Results 1 to 10 of about 20,316 (189)

Paediatric CSF acylcarnitine reference ranges [PDF]

open access: yesFrontiers in Molecular Biosciences
Acylcarnitines play a crucial role in energy metabolism pathways, primarily known for their involvement in the beta oxidation of fatty acids. However, their roles extend beyond mitochondrial transport; they also contribute to the synthesis of lipids in ...
Ontefetse Neo Plaatjie   +5 more
doaj   +2 more sources

Neonatal Hypoxic-Ischemic Brain Injury Alters Brain Acylcarnitine Levels in a Mouse Model

open access: yesMetabolites, 2022
Hypoxic-ischemic brain injury (HIBI) leads to depletion of ATP, mitochondrial dysfunction, and enhanced oxidant formation. Measurement of acylcarnitines may provide insight into mitochondrial dysfunction.
Amanda M. Dave   +3 more
doaj   +1 more source

Modulation of sleep by trafficking of lipids through the Drosophila blood-brain barrier

open access: yeseLife, 2023
Endocytosis through Drosophila glia is a significant determinant of sleep amount and occurs preferentially during sleep in glia of the blood-brain barrier (BBB).
Fu Li, Gregory Artiushin, Amita Sehgal
doaj   +1 more source

The association and prediction value of acylcarnitine on diabetic nephropathy in Chinese patients with type 2 diabetes mellitus

open access: yesDiabetology & Metabolic Syndrome, 2023
Background Acylcarnitines play a role in type 2 diabetes mellitus (T2DM), but the relationship between acylcarnitine and diabetic nephropathy was unclear.
Xuerui Li   +3 more
doaj   +1 more source

Management of pregnancy in a patient with long‐chain 3‐hydroxyacyl CoA dehydrogenase deficiency

open access: yesJIMD Reports, 2022
Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is a rare mitochondrial defect of β‐oxidation of long‐chain fatty acids. Patients may present with muscle pain, hypotonia, peripheral neuropathy, cardiomyopathy, recurrent rhabdomyolysis and ...
Loai A. Shakerdi   +8 more
doaj   +1 more source

Dataset from dried blood spot acylcarnitine for detection of Carnitine-Acylcarnitine Translocase (CACT) deficiency and Carnitine Palmitoyl Transferase 2 (CPT2) deficiency

open access: yesData in Brief, 2023
Clinical diagnosis of inborn errors of metabolism in the suspected patients is usually guided by the initial general investigations in the laboratory such as the concentration of ammonia, blood gases status, blood glucose and ketones.
Anasufiza Habib   +2 more
doaj   +1 more source

Comparison of serum acylcarnitine levels in patients with myalgic encephalomyelitis/chronic fatigue syndrome and healthy controls: a systematic review and meta-analysis

open access: yesJournal of Translational Medicine, 2023
Background Myalgic encephalomyelitis/chronic fatigue syndrome/systemic exertion intolerance disease (ME/CFS/SEID) is a condition diagnosed primarily based on clinical symptoms, including prolonged fatigue and post-exertional malaise; however, there is no
Ryuhei Jinushi   +11 more
doaj   +1 more source

High-throughput quantitation of amino acids and acylcarnitine in cerebrospinal fluid: identification of PCNSL biomarkers and potential metabolic messengers

open access: yesFrontiers in Molecular Biosciences, 2023
Background: Due to the poor prognosis and rising occurrence, there is a crucial need to improve the diagnosis of Primary Central Nervous System Lymphoma (PCNSL), which is a rare type of non-Hodgkin’s lymphoma. This study utilized targeted metabolomics of
Jingjing Ma   +20 more
doaj   +1 more source

Metabolomics profile and 10-year atherosclerotic cardiovascular disease (ASCVD) risk score

open access: yesFrontiers in Cardiovascular Medicine, 2023
BackgroundThe intermediate metabolites associated with the development of atherosclerotic cardiovascular disease (ASCVD) remain largely unknown. Thus, we conducted a large panel of metabolomics profiling to identify the new candidate metabolites that ...
Hojat Dehghanbanadaki   +17 more
doaj   +1 more source

Metabolomic Phenotype of Hepatic Steatosis and Fibrosis in Mexican Children Living with Obesity

open access: yesMedicina, 2023
Background and Objectives: Metabolic-dysfunction-associated steatotic liver disease or MASLD is the main cause of chronic liver diseases in children, and it is estimated to affect 35% of children living with obesity.
Nayely Garibay-Nieto   +12 more
doaj   +1 more source

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