Disease: Carnitine palmitoyltransferase I deficiency
- A case report of Carnitine Palmitoyltransferase deficiency type II
- A different perspective into clinical symptoms in CPT I deficiency
- A patient with atypical presentation of chronic hepatosteatosis harboring a novel variant in the CPT1A gene
- Ablation of fatty acid desaturase 2 (FADS2) exacerbates hepatic triacylglycerol and cholesterol accumulation in polyunsaturated fatty acid-depleted mice
- Acute insulin deprivation results in altered mitochondrial substrate sensitivity conducive to greater fatty acid transport
- Adaptation of AMPK-mTOR-signal pathways and lipid metabolism in response to low- and high-level rapeseed meal diet in Chinese perch (Siniperca chuatsi)
- An unusual case of cardiomyopathy showing carnitine palmitoyltransferase deficiency
- Analysis of a child with carnitine palmitoyl transferase 1A deficiency due to variant of CPT1A gene
- Angiotensin-converting enzyme 2 regulates endoplasmic reticulum stress and mitochondrial function to preserve skeletal muscle lipid metabolism
- Artemether Ameliorates Non-Alcoholic Steatohepatitis by Repressing Lipogenesis, Inflammation, and Fibrosis in Mice
- Atypical manifestation of carnitine palmitoyltransferase 1A deficiency: hepatosplenomegaly and nephromegaly
- Carbohydrate response element-binding protein regulates lipid metabolism via mTOR complex1 in diabetic nephropathy
- Cardiac-specific LRP6 knockout induces lipid accumulation through Drp1/CPT1b pathway in adult mice
- Cardiolipin Stabilizes and Increases Catalytic Efficiency of Carnitine Palmitoyltransferase II and Its Variants S113L, P50H, and Y479F
- Cardiologic evaluation of Turkish mitochondrial fatty acid oxidation disorders
- Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists
- Carnitine Palmitoyl Transferase Deficiency in a University Immunology Practice
- Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile
- Carnitine palmitoyltransferase II deficiency and post-COVID vaccination rhabdomyolysis
- Carnitine palmitoyltransferase-1A deficiency: a look at classic and arctic variants
- Carnitine palmitoyltransferase-II deficiency: case presentation and review of the literature
- Case 1: Lethal Pulmonary Hemorrhage in a 3-day-old Term Infant
- Case Study of an Elderly Patient With New Onset Weakness
- Cause of recurrent rhabdomyolysis, carnitine palmitoyltransferase II deficiency and novel pathogenic mutation
- Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy
- Clinical and Gene Analysis of Fatty Acid Oxidation Disorders Found in Neonatal Tandem Mass Spectrometry Screening
- Clinical features and gene mutations of 6 patients with carnitine palmitoyltransferase 1A deficiency
- Clinical features and genetic analysis of a case with carnitine palmitoyltransferase 1A deficiency
- Clinical features and genetic variants of a case with carnitine palmitoyltransferase 1A deficiency
- Clinical Reasoning: A 2-Day-Old Boy With Sudden Cardiac Arrest and Encephalopathy
- CPT1A-mediated Fat Oxidation, Mechanisms, and Therapeutic Potential
- CPT1C is required for synaptic plasticity and oscillatory activity that supports motor, associative and non-associative learning
- CPT1α maintains phenotype of tubules via mitochondrial respiration during kidney injury and repair
- Deciphering the pathogenesis of retinopathy associated with carnitine palmitoyltransferase I deficiency in zebrafish model
- Dietary copper supplementation enhances lipolysis in Rex rabbits
- Differences between acylcarnitine profiles in plasma and bloodspots
- Different Lipid Signature in Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders
- Discordant hepatic fatty acid oxidation and triglyceride hydrolysis leads to liver disease
- Disturbance of Fatty Acid Metabolism Promoted Vascular Endothelial Cell Senescence via Acetyl-CoA-Induced Protein Acetylation Modification
- Do renal and cardiac malformations in the fetus signal carnitine palmitoyltransferase II deficiency? A rare lethal fatty acid oxidation defect
- Does SARS-Cov-2 Trigger Rhabdomyolysis in Carnitine-Palmitoyltransferase-II Deficiency?
- Druggability of lipid metabolism modulation against renal fibrosis
- Effects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPD
- Evaluation of Metabolic Defects in Fatty Acid Oxidation Using Peripheral Blood Mononuclear Cells Loaded with Deuterium-Labeled Fatty Acids
- Fatty Acid oxidation disorders in a chinese population in taiwan
- Follow-up of fatty acid β-oxidation disorders in expanded newborn screening era
- Genetic characteristics and follow-up of patients with fatty acid β-oxidation disorders through expanded newborn screening in a Northern Chinese population
- Genetic deletion of Mas receptor in FVB/N mice impairs cardiac use of glucose and lipids
- Genistein Regulates Lipid Metabolism via Estrogen Receptor β and Its Downstream Signal Akt/mTOR in HepG2 Cells
- Hepatic carnitine palmitoyltransferase I deficiency: acylcarnitine profiles in blood spots are highly specific
- Homeostasis and transitional activation of regulatory T cells require c-Myc
- HRD1 inhibits fatty acid oxidation and tumorigenesis by ubiquitinating CPT2 in triple-negative breast cancer
- Hypercholesterolaemia treatment in a patient with family hypercholesterolaemia and myopathy due to carnitine palmitoyltransferase II deficiency with PCSK9 inhibitors
- Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency
- Imipramine activates FAM3A-FOXA2-CPT2 pathway to ameliorate hepatic steatosis
- Impaired fasting tolerance among Alaska native children with a common carnitine palmitoyltransferase 1A sequence variant
- Inhibition of carnitine palmitoyltransferase 1A in hepatic stellate cells protects against fibrosis
- Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1
- Knockdown of carnitine palmitoyltransferase I (CPT1) reduces fat body lipid mobilization and resistance to starvation in the insect vector <em>Rhodnius prolixus</em>
- Lethal neonatal presentation of carnitine palmitoyltransferase I deficiency
- Liver transplantation for acute-on-chronic liver failure due to carnitine palmitoyl transferase (CPT) 1A deficiency
- Medium branched chain fatty acids improve the profile of tricarboxylic acid cycle intermediates in mitochondrial fatty acid β-oxidation deficient cells: A comparative study
- Metabolic flexibility maintains proliferation and migration of FGFR signaling-deficient lymphatic endothelial cells
- miR204 potentially promotes non-alcoholic fatty liver disease by inhibition of cpt1a in mouse hepatocytes
- Mitochondrial carnitine palmitoyltransferase-II dysfunction: A possible novel mechanism for nonalcoholic fatty liver disease in hepatocarcinogenesis
- Mitochondrial Fatty Acid β-Oxidation Inhibition Promotes Glucose Utilization and Protein Deposition through Energy Homeostasis Remodeling in Fish
- Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach
- Neonatal Macrosomia is an Interfering Factor for Analytes on the Colorado State Newborn Screen
- Neutrophil trafficking to the site of infection requires Cpt1a-dependent fatty acid β-oxidation
- No effect of resveratrol on fatty acid oxidation or exercise capacity in patients with fatty acid oxidation disorders: A randomized clinical cross-over trial
- Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency
- Novel mutation in carnitine palmitoyltransferase 1A detected through newborn screening for a presymptomatic case in China: a case report
- Novel mutations associated with carnitine-acylcarnitine translocase and carnitine palmitoyl transferase 2 deficiencies in Malaysia
- Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency
- Octanoate is differentially metabolized in liver and muscle and fails to rescue cardiomyopathy in CPT2 deficiency
- Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic
- P2Y2R Deficiency Ameliorates Hepatic Steatosis by Reducing Lipogenesis and Enhancing Fatty Acid β-Oxidation through AMPK and PGC-1α Induction in High-Fat Diet-Fed Mice
- PARK7 deficiency inhibits fatty acid β-oxidation via PTEN to delay liver regeneration after hepatectomy
- PHDs/CPT1B/VDAC1 axis regulates long-chain fatty acid oxidation in cardiomyocytes
- Physiological aspects of muscular adaptations to training translated to neuromuscular diseases
- Prolonged neuraxial block following spinal anaesthesia in a patient with carnitine palmitoyl transferase II deficiency undergoing caesarean section
- REDD1 deficiency protects against nonalcoholic hepatic steatosis induced by high-fat diet
- Repeated and progressive rhabdomyolysis due to a novel carnitine palmitoyltransferase II gene variant in an adult male: A case report
- Rhabdomyolysis Associated with Recent <em>SARS-COV-2</em> Infection in a Patient with Carnitine Palmitoyltransferase II Deficiency
- Selective screening for fatty acid oxidation disorders by tandem mass spectrometry: difficulties in practical discrimination
- Skeletal muscle undergoes fiber type metabolic switch without myosin heavy chain switch in response to defective fatty acid oxidation
- Study of Carnitine/Acylcarnitine and Amino Acid Profile in Children and Adults With Acute Liver Failure
- Subclinical effects of long-chain fatty acid β-oxidation deficiency on the adult heart: A case-control magnetic resonance study
- Successful long-term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutation
- Successful orthotopic heart transplantation in CPTII deficiency
- Tandem mass spectrometry analysis and genetic diagnosis of neonates with fatty acid oxidation disorders in central and northern regions of Guangxi
- Tartronic acid promotes de novo lipogenesis and inhibits CPT-1β by upregulating acetyl-CoA and malonyl-CoA
- The Attenuation of Diabetic Nephropathy by Annexin A1 via Regulation of Lipid Metabolism Through the AMPK/PPARα/CPT1b Pathway
- The Carnitine Palmitoyl Transferase (CPT) System and Possible Relevance for Neuropsychiatric and Neurological Conditions
- The lactate receptor GPR81 mediates hepatic lipid metabolism and the therapeutic effect of metformin on experimental NAFLDs
- The role of increased FGF21 in VLDL-TAG secretion and thermogenic gene expression in mice under protein malnutrition
- The role of uncoupling protein 2 in macrophages and its impact on obesity-induced adipose tissue inflammation and insulin resistance
- Transcribed Ultraconserved Regions, Uc.323, Ameliorates Cardiac Hypertrophy by Regulating the Transcription of CPT1b (Carnitine Palmitoyl transferase 1b)