The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
about
The Contradictory Effects of Neuronal Hyperexcitation on Adult Hippocampal NeurogenesisMECP2 disorders: from the clinic to mice and backBDNF deregulation in Rett syndromeThe role of MeCP2 in brain development and neurodevelopmental disordersDendritic spine dysgenesis in Rett syndrome.A selective histone deacetylase-6 inhibitor improves BDNF trafficking in hippocampal neurons from Mecp2 knockout mice: implications for Rett syndrome.Investigation of modifier genes within copy number variations in Rett syndromeThe phenotype associated with a large deletion on MECP2.Peripheral administration of brain-derived neurotrophic factor to Rett syndrome animal model: a possible approach for the treatment of Rett syndromeA TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndromeModulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autismUpdating the profile of C-terminal MECP2 deletions in Rett syndromeThe best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease.Secreted factors as synaptic organizers.The neurotrophins and their role in Alzheimer's disease.Multiple approaches to investigate the transport and activity-dependent release of BDNF and their application in neurogenetic disorders.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.The BDNF val-66-met Polymorphism Affects Neuronal Morphology and Synaptic Transmission in Cultured Hippocampal Neurons from Rett Syndrome Mice.Stereotypical hand movements in 144 subjects with Rett syndrome from the population-based Australian database.Brain derived neurotrophic factor and serotonin transporter binding as markers of clinical response to fluoxetine therapy in children with autism.Longitudinal hand function in Rett syndrome.Environmental enrichment intervention for Rett syndrome: an individually randomised stepped wedge trial.Glial cell-derived neurotrophic factor gene polymorpisms affect severity and functionality of bipolar disorder.Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val⁶⁶Met polymorphism is associated with a better response to OROS-MPH in Korean ADHD children.MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.Rett syndrome: a neurological disorder with metabolic components.RettBASE: Rett syndrome database update.
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P2860
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
description
2009 nî lūn-bûn
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2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@ast
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@en
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@nl
type
label
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@ast
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@en
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@nl
prefLabel
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@ast
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@en
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@nl
P2093
P2860
P50
P1433
P1476
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
@en
P2093
P2860
P304
P356
10.1212/01.WNL.0000345664.72220.6A
P407
P577
2009-04-01T00:00:00Z