Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase deficiency; Paroxysmal exercise-induced dystonia; Brain MRS; Thiamine-responsive dystoniaMRS, magnetic resonance spectroscopy; MRI, magnetic resonance imaging; PDH, pyruvate dehydrogenase; WB, western blot; PED, paroxysmal exercise
مقالات ISI کمبود پیرووات دهیدروژناز (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: کمبود پیرووات دهیدروژناز; RC; respiratory chain; PDH; pyruvate dehydrogenase; BCAAs; branched chain amino acids; CK; creatine kinase; PC; pyruvate carboxylase; PDHc; pyruvate dehydrogenase complex; Primary human mitochondrial disease; Pyruvate dehydrogenase deficiency; Metabolites
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia
Keywords: کمبود پیرووات دهیدروژناز; Pontocerebellar hypoplasia type 1; Human RNA exosome complex; Pyruvate dehydrogenase deficiency; Complex I deficiency; Mitochondrial disease; Whole exome sequencing; Transcriptome analysis; mtDNA copy numbers;
Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency
Keywords: کمبود پیرووات دهیدروژناز; Leucoencephalopathy with cysts; Pyruvate dehydrogenase deficiency; Hyperglycinemia; NFU1; Lipoic acid;
Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patients
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase deficiency; PDHX gene; New mutation
A combined therapeutic approach for pyruvate dehydrogenase deficiency using self-complementary adeno-associated virus serotype-specific vectors and dichloroacetate
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase deficiency; AAV vector; Gene therapy; Dichloroacetate
Two silent substitutions in the PDHA1 gene cause exon 5 skipping by disruption of a putative exonic splicing enhancer
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase; Pyruvate dehydrogenase deficiency; PDHA1 gene; Somatic mosaicism; Synonymous mutations; Aberrant splicing; SRp55 binding
Mutations of the E1β subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase; Pyruvate dehydrogenase deficiency; β subunit; E1β; Mutations; PDHB; Lactic acidosis; Consanguinity; Protein structure modeling
Down-regulation of expression of rat pyruvate dehydrogenase E1α gene by self-complementary adeno-associated virus-mediated small interfering RNA delivery
Keywords: کمبود پیرووات دهیدروژناز; AAV; Gene therapy; RNAi; Pyruvate dehydrogenase deficiency
Sensorineural hearing loss and pyruvate dehydrogenase deficiency syndrome: Implications for cochlear implantation
Keywords: کمبود پیرووات دهیدروژناز; Cochlear implant; Glycolysis; Hearing loss; Internal auditory canal; Lactic acidosis; Pyruvate dehydrogenase deficiency
Somatic mosaicism in a male with an exon skipping mutation in PDHA1 of the pyruvate dehydrogenase complex results in a milder phenotype
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase deficiency; Splicing; Immunocytochemistry
Pyruvate dehydrogenase phosphatase deficiency: Orphan disease or an under-diagnosed condition?
Keywords: کمبود پیرووات دهیدروژناز; Pyruvate dehydrogenase phosphatase; Metabolism; Mitochondria; Pyruvate dehydrogenase deficiency