Keywords: 18S rRNA; eukaryotic 18S rRNA; ACL; American cutaneous leishmaniasis; B2M; beta-2-microbolin; cDNA; complementary DNA; CYCA; cyclophilin A; FFPE; formalin-fixed paraffin-embedded; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; HIV; human immunodeficienc
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: LVNC; left ventricular non-compaction cardiomyopathy; mtDNA; mitochondrial DNA; rCRS; revised Cambridge Reference Sequence; CI; conversation index; MT-CO3; cytochrome c oxidase subunit 3 gene; MT-ATP6; ATPase subunit 6 gene; MT-ND5; NADH dehydrogenase sub
AMC-Bio-Artificial Liver culturing enhances mitochondrial biogenesis in human liver cell lines: The role of oxygen, medium perfusion and 3D configuration
Keywords: Mitochondrial biogenesis; Bio-artificial liver; HepaRG; C3A; Hepatocyte; ABCA12; ATP binding cassette subfamily A member 12; ACO2; aconitase 2; AMC; Amsterdam Medical Center; BAL; bio-artificial liver; BALIAD; bio-artificial liver-in-a-dish; CEBPa; CCAAT/
Centella asiatica attenuates hippocampal mitochondrial dysfunction and improves memory and executive function in β-amyloid overexpressing mice
Keywords: AD; Alzheimer's Disease; ADP; Adenosine diphosphate; Aβ; β-amyloid; CAW; Water extract of Centella asiatica; CFR; Conditioned fear response; ETC; Electron transport chain; FCCP; Carbonyl cyanide p-(trifluoromethoxy)phenylhydrazone; GAPDH; Glyceraldehyde
A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy
Keywords: MT-ATP6; ATP synthase; Mitochondrial disease; Mitochondrial DNA (mtDNA); Complex V deficiency;
Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
Keywords: Mitochondrial mutations; mtDNA; Mitochondrial duplication; m.9157G>A; m.14924T>C; MT-ATP6;
Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA
Keywords: 5-aza-dC; 5-aza-2â²-deoxycytidine; AD; Alzheimer's disease; AMD; Age-related Macular Degeneration; APOE; apolipoprotein E; ARPE-19; retinal pigmented epithelium cell line; ATP; adenosine triphosphate; BSA; bovine serum albumin; DMEM; Dulbecco's modified
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome
Keywords: Mitochondrial genome; Exome; Next-generation sequencing; Leigh syndrome; Homoplasmy; MT-ATP6; Lactic academia; Mitochondrial complex I; Inborn error of metabolism; CoQ10 deficiency; Molecular diagnostics