Keywords: آتروفی غالب اپتیکی; ONH; optic nerve head; VD; vessel density; N; nasal; IN; inferonasal; IT; inferotemporal; T; temporal; IT; inferotemporal; IN; inferonasal; Dominant optic atrophy; DOA; Optical coherence tomography angiography; Vessel density; Inherited mitochondrial opti
مقالات ISI آتروفی غالب اپتیکی (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: آتروفی غالب اپتیکی; Melanopsin; Retinal ganglion cells; Mitochondria; Leber's hereditary optic neuropathy; Dominant optic atrophy; Optic atrophy; Light; Robustness; Alzheimer;
Keywords: آتروفی غالب اپتیکی; Inherited optic neuropathies; Leber's Hereditary Optic Neuropathy; Dominant optic atrophy; Incomplete penetrance; Genetic modifiers; Environmental triggers;
Keywords: آتروفی غالب اپتیکی; Neuropathies optiques; Neuropathie optique héréditaire de Leber; Atrophie optique dominante; Maladie de Kjer; Syndrome de Wolfram; Optic neuropathy; Chronic progressive external ophthalmoplegia; Retinitis pigmentosa; Leber's hereditary optic neuropathy;
Keywords: آتروفی غالب اپتیکی; Mitochondria; Mitochondrial fission; Mitochondrial fusion; DRP1; OPA1; MFN1; MFN2; GDAP1; Neurodegeneration; Charcot-Marie-Tooth disease; Dominant Optic Atrophy; Neuronal maturation; Neuronal plasticity; Synapse; Dendrite; Axon;
Keywords: آتروفی غالب اپتیکی; Hereditary optic neuropathies; Dominant optic atrophy; Wolfram syndrome; Diabetes mellitus; Deafness
Neuropathies optiques héréditaires en ophtalmo-pédiatrie
Keywords: آتروفی غالب اپتیکی; Atrophie optique dominante; Enfant; Neuropathie optique de Leber; Neuropathie optique héréditaire; Syndrome de Wolfram; Syndrome de Wolfram-like; Dominant optic atrophy; Child; Leber's optic neuropathy; Hereditary optic neuropathy; Wolfram's syndrome; W
OPA1: How much do we know to approach therapy?
Keywords: آتروفی غالب اپتیکی; OPA1 mutations; Dominant optic atrophy; Mitochondria dynamics; DOA therapy;
Research PaperAge-related accumulation of phosphorylated mitofusin 2 protein in retinal ganglion cells correlates with glaucoma progression
Keywords: آتروفی غالب اپتیکی; CMT; Charcot-Marie-Tooth; DBA; DBA/2J; DOA; dominant optic atrophy; D2G; DBA/2JGpnmb +;  IOP; intraocular pressure; Mfn1; mitofusin 1; Mfn2; mitofusin 2; NICIF; nanoimmuno capillary isoelectric focusing; NP; NanoPro; ON; optic nerve; Opa1; optic atrophy
Deficiencies in mitochondrial dynamics sensitize Caenorhabditis elegans to arsenite and other mitochondrial toxicants by reducing mitochondrial adaptability
Keywords: آتروفی غالب اپتیکی; OMM; outer mitochondrial membrane; DRP1; dynamin-related protein-1; MFN1; mitofusin 1; MFN2; mitofusin 2; mtDNA; mitochondrial DNA; PINK1; PTEN-induced putative kinase 1; PARK2; parkin; DOA; dominant optic atrophy; CMT2A; Charcot-Marie-Tooth neuropathy ty
OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology
Keywords: آتروفی غالب اپتیکی; DOA; Dominant Optic Atrophy; DOAD; Dominant Optic Atrophy and Deafness; mtDNA; Mitochondrial DNA; OCT; Optical Coherence Tomography; OPA1; Optic Atrophy 1; OXPHOS; Oxidative Phosphorylation; RGC; Retinal Ganglion Cell; Mitochondria; Mitochondrial dynamics
Analysis of mitochondrial structure and function in the Drosophila larval musculature
Keywords: آتروفی غالب اپتیکی; ATP; adenosine triphosphate; AEL; after egg laying; CMT2A; Charcot-Marie-Tooth Type 2A; ConA; concanavalin A; Drp1; dynamin-related protein; DOA; dominant optic atrophy; GFP; green fluorescent protein; IFM; indirect flight muscle; IMF; intermyofibrill
Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction
Keywords: آتروفی غالب اپتیکی; Dominant optic atrophy; Brain imaging; Mitochondrial disorders; Magnetic resonance spectroscopy; OPA1; Optic nerve;
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy
Keywords: آتروفی غالب اپتیکی; CC; coiled coil; CMV; cytomegalovirus; COX; cytochrome c oxidoreductase; DOA; Dominant Optic Atrophy; DOA plus; Dominant Optic Atrophy plus phenotype; GED; GTPase effector domain; MPS; mitochondrial peptide signal; NCCR; NADH-cytochrome c oxidoreductase;
The dynamin GTPase OPA1: More than mitochondria?
Keywords: آتروفی غالب اپتیکی; OPA1; Mitochondria; Membrane dynamics; Apoptosis; mtDNA; Dominant optic atrophy;
D. melanogaster, mitochondria and neurodegeneration: small model organism, big discoveries
Keywords: آتروفی غالب اپتیکی; AD; Alzeheimer's disease; ADOA; Autosomal dominant optic atrophy; AP; Amyloid plaque; APP; Amyloid precursor protein; Aβ; Amino acids amyloid β-peptides; CaMKIIa; Calcium/calmodulin dependent protein kinase II alpha; CMTIIa; Charcot-Marie-Tooth type
Les neuropathies optiques héréditaires : du signe clinique au diagnostic
Keywords: آتروفی غالب اپتیکی; Atrophie optique dominante; Neuropathie optique de Leber; OPA1; ADN mitochondrial; Syndrome de Wolfram; Télangiectasies papillaires; Dominant optic atrophy; Leber's optic atrophy; OPA1; Mitochondrial DNA; Wolfram syndrome; Optic nerve head telangiectasia
Mitochondrial optic neuropathies - Disease mechanisms and therapeutic strategies
Keywords: آتروفی غالب اپتیکی; Dominant optic atrophy; Glaucoma; Hereditary spastic paraplegia; Leber hereditary optic neuropathy; Mitochondrial DNA; Mitofusin; Multiple sclerosis; Neuroprotection; Optic neuritis; Optic neuropathy; Retinal ganglion cell;
The Neuro-ophthalmology of Mitochondrial Disease
Keywords: آتروفی غالب اپتیکی; chronic progressive external ophthalmoplegia; dominant optic atrophy; Kearns-Sayre syndrome; Leber hereditary optic neuropathy; MELAS; mitochondria; NARP; neuro-ophthalmology; pigmentary retinopathy
OPA1 expression in the human retina and optic nerve
Keywords: آتروفی غالب اپتیکی; dominant optic atrophy; mitochondria; OPA1