Keywords: Sciatic nerve crush; Curcumin; Oxidative stress; Myelin; ARE; Antioxidant responsive element; APL; Area per lipid; BW; Beam walking; CMAP; Compound muscle action potential; GST-P; Glutathione S-transferase P; HES; Haematoxylin-eosin-safran; HO-1; Heme-oxy
مقالات ISI (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: Leprosy; MPZ; MBL2; Gene polymorphisms; Immune response; Allelic transmission;
Keywords: PPI; protein-protein interactions; TM; transmembrane; GPCR; G-protein coupled receptor; RTK; receptor tyrosine kinase; TLR; Toll-like receptor; ErbB-2; EGFR epidermal growth factor receptor; NRP1; neuropilin-1; MPZ; myelin protein zero; gp41; glycoprote
Keywords: CFL; Courant-Friedrichs-Lewy; CSF; Continuum surface force; AMP; 2-aminomethylpropanol; MDEA; N-methyldiethanolamine; MEA; Monoethanolamine; MPZ; 1-methylepiperazine; PISO; Pressure implicit with split of operators; PLIC; Piecewise linear interface ca
Keywords: CMT; Charcot Marie Tooth disease; AD; Autosomal dominant; AR; Autosomal recessive; MNCV; Motor nerve conduction velocity; CMAP; Compound muscle action potential; PMP22; Peripheral myelin protein 22; HMSN; Hereditary motor sensory neuropathy; LITAF; lipopo
Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs
Keywords: Cross sectional area (CSA); High resolution ultrasound (HRUS); Inherited neuropathy; Nerve conduction study (NCS); Nerve ultrasound; Phenotypical spectrum; PMP22; peripheral myelin protein 22; GJB1; gap-junction protein beta-1; Cx32; connexin 32; MPZ; mye
Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo
Keywords: CMT; Charcot-Marie-Tooth disease; siRNA; small interfering RNA; PMP22; peripheral myelin protein 22Â kD; MBP; myelin basic protein; MPZ; myelin protein zero; IPN; Inherited peripheral neuropathy; HMSN; hereditary motor and sensory neuropathy; HNPP; heredi
The protective effect of the active components of ERPC on diabetic peripheral neuropathy in rats
Keywords: DPN; diabetic peripheral neuropathy; PKC; protein kinase C; TCM; traditional Chinese medicine; MNCV; motor nerve conduction velocity; AGE; advanced glycation end products; RAGE; receptor of advanced glycation end products; NF-κB; nuclear factor-κB; MDA;
Case reportA novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b
Keywords: CMT; P0; MPZ; RNA splicing; Synonymous mutation;
The shifting paradigm of Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Hereditary polyneuropathy; Maladie de Charcot-Marie-Tooth; Polyneuropathie héréditaire; AD; autosomal dominant; AR; autosomal recessive; CMT; Charcot-Marie-Tooth disease; CMT1; autosomal dominant demyelinating CMT; CMT2; aut
Impact of I30T and I30M substitution in MPZ gene associated with Dejerine-Sottas syndrome type B (DSSB): A molecular modeling and dynamics
Keywords: DSSB; MPZ; nsSNPs; I30T; I30M; Molecular dynamics;
Demyelinating CMT–what’s known, what’s new and what’s in store?
Keywords: Charcot–Marie–Tooth disease; Inherited neuropathies; Demyelinating neuropathies; PMP22; MPZ; Cx32; Unfolded protein response
Short communicationPOLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria
Keywords: POLG; Polymerase gamma; MRI; Magnetic resonance imaging; EKG; Electrocardiogram; EEG; Electroencephalogram; GALT; Galactose-1-phosphate uridylyltransferase; GJB1; Gap junction beta-1; MPZ; Myelin protein zero; DNA; Deoxyribose nucleic acid; STR; Short tan
Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family
Keywords: EGR2; CMT; MPZ; Demyelinating neuropathy; Linkage analysis;
Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain
Keywords: Peripheral neuropathy; MPZ; Charcot-Marie-Tooth disease; Neuropathic pain; Quantitative sensory testing; Intraepidermal nerve fibre density;
Clinical and cellular characterization of two novel MPZ mutations, p.I135M and p.Q187PfsX63
Keywords: MPZ; P0; CMT; CMT1B; Charcot–Marie–Tooth disease
A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia
Keywords: HyperCKemia; Inherited neuropathy; MPZ; Sural nerve biopsy; Electromyography
Human cytomegalovirus (HCMV) and hearing impairment: Infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49—Both involved in dominantly inherited, sensorineural, hearing impairment
Keywords: HCMV; Cytomegalovirus; Hearing impairment; DFNA7; DFNA49; MPZ; Chromosome break; Chromosome gap
Molecular characterization of myelin protein zero in Xenopus laevis peripheral nerve: Equilibrium between non-covalently associated dimer and monomer
Keywords: CAD; collision-activated dissociation; α-CHCA; α-cyano-4-hydroxycinnamic acid; CHAPSO; 3-[(3-cholamidopropyl) dimethylammonio]-2-hydroxy-1-propane sulfonate; CHN; congenital hypomyelination neuropathy; CID; collision-induced decomposition; CMT1B; Charco
Peripheral neuropathies caused by mutations in the myelin protein zero
Keywords: MPZ; Early onset neuropathy; Late onset neuropathy; Myelination; Demyelination