(Q28209903)

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

9 April 2017

0 references

2

H Y Zoghbi

0 references

Huda Zoghbi

series ordinal

2

0 references

author name string

I B Van den Veyver

series ordinal

1

0 references

Ignatia B. Van den Veyver

series ordinal

1

1 reference

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

9 April 2017

language of work or name

English

0 references

publication date

December 2001

1 reference

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

9 April 2017

published in

Brain and Development

1 reference

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

9 April 2017

volume

23 Suppl 1

0 references

23

1 reference

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

9 April 2017

page(s)

S147-51

0 references

S147-S151

1 reference

https://doi.org/10.1016%2FS0387-7604%2801%2900376-X

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

9 April 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Clinical delineation of Rett syndrome variants

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

In search of a genetic basis for the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

X chromosome linkage studies in familial Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

7 January 2021

Methylation-induced repression--belts, braces, and chromatin

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Identification and characterization of a family of mammalian methyl-CpG binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

DNA methyltransferases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

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%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

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

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Cytosine methylation and mammalian development

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021

Nonsense-mediated mRNA decay in health and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900376-X

7 January 2021