Keywords: BSA; bovine serum albumin; CPT1; carnitine palmitoyltransferase 1; DMEM; Dulbecco's modified eagle medium; ETX; etomoxir; FAO; fatty acid β-oxidation; LC; long-chain; LCFA; long-chain fatty acid; LCHAD; long-chain 3-hydroxyacyl-CoA dehydrogenase; LKAT; l
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: AD; autosomal dominant; ADNIV; autosomal dominant neovascular inflammatory vitreoretinopathy; AR; autosomal recessive; AR-1; autosomal recessive-1 allele identified; ARMS; amplification refractory mutation system; AZOOR; acute zonal occult outer retinopat
Keywords: GC-MS; gas chromatography mass spectrometry; LC-MS; liquid chromatography mass spectrometry; CSF; Cerebrospinal fluid; IEM; inborn errors of metabolism; MALDI; matrix-assisted laser desorption ionization; SELDI; Surface-enhanced laser desorption/ionizatio
Keywords: CACT; carnitine acylcarnitine translocase; CM; cardiomyopathy; CRF; case report forms; ECHO; echocardiography; ER; emergency room; LC-FAOD; long chain fatty acid oxidation disorder; MCT; Medium Chain Triglyceride; TFP; trifunctional protein; CK; creatine
Keywords: DBSs; dried blood spots; CPT-1; carnitine palmitoyltransferase 1; VLCAD; very-long-chain acyl-CoA dehydrogenase; LCHAD; long-chain 3-hydroxyacyl-CoA dehydrogenase; MCAD; medium-chain acyl-CoA dehydrogenase; PA; propionic acidemia; MMA; methylmalonic acide
UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24 weeks of treatment
Keywords: Metabolic disorders; Fatty acid oxidation disorders; Triheptanoin; UX007; FAOD; LC-FAOD; VLCAD; LCHAD;
Uncoupling, metabolic inhibition and induction of mitochondrial permeability transition in rat liver mitochondria caused by the major long-chain hydroxyl monocarboxylic fatty acids accumulating in LCHAD deficiency
Keywords: Alm; alamethicin; ANT; adenine nucleotide translocator; ATC; atractyloside; BSA; bovine serum albumin; CCCP; carbonyl cyanide 3-chlorophenyl hydrazine; CsA; cyclosporin A; DTT; dithiothreitol; EGTA; ethylene glycol-bis (2-aminoethylether)-N,N,Nâ²,Nâ²-te
Mitochondrial bioenergetics deregulation caused by long-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies in rat brain: A possible role of mPTP opening as a pathomechanism in these disorders?
Keywords: Alm; alamethicin; AA; antimycin A; BBB; blood brain barrier; BSA; bovine serum albumin; CCCP; carbonyl cyanide 3-chlorophenyl hydrazine; CsA; cyclosporin A; EGTA; ethylene glycol-bis(2-aminoethylether)-N,N,Nâ²,Nâ²-tetraacetic acid; FAU; fluorescence arb
Substrate oxidation and cardiac performance during exercise in disorders of long chain fatty acid oxidation
Keywords: AUC; area under the curve; A-VO2; arteriovenous oxygen; BMI; body mass index; BP; blood pressure; CHO; carbohydrate; CK; creatine kinase; CPT II; carnitine palmitoyl-transferase II; CTRC; Clinical & Translational Research Center; DEXA; dual energy X-ray a
Carnitine palmitoyltransferase 2: New insights on the substrate specificity and implications for acylcarnitine profiling
Keywords: mFAO; mitochondrial fatty acid β-oxidation; CPT1; carnitine palmitoyltransferase 1; CPT2; carnitine palmitoyltransferase 2; CACT; carnitine/acylcarnitine translocase; MTP; mitochondrial trifunctional protein; LCHAD; long-chain 3-hydroxyacyl-CoA dehydroge
ESI-MS/MS measurement of free carnitine and its precursor γ-butyrobetaine in plasma and dried blood spots from patients with organic acidurias and fatty acid oxidation disorders
Keywords: CPT; carnitine palmitoyltransferase; DBS; dried blood spots; FAOD; fatty acid oxidation disorder; IVA; isovaleric aciduria; GA-I; glutaric aciduria; LCHAD; long-chain 3-hydroxyacyl-CoA dehydrogenase; MA; malonic aciduria; MAD; multiple acyl-CoA dehydrogen
162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28-30 November 2008, Bussum, The Netherlands
Keywords: CPT; carnitine palmitoyl transferase; ETF; electron transfer flavoprotein; ETF-QO; electron transfer flavoprotein ubiquinone-oxidoreductase; LCEH; long-chain-2-enoyl-CoA hydratase; LCHAD; long-chain-3-hydroxyacyl-CoA dehydrogenase; LCKAT; long-chain-3-ket
Mitochondrial trifunctional protein defects: Clinical implications and therapeutic approaches
Keywords: Fatty acids; β-oxidation; Mitochondrial trifunctional protein; LCHAD; Mitochondria; TAT; PTD; Fusion proteins; Protein transduction domain; Cell penetrant peptide
Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts
Keywords: Carnitine-acylcarnitine translocase; Carnitine palmitoyltransferase II; LCHAD; Mitochondrial trifunctional protein; Acylcarnitines; Enzyme assays; Fatty acid oxidation; Fibroblasts; Pristanic
Mice Heterozygous for a Defect in Mitochondrial Trifunctional Protein Develop Hepatic Steatosis and Insulin Resistance
Keywords: AUC; area under curve; GPx; glutathione peroxidase; GSH; glutathione; GTT; glucose tolerance test; ITT; insulin tolerance test; LCHAD; long chain 3-hydroxyacyl-CoA dehydrogenase; MTP; mitochondrial trifunctional protein; NAFLD; nonalcoholic fatty liver di
Screening of newborns and high-risk group of children for inborn metabolic disorders using tandem mass spectrometry in South Korea: a three-year report
Keywords: PA; propionyl-CoA carboxylase deficiency; MMA; methylmalonyl-CoA mutase deficiency; GA 1; glutaryl-CoA dehydrogenase deficiency; GA 2; multiple-CoA dehydrogenase deficiency; MCC; multiple-CoA carboxylase deficiency; HMG; 3-hydroxy-3-methylglutaryl-CoA lya