Keywords: نوروژنتیک; Neurobiology; Pathogenesis; Pathophysiology; Neurogenetics; Neuroanatomy; Neurophysiology;
مقالات ISI نوروژنتیک (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: نوروژنتیک; Ischemic stroke; neurogenetics; genome-wide expression; bioinformatics; meta-analysis; computational biology;
Keywords: نوروژنتیک; Motor neuron disease; Amyotrophic lateral sclerosis; Inborn errors of metabolism; Neurogenetics; Neurometabolic disorders;
Keywords: نوروژنتیک; Individual differences; Language learning; Neurogenetics; Personalized learning;
Keywords: نوروژنتیک; Antisocial behavior; Early life adversity; fMRI; Harsh parenting; Neurogenetics; Stress;
Keywords: نوروژنتیک; Candidate; Genetics; Genomics; Imaging; MRI; Neurogenetics; Polygenic;
Keywords: نوروژنتیک; reading; neural oscillation; neurogenetics; excitability; glutamate;
Keywords: نوروژنتیک; Hereditary spastic paraplegia; Spastic ataxia; Neurogenetics; Spasticity;
Keywords: نوروژنتیک; Carrier testing; confidentiality; consent; diagnostic testing; genetic testing; neurogenetics; neurology; next-generation sequencing; pre-symptomatic testing
Keywords: نوروژنتیک; Intermediate phenotype; MRI; Neural circuit; Neurogenetics; Neuroimaging genetics; PTSD; Risk polymorphism; Trauma;
Keywords: نوروژنتیک; Schizophrenia; Dysconnection; Neuromodulation; Bayesian; Predictive coding; Neurogenetics;
Keywords: نوروژنتیک; Amyotrophic lateral sclerosis; ALS; Diagnosis; Genetic; Sequencing; Next-generation sequencing; NGS; MiSeq; Neurogenetics;
Keywords: نوروژنتیک; Dementia; Diagnosis; Neurogenetics; Genetic; Sequencing; Next-generation sequencing; NGS; Ion torrent; MiSeq;
Keywords: نوروژنتیک; 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-
A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members
Keywords: نوروژنتیک; Neurogenetics; Mitochondrial DNA mutation; Genotype-driven treatment; Klinefelter syndrome; MERRF/Leigh-like syndrome;
Les mouvements anormaux : mise au point
Keywords: نوروژنتیک; Mouvements anormaux; Ganglions de la base; Maladies métaboliques traitables; Neurogénétique; Stimulation cérébrale profonde; Movement disorders; Basal ganglia; Treatable metabolic diseases; Neurogenetics; Deep brain stimulation;
Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy
Keywords: نوروژنتیک; Spinocerebellar ataxia; Parkinson's disease; Epilepsy; Cognitive disorders; KCND3 mutation; Neurogenetics; Neuropsychiatric disorder;
SCA13 causes dominantly inherited non-progressive myoclonus ataxia
Keywords: نوروژنتیک; Cerebellar ataxia; Myoclonus; Neurogenetics; Movement disorder;
The clinical, neuroanatomical, and neuropathologic phenotype of TBK1-associated frontotemporal dementia: A longitudinal case report
Keywords: نوروژنتیک; TBK1; Neurogenetics; Neuropathology; Frontotemporal dementia;
The BDNF Val66Met polymorphism is associated with structural neuroanatomical differences in young children
Keywords: نوروژنتیک; BDNF; rs6265; Neurogenetics; sMRI neuroimaging; Gray matter volume; Cortical thickness; Surface area; Development;
Meta-analysis of six genes (BDNF, DRD1, DRD3, DRD4, GRIN2B and MAOA) involved in neuroplasticity and the risk for alcohol dependence
Keywords: نوروژنتیک; Candidate genes; Neurogenetics; Addiction; Alcoholism;
FMRFamide signaling promotes stress-induced sleep in Drosophila
Keywords: نوروژنتیک; Sleep; Stress; Neuropeptides; Drosophila; Circadian rhythms; Neurogenetics;
Oxytocin receptor gene sequences in owl monkeys and other primates show remarkable interspecific regulatory and protein coding variation
Keywords: نوروژنتیک; OXTR; Behavioral genetics; Night monkey; Neurogenetics; Evolution
Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts
Keywords: نوروژنتیک; Parkinson's disease; PARK10; Whole exome sequencing; NeuroX; Neurogenetics;
A functional polymorphism in the promoter region of MAOA gene is associated with daytime sleepiness in healthy subjects
Keywords: نوروژنتیک; Neurogenetics; Latin America; Neuropsychiatric genetics; Candidate genes; Endophenotypes; Daytime sleepiness; Monoamine Oxidase A;
Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxia
Keywords: نوروژنتیک; Myoclonus; Progressive myoclonic ataxia; Tremor; Ataxia-telangiectasia-like disorder; Neurogenetics; MRE11;
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
Keywords: نوروژنتیک; Amyotrophic lateral sclerosis; Frontotemporal lobar degeneration; C9orf72; Progressive supranuclear palsy; Corticobasal syndrome; Neurogenetics;
Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion
Keywords: نوروژنتیک; Frontotemporal dementia; C9ORF72 gene; Hexanucleotide expansion; Neurogenetics;
Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain
Keywords: نوروژنتیک; CLN; Development; Neurogenesis; Neuronal progenitor; Neuropathology; Neurogenetics;
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26
Keywords: نوروژنتیک; Temporal lobe epilepsy; Neurogenetics; Linkage analysis; Exome sequencing;
A novel association of two non-synonymous polymorphisms in PER2 and PER3 genes with specific diurnal preference subscales
Keywords: نوروژنتیک; Molecular genetics; Endophenotypes; Sleep; Candidate genes; Neurogenetics;
Genetic ablation of phospholipase C delta 1 increases survival in SOD1G93A mice
Keywords: نوروژنتیک; ALS; amyotrophic lateral sclerosis; AMPA; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid; C9orf72; chromosome 9 open reading frame 72; DPP6; dipeptidyl-peptidase 6; ELP3; elongator protein 3; ER; endoplasmic reticulum; FUS/TLS; fused in sarcoma/tra
PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins
Keywords: نوروژنتیک; Movement disorders; Hemiplegic migraine; Neurogenetics; Paroxysmal kinesigenic dyskinesia
Systematic review, structural analysis, and new theoretical perspectives on the role of serotonin and associated genes in the etiology of psychopathy and sociopathy
Keywords: نوروژنتیک; Behavioral neurophysiology; Behavioral genetics; Neurogenetics; Temperament; Psychopathy; Cluster B personality disorders; Sociopathy; Homeostasis; Allostasis; Serotonin; TPH; 5HTT; 5HT1A; 5HT2C; 5HT3; GABA-A; Testosterone; Gene–gene interactions; Gene–en
Genetic testing in neurology
Keywords: نوروژنتیک; carrier testing; confidentiality; consent; diagnostic testing; genetic testing; neurogenetics; neurology; presymptomatic testing;
Micro-duplications of 1q32.1 associated with neurodevelopmental delay
Keywords: نوروژنتیک; Neurogenetics; Developmental delay; Duplication syndrome; 1q
Linking neurogenetics and individual differences in language learning: The dopamine hypothesis
Keywords: نوروژنتیک; Neurogenetics; Procedural learning; Dopamine;
Transcription factor PITX3 gene in Parkinson's disease
Keywords: نوروژنتیک; Single nucleotide polymorphisms; Dopaminergic neurons; Substantia nigra; Neurogenetics
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: نوروژنتیک; Hereditary spastic paraplegia; Spastin; SPAST gene; SPG4 gene; Neurogenetics
Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like disease
Keywords: نوروژنتیک; Neurogenetics;
Genetic counselling in Neurology: A complex problem that requires regulation
Keywords: نوروژنتیک; Genetic tests; Genetic counselling; Neurogenetics; Legislation; Rare disorders; Predictive testing; Análisis genéticos; Asesoramiento genético; Neurogenética; Legislación; Enfermedades raras; Test predictivos;
Asesoramiento genético en NeurologÃa: un problema complejo que necesita regulación
Keywords: نوروژنتیک; Análisis genéticos; Asesoramiento genético; Neurogenética; Legislación; Enfermedades raras; Test predictivos; Genetic tests; Genetic counseling; Neurogenetics; Legislation; Rare disorders; Predictive testing;
Genetic differences in emotionally enhanced memory
Keywords: نوروژنتیک; Emotional memory; Episodic memory; Amygdala; Neurogenetics; Motivated attention;
Siblings with the adult-onset slowly progressive type of pantothenate kinase-associated neurodegeneration and a novel mutation, Ile346Ser, in PANK2: Clinical features and 99mTc-ECD brain perfusion SPECT findings
Keywords: نوروژنتیک; Neuroimaging; Neurogenetics; Pantothenate kinase-associated neurodegeneration; Pantothenate kinase 2 gene (PANK2); Hallervorden–Spatz syndrome
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations
Keywords: نوروژنتیک; X-linked myopathy; Scapuloperoneal; FHL1; Neurogenetics; Muscular dystrophy; Genetic diagnosis;
Approaches to the Patient with Neurogenetic Disease
Keywords: نوروژنتیک; Neurogenetics; Genetic counseling; Genetic testing; Neurologic diseases;
Neurobiología y neurogenética de la dislexia
Keywords: نوروژنتیک; Comorbilidad; Dislexia; Neurobiología; Neurogenética; Modelos animalesAnimal models; Comorbidity; Dyslexia; Neurobiology; Neurogenetics
Brief ReportBcl-2 Polymorphism Influences Gray Matter Volume in the Ventral Striatum in Healthy Humans
Keywords: نوروژنتیک; Accumbens; magnetic resonance imaging; neurogenetics; neuroplasticity; voxel-based morphometry (VBM);
Elevated forebrain excitatory l-glutamate, l-aspartate and d-aspartate in the Naples high-excitability rats
Keywords: نوروژنتیک; Behaviour; Animal model; Neurogenetics; Amino acids
Excitatory amino acids in the forebrain of the Naples high-excitability rats: neurochemical and behavioural effects of subchronic d-aspartate and its diethyl ester prodrug
Keywords: نوروژنتیک; Animal model; Neurogenetics; Prodrug; HPLC