Keywords: Arterivirus; Simian hemorrhagic fever virus; PLP1; nsp1; Minor structural proteins; Infectious clone
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: ACP33; Maspardin gene; AD; Autosomal dominant; AP4B1; Adaptor-related protein complex 4, epsilon 1 subunit gene; AP4M1; Adaptor-related protein complex 4, Mu 1 subunit gene; AP4E1; Adaptor-related protein complex 4, Epsilon 1 subunit gene; AP4S1; Adaptor-
Keywords: DHA; docosahexaenoic acid; E1; estrone; E2; estradiol; E3; estriol; EPA; eicosapentaenoic acid; GST; galactocereboside sulfotransferase; IGF-1; insulin-like growth factor-I; MBP; myelin basic protein; MOG; myelin oligodendrocyte glycoprotein; PLP; proteol
Keywords: PLP1; DM20; Hypomyelinating leukodystrophy; Intronic mutation
Mice overexpressing lamin B1 in oligodendrocytes recapitulate the age-dependent motor signs, but not the early autonomic cardiovascular dysfunction of autosomal-dominant leukodystrophy (ADLD)
Keywords: ADLD; adult-onset autosomal dominant leukodystrophy; BRS; index of cardiac baroreflex sensitivity; EEG; electroencephalogram; EMG; electromyogram; HP; heart period; LMNB1; lamin B1 gene; N; non-rapid-eye-movement sleep; PBS; phosphate buffered saline; Plp
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing
Keywords: Hereditary spastic paraparesis; PLP1; Multiple sclerosis; MRI;
Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation
Keywords: Spastic paraplegia 2; Pelizaeus–Merzbacher disease; PLP1; Dysmyelination; Auditory brainstem response
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus–Merzbacher disease
Keywords: PMD; PLP1; Missense mutation; Subcellular localization
Plp1 gene duplication inhibits airway responsiveness and induces lung inflammation
Keywords: Pelizaeus-Merzbacher disease; Airway pharmacology; Lung mechanics; Phase angle; CNS; central nervous system; Cdyn; dynamic lung compliance; Cst; static lung compliance; IL; interleukin; LBI; labored breathing index; PMD; Pelizaeus-Merzbacher disease; PLP;
Oligodendrocyte morphometry and expression of myelin - Related mRNA in ventral prefrontal white matter in major depressive disorder
Keywords: Postmortem; Myelin; CNPase; MOG; PLP1; OLIG1;
Modeling the natural history of Pelizaeus-Merzbacher disease
Keywords: PMD; Pelizaeus-Merzbacher Disease; PLP1/Plp1; proteolipid protein 1 gene; TUNEL; Terminal deoxynucleotidyl transferase-mediated dUTP Nick End Labeling; OL; Oligdendrocyte; GFAP; Glial Fibrillary Acidic Protein.; X-linked; Hypomyelination; PLP1; Oligoden
Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease
Keywords: CNS; central nervous system; PMD; Pelizaeus-Merzbacher disease; PMLD; Pelizaeus-Merzbacher like disease; PLP1; proteolipid protein 1; GJC2; gap junction protein, gamma 2; Cx47; connexin 47; MRI; magnetic resonance imaging; PCR; polymerase chain reacti
Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion
Keywords: Pelizaeus–Merzbacher disease; PLP1; PLP1-null syndrome; Nonhomologous end joining
Pelizaeus–Merzbacher disease-associated proteolipid protein 1 inhibits oligodendrocyte precursor cell differentiation via extracellular-signal regulated kinase signaling
Keywords: PLP1; ERK; Oligodendrocyte precursor cells; Differentiation; Primary culture system
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Keywords: ACP33; Maspardin gene; AD; Autosomal dominant; ALS; Amyotrophic lateral sclerosis; AP; Adaptor Protein complex; AR; Autosomal recessive; ATL1; Atlastin-1 gene; BMP; Bone morphogenic protein; BSCL2; Berardinelli-Seip congenital lipodystrophy gene; CYP7B1;
Characterization of a PLP-overexpressing transgenic rat, a model for the connatal form of Pelizaeus–Merzbacher disease
Keywords: Pelizaeus–Merzbacher disease; Proteolipid protein; Myelination; Plp1; Apoptosis; Connatal PMD; Gene duplication
Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation
Keywords: Pelizaeus-Merzbacher disease; Proteolipid protein 1; PLP1;
PLP1 gene duplication as a cause of the classic form of Pelizaeus-Merzbacher disease – case report
Keywords: Pelizaeus-Merzbacher disease; dysmyelination disorder; leukodystrophy; PLP1; gene duplication; MLPAchoroba Pelizaeusa-Merzbachera; choroba dysmielinizacyjna; leukodystrofia; PLP1; duplikacja genu; MLPA
PLP1 gene duplication causes overexpression and alteration of the PLP/DM20 splicing balance in fibroblasts from Pelizaeus–Merzbacher disease patients
Keywords: Gene duplication; Gene expression; PLP1; PMD; Fibroblast; Alternative splicing
Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNA
Keywords: Pelizaeus-Merzbacher disease; PLP1 gene; splice mutation; CT; computed tomography; ER; endoplasmatic reticulum; MRI; magnetic resonance imaging; PLP1; proteolipid protein gene; PMD; Pelizaeus-Merzbacher disease; SPG; spastic paraplegia; SSCP; single stran