(Q34194830)

31 July 2017

title

Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease (English)

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31 July 2017

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Cristina Tufarelli

1

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author name string

Jackie A Sloane Stanley

2

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31 July 2017

David Garrick

3

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31 July 2017

Jackie A Sharpe

4

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31 July 2017

Helena Ayyub

5

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31 July 2017

William G Wood

6

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31 July 2017

Douglas R Higgs

7

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31 July 2017

language of work or name

English

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publication date

1 June 2003

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31 July 2017

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31 July 2017

volume

34

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31 July 2017

issue

2

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31 July 2017

page(s)

157-165

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Good genes in bad neighbourhoods.

31 July 2017

cites work

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7 January 2021

Position effect in human genetic disease

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7 January 2021

The relationship between chromosome structure and function at a human telomeric region

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7 January 2021

The pattern of replication at a human telomeric region (16p13.3): its relationship to chromosome structure and gene expression

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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

Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domain

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7 January 2021

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

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7 January 2021

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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7 January 2021

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

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7 January 2021

An imprinted antisense transcript at the human GNAS1 locus

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7 January 2021

Targeted mutagenesis of Tsix leads to nonrandom X inactivation.

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7 January 2021

A major positive regulatory region located far upstream of the human alpha-globin gene locus

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7 January 2021

Analysis of the human alpha-globin gene cluster in transgenic mice

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7 January 2021

RNA: guiding gene silencing

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7 January 2021

Both X chromosomes function before visible X-chromosome inactivation in female mouse embryos

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7 January 2021

Sequential X chromosome inactivation coupled with cellular differentiation in early mouse embryos

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7 January 2021

X chromosome inactivation is mediated by Xist RNA stabilization

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7 January 2021

Stabilization of Xist RNA mediates initiation of X chromosome inactivation.

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7 January 2021

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

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7 January 2021

Transcription of tissue-specific genes in human preimplantation embryos.

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7 January 2021

The human ubiquitin C promoter directs high ubiquitous expression of transgenes in mice

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7 January 2021

The non-coding Air RNA is required for silencing autosomal imprinted genes

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7 January 2021

The uniqueness of the imprinting mechanism

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7 January 2021

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

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7 January 2021

Tsix, a gene antisense to Xist at the X-inactivation centre

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7 January 2021

Role for DNA methylation in the control of cell type specific maspin expression

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7 January 2021

Transcriptional activation of human adult alpha-globin genes by hypersensitive site-40 enhancer: function of nuclear factor-binding motifs occupied in erythroid cells

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7 January 2021

Activation of EGFP expression by Cre-mediated excision in a new ROSA26 reporter mouse strain

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7 January 2021

Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene

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7 January 2021

Hematopoietic commitment during embryonic stem cell differentiation in culture

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7 January 2021

Two different theta (theta) globin gene deletions observed among black newborn babies

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7 January 2021

Identifiers

DOI

10.1038/NG1157

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31 July 2017

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