Experience-dependent retinogeniculate synapse remodeling is abnormal in MeCP2-deficient mice (Q34856164)

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28 January 2020

title

Experience-dependent retinogeniculate synapse remodeling is abnormal in MeCP2-deficient mice (English)

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28 January 2020

4

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28 January 2020

author name string

Joao Noutel

1

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28 January 2020

Y Kate Hong

2

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28 January 2020

Byunghee Leu

3

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28 January 2020

Chinfei Chen

5

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28 January 2020

language of work or name

English

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publication date

1 April 2011

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28 January 2020

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28 January 2020

volume

70

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28 January 2020

issue

1

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28 January 2020

page(s)

35-42

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Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

28 January 2020

cites work

1 reference

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Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a

8 July 2018

1 reference

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MeCP2 is required for normal development of GABAergic circuits in the thalamus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

8 July 2018

1 reference

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Critical period plasticity is disrupted in the barrel cortex of FMR1 knockout mice.

8 July 2018

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Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in an RNA interference model of methyl-CpG-binding protein 2 deficiency

8 July 2018

1 reference

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LTD and LTP at the developing retinogeniculate synapse

8 July 2018

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Intact long-term potentiation but reduced connectivity between neocortical layer 5 pyramidal neurons in a mouse model of Rett syndrome

8 July 2018

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

8 July 2018

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Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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Circuit and plasticity defects in the developing somatosensory cortex of FMR1 knock-out mice.

8 July 2018

1 reference

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

8 July 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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Excitatory-inhibitory balance and critical period plasticity in developing visual cortex

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

8 July 2018

1 reference

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Vision, cognition and developmental characteristics of girls and women with Rett syndrome.

8 July 2018

1 reference

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Enhancement of transmission at the developing retinogeniculate synapse.

8 July 2018

1 reference

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Prenatal and postnatal development of retinogeniculate and retinocollicular projections in the mouse

8 July 2018

1 reference

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Neurophysiological findings in the Rett syndrome, II: Visual and auditory brainstem, middle and late evoked responses

8 July 2018

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

8 July 2018

1 reference

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Vision triggers an experience-dependent sensitive period at the retinogeniculate synapse

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Distinct roles for spontaneous and visual activity in remodeling of the retinogeniculate synapse

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

The development of visual- and auditory processing in Rett syndrome: an ERP study

26 October 2018

1 reference

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Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

MeCP2-dependent transcriptional repression regulates excitatory neurotransmission

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Structural and functional composition of the developing retinogeniculate pathway in the mouse

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Unbiased analysis of bulk axonal segregation patterns

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

Developmental remodeling of the retinogeniculate synapse

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082316

10.1016/J.NEURON.2011.03.001

26 October 2018

Identifiers

DOI

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28 January 2020

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28 January 2020

PubMed publication ID

21482354

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