(Q35671678)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

review article

1 reference

title

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

author name string

Janine M LaSalle

series ordinal

1

1 reference

9 August 2017

publication date

1 January 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

Current Topics in Developmental Biology

24 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

volume

59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

page(s)

61-86

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex

24 November 2019

cites work

1 reference

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7 January 2021

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

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7 January 2021

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

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7 January 2021

Review of Rett syndrome.

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7 January 2021

Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21.

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7 January 2021

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

1 reference

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7 January 2021

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

1 reference

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7 January 2021

Creation of genomic methylation patterns

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7 January 2021

Mutation analysis of the coding sequence of the MECP2 gene in infantile autism

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7 January 2021

MECP2 mutations account for most cases of typical forms of Rett syndrome.

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7 January 2021

Difference in early development of presumed monozygotic twins with Rett syndrome

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7 January 2021

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

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7 January 2021

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

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7 January 2021

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

1 reference

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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

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males

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7 January 2021

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

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MECP2 is highly mutated in X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

1 reference

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7 January 2021

A Rett syndrome MECP2 mutation that causes mental retardation in men.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett syndrome: a surprising result of mutation in MECP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methylation-dependent silencing at the H19 imprinting control region by MeCP2

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Amount and distribution of 5-methylcytosine in human DNA from different types of tissues of cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett syndrome: clinical update and review of recent genetic advances.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

DNA hypomethylation perturbs the function and survival of CNS neurons in postnatal animals.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Parental origin of de novo MECP2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Human diseases with underlying defects in chromatin structure and modification.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Maintenance-type DNA methyltransferase is highly expressed in post-mitotic neurons and localized in the cytoplasmic compartment

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Translating the Histone Code

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MeCP2 driven transcriptional repression in vitro: selectivity for methylated DNA, action at a distance and contacts with the basal transcription machinery

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase, Dnmt1

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Parental imprinting and human disease

1 reference

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7 January 2021

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Absence of MeCP2 mutations in patients from the South Carolina autism project

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methylation-mediated proviral silencing is associated with MeCP2 recruitment and localized histone H3 deacetylation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Microarray applications in neuroscience

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methylation of the cyclin A1 promoter correlates with gene silencing in somatic cell lines, while tissue-specific expression of cyclin A1 is methylation independent

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MECP2 mutation in male patients with non-specific X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett and Angelman's syndromes: models of arrested development

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Skewed X inactivation and recurrent spontaneous abortion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

[Rett phenotype in patient with XXY karyotype: case report]

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett syndrome and MeCP2: linking epigenetics and neuronal function

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Balanced X chromosome inactivation patterns in the Rett syndrome brain

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methylated cytosine and the brain: a new base for neuroscience

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Methyl-CpG-binding protein 2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Two affected boys in a Rett syndrome family: clinical and molecular findings

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Mutation screening in Rett syndrome patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Preserved speech variants of the Rett syndrome: molecular and clinical analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2959003-8

7 January 2021

10.1016/S0070-2153(04)59003-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14975247%20AND%20SRC:MED&resulttype=core&format=json

24 November 2019

1 reference