Rett syndrome and MeCP2: linking epigenetics and neuronal function (Q24616417)

American Journal of Human Genetics

Europe PubMed Central

title

Rett syndrome and MeCP2: linking epigenetics and neuronal function (English)

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2

Huda Y Zoghbi

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author name string

Mona D Shahbazian

series ordinal

1

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language of work or name

English

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publication date

December 2002

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published in

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volume

71

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page(s)

1259-72

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issue

6

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cites work

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7 April 2017

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Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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Methyl-CpG-binding protein 2 represses LINE-1 expression and retrotransposition but not Alu transcription

27 September 2017

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27 September 2017

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27 September 2017

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

27 September 2017

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Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.

27 September 2017

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DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.

27 September 2017

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Parental origin of de novo MECP2 mutations in Rett syndrome

27 September 2017

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MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern

27 September 2017

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Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

27 September 2017

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Functional consequences of Rett syndrome mutations on human MeCP2.

27 September 2017

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

27 September 2017

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DNA recognition by the methyl-CpG binding domain of MeCP2.

27 September 2017

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

27 September 2017

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

27 September 2017

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Mutation screening in Rett syndrome patients.

27 September 2017

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Molecular approaches to the Rett syndrome gene

27 September 2017

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

27 September 2017

1 reference

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Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28

27 September 2017

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Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution

27 September 2017

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Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated

27 September 2017

1 reference

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Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

27 September 2017

1 reference

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High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders

27 September 2017

1 reference

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COX-2, a synaptically induced enzyme, is expressed by excitatory neurons at postsynaptic sites in rat cerebral cortex

27 September 2017

1 reference

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The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

DNA methylation specifies chromosomal localization of MeCP2.

27 September 2017

1 reference

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Epidemiology of Rett syndrome: a population-based registry.

27 September 2017

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Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

27 September 2017

1 reference

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Selective dendritic alterations in the cortex of Rett syndrome

27 September 2017

1 reference

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Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome

27 September 2017

1 reference

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The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

27 September 2017

1 reference

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A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

27 September 2017

1 reference

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Two DNA methyltransferases from murine erythroleukemia cells: purification, sequence specificity, and mode of interaction with DNA.

27 September 2017

1 reference

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Hyperventilation in the awake state: potentially treatable component of Rett syndrome

27 September 2017

1 reference

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On the genetics of Rett syndrome: analysis of family and pedigree data.

27 September 2017

1 reference

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Genetic aspects of Rett syndrome

27 September 2017

1 reference

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Electroencephalographic findings in Rett syndrome

27 September 2017

1 reference

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Rett's syndrome in the west of Scotland

27 September 2017

1 reference

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Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

The neuropathology of the Rett syndrome

27 September 2017

1 reference

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The Rett girls with preserved speech

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Patterns of X chromosome inactivation in the Rett syndrome

27 September 2017

1 reference

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Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome.

27 September 2017

1 reference

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Preserved speech variant is allelic of classic Rett syndrome

30 May 2018

1 reference

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Substance P immunoreactivity in Rett syndrome

30 May 2018

1 reference

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DNA methyltransferase contributes to delayed ischemic brain injury.

30 May 2018

1 reference

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Organ growth in Rett syndrome: a postmortem examination analysis.

30 May 2018

1 reference

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

30 May 2018

1 reference

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Cyclooxygenase-2 expression during rat neocortical development and in Rett syndrome

30 May 2018

1 reference

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Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Brain perfusion SPECT and EEG findings in Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Assignment of the gene for methyl-CpG-binding protein 2 (MECP2) to human chromosome band Xq28 by in situ hybridization.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Neuroanatomy of Rett syndrome: a volumetric imaging study

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Trichostatin A inhibits both ras-induced neurite outgrowth of PC12 cells and morphological transformation of NIH3T3 cells.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Underpigmentation of the substantia nigra in chronic disease in children

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Abnormal breathing in the Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

The clinical pattern of the Rett syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

The nutritional aspects of Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome. History and general overview

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome and the electroencephalogram.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Atypical forms of Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Breathing impairment in Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Immature pattern of brain activity in Rett syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Growth and nutrition in 10 girls with Rett syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Light induces chromatin modification in cells of the mammalian circadian clock.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Balanced X chromosome inactivation patterns in the Rett syndrome brain.

19 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome: clinical manifestations in males with MECP2 mutations.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

MECP2 mutation in a boy with language disorder and schizophrenia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome in Spain: mutation analysis and clinical correlations.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Spectrum of MECP2 mutations in Rett syndrome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

DHPLC analysis of the MECP2 gene in Italian Rett patients.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Occurrence of Rett syndrome in boys.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

MECP2 is highly mutated in X-linked mental retardation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Evaluation of two X chromosomal candidate genes for Rett syndrome: glutamate dehydrogenase-2 (GLUD2) and rab GDP-dissociation inhibitor (GDI1).

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Neonatal encephalopathy in two boys in families with recurrent Rett syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Expression of DNA methyltransferase gene in mature and immature neurons as well as proliferating cells in mice.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett variants: a suggested model for inclusion criteria.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Studies on neuromelanin: II. Melanin in the brainstems of infants and children

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Rett's syndrome. Correlation of electroencephalographic characteristics with clinical staging

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378559

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

28 November 2018

1 reference

12 December 2020

MECP2 mutation screening in Swedish classical Rett syndrome females

1 reference

12 December 2020

Neurotrophic effects of substance P on hippocampal neurons in vitro

1 reference

12 December 2020

Electrocardiographic findings in Rett syndrome: an explanation for sudden death?

1 reference

12 December 2020

Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

1 reference

12 December 2020

GFAP gene methylation in different neural cell types from rat brain

1 reference

12 December 2020

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

1 reference

12 December 2020

A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA

1 reference

12 December 2020

Physical growth and development in patients with Rett syndrome

1 reference

12 December 2020

Neuropathology of Rett syndrome

1 reference

12 December 2020

Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence

1 reference

12 December 2020

Rett syndrome--natural history in 70 cases

1 reference

12 December 2020

Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation

1 reference

12 December 2020

Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation

1 reference

12 December 2020

Mitochondrial alterations in Rett syndrome

1 reference

12 December 2020

X chromosome linkage studies in familial Rett syndrome

1 reference

12 December 2020

Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients

1 reference

12 December 2020

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

1 reference

12 December 2020

Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death

1 reference

12 December 2020

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy

1 reference

12 December 2020

Nerve growth factor induced differentiation of neuronal cells requires gene methylation

1 reference

12 December 2020

The DNA methyltransferase inhibitor 5-azacytidine specifically alters the expression of helix-loop-helix proteins Id1, Id2 and Id3 during neuronal differentiation

1 reference

12 December 2020

Rett syndrome: analysis of deaths in the British survey

1 reference

12 December 2020

https://api.crossref.org/works/10.1086%2F345360

1 reference

7 January 2021

inferred from DOI database lookup

Spino-cerebellar degeneration with polyneuropathy associated with ceroid lipofuscinosis in one family.

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F345360

7 January 2021

inferred from DOI database lookup

Computerized real-time neuromuscular sonography: a new application, techniques and methods

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F345360

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/345360

1 reference

1450459

1450459

1 reference

1 reference

1 reference