(Q40372504)

19 September 2017

Fragile X mental retardation protein is required for synapse elimination by the activity-dependent transcription factor MEF2. (English)

1 reference

19 September 2017

Brad E Pfeiffer

1 reference

19 September 2017

Tong Zang

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19 September 2017

Julia R Wilkerson

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19 September 2017

Makoto Taniguchi

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19 September 2017

Marina A Maksimova

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19 September 2017

Laura N Smith

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19 September 2017

Christopher W Cowan

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19 September 2017

Kimberly M Huber

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19 September 2017

language of work or name

English

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publication date

1 April 2010

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19 September 2017

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19 September 2017

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19 September 2017

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19 September 2017

191-197

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describes a project that uses

19 September 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2864778/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

22 September 2017

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Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection

22 September 2017

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The self-tuning neuron: synaptic scaling of excitatory synapses

22 September 2017

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Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

22 September 2017

1 reference

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Cocaine regulates MEF2 to control synaptic and behavioral plasticity

22 September 2017

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Identifying autism loci and genes by tracing recent shared ancestry

22 September 2017

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MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function

22 September 2017

1 reference

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Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo

22 September 2017

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

22 September 2017

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Advances in autism genetics: on the threshold of a new neurobiology

22 September 2017

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Developmental presence and disappearance of postsynaptically silent synapses on dendritic spines of rat layer 2/3 pyramidal neurons

22 September 2017

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MEF2C transcription factor controls chondrocyte hypertrophy and bone development

22 September 2017

1 reference

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Developmental homeostasis of mouse retinocollicular synapses

22 September 2017

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Temporal regulation of the expression locus of homeostatic plasticity.

22 September 2017

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A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation

22 September 2017

1 reference

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Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number

22 September 2017

1 reference

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FMRP RNA targets: identification and validation

22 September 2017

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Long-term sensory deprivation prevents dendritic spine loss in primary somatosensory cortex

22 September 2017

1 reference

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Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes

22 September 2017

1 reference

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Neural activity and the dynamics of central nervous system development

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

MEF2: a calcium-dependent regulator of cell division, differentiation and death

22 September 2017

1 reference

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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

22 September 2017

1 reference

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The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

22 September 2017

1 reference

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Abnormal development of dendritic spines in FMR1 knock-out mice

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Evidence that fragile X mental retardation protein is a negative regulator of translation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Overview on the structure, composition, function, development, and plasticity of hippocampal dendritic spines

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Development of the vertebrate neuromuscular junction

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Mutational analysis of the DNA binding, dimerization, and transcriptional activation domains of MEF2C

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Postnatal development of the visual cortex and the influence of environment

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Concurrent overproduction of synapses in diverse regions of the primate cerebral cortex

22 September 2017

1 reference

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A simple method for organotypic cultures of nervous tissue

22 September 2017

1 reference

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A point mutation in the FMR-1 gene associated with fragile X mental retardation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Sequence of abnormal dendritic spine development in primary somatosensory cortex of a mouse model of the fragile X mental retardation syndrome.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Biolistic transfection of cultured organotypic brain slices.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2864778

10.1016/J.NEURON.2010.03.017

20 August 2018

Identifiers

DOI

1 reference

19 September 2017

1 reference

19 September 2017

PubMed publication ID

20434996

1 reference