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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Keywords: AD; Alzheimer's disease; ADF; alternate day fasting; ALS; amyotrophic lateral sclerosis; APP; β-amyloid precursor protein; BDNF; brain-derived neurotrophic factor; CER; continuous energy restriction; CR; caloric restriction; CREB; cyclic AMP response e
Keywords: Action potential; Nerve conduction study; Sensory nerve action potential; Compound muscle action potential; Ion channel; Voltage-gated sodium channel; Voltage-gated potassium channel; Node of Ranvier; Paranode; Juxtaparanode; Septate-like junction; Tight
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
Keywords: Progesterone; Testosterone; Metabolites; Streptozotocin; Peripheral nerve; 3α-diol; 5α-androstane-3α,17β-diol; ACC; acetyl-CoA carboxylase α; AR; androgen receptor; DPN; diabetic peripheral neuropathy; DHP; dihydroprogesterone; ESI; electrospray ioni
Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP)
Keywords: PMP22; LITAF; MRI; Cervical spine; Han Chinese;
Lycium barbarum polysaccharide protects diabetic peripheral neuropathy by enhancing autophagy via mTOR/p70S6K inhibition in Streptozotocin-induced diabetic rats
Keywords: LBP; Lycium barbarum polysaccharide; DM; diabetes mellitus; DPN; diabetic peripheral neuropathy; LC3-II; microtubule-associated protein 1 light chain 3-II; HDL; high density lipoprotein; SC; Schwarm cell; STZ; streptozotocin; LA; lipoic acid; PWT; paw wit
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
Case reportCongenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion
Keywords: PMP22; Congenital hypomyelinating neuropathy; CMT; Nerve biopsy;
Temporal and spatial expression analysis of peripheral myelin protein 22 (Pmp22) in developing Xenopus
Keywords: Pmp22; Trigeminal ganglia; Cranio-facial cartilages; Otic vesicle; Xenopus;
Co-occurrence of Xp21 microduplication encompassing the DMD locus in conjunction with 17p12/PMP22 microduplication in a female with Charcot–Marie–Tooth disease type 1A
Keywords: CMT1A; DMD; PMP22; Combined microduplications; Dystrophin gene; Array comparative genomic hybridization (array CGH); Chromosomal microarray
Molecular and clinical features of inherited neuropathies due to PMP22 duplication
Keywords: PMP22; Duplication; Myelin; Nerve; Neuropathies; CMT1A
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
Fingolimod induces the transition to a nerve regeneration promoting Schwann cell phenotype
Keywords: Akt; PKB, protein kinase B; BDNF; brain derived neurotrophic factor; cAMP; cyclic adenosine monophosphate; CIDP; chronic inflammatory demyelinating polyneuropathy; CNS; central nervous system; Cx32; connexin-32; DMSO; dimethyl sulfoxide; DRG; dorsal root
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
Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in mice
Keywords: miR; microRNA; BACE1; beta secreatase; AD; Alzheimer's disease; NAV3; neuronal navigator 3; SCA17; spinocerebellar ataxia 17; FISH; fluorescence in situ hybridization; LNA; locked nucleic acid; APP; amyloid precursor protein; PMP22; peripheral myelin prot
Peripheral Myelin Protein 22 gene duplication with atypical presentations: A new example of the wide spectrum of Charcot-Marie-Tooth 1A disease
Keywords: Charcot-Marie-Tooth disease; CMT1A; HNPP; PMP22; Tomacula;
Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation
Keywords: Hereditary neuropathy with liability to pressure palsies; Novel mutation; MRI; PMP22; No recurrent palsies with pain;
Biopsy in a patient with PMP22 exon 2 mutation recapitulates pathology of Trembler-J mouse
Keywords: PMP22; DSD; Congenital hypomyelinating neuropathies; Genotype/phenotype correlations;
Variable phenotypes are associated with PMP22 missense mutations
Keywords: Charcot-Marie-Tooth disease; PMP22; HNPP
Sex-dimorphic effects of dehydroepiandrosterone in diabetic neuropathy
Keywords: liquid chromatography-tandem mass spectrometry; neuroactive steroids; myelin proteins; peripheral nerve; rat; streptozotocin; 3α-diol; α-androstane-3α, 17β-diol; 3β-diol; α-androstane-3β, 17β-diol; 17α-E; α-estradiol; 17β-E; β-estradiol; D9-PR
A new long term in vitro model of myelination
Keywords: Co-culture; Myelination; MBP; MAG; P0; PMP22
Overexpression and purification of rat peroxisomal membrane protein 22, PMP22, in Pichia pastoris
Keywords: PMP22; Pichia pastoris; Heterologous expression; Membrane protein; Fed-batch fermentation; Peroxisome
The α-chemokine CXCL14 is up-regulated in the sciatic nerve of a mouse model of Charcot–Marie–Tooth disease type 1A and alters myelin gene expression in cultured Schwann cells
Keywords: CMT1A; Pmp22; C61 mouse mutant; Myelin; Schwann cells; Cyclin D1; Ninjurin 1; Tenascin; CXCL14; Myelination
Different clinical and magnetic resonance imaging features between Charcot–Marie–Tooth disease type 1A and 2A
Keywords: Charcot–Marie–Tooth disease; PMP22; Mitofusin 2; Magnetic resonance imaging; Fatty infiltration
Altered peripheral myelination in mice lacking GABAB receptors
Keywords: Sciatic nerve; P0; PMP22; Nociception; Aδ fibers; DRG
Neuroprotective effects of dihydroprogesterone and progesterone in an experimental model of nerve crush injury
Keywords: rat sciatic nerve; neuroactive steroids; myelin proteins; reelin; morphology; nociception; ANOVA; analysis of variance; Ct; cycle threshold; Cx32; connexin 32; DHP; dihydroprogesterone; MAG; myelin-associated glycoprotein; MAL; myelin and lymphocyte prote
Ascorbic acid inhibits PMP22 expression by reducing cAMP levels
Keywords: CMT, Charcot-Marie-Tooth disease; PMP22, peripheral myelin protein 22 kDa; AA, ascorbic acid; dbcAMP, dibutyrylcyclic adenosine monophosphateCharcot-Marie-Tooth; Ascorbic acid; PMP22; Schwann cells; Cyclic AMP
Peripheral myelin protein 22 is expressed in human central nervous system
Keywords: PMP22; Gene expression; CNS; CMT1A; Motor neuron; Pia mater
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): The study protocol [EudraCT no.: 2006-000032-27]
Keywords: Charcot-Marie-Tooth disease; Ascorbic acid; Randomized controlled trial; Neuropathy; Genetic disorders; PMP22
Co-segregation of LMNA and PMP22 gene mutations in the same family
Keywords: LGMD1B; HNPP; LMNA; PMP22;
Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation
Keywords: Pmp22; Myelin; Trembler; Microarrays; E2F; Heat shock proteins 1A and 1B; Cholesterol synthesis; Cell cycle;