Keywords: آتروفی عضلانی نخاعی (SMA); Biosensor; Cystic Fibrosis (CF); Duchenne Muscular Dystrophy (DMD); Dystrophin; Spinal muscular atrophy (SMA); Square wave voltammetry; Survival motor neuron 1 (SMN1); Voltammetry;
مقالات ISI آتروفی عضلانی نخاعی (SMA) (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.
Electrochemical immunosensors for the detection of survival motor neuron (SMN) protein using different carbon nanomaterials-modified electrodes
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Immunosensor; Carbon nanofiber;
CNS uptake of bortezomib is enhanced by P-glycoprotein inhibition: implications for spinal muscular atrophy
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); P-glycoprotein (P-gp); Blood brain barrier (BBB); Bortezomib; Tariquidar; Proteasome;
Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron 1 gene (SMN1); Survival motor neuron 2 gene (SMN2); Neuronal apoptosis inhibitory protein gene (NAIP); Small EDRK-rich factor 1A (SERF1A); Multiplex Ligation-dependent Probe Amplification (MLPA);
SMN control of RNP assembly: From post-transcriptional gene regulation to motor neuron disease
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Small nuclear RNA (snRNA); Ribonucleoprotein complexes (RNPs); Sm and LSm proteins; RNA processing;
Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Muscle ubiquitin ligases; Muscle atrophy F-box; MAFbx (Atrogin1); Muscle RING Finger 1; MuRF1 (Trim63)
Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); SMN1 gene; Infantile-onset X-linked SMA (SMAX2); UBA1 gene; Ubiquitin–proteasome system (UPS); Motor sensory neuronopathy; Cerebellum
Spinal muscular atrophy: going beyond the motor neuron
Keywords: آتروفی عضلانی نخاعی (SMA); motor neuron; multi-system disorder; spinal muscular atrophy (SMA); mouse; gene therapy; SMN
Analysis of a read-through promoting compound in a severe mouse model of spinal muscular atrophy
Keywords: آتروفی عضلانی نخاعی (SMA); SMA; spinal muscular atrophy; SMN; survival motor neuron; CNS; central nervous system; ICV; intracerebral ventricular injection; BBB; blood-brain-barrier; Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Read-through; Aminoglycoside;
Direct central nervous system delivery provides enhanced protection following vector mediated gene replacement in a severe model of Spinal Muscular Atrophy
Keywords: آتروفی عضلانی نخاعی (SMA); Survival Motor Neuron (SMN); Spinal Muscular Atrophy (SMA); scAAV; Gene therapy; Neurodegeneration; Therapeutics
Stabilization of the survival motor neuron protein by ASK1
Keywords: آتروفی عضلانی نخاعی (SMA); Apoptosis signal-regulating kinase 1 (ASK1); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Ubiquitination
Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Plastin 3 (PLS3); Discordant siblings; Modifier genes
New insights into the pathogenesis of spinal muscular atrophy
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Clinicopathological study; Ballooned neuron; Survival motor neuron (SMN); Programmed cell death
Inflammation in ALS and SMA: Sorting out the good from the evil
Keywords: آتروفی عضلانی نخاعی (SMA); Neuroinflammation; Gliosis; Astrocytosis; Astrocytes; Microgliosis; Microglia; Amyotrophic lateral sclerosis (ALS); Superoxide dismutase 1 (SOD1); Spinal muscular atrophy (SMA)
The spinal muscular atrophy protein SMN affects Drosophila germline nuclear organization through the U body–P body pathway
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); U body; P body; Drosophila; Nurse cell; Oocyte; Cajal body; Histone locus body
A SMNΔ7 read-through product confers functionality to the SMNΔ7 protein
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Read-through
Identification and characterisation of a nuclear localisation signal in the SMN associated protein, Gemin4
Keywords: آتروفی عضلانی نخاعی (SMA); Gemin4; Survival motor neuron; SMN; Spinal muscular atrophy (SMA); Nuclear localisation signal (NLS); Import receptors
SMN protects cells against mutant SOD1 toxicity by increasing chaperone activity
Keywords: آتروفی عضلانی نخاعی (SMA); Spinal muscular atrophy (SMA); The survival of motor neuron (SMN); Superoxide dismutase 1 (SOD1); Amyotrophic lateral sclerosis (ALS); Chaperone