(Q22337290)

7 February 2023

5

Uta Francke

Uta

Francke

1 reference

7 February 2023

Ruthie E. Amir

1

Ruthie E.

Amir

1 reference

7 February 2023

Ignatia B. Van den Veyver

series ordinal

2

author given names

Ignatia B.

author last names

Van den Veyver

1 reference

7 February 2023

Mimi Wan

series ordinal

3

author given names

Mimi

author last names

Wan

1 reference

7 February 2023

Charles Q. Tran

series ordinal

4

author given names

Charles Q.

author last names

Tran

1 reference

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

7 February 2023

language of work or name

English

0 references

publication date

1 October 1999

0 references

published in

Nature Genetics

0 references

volume

23

0 references

issue

2

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page(s)

185-188

0 references

cites work

1 reference

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

7 January 2021

Genetic aspects of Rett syndrome

1 reference

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

7 January 2021

X chromosome linkage studies in familial Rett syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

1 reference

7 January 2021