolism and Energetic Control
inferred← citeshttps://doi.org/10.1007/978-3-319-40458-5_30openalex-snapshot
Linoleic Acid and Alpha-Linolenic Acid Have Central Roles in Brain Energy Substrate Provision, Endogenous Lipid Production, Immune and Repair Function, via Peroxisomal Beta-Oxidation-Related Pathways?
inferred← citeshttps://doi.org/10.1007/978-3-319-55330-6_21openalex-snapshot
Mitochondria and Angiogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-55530-0_108openalex-snapshot
Methylation in CPT1A, Lipoproteins, and Epigenetics
inferred← citeshttps://doi.org/10.1007/978-3-319-61401-4_12openalex-snapshot
Other Metabolic Syndromes
inferred← citeshttps://doi.org/10.1007/978-3-319-66816-1_1329-1openalex-snapshot
Carnitine Palmitoyltransferase Deficiency
inferred← citeshttps://doi.org/10.1007/978-3-540-29676-8_421openalex-snapshot
Carnitine Palmitoyltransferase II Deficiency
inferred← citeshttps://doi.org/10.1007/978-3-540-76698-8_10openalex-snapshot
Acylcarnitines, Including In Vitro Loading Tests
inferred← citeshttps://doi.org/10.1007/978-981-13-2297-6_6openalex-snapshot
Metabolic Autopsy and Molecular Autopsy in Sudden Unexpected Death in Infancy
inferred← citeshttps://doi.org/10.1007/978-981-95-2286-6_2openalex-snapshot
Genetics of Metabolic Diseases
inferred← citeshttps://doi.org/10.1007/s00018-020-03624-6openalex-snapshot
Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy
inferred← citeshttps://doi.org/10.1007/s00018-025-05696-8openalex-snapshot
Direct regulation of Per2 by Roraa: insights into circadian and metabolic interplay in zebrafish
inferred← citeshttps://doi.org/10.1007/s00059-012-3659-0openalex-snapshot
Genetics and metabolic cardiomyopathies
inferred← citeshttps://doi.org/10.1007/s00109-024-02512-xopenalex-snapshot
Deciphering metabolic shifts in Gaucher disease type 1: a multi-omics study
inferred← citeshttps://doi.org/10.1007/s00125-009-1284-0openalex-snapshot
Enhanced susceptibility of Cpt1c knockout mice to glucose intolerance induced by a high-fat diet involves elevated hepatic gluconeogenesis and decreased skeletal muscle glucose uptake
inferred← citeshttps://doi.org/10.1007/s00204-019-02626-zopenalex-snapshot
Doxorubicin persistently rewires cardiac circadian homeostasis in mice
inferred← citeshttps://doi.org/10.1007/s00240-022-01384-5openalex-snapshot
Integrated analysis of mRNA-seq and miRNA-seq reveals the potential roles of Egr1, Rxra and Max in kidney stone disease
inferred← citeshttps://doi.org/10.1007/s00394-019-02071-9openalex-snapshot
Early weaning alters the thermogenic capacity of brown adipose tissue in adult male and female rats
inferred← citeshttps://doi.org/10.1007/s00395-026-01172-xopenalex-snapshot
ATP5A1 succinylation as a key driver for the transition of myocardial ischemia to development of heart failure
inferred← citeshttps://doi.org/10.1007/s00401-020-02152-8openalex-snapshot
Biological sex and DNA repair deficiency drive Alzheimer’s disease via systemic metabolic remodeling and brain mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1007/s00421-024-05684-zopenalex-snapshot
The first case of a competitive basketball player affected by carnitine palmitoyl transferase II deficiency presenting an undescribed compound heterozygous genetic mutation
inferred← citeshttps://doi.org/10.1007/s00439-019-01998-7openalex-snapshot
Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals
inferred← citeshttps://doi.org/10.1007/s00467-011-1767-3openalex-snapshot
A 10-year-old boy with dark urine and acute kidney injury: answer
inferred← citeshttps://doi.org/10.1007/s00705-016-2785-zopenalex-snapshot
Carnitine palmitoyl transferase 2 polymorphism may be associated with enterovirus 71 severe infection in a Chinese population
inferred← citeshttps://doi.org/10.1007/s10499-025-02342-9openalex-snapshot
Novel insights into the interaction between Litopenaeus vannamei and Enterocytozoon hepatonaei via histopathology and transcriptomic analysis
inferred← citeshttps://doi.org/10.1007/s10545-007-0536-8openalex-snapshot
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation
inferred← citeshttps://doi.org/10.1007/s10545-008-0844-7openalex-snapshot
PPARs as therapeutic targets for correction of inborn mitochondrial fatty acid oxidation disorders
inferred← citeshttps://doi.org/10.1007/s10545-010-9061-2openalex-snapshot
A general introduction to the biochemistry of mitochondrial fatty acid β‐oxidation
inferred← citeshttps://doi.org/10.1007/s10545-010-9090-xopenalex-snapshot
Mitochondrial fatty acid oxidation disorders: clinical presentation of long‐chain fatty acid oxidation defects before and after newborn screening
inferred← citeshttps://doi.org/10.1007/s10545-010-9162-yopenalex-snapshot
Metabolic manipulators: a well founded strategy to combat mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1007/s10545-015-9819-7openalex-snapshot
Peroxisome‐mitochondria interplay and disease
inferred← citeshttps://doi.org/10.1007/s10695-018-0589-7openalex-snapshot
Lipid accumulation in grass carp (Ctenopharyngodon idellus) fed faba beans (Vicia faba L.)
inferred← citeshttps://doi.org/10.1007/s11010-011-0847-9openalex-snapshot
Acyl-CoA binding proteins interact with the acyl-CoA binding domain of mitochondrial carnitine palmitoyl transferase I
inferred← citeshttps://doi.org/10.1007/s11154-018-9448-1openalex-snapshot
Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle
inferred← citeshttps://doi.org/10.1007/s11356-023-31086-3openalex-snapshot
Lead exposure induced lipid metabolism disorders by regulating the lipophagy process in microglia
inferred← citeshttps://doi.org/10.1007/s11626-016-0018-0openalex-snapshot
Establishment and characterisation of a novel bovine SV40 large T-antigen-transduced foetal hepatocyte-derived cell line
inferred← citeshttps://doi.org/10.1007/s11745-015-3992-1openalex-snapshot
Lutein Prevents High Fat Diet‐Induced Atherosclerosis in ApoE‐Deficient Mice by Inhibiting NADPH Oxidase and Increasing PPAR Expression
inferred← citeshttps://doi.org/10.1007/s11745-015-4070-4openalex-snapshot
Forms of n‐3 (ALA, C18:3n‐3 or DHA, C22:6n‐3) Fatty Acids Affect Carcass Yield, Blood Lipids, Muscle n‐3 Fatty Acids and Liver Gene Expression in Lambs
inferred← citeshttps://doi.org/10.1007/s11886-024-02162-yopenalex-snapshot
Cardiac Regeneration in Adult Zebrafish: A Review of Signaling and Metabolic Coordination
inferred← citeshttps://doi.org/10.1007/s12035-015-9238-7openalex-snapshot
The Carnitine Palmitoyl Transferase (CPT) System and Possible Relevance for Neuropsychiatric and Neurological Conditions
inferred← citeshttps://doi.org/10.1007/s13105-025-01121-7openalex-snapshot
Elevated hydrostatic pressure dysregulates lipid metabolism of hepatocytes
inferred← citeshttps://doi.org/10.1007/s13679-026-00756-xopenalex-snapshot
Adipose Tissue Remodeling Beyond Weight Loss: New Insights Into Incretin-Based Therapies and Bariatric Surgery
inferred← citeshttps://doi.org/10.1007/s13730-017-0292-zopenalex-snapshot
Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult life
inferred← citeshttps://doi.org/10.1007/springerreference_109300openalex-snapshot
Carnitine Palmitoyltransferase II Deficiency
inferred← citeshttps://doi.org/10.1016/b978-0-12-381510-1.00075-2openalex-snapshot
Metabolic and Mitochondrial Myopathies
inferred← citeshttps://doi.org/10.1016/b978-0-12-384878-9.00010-8openalex-snapshot
Modeling Disorders of Fatty Acid Metabolism in the Mouse
inferred← citeshttps://doi.org/10.1016/b978-0-12-404599-6.00016-0openalex-snapshot
Post-Genomic Analysis of Fatty Acid and Glucose Metabolism in Cardiovascular Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-410529-4.00050-4openalex-snapshot
Disorders of Lipid Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-800040-3.00013-3openalex-snapshot
Mitochondrial Disorders Causing Cardioskeletal Myopathies in Childhood
inferred← citeshttps://doi.org/10.1016/b978-0-12-801585-8.00028-2openalex-snapshot
Hepatic Mitochondrial Fatty Acid Oxidation and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-811230-4.00003-xopenalex-snapshot
Polyunsaturated Fatty Acid Biosynthesis and Metabolism in Fish
inferred← citeshttps://doi.org/10.1016/b978-0-12-813955-4.00054-4openalex-snapshot
Disorders of lipid metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-824412-8.00006-0openalex-snapshot
Nutrigenomics in the management and prevention of metabolic disorders
inferred← citeshttps://doi.org/10.1016/b978-0-323-03354-1.50092-4openalex-snapshot
METABOLIC MYOPATHIES (INCLUDING MITOCHONDRIAL DISEASES)
inferred← citeshttps://doi.org/10.1016/b978-0-323-18907-1.00047-0openalex-snapshot
Hypoglycemia and Hypoglycemic Syndromes
inferred← citeshttps://doi.org/10.1016/b978-0-323-40139-5.00022-xopenalex-snapshot
Inborn Errors of Carbohydrate, Ammonia, Amino Acid, and Organic Acid Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-323-71317-7.00023-8openalex-snapshot
Treatment and Management of Hereditary Metabolic Myopathies
inferred← citeshttps://doi.org/10.1016/b978-0-323-82823-9.00029-5openalex-snapshot
Inborn Errors of Carbohydrate, Ammonia, Amino Acid, and Organic Acid Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-323-90528-2.00012-6openalex-snapshot
Lipid metabolism part II
inferred← citeshttps://doi.org/10.1016/b978-0-323-90528-2.00013-8openalex-snapshot
Lipid metabolism part I
inferred← citeshttps://doi.org/10.1016/b978-0-443-19176-3.00050-9openalex-snapshot
Disorders of lipid metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-443-41379-7.00003-2openalex-snapshot
Disorders of the carnitine cycle and mitochondrial fatty acid oxidation
inferred← citeshttps://doi.org/10.1016/b978-012373698-7/50016-4openalex-snapshot
Fatty Acid and Glucose Metabolism in Cardiac Disease
inferred← citeshttps://doi.org/10.1016/b978-1-4160-2450-7.50088-8openalex-snapshot
10.1016/b978-1-4160-2450-7.50088-8
inferred← citeshttps://doi.org/10.1016/b978-1-4160-5583-9.00047-2openalex-snapshot
Hypoglycemia and Hypoglycemic Syndromes
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6164-9.00058-5openalex-snapshot
Newborn Screening and Inborn Errors of Metabolism
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0372-6.00022-0openalex-snapshot
Treatment and Management of Hereditary Metabolic Myopathies
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0774-8.10071-5openalex-snapshot
Mitochondrial Hepatopathies
inferred← citeshttps://doi.org/10.1016/j.abb.2007.06.026openalex-snapshot
Hormonal and nutritional regulation of muscle carnitine palmitoyltransferase I gene expression in vivo
inferred← citeshttps://doi.org/10.1016/j.advnut.2023.04.012openalex-snapshot
Nutritional Considerations for the Vegan Athlete
inferred← citeshttps://doi.org/10.1016/j.aninu.2024.11.002openalex-snapshot
Transcriptomics and non-targeted metabolomics provide mechanistic insights into the improvement of the growth performance and meat quality of lambs supplemented with fermented Lycium barbarum residues
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2020.106665openalex-snapshot
Physiological and molecular aspects of heat-treated cultured granulosa cells of Egyptian buffalo (Bubalus bubalis)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.740827openalex-snapshot
Acute hypoxia and reoxygenation alters glucose and lipid metabolic patterns in Hulong hybrid grouper (Epinephelus fuscoguttatus♀ × E. lanceolatus♂)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2025.743256openalex-snapshot
Combined ammonia and nitrite exposure aggravated nitric oxide accumulation, liver glucose and lipid metabolism disturbance, intestinal barrier dysfunction and inflammation in high fat-fed largemouth bass (Micropterus salmoides)
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2009.11.033openalex-snapshot
The genetics of statin-induced myopathy
inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.01.003openalex-snapshot
Speract, a sea urchin egg peptide that regulates sperm motility, also stimulates sperm mitochondrial metabolism
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.04.006openalex-snapshot
Altered mitochondrial and peroxisomal integrity in lipocalin-2-deficient mice with hepatic steatosis
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.04.008openalex-snapshot
Metabolic activation triggered by cAMP in MCF-7 cells generates lethal vulnerability to combined oxamate/etomoxir
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.04.008openalex-snapshot
Regulation of the subcellular trafficking of CD36, a major determinant of cardiac fatty acid utilization
inferred← citeshttps://doi.org/10.1016/j.bbapap.2011.07.001openalex-snapshot
Role of host cellular proteases in the pathogenesis of influenza and influenza-induced multiple organ failure
inferred← citeshttps://doi.org/10.1016/j.bbi.2015.08.004openalex-snapshot
The impact of mitochondrial aldehyde dehydrogenase (ALDH2) activation by Alda-1 on the behavioral and biochemical disturbances in animal model of depression
inferred← citeshttps://doi.org/10.1016/j.bbr.2013.08.004openalex-snapshot
Carnitine palmitoyltransferase 1C deficiency causes motor impairment and hypoactivity
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.06.006openalex-snapshot
Crystal structure of rat carnitine palmitoyltransferase II (CPT-II)
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.01.102openalex-snapshot
NR4A nuclear receptors mediate carnitine palmitoyltransferase 1A gene expression by the rexinoid HX600
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.08.042openalex-snapshot
Mitoxantrone alleviates hepatic steatosis induced by high-fat diet in broilers
inferred← citeshttps://doi.org/10.1016/j.biochi.2013.05.012openalex-snapshot
Regulation of mitochondrial fatty acid β-oxidation in human: What can we learn from inborn fatty acid β-oxidation deficiencies?
inferred← citeshttps://doi.org/10.1016/j.biochi.2020.03.007openalex-snapshot
In vivo evidence that bezafibrate prevents oxidative stress and mitochondrial dysfunction caused by 3-methylglutaric acid in rat liver
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.116092openalex-snapshot
Macrophage fatty acid oxidation in atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.01.045openalex-snapshot
The molecular structure of thio-ether fatty acids influences PPAR-dependent regulation of lipid metabolism
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.09.111openalex-snapshot
Synthesis and structure–activity relationships of fibrate-based analogues inside PPARs
inferred← citeshttps://doi.org/10.1016/j.braindev.2010.12.012openalex-snapshot
Thermolabile CPT II variants and low blood ATP levels are closely related to severity of acute encephalopathy in Japanese children
inferred← citeshttps://doi.org/10.1016/j.braindev.2013.07.011openalex-snapshot
Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy
inferred← citeshttps://doi.org/10.1016/j.canlet.2015.11.020openalex-snapshot
Perturbation of energy metabolism by fatty-acid derivative AIC-47 and imatinib in BCR-ABL-harboring leukemic cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.08.006openalex-snapshot
Fatty acid oxidation: An emerging facet of metabolic transformation in cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2019.12.036openalex-snapshot
Inhibition of fatty acid catabolism augments the efficacy of oxaliplatin-based chemotherapy in gastrointestinal cancers
inferred← citeshttps://doi.org/10.1016/j.canlet.2025.217991openalex-snapshot
Inhibition of CPT1A activates the cGAS/STING pathway to enhance neutrophil-mediated tumor abrogation in triple-negative breast cancer
inferred← citeshttps://doi.org/10.1016/j.cbpa.2009.09.031openalex-snapshot
The unusual energy metabolism of elasmobranch fishes
inferred← citeshttps://doi.org/10.1016/j.cca.2013.07.018openalex-snapshot
Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient
inferred← citeshttps://doi.org/10.1016/j.ccm.2018.02.001openalex-snapshot
Metabolic Myopathies and the Respiratory System
inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102336openalex-snapshot
Role of mitochondria in liver metabolic health and diseases
inferred← citeshttps://doi.org/10.1016/j.cellsig.2022.110267openalex-snapshot
Downregulation of CPT2 promotes proliferation and inhibits apoptosis through p53 pathway in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.cellsig.2023.110838openalex-snapshot
CPT2-mediated fatty acid oxidation inhibits tumorigenesis and enhances sorafenib sensitivity via the ROS/PPARγ/NF-κB pathway in clear cell renal cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.05.040openalex-snapshot
Histopathological changes and lipid metabolism in the liver of Bufo gargarizans tadpoles exposed to Triclosan
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2012.10.006openalex-snapshot
Acylcarnitine profile in thyroid disease
inferred← citeshttps://doi.org/10.1016/j.cmet.2025.09.012openalex-snapshot
Adipocyte lipolysis activates epithelial stem cells for hair regeneration through fatty acid metabolic signaling
inferred← citeshttps://doi.org/10.1016/j.drudis.2022.05.003openalex-snapshot
Key regulatory miRNAs in lipid homeostasis: Implications for cardiometabolic diseases and development of novel therapeutics
inferred← citeshttps://doi.org/10.1016/j.ebiom.2016.08.027openalex-snapshot
Transgenic Adipose-specific Expression of the Nuclear Receptor RORα Drives a Striking Shift in Fat Distribution and Impairs Glycemic Control
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.08.058openalex-snapshot
Chronic effects of mercury on Bufo gargarizans larvae: Thyroid disruption, liver damage, oxidative stress and lipid metabolism disorder
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.110055openalex-snapshot
The effects of chronic lead exposure on the liver of female Japanese quail (Coturnix japonica): Histopathological damages, oxidative stress and AMP-activated protein kinase based lipid metabolism disorder
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.111957openalex-snapshot
Cadmium induced skeletal underdevelopment, liver cell apoptosis and hepatic energy metabolism disorder in Bufo gargarizans larvae by disrupting thyroid hormone signaling
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116922openalex-snapshot
Gut dysbiosis of Rana zhenhaiensis tadpoles after lead (Pb) exposure based on integrated analysis of microbiota and gut transcriptome
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116408openalex-snapshot
Modulators for palmitoylation of proteins and small molecules
inferred← citeshttps://doi.org/10.1016/j.ejmg.2020.104034openalex-snapshot
A patient with atypical presentation of chronic hepatosteatosis harboring a novel variant in the CPT1A gene
inferred← citeshttps://doi.org/10.1016/j.ejphar.2009.02.016openalex-snapshot
Metoprolol represses PGC1α-mediated carnitine palmitoyltransferase-1B expression in the diabetic heart
inferred← citeshttps://doi.org/10.1016/j.ejpn.2024.02.003openalex-snapshot
Impact of newborn screening for fatty acid oxidation disorders on neurological outcome: A Belgian retrospective and multicentric study
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.113052openalex-snapshot
Effects of fluoride on the histology, lipid metabolism, and bile acid secretion in liver of Bufo gargarizans larvae
inferred← citeshttps://doi.org/10.1016/j.fct.2020.111328openalex-snapshot
Nicotine exposure during breastfeeding reduces sympathetic activity in brown adipose tissue and increases in white adipose tissue in adult rats: Sex-related differences
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2009.01.104openalex-snapshot
Mitochondrial fatty acid transport enzyme deficiency—implications for in vitro fertilization
inferred← citeshttps://doi.org/10.1016/j.fob.2013.04.003openalex-snapshot
Isothermal titration calorimetry with micelles: Thermodynamics of inhibitor binding to carnitine palmitoyltransferase 2 membrane protein
inferred← citeshttps://doi.org/10.1016/j.fsi.2017.07.058openalex-snapshot
Inhibited fatty acid β-oxidation impairs stress resistance ability in Nile tilapia (Oreochromis niloticus)
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109666openalex-snapshot
Effects of dietary glycerol monolaurate on growth and digestive performance, lipid metabolism, immune defense and gut microbiota of shrimp (Penaeus vannamei)
inferred← citeshttps://doi.org/10.1016/j.gendis.2021.01.005openalex-snapshot
Critical roles of FTO-mediated mRNA m6A demethylation in regulating adipogenesis and lipid metabolism: Implications in lipid metabolic disorders
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e35961openalex-snapshot
Dysfunction of the carnitine cycle in tumor progression
inferred← citeshttps://doi.org/10.1016/j.identj.2025.100837openalex-snapshot
Expression of Carnitine Palmitoyltransferase I Isotypes in Gingival Tissues of Human Periodontitis
inferred← citeshttps://doi.org/10.1016/j.ijoa.2023.103895openalex-snapshot
Prolonged neuraxial block following spinal anaesthesia in a patient with carnitine palmitoyl transferase II deficiency undergoing caesarean section
inferred← citeshttps://doi.org/10.1016/j.ijoa.2024.104246openalex-snapshot
Neuraxial labor analgesia in a parturient with carnitine palmitoyl transferase type II deficiency: a case report
inferred← citeshttps://doi.org/10.1016/j.intimp.2017.05.026openalex-snapshot
Rutin exhibits hepatoprotective effects in a mouse model of non-alcoholic fatty liver disease by reducing hepatic lipid levels and mitigating lipid-induced oxidative injuries
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112730openalex-snapshot
Specific small interfering RNAs (siRNAs) for targeting the metastasis, immune responses, and drug resistance of colorectal cancer cells (CRC)
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102485openalex-snapshot
CLICK-enabled analogues reveal pregnenolone interactomes in cancer and immune cells
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108109openalex-snapshot
Host macrocyclic acylcarnitines mediate symbiotic interactions between frogs and their skin microbiome
inferred← citeshttps://doi.org/10.1016/j.jelectrocard.2012.02.003openalex-snapshot
Arrhythmia-related workup in hereditary myopathies
inferred← citeshttps://doi.org/10.1016/j.jhep.2011.10.008openalex-snapshot
Enhancing liver mitochondrial fatty acid oxidation capacity in obese mice improves insulin sensitivity independently of hepatic steatosis
inferred← citeshttps://doi.org/10.1016/j.jlr.2025.100861openalex-snapshot
Arachidonoyl-carnitine and arachidonoyl-coenzyme A are suitable substrates for mammalian ALOX isoforms
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2021.577657openalex-snapshot
Mitochondria–A target for attenuation of astrocyte pathology
inferred← citeshttps://doi.org/10.1016/j.jns.2015.11.043openalex-snapshot
Drugs indicated for mitochondrial dysfunction as treatments for acute encephalopathy with onset of febrile convulsive status epileptics
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2005.03.027openalex-snapshot
Acetylcarnitine and cellular stress response: roles in nutritional redox homeostasis and regulation of longevity genes
inferred← citeshttps://doi.org/10.1016/j.jss.2012.05.053openalex-snapshot
Stimulation of carnitine palmitoyltransferase 1 improves renal function and attenuates tissue damage after ischemia/reperfusion
inferred← citeshttps://doi.org/10.1016/j.jtemb.2021.126851openalex-snapshot
Dietary copper supplementation enhances lipolysis in Rex rabbits
inferred← citeshttps://doi.org/10.1016/j.labcli.2008.06.004openalex-snapshot
Identificación de mutaciones en el gen CPT2 en un caso con déficit muscular de carnitina palmitoiltransferasa II,
inferred← citeshttps://doi.org/10.1016/j.legalmed.2016.07.005openalex-snapshot
A case of sudden unexpected infant death involving a homozygotic twin with the thermolabile CPT2 variant, accompanied by rotavirus infection and treatment with an antibiotic containing pivalic acid
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119668openalex-snapshot
Berteroin ameliorates lipid accumulation through AMPK-mediated regulation of hepatic lipid metabolism and inhibition of adipocyte differentiation
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.120103openalex-snapshot
Determination of metabolic phenotype and potential biomarkers in the liver of heroin addicted mice with hepatotoxicity
inferred← citeshttps://doi.org/10.1016/j.lfs.2022.120838openalex-snapshot
The Role and Mechanism of CREBH Regulating SIRT3 in Metabolic Associated Fatty Liver Disease
inferred← citeshttps://doi.org/10.1016/j.mce.2013.06.020openalex-snapshot
Genes involved in fatty acid metabolism: Molecular characterization and hypothalamic mRNA response to energy status and neuropeptide Y treatment in the orange-spotted grouper Epinephelus coioides
inferred← citeshttps://doi.org/10.1016/j.mce.2018.12.001openalex-snapshot
Novel metabolic disorders in skeletal muscle of Lipodystrophic Bscl2/Seipin deficient mice
inferred← citeshttps://doi.org/10.1016/j.mcpro.2021.100101openalex-snapshot
Normothermic Ex-vivo Kidney Perfusion in a Porcine Auto-Transplantation Model Preserves the Expression of Key Mitochondrial Proteins: An Unbiased Proteomics Analysis
inferred← citeshttps://doi.org/10.1016/j.meatsci.2017.05.003openalex-snapshot
Identification of the bovine HSL gene expression profiles and its association with fatty acid composition and fat deposition traits
inferred← citeshttps://doi.org/10.1016/j.meatsci.2017.10.012openalex-snapshot
Effects of dietary lecithin and l-carnitine on fatty acid composition and lipid-metabolic genes expression in subcutaneous fat and longissimus thoracis of growing-finishing pigs
inferred← citeshttps://doi.org/10.1016/j.meatsci.2019.06.008openalex-snapshot
Effects of algae supplementation in high-energy dietary on fatty acid composition and the expression of genes involved in lipid metabolism in Hu sheep managed under intensive finishing system
inferred← citeshttps://doi.org/10.1016/j.metabol.2022.155292openalex-snapshot
Imipramine activates FAM3A-FOXA2-CPT2 pathway to ameliorate hepatic steatosis
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.01.010openalex-snapshot
A Metabolic Basis for Endothelial-to-Mesenchymal Transition
inferred← citeshttps://doi.org/10.1016/j.molmet.2015.01.004openalex-snapshot
Central nervous system neuropeptide Y regulates mediators of hepatic phospholipid remodeling and very low-density lipoprotein triglyceride secretion via sympathetic innervation
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102237openalex-snapshot
ACAA1 knockout increases the survival rate of KPC mice by activating autophagy
inferred← citeshttps://doi.org/10.1016/j.ncl.2014.05.001openalex-snapshot
Metabolic and Mitochondrial Myopathies
inferred← citeshttps://doi.org/10.1016/j.neures.2019.07.006openalex-snapshot
A PRIMPOL mutation and variants in multiple genes may contribute to phenotypes in a familial case with chronic progressive external ophthalmoplegia symptoms
inferred← citeshttps://doi.org/10.1016/j.npep.2016.03.006openalex-snapshot
Temperature dependence of the control of energy homeostasis requires CART signaling
inferred← citeshttps://doi.org/10.1016/j.nucmedbio.2015.08.005openalex-snapshot
Synthesis and preliminary evaluation of an 18 F-labeled oleic acid analog for PET imaging of fatty acid uptake and metabolism
inferred← citeshttps://doi.org/10.1016/j.nurt.2008.08.006openalex-snapshot
Therapeutic Options in Other Metabolic Myopathies
inferred← citeshttps://doi.org/10.1016/j.nutres.2023.07.003openalex-snapshot
Type 2–resistant starch and Lactiplantibacillus plantarum NCIMB 8826 result in additive and interactive effects in diet-induced obese mice
inferred← citeshttps://doi.org/10.1016/j.orcp.2021.06.008openalex-snapshot
The impact of CPT1B rs470117, LEPR rs1137101 and BDNF rs6265 polymorphisms on the risk of developing obesity in an Italian population
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2025.11.002openalex-snapshot
Rewiring lipid Metabolism: The central role of CPT1 in metabolic dysfunction
inferred← citeshttps://doi.org/10.1016/j.pharmr.2025.100051openalex-snapshot
International Union of Basic and Clinical Pharmacology. CXIX. Fundamental insights and clinical relevance regarding the carnitine palmitoyltransferase family of enzymes
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2017.11.003openalex-snapshot
Role of kinase-coupled TRP channels in mineral homeostasis
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