Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome (Q33572334)

28 July 2017

title

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome (English)

1 reference

MECP2 duplication syndrome

28 July 2017

0 references

1 reference

Feng Zhang

4

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Huda Zoghbi

object named as

Huda Y Zoghbi

11

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James R. Lupski

10

object named as

James R Lupski

1 reference

28 July 2017

9

Daniel G Glaze

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28 July 2017

1

Melissa B Ramocki

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3

Y Jane Tavyev

1 reference

28 July 2017

Sarika U Peters

2

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Claudia M B Carvalho

5

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28 July 2017

Christian P Schaaf

6

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Ronald Richman

7

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28 July 2017

Ping Fang

8

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28 July 2017

publication date

1 December 2009

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28 July 2017

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28 July 2017

volume

66

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28 July 2017

issue

6

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28 July 2017

page(s)

771-782

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describes a project that uses

28 July 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2801873/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

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 June 2018

1 reference

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

21 June 2018

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A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

21 June 2018

1 reference

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

21 June 2018

1 reference

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IRAK1: a critical signaling mediator of innate immunity

21 June 2018

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Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome

21 June 2018

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

21 June 2018

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The pattern of inheritance of X-linked traits is not dominant or recessive, just X-linked

21 June 2018

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MeCP2 dysfunction in Rett syndrome and related disorders

21 June 2018

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Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

21 June 2018

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Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

21 June 2018

1 reference

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Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication.

21 June 2018

1 reference

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Rett syndrome: a prototypical neurodevelopmental disorder

21 June 2018

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DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 June 2018

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Identification of MeCP2 mutations in a series of females with autistic disorder

21 June 2018

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

21 June 2018

1 reference

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A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

21 June 2018

1 reference

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

21 June 2018

1 reference

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Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

21 June 2018

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Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections

21 June 2018

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Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males

31 October 2018

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31 October 2018

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Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.

31 October 2018

1 reference

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Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

31 October 2018

1 reference

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31 October 2018

1 reference

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MECP2 is highly mutated in X-linked mental retardation

31 October 2018

1 reference

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31 October 2018

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Psychiatric disorder and the broad autism phenotype: evidence from a family study of multiple-incidence autism families

31 October 2018

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Autism, affective and other psychiatric disorders: patterns of familial aggregation

31 October 2018

1 reference

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31 October 2018

1 reference

PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/ANA.21715

1 reference

28 July 2017

1 reference

28 July 2017

1 reference