Keywords: 3D genome; Chromosome; Chromatin loop; Nucleus; Cohesin; 3C; chromosome conformation capture; CTCF; CCCTC-binding factor; SMC; structural maintenance of chromosomes; CdLS; Cornelia de Lange syndrome; FISH; fluorescent in situ hybridization; Hi-C; high-thr
مقالات ISI (ترجمه نشده)
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Keywords: Maternal high fat; Neurodevelopmental programming; Mecp2; Tbr1; Glutamate; Anxiety;
Keywords: 5mC; 5-methylcytosine; a-DMR; age-differentially methylated region; Avy; agouti viable yellow; cfDNAs; cell-free DNA; COBRA; combined bisulfite restriction analysis; ERE; endogenous retroelement; ETns; early transposons; hADSC; human adipose derived mesen
Keywords: ALS; amyotrophic lateral sclerosis; BDNF; brain-derived neurotropic factor; CerS; ceramide synthase; CNS; central nervous system; CPL; cecal ligation and puncture; cPLA2; cytosolic phospholipase A2; CSA; cyclosporine A; CTL; cytotoxic T lymphocytes; CYP45
Keywords: ADA2; Adenosine deaminase 2; ASH1L; Absent, Small, or Homeotic 1-like; BAF; BRG1 associated factor; BAH; Bromoadjacent homology; BAZ2A; Bromodomain adjacent to zinc finger domain protein 2A; BET; Bromodomain and Extra-Terminal domain; BRPF1; Bromodomain a
Keywords: ASD; autism spectrum disorders; BTBR; BTBR T+Itpr3tf/J mouse strain; cKO; conditional knockout; CNS; central nervous system; CNTNAP2; contactin-associated protein-like 2; DREADD; designer receptors exclusively activated by designer drugs; DSM-5; Diagnosti
Keywords: Norepinephrine transporter; Postural tachycardia syndrome; Epigenetics; Gene regulation; MeCP2; Histone modifications; Chromatin;
Keywords: 5-HT(2B); 5-hydroxytryptamine 2B receptor; ACE; angiotensin-converting enzyme; AMPK; AMP-activated protein kinase; ARB; AT1R blocker; ASK1; apoptosis signal-regulating kinase 1; AT1R; angiotensin II type 1 receptor; ATX; autotaxin; BDL; bile duct ligation
Keywords: Aza; 5-aza 2 deoxycytidine; TSA; trichostatin A; MeCP2; methyl CpG binding protein 2; SLE; systemic lupus erythematosus; RA; rheumatoid arthritis; DNMTs; DNA methyltransferases; HDACs; histone deacetylases; HAT; histones acetyl transferases; HMT; histone
Keywords: MECP2; Inflammation; Aberrant N-glucosylation; Synthetic antigenic peptides; Autoimmunity
Keywords: AMPA; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid; dendritic spine; spine or postsynaptic terminal or postsynapse; DHA; docosahexaenoic acid; ECM; extracellular matrix; EEG; electroencephalogram; EPSP; excitatory postsynaptic potential; GABA; ga
Keywords: Estradiol; Estrogens; Androgen; Neuroactive steroids; MeCP2; FMRP; Trisomy 21; Reelin; Behavior; Animal models
Keywords: ASDs; Autism spectrum disorders; CNV; copy number variant; eIPSC; evoked IPSC; FMRP; fragile X mental retardation protein; FXS; fragile X syndrome; LOH; loss of heterozygosity; LTD; long-term depression; LTP; long-term potentiation; mEPSCs; miniature exci
Keywords: M1 macrophage activation; Iron; Hepatic stellate cells; Morphogens; Wnt; MeCP2;
Keywords: ALD; alcoholic liver disease; ASH1; absent, small or homeotic disc 1; ChIP; chromatin immunoprecipitation; ECM; extra cellular matrix; H3K4; lysine 4 histone 3; HSC; hepatic stellate cell; MeCP2; methyl-CpG binding protein 2; MLL1; myeloid/lymphoid, or mi
Keywords: ADHD; Epigenetic; DNA methylation; Histone acetylation; MeCP2;
Keywords: 5-aza-CdR; 5-aza-2â²-deoxycytidine; AML; acute myeloid leukemia; ANRIL; antisense non-coding RNA in the INK4 locus; CBP; CREB-binding protein; CDKN2A; Cyclin-Dependent Kinase Inhibitor 2A; CoREST; co-repressor for element-1-silencing transcription factor
Keywords: Dendritic spine; Synaptic plasticity; Neurodegenerative diseases; Psychiatric disorders; Glutamate receptor; Calcium signaling; ADHD; attention deficit hypersensitive disorders; FXS; Fragile X-syndrome; CNS; central nervous system; GABA; gamma amino butyr
Keywords: 4HNE; 4-hydroxy-2-nonena 1; AA-NAT; arylalkylamine N-acetylatransferase; AFMK; N1-acetyl-N2-formyl-5-methoxykynuramine; AHr; aryl hydrocarbon receptor; AMK; N1-acetyl-5-methoxykynuramine; Apo; apolipoprotein; cAMP; cyclic adenosine monophosphate; B2-adr;
Keywords: Transcription; MeCP2; REST; HDACs; CNS; Behavior; Synapse
Keywords: Addiction; AMPAR; CoREST; HDAC2; MeCP2; NMDAR; REST; valproic acid;
Keywords: BLA; basolateral amygdala; CBP; CREB binding protein; CREB; cyclic AMP-responsive element binding factor; DG; dentate gyrus; Dnmt; DNA methyl transferase; GR; glucocorticoid receptor; HAT; histone acetyltransferase; HDACs; histone deacetylases; LTD; long-
Keywords: cDNA; complementary DNA; DAPI; 4',6'-Diamino-2-Phenylindole; DNMT; DNA methyltransferase; DMEM; Dulbecco's minimal essential medium; FCS; fetal calf serum; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; GS; glutamine synthetase; MeCP2; methyl-CpG-
Keywords: BDNF; brain derived neurotrophic factor; CAMKII; calmodulin-dependent protein kinase II; Ca2+; calcium; cAMP; cyclic adenosine monophosphate; CBS; cystathionine-β-synthase; CCI; chronic constriction injury; CFA; complete Freund's adjuvant; cGMP; cyclic
Keywords: Small ubiquitin-like modifier; SUMO; MeCP2; Neurons; Sequential quantitative chromatin immunoprecipitation; Seq-ChIP; Chromatin biochemistry
Anti-MOG antibody encephalitis mimicking neurological deterioration in a case of Rett syndrome with MECP2 mutation
Keywords: Anti-MOG antibody encephalitis; Rett syndrome; MECP2; Mutation; MRI;
MECP2 mutation in a boy with severe apnea and sick sinus syndrome
Keywords: MECP2; Male; Neonatal encephalopathy; Apnea; Sick sinus syndrome;
LPS-induces IL-6 and IL-8 gene expression in bovine endometrial cells “through DNA methylation”
Keywords: LPS; Lipopolysaccharide; TLR4; Toll-Like Receptor 4; IL-6; interleukin 6; IL-8; interleukin 8; MeCP2; methyl CpG-binding protein 2; ELISA; Enzyme-linked immunosorbent assay; qRT-PCR; RNA extraction and quantitative real-time PCR; cDNA; complementary DNA;
First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation
Keywords: Rett syndrome; MECP2; (c.695G>T;p.G232V); (c.880â¯C>T;p.R294X); TRD (transcription repression domain);
Impact of Gastrostomy Placement on Nutritional Status, Physical Health, and Parental Well-Being of Females with Rett Syndrome: A Longitudinal Study of an Australian Population
Keywords: BMI; Body mass index; IRR; Incidence rate ratio; MCS; Mental Component Summary; MECP2; Methyl CpG binding protein 2; PCS; Physical Component Summary; WAZ; Weight-for-age z score;
The course of awake breathing disturbances across the lifespan in Rett syndrome
Keywords: CDKL5; human cyclin-dependent kinase-like 5 gene; MeCP2; human methyl-CpG-binding protein 2; MECP2; human methyl-CpG-binding protein 2 gene; Mecp2; murine methyl-CpG-binding protein 2 gene; Rett syndrome; MECP2; Periodic breathing; Dysautonomia; Natural H
Whole exome sequencing identifies a novel 5â¯Mb deletion at 14q12 region in a patient with global developmental delay, microcephaly and seizures
Keywords: RTT; Rett syndrome; MECP2; Methyl-CpG-Binding Protein 2; CDKL5; Cyclin Dependent Kinase Like 5; FOXG1; Forkhead Box G1; OMIM; Online Mendelian Inheritance in Man; PRKD1; Protein Kinase D1; NOVA1; Neurooncologic Ventral Antigen 1; c14orf23; Chromosome 14 O
MeCP2 overexpression inhibits proliferation, migration and invasion of C6 glioma by modulating ERK signaling and gene expression
Keywords: MeCP2; C6 glioma; ERK; ChIP;
Regulation of seizure-induced MeCP2 Ser421 phosphorylation in the developing brain
Keywords: MeCP2; methyl CpG binding protein 2; CP-AMPARs; calcium-permeable α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPAR) receptors; NMDARs; N-methyl-d-aspartate receptor; LT-VGCCs; l-type voltage gated calcium channels; HS; hypoxic seizures; ASD; a
MeCP2 Expression in a Rat Model of Risky Decision Making
Keywords: BLA; basolateral amygdala; CeA; central amygdala; dmPFC; dorsal mPFC; MeCP2; Methyl CpG-binding protein 2; mPFC; medial prefrontal cortex; NAc; nucleus accumbens; pMeCP2; phospho-MeCP2; RDT; Risky Decision-making Task; epigenetics; MeCP2; DNA methylation;
Correcting deregulated Fxyd1 expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male mice
Keywords: RTT; Rett Syndrome; MeCP2; methyl-CpG binding protein 2; FXYD1; FXYD (phenyl alanine-any amino acid, tyrosine, aspartic acid domain-containing transport regulator 1; NKA; Sodium/potassium adenosine triphosphatase; Mecp2 deficiency; Neuronal morphology; Po
Disruption of AT-hook 1 domain in MeCP2 protein caused behavioral abnormality in mice
Keywords: Ab; antibody; bp; base pair; CRISPR/Cas9; clustered regularly interspaced short palindromic repeat/CRISPR associated proteins 9; CREB/miR132; cAMP-response element binding protein/micro RNA 132; hmC; hydroxymethylcytosine; GFAP; glial fibrillary acidic pr
High phosphate-induced downregulation of PPARγ contributes to CKD-associated vascular calcification
Keywords: CKD; chronic kidney disease; PPARγ; peroxisome proliferator-activated receptor-gamma; VMSCs; mouse vascular smooth muscle cells; Mecp2; methyl-CpG binding protein 2; Runx2; runt-related transcription factor 2; BMP-2; bone morphogenic proteins-2; BUN; blo
Multi-PK antibodies: Powerful analytical tools to explore the protein kinase world
Keywords: 2D-PAGE; two-dimensional polyacrylamide gel electrophoresis; CaMK; Ca2+/calmodulin-dependent protein kinase; CDKL5; cyclin-dependent kinase-like 5; CNBr; cyanogen bromide; DCLK; double-cortin like protein kinase; Dnmt1; DNA methyltransferase 1; FAK; focal
Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene
Keywords: adFNDI; autosomal dominant familial neurohypophyseal diabetes insipidus; AVP; arginine vasopressin; DI; diabetes insipidus; ER; endoplasmic reticulum; MeCP2; methyl-CpG binding protein 2; OXT; oxytocin;
CpG methylation and the methyl CpG binding protein 2 (MeCP2) are required for restraining corticotropin releasing hormone (CRH) gene expression
Keywords: CRH gene; CpG methylation; Glucocorticoids; MeCP2;
Comprehensive Evaluation on Effect of IMPX977 on Expression of Methyl-CpG-binding Protein 2 in Rats
Keywords: cerebellum; homeostasis; IMPX977; MeCP2; Rett syndrome;
Zoledronic acid improves bone histomorphometry in a murine model of Rett syndrome
Keywords: Ïapp; apparent density; BFR/BS; bone formation rate per unit of bone surface; BV/TV; bone volume fraction; Ct.Th; cortical thickness; Mecp2-null; hemizygous male missing Mecp2; HET; heterozygous female; MeCP2; human and mouse protein methyl CpG binding p
Research reportDistinguishing response to names in Rett and MECP2 Duplication syndrome: An ERP study of auditory social information processing
Keywords: Rett; Electroencephalography; MECP2; Auditory processing;
Breathing abnormalities in animal models of Rett syndrome a female neurogenetic disorder
Keywords: Rett syndrome; Mecp2; Breathing; Autonomic function; CO2 chemosensitivity; Brainstem; Animal models;
Reduced axonal diameter of peripheral nerve fibers in a mouse model of Rett syndrome
Keywords: Rett syndrome; MECP2; sciatic nerve; mitochondria;
Research reportSelective preservation of cholinergic MeCP2 rescues specific Rett-syndrome-like phenotypes in MeCP2stop mice
Keywords: RTT; Rett syndrome; MeCP2; methyl CpG-binding protein 2; Chat; choline acetyltrasferase; MS; medial septal nucleus; VDB; nucleus of the vertical limb of the diagonal band; HDB; nucleus of the horizontal limb of the diagonal band; PPTg; primarily pedunculo
Original articleExome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes
Keywords: Whole exome sequencing; WES; Skewed X-inactivation; ATRX; DMD; RPS6KA3; MECP2;
4-hydroxynonenal protein adducts: Key mediator in Rett syndrome oxinflammation
Keywords: Inflammation; Isoprostanes; Oxidative stress; Rare disease; Orphan disease; CDKL5; FOXG1; MecP2;
CX3CR1 ablation ameliorates motor and respiratory dysfunctions and improves survival of a Rett syndrome mouse model
Keywords: Rett syndrome; MeCP2; Microglia; CX3CR1;