The role of X-chromosome inactivation in the manifestation of Rett syndrome (Q34460601)

2 August 2017

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title

The role of X-chromosome inactivation in the manifestation of Rett syndrome (English)

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2 August 2017

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Takagi N

1

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2 August 2017

publication date

1 December 2001

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2 August 2017

published in

Brain and Development

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2 August 2017

volume

23 Suppl 1

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2 August 2017

page(s)

S182-5

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

2 August 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-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%2900362-X

7 January 2021

Methyl-CpG-binding protein 2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-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%2900362-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%2900362-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%2900362-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%2900362-X

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%2FS0387-7604%2801%2900362-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%2900362-X

7 January 2021

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

X-chromosome inactivation in mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

A 450 kb transgene displays properties of the mammalian X-inactivation center.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Long-range cis effects of ectopic X-inactivation centres on a mouse autosome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Xist has properties of the X-chromosome inactivation centre

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Xist yeast artificial chromosome transgenes function as X-inactivation centers only in multicopy arrays and not as single copies

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Human XIST yeast artificial chromosome transgenes show partial X inactivation center function in mouse embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Requirement for Xist in X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Xist-deficient mice are defective in dosage compensation but not spermatogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Preferential expression of the maternally derived X chromosome in the mouse yolk sac

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Escape from X inactivation in human and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

A first-generation X-inactivation profile of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

A chemically-induced variegated-type position effect in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

The applications of genetic mosaicism to developmental problems

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Controlling elements in the mouse: IV. Evidence of non-randomX-inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Mapping the murine Xce locus with (CA)n repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Translocation breakpoint possibly predisposes to nonrandom X-chromosome inactivation in mouse embryos bearing Searle's T(X;16)16H translocation.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

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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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

Patterns of X chromosome inactivation in the Rett syndrome

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900362-X

7 January 2021

10.1016/S0387-7604(01)00362-X

Identifiers

DOI

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2 August 2017

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