Keywords: اسپاستین; Hereditary spastic paraplegia; Spastic paraplegia; Spastin; SPAST; SPG4; SPG7; Ethnic distribution;
مقالات ISI اسپاستین (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: اسپاستین; Curvature elasticity concept of biomembrane functions; Endoplasmatic reticulum shaping proteins; Membrane fusion; Membrane microtubule coupling; Lipid protein interaction; Reticulons; Atlastin; Spastin;
Missense mutation of SPAST protein (I344K) results in loss of ATPase activity and prolonged the half-life, implicated in autosomal dominant hereditary spastic paraplegia
Keywords: اسپاستین; Hereditary spastic paraplegia; Spastin; Missense mutation; ATPase activity; Axonal abnormality; Gene therapy;
Microtubules in health and degenerative disease of the nervous system
Keywords: اسپاستین; Microtubule; Neuron; Axon; Dendrite; Katanin; Spastin; Fidgetin; Dynein; Kinesin; Neurodegeneration; Alzheimer's disease; Tau; Tauopathy; Microtubule-associated proteins; Molecular motor proteins; Axonal transport; CAMSAP; Tubulin; Tubulin code; Microtu
Novel and recurrent spastin mutations in a large series of SPG4 Italian families
Keywords: اسپاستین; Spastin; SPG4; Hereditary spastic paraplegia (HSP); Mutations
The C-terminal α-helix of SPAS-1, a Caenorhabditis elegans spastin homologue, is crucial for microtubule severing
Keywords: اسپاستین; AAA ATPase; Caenorhabditis elegans; Chaperone; Hereditary spastic paraplegia; Microtubule; Spastin;
Crystal structure of the human spastin AAA domain
Keywords: اسپاستین; AAA ATPase; Microtubule severing; HSP; Spastin;
Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation – A neurophysiological study using excitability techniques
Keywords: اسپاستین; Hereditary spastic paraplegia; Spastin; Sensory dysfunction; Axonal excitability; Threshold electrotonus; Nerve conduction; Peripheral neuropathy
Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia
Keywords: اسپاستین; hereditary spastic paraplegia; multiplex ligation-dependent probe amplification; SPG4; spastin
Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males
Keywords: اسپاستین; Hereditary spastic paraplegia; Spastin; SPAST gene; SPG4 gene; Neurogenetics
A potential link between autoimmunity and neurodegeneration in immune-mediated neurological disease
Keywords: اسپاستین; Neurodegeneration; Autoimmunity; Multiple sclerosis; Spastin; Bioinformatics
Drosophila Atlastin regulates the stability of muscle microtubules and is required for synapse development
Keywords: اسپاستین; Drosophila; Atl; Spastin; Synaptic growth; Neuromuscular junction; ER and Golgi morphogenesis; Microtubule stability; Hereditary spastic paraplegia
Microtubule stabilizing effect of notch activation in primary cortical neurons
Keywords: اسپاستین; Jagged1; acetylated tubulin; Spastin; microtubules dynamicscDNA, complementary DNA; DIV, days in vitro
The C. elegans homologue of the spastic paraplegia protein, spastin, disassembles microtubules
Keywords: اسپاستین; AAA ATPase; C. elegans; Chaperone; Hereditary spastic paraplegia; Microtubule; Spastin
Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis
Keywords: اسپاستین; Spastic paraplegia; Spastin; Endoplasmic reticulum; Spinal cord; Motor neurons; HEK293 cells; Cortical neurons; Brefeldin A
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia
Keywords: اسپاستین; Hereditary spastic paraplegia; Spastin; SPG4; DHPLC
Spastin in the human and mouse central nervous system with special reference to its expression in the hippocampus of mouse pilocarpine model of status epilepticus and temporal lobe epilepsy
Keywords: اسپاستین; Spastin; Human; Mouse; Central nervous system; Distribution; Hippocampus; Epilepsy
Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons
Keywords: اسپاستین; Hereditary spastic paraplegia; SPG20; Neurodegeneration; Spartin; Spastin; Synaptotagmin
Spastin related hereditary spastic paraplegia with dysplastic corpus callosum
Keywords: اسپاستین; Hereditary spastic paraplegia; Dysplasia; Corpus callosum; Spastin; SPG4;
Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus
Keywords: اسپاستین; Hereditary spastic paraplegia; Spastin; Axonal degeneration; Nuclear-cytoplasmic shuttle; Leptomycin B; Initiation of translation;