(Q37801244)

23 August 2017

title

The role of calcium-dependent gene expression in autism spectrum disorders: lessons from MeCP2, Ube3a and beyond (English)

1 reference

23 August 2017

main subject

autism spectrum disorder

0 references

autism

0 references

author name string

Zilong Qiu

series ordinal

1

1 reference

23 August 2017

Ju Cheng

series ordinal

2

1 reference

23 August 2017

publication date

19 October 2010

1 reference

23 August 2017

1 reference

23 August 2017

volume

18

1 reference

23 August 2017

issue

2

1 reference

23 August 2017

page(s)

72-81

1 reference

Disorders of the autism spectrum.

23 August 2017

cites work

1 reference

The Epidemiology of Autism Spectrum Disorders *

21 January 2018

1 reference

Genetic markers in autism: association study on short arm of chromosome 11.

21 January 2018

1 reference

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

Deletion of chromosome 2q37 and autism: a distinct subtype?

21 January 2018

1 reference

Chromosome 7q: where autism meets language disorder?

21 January 2018

1 reference

Brief report: A case of autism with interstitial deletion of chromosome 13.

21 January 2018

1 reference

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

21 January 2018

1 reference

Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.

21 January 2018

1 reference

Rationale for further investigation of chromosome 16p13.3, a region implicated for autism

21 January 2018

1 reference

Early exploration of the visual cortex.

21 January 2018

1 reference

Synaptic activity and the construction of cortical circuits

21 January 2018

1 reference

Communication between the synapse and the nucleus in neuronal development, plasticity, and disease

21 January 2018

1 reference

Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system

21 January 2018

1 reference

Dendrite development regulated by CREST, a calcium-regulated transcriptional activator

21 January 2018

1 reference

Regulation of thalamocortical patterning and synaptic maturation by NeuroD2

21 January 2018

1 reference

Calcium activation of the LMO4 transcription complex and its role in the patterning of thalamocortical connections.

21 January 2018

1 reference

A calcium-dependent switch in a CREST-BRG1 complex regulates activity-dependent gene expression

21 January 2018

1 reference

A brief history of neuronal gene expression: regulatory mechanisms and cellular consequences

21 January 2018

1 reference

Regulation of dendritic development by neuron-specific chromatin remodeling complexes

21 January 2018

1 reference

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

21 January 2018

1 reference

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

21 January 2018

1 reference

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

21 January 2018

1 reference

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

The story of Rett syndrome: from clinic to neurobiology

21 January 2018

1 reference

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

21 January 2018

1 reference

MeCP2, a key contributor to neurological disease, activates and represses transcription

21 January 2018

1 reference

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 January 2018

1 reference

Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA

21 January 2018

1 reference

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

21 January 2018

1 reference

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

1 reference

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

1 reference

Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

21 January 2018

1 reference

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

21 January 2018

1 reference

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

21 January 2018

1 reference

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

21 January 2018

1 reference

MeCP2-dependent transcriptional repression regulates excitatory neurotransmission.

21 January 2018

1 reference

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

21 January 2018

1 reference

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

21 January 2018

1 reference

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

21 January 2018

1 reference

UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

21 January 2018

1 reference

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples

21 January 2018

1 reference

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues

21 January 2018

1 reference

Huntington's disease and repeating trinucleotides

21 January 2018

1 reference

Polyglutamine diseases: emerging concepts in pathogenesis and therapy

21 January 2018

1 reference

Progress in pathogenesis studies of spinocerebellar ataxia type 1.

21 January 2018

1 reference

Ube3a is required for experience-dependent maturation of the neocortex.

21 January 2018

1 reference

The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53

21 January 2018

1 reference

Localization of the E6-AP regions that direct human papillomavirus E6 binding, association with p53, and ubiquitination of associated proteins

21 January 2018

1 reference

The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.

21 January 2018

1 reference

Arc/Arg3.1 mediates homeostatic synaptic scaling of AMPA receptors

21 January 2018

1 reference

Increased expression of the immediate-early gene arc/arg3.1 reduces AMPA receptor-mediated synaptic transmission

21 January 2018

1 reference

Arc/Arg3.1 interacts with the endocytic machinery to regulate AMPA receptor trafficking

21 January 2018

1 reference

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

1 reference

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection

21 January 2018

1 reference

Autism: the ups and downs of neuroligin

21 January 2018

1 reference

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

21 January 2018

1 reference

Regulation of dendritic spine morphology and synaptic function by Shank and Homer

21 January 2018

1 reference

Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.

21 January 2018

1 reference

Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin

21 January 2018

1 reference

Neuroligin 1: a splice site-specific ligand for beta-neurexins

21 January 2018

1 reference

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

21 January 2018

1 reference

Control of excitatory and inhibitory synapse formation by neuroligins

21 January 2018

1 reference

Neuroligins determine synapse maturation and function

21 January 2018

1 reference

Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

21 January 2018

1 reference

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

21 January 2018

1 reference

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

21 January 2018

1 reference

Copy number variation in human health, disease, and evolution

21 January 2018

1 reference

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

21 January 2018

1 reference

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

21 January 2018

1 reference

The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing

21 January 2018

1 reference

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

21 January 2018

1 reference

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

21 January 2018

1 reference

Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

1 reference

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

21 January 2018

1 reference

Directed evolution of a novel adeno-associated virus (AAV) vector that crosses the seizure-compromised blood-brain barrier (BBB).

21 January 2018

1 reference

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation.

21 January 2018

1 reference

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

21 January 2018

1 reference

Therapeutic silencing of microRNA-122 in primates with chronic hepatitis C virus infection

21 January 2018

1 reference

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000320970

1 reference

23 August 2017

1 reference