Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism (Q34499035)

2 August 2017

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title

Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism (English)

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ORCID Public Data File 2021

2 August 2017

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author name string

Janine M LaSalle

series ordinal

1

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2 August 2017

Amber Hogart

series ordinal

2

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2 August 2017

Karen N Thatcher

series ordinal

3

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2 August 2017

language of work or name

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1 January 2005

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International Review of Neurobiology

2 August 2017

published in

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2 August 2017

volume

71

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2 August 2017

page(s)

131-165

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

2 August 2017

cites work

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7 January 2021

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

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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

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

1 reference

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7 January 2021

Interphase cytogenetics reveals somatic pairing of chromosome 17 centromeres in normal human brain tissue, but no trisomy 7 or sex-chromosome loss

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7 January 2021

Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum

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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.

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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

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

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

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7 January 2021

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD

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7 January 2021

What's going on? The question of time trends in autism

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7 January 2021

Movement of the X chromosome in epilepsy

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7 January 2021

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

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7 January 2021

Expression of alpha- and beta-globin genes occurs within different nuclear domains in haemopoietic cells.

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7 January 2021

Dynamic repositioning of genes in the nucleus of lymphocytes preparing for cell division

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7 January 2021

Association of Transcriptionally Silent Genes with Ikaros Complexes at Centromeric Heterochromatin

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7 January 2021

Disruption of the bipartite imprinting center in a family with Angelman syndrome

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7 January 2021

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect

1 reference

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7 January 2021

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

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7 January 2021

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome

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7 January 2021

Association between a GABRB3 polymorphism and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Visualization of chromatin domains created by the gypsy insulator of Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Minicolumnar pathology in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Differential expression of the methyl-cytosine binding protein 2 gene in embryonic and adult brain of zebrafish

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Role of Chromosome Territories in the Functional Compartmentalization of the Cell Nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Phenotypic consequences of deletion of the gamma 3, alpha 5, or beta 3 subunit of the type A gamma-aminobutyric acid receptor in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Spatial organization of gene expression: the active chromatin hub.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

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https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

A functional enhancer suppresses silencing of a transgene and prevents its localization close to centrometric heterochromatin.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Disruption of the mouse necdin gene results in early post-natal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Parental origin of de novo MECP2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The dynamics of X-inactivation skewing as women age.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Arrangement of kinetochore proteins and satellite DNA in neuronal interphase nuclei: changes induced by gamma-aminobutyric acid (GABA)

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Visualization of focal sites of transcription within human nuclei.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Translating the Histone Code

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Human disorders of ubiquitination and proteasomal degradation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

MeCP2 and other methyl-CpG binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Increased dendritic complexity and axonal length in cultured mouse cortical neurons overexpressing methyl-CpG-binding protein MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mutation screening and transmission disequilibrium study of ATP10C in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Gene order and dynamic domains

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Parental imprinting and human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Homologous association of oppositely imprinted chromosomal domains

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. II. Olfactory bulb and cerebellum.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Identifying environmental contributions to autism: provocative clues and false leads

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Higher levels of organization in the interphase nucleus of cycling and differentiated cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

A view of interphase chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Reproducible compartmentalization of individual chromosome domains in human CNS cells revealed by in situ hybridization and three-dimensional reconstruction

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Nuclear topology of murine, cerebellar Purkinje neurons: changes as a function of development.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mapping of the alpha 4 subunit gene (GABRA4) to human chromosome 4 defines an alpha 2-alpha 4-beta 1-gamma 1 gene cluster: further evidence that modern GABAA receptor gene clusters are derived from an ancestral cluster.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Evidence for Uniparental, Paternal Expression of the Human GABAA Receptor Subunit Genes, Using Microcell-Mediated Chromosome Transfer

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The genetics of autism

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https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Imprinting evolution and the price of silence.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Oct-1 maintains an intermediate, stable state of HLA-DRA promoter repression in Rb-defective cells: an Oct-1-containing repressosome that prevents NF-Y binding to the HLA-DRA promoter

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Multiple interactions between regulatory regions are required to stabilize an active chromatin hub.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Autism in Angelman syndrome: implications for autism research

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

GABA(A) receptors: immunocytochemical distribution of 13 subunits in the adult rat brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Toward a developmental neurobiology of autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Genomic imprinting: parental influence on the genome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Rethinking the fate of males with mutations in the gene that causes Rett syndrome

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https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Autism and maternally derived aberrations of chromosome 15q

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Imprinting centers, chromatin structure, and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Looping and interaction between hypersensitive sites in the active beta-globin locus

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Genomic imprinting: intricacies of epigenetic regulation in clusters.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

1 reference

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%2FS0074-7742%2805%2971006-0

7 January 2021

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

The molecular genetics of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

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%2FS0074-7742%2805%2971006-0

7 January 2021

Chromosomal subunits in active genes have an altered conformation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Chicken MAR-Binding Protein ARBP Is Homologous to Rat Methyl-CpG-Binding Protein MeCP2

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Integration of Runx and Smad regulatory signals at transcriptionally active subnuclear sites

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2805%2971006-0

7 January 2021

10.1016/S0074-7742(05)71006-0

Identifiers

DOI

1 reference

2 August 2017

1 reference