(Q35823293)

English

MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder

scientific article published on 9 January 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

autism spectrum disorder

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1 reference

based on heuristic

inferred from title

author name string

Wenlin Liao

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Michael J Gandal

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Richard S Ehrlichman

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Steven J Siegel

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Greg C Carlson

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

publication date

9 January 2012

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Neurobiology of Disease

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

46

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

88-92

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Dysbindin-1 mutant mice implicate reduced fast-phasic inhibition as a final common disease mechanism in schizophrenia

1 reference

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1 reference

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Auditory magnetic mismatch field latency: a biomarker for language impairment in autism

1 reference

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Validating γ oscillations and delayed auditory responses as translational biomarkers of autism

1 reference

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Contrasting patterns of language-associated brain activity in autism and Williams syndrome

1 reference

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Abnormal neural oscillations and synchrony in schizophrenia

1 reference

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MEG detection of delayed auditory evoked responses in autism spectrum disorders: towards an imaging biomarker for autism

1 reference

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Assessment of NMDA receptor NR1 subunit hypofunction in mice as a model for schizophrenia

1 reference

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Event related potentials in the understanding of autism spectrum disorders: an analytical review

1 reference

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Reduced neural synchronization of gamma-band MEG oscillations in first-degree relatives of children with autism

1 reference

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Behavioral states, network states, and sensory response variability

1 reference

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1 reference

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The gamma cycle

1 reference

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Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

1 reference

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Epigenetics of autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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Children and adolescents with autism exhibit reduced MEG steady-state gamma responses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

11 July 2018

EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

11 July 2018

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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Inhibition of auditory evoked potentials and prepulse inhibition of startle in DBA/2J and DBA/2Hsd inbred mouse substrains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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Brain stem and spinal cord impairment in Rett syndrome: somatosensory and auditory evoked responses investigations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

11 July 2018

Auditory brainstem response findings in Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3299908

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Brainstem auditory evoked potentials in receptive developmental language disorder.

1 reference

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11 July 2018

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

1 reference

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Evoked potentials in the Rett syndrome.

1 reference

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Giant somatosensory evoked potentials in the Rett syndrome.

1 reference

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1 reference

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1 reference

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Auditory evoked fields predict language ability and impairment in children.

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1 reference

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Midlatency auditory event-related potentials in mice: comparison to midlatency auditory ERPs in humans.

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1 reference

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Auditory evoked potentials in Rett syndrome.

1 reference

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1 reference

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12 December 2020

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10.1016/J.NBD.2011.12.048

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

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