Keywords: بیماری الکساندر; Enfermedad de Alexander; Mielinización; ProteÃna acidica fibrilar glial; CondroitÃn sulfato proteoglicano-NG2; Epigenética; Astrocitos; Alexander disease; Myelination; Glial fibrilar acidic protein; Chondroitin sulfate proteoglycan-NG2; Epigenetics; A
مقالات ISI بیماری الکساندر (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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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: بیماری الکساندر; Alexander disease; Myelination; Glial fibrillar acidic protein; Chondroitin sulfate proteoglycan-NG2; Epigenetics; Astrocytes; Enfermedad de Alexander; Mielinización; ProteÃna acidica fibrilar glial; CondroitÃn sulfato proteoglicano-NG2; Epigenética;
Keywords: بیماری الکساندر; Neurodegenerative disorder; Leukodystrophy; Alexander disease; Magnetic resonance; GFAP gene; Enfermedad neurodegenerativa; Leucodristrofia; Enfermedad de Alexander; Resonancia magnética; Gen GFAP;
Keywords: بیماری الکساندر; direct conversion; chemical reprogramming; induced astrocytes; small molecules; Alexander disease
Keywords: بیماری الکساندر; gLE; genetic leukoencephalopathy; CNS; central nervous system; MRI; magnetic resonance imaging; MSUD; Maple Syrup Urine Disease; ClC-2; Chloride Ion Channel 2; MLC; Megalencephalic Leukoencephalopathy with subcortical cysts; X-ALD; X-linked Adrenoleukodys
Keywords: بیماری الکساندر; X-ALD; X-linked adrenoleukodystrophy; ADLD; Adult onset autosomal dominant leukodystrophy; AGS; Aicardi-Goutières syndrome; AxD; Alexander disease; CER; Comparative effectiveness research; CT; Computed tomography; CTX; Cerebrotendinous xanthomatosis; G
Keywords: بیماری الکساندر; Astrocytes; Glial scar; Transcription factors; Brain pathology; IF; intermediate filament; GFAP; glial fibrillary acidic protein; AxD; Alexander disease; AD; Alzheimer disease; ECM; extracellular matrix; FAK; focal adhesion kinase; FA; focal adhesion; MMP
Keywords: بیماری الکساندر; Leukoencephalopathy; Alexander disease; Mitochondrial disorders; Lactic acid
Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis
Keywords: بیماری الکساندر; Alexander disease; Leukodystrophy; GFAP; Spinal manifestation;
Review articleChildhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management
Keywords: بیماری الکساندر; ADLD; adult-onset autosomal dominant leukodystrophy; AGS; aicardi-goutieres syndrome; AMN; adrenomyeloneuropathy; AxD; alexander disease; CIC-2 related disease; chloride ion channel 2-related disease; CRMCC; cerebroretinal microangiopathy with calcificati
Screening for GFAP rearrangements in a cohort of Alexander disease and undetermined leukoencephalopathy patients
Keywords: بیماری الکساندر; Alexander disease; Undetermined hypomyelinating leukodystrophies; GFAP copy number variations; QMPSF
Disease specific therapies in leukodystrophies and leukoencephalopathies
Keywords: بیماری الکساندر; X-ALD; X-linked Adrenoleukodystrophy; AGS; Aicardi-Goutières Syndrome; CSF; cerebrospinal fluid; IFNα; α-interferon; RNA; ribonucleic acid; DNA; deoxyribonucleic acid; SLE; systemic lupus erythematosus; AxD; Alexander disease; GFAP; growth factor ass
Alexander disease with mild dorsal brainstem atrophy and infantile spasms
Keywords: بیماری الکساندر; Alexander disease; Glial fibrillary acidic protein gene; Infantile spasms; Brainstem; Hypsarrhythmia; Novel mutation
Beneficial effects of curcumin on GFAP filament organization and down-regulation of GFAP expression in an in vitro model of Alexander disease
Keywords: بیماری الکساندر; Alexander disease; Curcumin; GFAP; Autophagy; Heat shock proteins
Alexander disease causing mutations in the C-terminal domain of GFAP are deleterious both to assembly and network formation with the potential to both activate caspase 3 and decrease cell viability
Keywords: بیماری الکساندر; IF, intermediate filament; sHSPs, small heat shock proteins; GFAP, glial fibrillary acidic protein; TEM, transmission electron microscopy; ULF, unit length filament; WT, wild typeGFAP; Mutation; Alexander disease; Intermediate filament; Stress; Small heat
The process of inducing GFAP aggregates in astrocytoma-derived cells is different between R239C and R416W mutant GFAP. A time-lapse recording study
Keywords: بیماری الکساندر; Alexander disease; Glial fibrillary acidic protein; Astrocytes; Time-lapse recording
Tumor-like enlargement of the optic chiasm in an infant with Alexander disease
Keywords: بیماری الکساندر; Alexander disease; GFAP mutation; Optic pathway glioma;
Review of Alexander disease: Beyond the classical concept of leukodystrophy
Keywords: بیماری الکساندر; Alexander disease; GFAP; Rosenthal fiber; Leukodystrophy
Properties of astrocytes cultured from GFAP over-expressing and GFAP mutant mice
Keywords: بیماری الکساندر; Glial fibrillary acidic protein (GFAP); Alexander disease; Rosenthal fiber (RF); Astrocytes
GFAP aggregates in the cochlear nerve increase the noise vulnerability of sensory cells in the organ of Corti in the murine model of Alexander disease
Keywords: بیماری الکساندر; Alexander disease; Astrocyte; Cochlear nerve; GFAP aggregates; Glia; Hair cell; Noise-induced hearing loss;
A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis
Keywords: بیماری الکساندر; Alexander disease; Infantile type; GFAP; R239H; MRI
Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease
Keywords: بیماری الکساندر; Alexander disease; Astrocytes; Demyelinating disease; Glial fibrillary acid protein; Intermediate filaments; Hereditary neurodegenerative diseases;
Fluoro-Jade: New fluorescent marker of Rosenthal fibers
Keywords: بیماری الکساندر; Fluoro-Jade; Rosenthal fibers; GFAP; Aggregates; Alexander disease;