(Q51820369)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

0 references

11

1 reference

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19 January 2020

Maurizio Giustetto

12

1 reference

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19 January 2020

Sara Ricciardi

1

1 reference

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19 January 2020

Stefano Grosso

3

1 reference

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19 January 2020

Greta Forlani

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Nicoletta Landsberger

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Stefano Biffo

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Vania Broccoli

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Elena M Boggio

2

1 reference

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19 January 2020

Giuseppina Lonetti

4

1 reference

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19 January 2020

Gilda Stefanelli

6

1 reference

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19 January 2020

Eleonora Calcagno

7

1 reference

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19 January 2020

Noemi Morello

8

1 reference

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19 January 2020

publication date

6 January 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

published in

Human Molecular Genetics

1 reference

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19 January 2020

volume

20

1 reference

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19 January 2020

issue

6

1 reference

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19 January 2020

page(s)

1182-1196

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212100%20AND%20SRC:MED&resulttype=core&format=json

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

19 January 2020

cites work

1 reference

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The story of Rett syndrome: from clinic to neurobiology

21 January 2018

1 reference

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Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons

21 January 2018

1 reference

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Clinical manifestations and stages of Rett syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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Mechanisms of disease: neurogenetics of MeCP2 deficiency

21 January 2018

1 reference

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Evolving role of MeCP2 in Rett syndrome and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

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

21 January 2018

1 reference

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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

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Dissecting MECP2 function in the central nervous system

21 January 2018

1 reference

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MeCP2 dysfunction in Rett syndrome and related disorders

21 January 2018

1 reference

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

21 January 2018

1 reference

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Rett syndrome and the impact of MeCP2 associated transcriptional mechanisms on neurotransmission

21 January 2018

1 reference

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

21 January 2018

1 reference

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The Autistic Neuron: Troubled Translation?

21 January 2018

1 reference

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A synaptic trek to autism

21 January 2018

1 reference

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Oncogenes on my mind: ERK and MTOR signaling in cognitive diseases

21 January 2018

1 reference

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mTOR signaling: at the crossroads of plasticity, memory and disease

21 January 2018

1 reference

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Fragile X: translation in action

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Translational regulatory mechanisms in persistent forms of synaptic plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

The growing role of mTOR in neuronal development and plasticity.

21 January 2018

1 reference

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Making synaptic plasticity and memory last: mechanisms of translational regulation

21 January 2018

1 reference

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Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets

21 January 2018

1 reference

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Mecp2-null mice provide new neuronal targets for Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Ribosomal protein S6 phosphorylation: from protein synthesis to cell size.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

RAS/ERK signaling promotes site-specific ribosomal protein S6 phosphorylation via RSK and stimulates cap-dependent translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

NMDA receptor activation results in PKA- and ERK-dependent Mnk1 activation and increased eIF4E phosphorylation in hippocampal area CA1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Regulation of eukaryotic initiation factor 4E by converging signaling pathways during metabotropic glutamate receptor-dependent long-term depression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

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

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Early environmental enrichment moderates the behavioral and synaptic phenotype of MeCP2 null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

PKCbetaII modulates translation independently from mTOR and through RACK1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Ribosomal S6 kinase signaling and the control of translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Upstream and downstream of mTOR

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Molecular mechanisms of mTOR-mediated translational control

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

Rett syndrome: what do we know for sure?

21 January 2018

1 reference

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Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

21 January 2018

1 reference

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Translational control of long-lasting synaptic plasticity and memory

21 January 2018

1 reference

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mTOR signaling at a glance

21 January 2018

1 reference

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Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

21 January 2018

1 reference

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Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

21 January 2018

1 reference

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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

21 January 2018

1 reference

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Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells.

21 January 2018

1 reference

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Regulation of translation initiation in eukaryotes: mechanisms and biological targets

21 January 2018

1 reference

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

21 January 2018

1 reference

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Visual stimulation activates ERK in synaptic and somatic compartments of rat cortical neurons with parallel kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ563

ERK activation in axonal varicosities modulates presynaptic plasticity in the CA3 region of the hippocampus through synapsin I

21 January 2018

1 reference

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Release of eIF6 (p27BBP) from the 60S subunit allows 80S ribosome assembly

21 January 2018

1 reference

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