(Q46146028)

19 December 2017

title

Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome (English)

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19 December 2017

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Nadia P Belichenko

1

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19 December 2017

Pavel V Belichenko

2

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19 December 2017

Hong Hua Li

3

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19 December 2017

William C Mobley

4

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19 December 2017

Uta Francke

5

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19 December 2017

language of work or name

English

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publication date

1 May 2008

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19 December 2017

The Journal of Comparative Neurology

published in

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19 December 2017

volume

508

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19 December 2017

issue

1

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19 December 2017

page(s)

184-195

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19 December 2017

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

cites work

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Rett syndrome: Criteria for inclusion and exclusion

21 January 2018

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Does genotype predict phenotype in Rett syndrome?

21 January 2018

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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

21 January 2018

1 reference

Cerebellar and cerebral abnormalities in Rett syndrome: a quantitative MR analysis

21 January 2018

1 reference

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

21 January 2018

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

21 January 2018

1 reference

7 January 2021

Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation.

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7 January 2021

Neuropathology of Rett syndrome

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7 January 2021

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

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7 January 2021

Microscopic Observations of the Brain in Rett Syndrome

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7 January 2021

Morphological study of neocortical areas in Rett syndrome

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7 January 2021

Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice

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7 January 2021

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

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7 January 2021

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

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7 January 2021

Differential distribution of the MeCP2 splice variants in the postnatal mouse brain

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7 January 2021

Rett syndrome: investigation of nine patients, including PET scan

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7 January 2021

Abnormal general movements in girls with Rett disorder: the first four months of life.

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7 January 2021

Magnetic resonance imaging and clinical findings examined in adulthood-studies on three adults with Rett syndrome.

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7 January 2021

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

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7 January 2021

Reversal of neurological defects in a mouse model of Rett syndrome

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7 January 2021

Rett syndrome: clinical peculiarities, diagnostic approach, and possible cause

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7 January 2021

Rett syndrome: clinical peculiarities and biological mysteries

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7 January 2021

Neuropathology of Rett syndrome

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7 January 2021

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

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7 January 2021

Genome-wide atlas of gene expression in the adult mouse brain

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7 January 2021

Morphological study of the entorhinal cortex, hippocampal formation, and basal ganglia in Rett syndrome patients

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7 January 2021

Temporal shift in methyl-CpG binding protein 2 expression in a mouse model of Rett syndrome.

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7 January 2021

Estimating mean glomerular volume using two arbitrary parallel sections

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7 January 2021

Rett syndrome: cerebellar pathology.

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7 January 2021

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

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7 January 2021

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

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7 January 2021

Neuroanatomy of Rett syndrome: a volumetric imaging study

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7 January 2021

Evidence for abnormal early development in a mouse model of Rett syndrome.

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7 January 2021

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

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7 January 2021

Rett syndrome and MeCP2: linking epigenetics and neuronal function

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Identifiers

DOI

10.1002/CNE.21673

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19 December 2017

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19 December 2017