(Q34004048)

30 July 2017

title

Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice (English)

1 reference

30 July 2017

2

Walter E Kaufmann

1 reference

30 July 2017

Mary E Blue

1

1 reference

30 July 2017

Joseph Bressler

3

1 reference

30 July 2017

Charlotte Eyring

4

1 reference

30 July 2017

Cliona O'driscoll

5

1 reference

30 July 2017

Sakkubai Naidu

6

1 reference

30 July 2017

Michael V Johnston

7

1 reference

30 July 2017

publication date

8 September 2011

1 reference

30 July 2017

number of pages

11

1 reference

based on heuristic

inferred from page(s)

published in

The Anatomical Record

1 reference

30 July 2017

volume

294

1 reference

30 July 2017

issue

10

1 reference

30 July 2017

page(s)

1624-1634

1 reference

Rett syndrome: revised diagnostic criteria and nomenclature

30 July 2017

cites work

1 reference

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The insular cortex and cardiovascular system: a new insight into the brain-heart axis

28 July 2018

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The contribution(s) of the insula to speech production: a review of the clinical and functional imaging literature

28 July 2018

1 reference

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Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Advances in the treatment of fragile X syndrome

28 July 2018

1 reference

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Enhanced hypoxia susceptibility in hippocampal slices from a mouse model of rett syndrome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Enhanced cell death in MeCP2 null cerebellar granule neurons exposed to excitotoxicity and hypoxia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Rett syndrome and neuronal development

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

The transcriptional repressor Mecp2 regulates terminal neuronal differentiation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Development of amino acid receptors in frontal cortex from girls with Rett syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Rett syndrome: a disorder affecting early brain growth

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Choline acetyltransferase activity and vesamicol binding in Rett syndrome and in rats with nucleus basalis lesions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Glutamate dehydrogenase improves binding of [3H]CGP39653 to NMDA receptors in the autoradiographic assay.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

On a unusual brain atrophy syndrome in hyperammonemia in childhood

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Rett syndrome: Criteria for inclusion and exclusion

28 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

28 July 2018

Elevated CSF glutamate in Rett syndrome

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions.

28 July 2018

1 reference

Status epilepticus induces region-specific changes in dendritic spines, dendritic length and TrkB protein content of rat brain cortex.

21 January 2018

1 reference

Ontogeny of non-NMDA glutamate receptors in rat barrel field cortex: II. Alpha-AMPA and kainate receptors.

21 January 2018

1 reference

Retrosplenial granular b cortex in normal and epileptic rats: a stereological study

21 January 2018

1 reference

Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

21 January 2018

1 reference

Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice.

21 January 2018

1 reference

MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.

21 January 2018

1 reference

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations

21 January 2018

1 reference

Neurobiology of Rett syndrome: a genetic disorder of synapse development

21 January 2018

1 reference

Neurobiology of Rett syndrome

21 January 2018

1 reference

Involvement of histamine 1 receptor in seizure susceptibility and neuroprotection in immature mice.

21 January 2018

1 reference

Diminished prevalence but preserved synaptic distribution of N-methyl-D-aspartate receptor subunits in the methyl CpG binding protein 2(MeCP2)-null mouse brain

21 January 2018

1 reference

Rett syndrome: 1H spectroscopic imaging at 4.1 Tesla.

21 January 2018

1 reference

Olfactory biopsies demonstrate a defect in neuronal development in Rett's syndrome.

21 January 2018

1 reference

Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism

21 January 2018

1 reference

Annexin-1 is abnormally expressed in fragile X syndrome: two-dimensional electrophoresis study in lymphocytes.

21 January 2018

1 reference

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

21 January 2018

1 reference

Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

Ontogeny of non-NMDA glutamate receptors in rat barrel field cortex: I. Metabotropic receptors.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4122218

High levels of cerebrospinal fluid glutamate in Rett syndrome

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21901842

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

MeCP2 mutations in children with and without the phenotype of Rett syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21901842

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AR.21380

1 reference

30 July 2017

1 reference

30 July 2017

1 reference