Keywords: اختلال بیوژنز پراکسسیوم; ACOX; acyl-CoA oxidase; DCA; dicarboxylic fatty acid; DHA; docosahexaenoic acid; DHCA; 3α,7α-dihydroxycholestanoic acid; MCK; muscle creatine kinase; MFP; multifunctional protein; PBD; peroxisome biogenesis disorder; PUFA; polyunsaturated fatty acid; RO
مقالات ISI اختلال بیوژنز پراکسسیوم (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: اختلال بیوژنز پراکسسیوم; ABC; ATP-binding cassette; ACAA1; acetyl-CoA acyltransferase; ACOX; acyl-CoA oxidase; BAAT; bile acid CoA-amino acid N-acyl transferase; C24-bile acid; cholanoic acid; C27-bile acid; cholestanoic acid; CDCA; chenodeoxycholic acid; Cn-DCA; straight chain d
Keywords: اختلال بیوژنز پراکسسیوم; AA; arachidonic acid; ABCD1; ATP-binding cassette transporter subfamily D member 1; AlkCho; plasmanylcholine; AOx; acyl-CoA oxidase1; CG; complementation group; CHO; Chinese hamster ovary; CNS; central nervous system; D-BP; D-bifunctional protein; DHA; do
Disruption of peroxisome function leads to metabolic stress, mTOR inhibition, and lethality in liver cancer cells
Keywords: اختلال بیوژنز پراکسسیوم; Peroxisome; Peroxisomal biogenesis factor 2; Mammalian target of rapamycin complex 1; Metabolic stress; Human hepatocellular carcinoma; PEXs; peroxins; PTS; peroxisome targeting signal; PBD; peroxisome biogenesis disorder; ZS; Zellweger syndrome; HCC; hum
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
Keywords: اختلال بیوژنز پراکسسیوم; Peroxisome biogenesis disorder; Peroxisome biogenesis factor 10 (PEX10); Compound heterozygote; Point mutation; Cerebellar ataxia; Zellweger syndrome; AFP; alpha fetoprotein; BWA; Burrows Wheeler Aligner; DHA; docosahexaenoic acid; dma; dimethyl acetal; F
Phytol-induced pathology in 2-hydroxyacyl-CoA lyase (HACL1) deficient mice. Evidence for a second non-HACL1-related lyase
Keywords: اختلال بیوژنز پراکسسیوم; 2OH-FA; 2-hydroxy fatty acid; ARD; adult Refsum disease; CNS; central nervous system; DEXA; dual energy X-ray absorptiometry; ER; endoplasmic reticulum; GC; gas chromatography; KO; knockout; LC; liquid chromatography; MEF; mouse embryonic fibroblasts; MFP
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Keywords: اختلال بیوژنز پراکسسیوم; AAV; adeno-associated virus; AED; anti-epileptic drug(s); DHA; docosahexaenoic acid; DHCA; dihydroxycholestanoic acid; ERG; electroretinogram; G-tube; gastrostomy tube; IRD; infantile Refsum disease; LC-MS/MS; liquid chromatography/tandem mass spectrometr
De novo peroxisome biogenesis: Evolving concepts and conundrums
Keywords: اختلال بیوژنز پراکسسیوم; aa; amino acids; ARF1; ADP-ribosylation-factor 1; APX; ascorbate peroxidase; BFA; brefeldin A; BY-2; bright yellow-2; COP; coatomer protein; ER; endoplasmic reticulum; ERES; endoplasmic reticulum exit sites; ERPIC; ER-peroxisome intermediate compartment;
Late-Onset Zellweger Spectrum Disorder Caused by PEX6 Mutations Mimicking X-Linked Adrenoleukodystrophy
Keywords: اختلال بیوژنز پراکسسیوم; peroxisome biogenesis disorder; Zellweger spectrum disorder; X-linked adrenoleukodystrophy; PEX6 gene; late onset
New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis
Keywords: اختلال بیوژنز پراکسسیوم; CG; complementation group; CHO; Chinese hamster ovary; NSF; N-ethylmaleimide-sensitive fusion protein; PBDs; peroxisome biogenesis disorders; PTS1 and PTS2; peroxisome targeting signal types 1 and 2; VCP; valocin-containing protein; AAA peroxin; CHO cell
Genetics and molecular basis of human peroxisome biogenesis disorders
Keywords: اختلال بیوژنز پراکسسیوم; Peroxisome biogenesis disorder; Zellweger syndrome spectrum; PEX genes; Peroxisome assembly; Genetic testing
A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton
Keywords: اختلال بیوژنز پراکسسیوم; Pex7; Mouse models; Peroxisome biogenesis disorder; Rhizomelic chondrodysplasia punctata; Plasmalogens; Phytanic acid