(Q52163717)

25 April 2018

title

Disruption of imprinted X inactivation by parent-of-origin effects at Tsix. (English)

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25 April 2018

author name string

Lee JT

series ordinal

1

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25 April 2018

language of work or name

English

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publication date

1 September 2000

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25 April 2018

published in

Cell

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25 April 2018

volume

103

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25 April 2018

page(s)

17-27

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25 April 2018

issue

1

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25 April 2018

Derivation of embryonic stem cell lines

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Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

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Double-stranded RNA as a template for gene silencing

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Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

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7 January 2021

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

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7 January 2021

The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

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7 January 2021

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

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7 January 2021

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

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7 January 2021

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

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7 January 2021

Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist

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7 January 2021

Functional analysis of the DXPas34 locus, a 3' regulator of Xist expression

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7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

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7 January 2021

Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting

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7 January 2021

Mammals that break the rules: genetics of marsupials and monotremes

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CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

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7 January 2021

Retarded postimplantation development of X0 mouse embryos: impact of the parental origin of the monosomic X chromosome.

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7 January 2021

Igf2 imprinting does not require its own DNA methylation or H19 RNA.

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7 January 2021

DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation

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7 January 2021

Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation

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7 January 2021

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development

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X chromosome imprinting and inactivation in the early mammalian embryo

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Highly localized tracks of specific transcripts within interphase nuclei visualized by in situ hybridization

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

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7 January 2021

Targeted mutagenesis of Tsix leads to nonrandom X inactivation.

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7 January 2021

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

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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

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

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7 January 2021

Role for DNA methylation in genomic imprinting

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7 January 2021

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

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7 January 2021

Possible mechanisms of X chromosome inactivation.

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7 January 2021

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

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7 January 2021

Frequent derepression of G6PD and HPRT on the marsupial inactive X chromosome associated with cell proliferation in vitro

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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

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

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7 January 2021

X chromosome inactivation is mediated by Xist RNA stabilization

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7 January 2021

Requirement for Xist in X chromosome inactivation

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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

Enhancer competition between H19 and Igf2 does not mediate their imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

Stabilization of Xist RNA mediates initiation of X chromosome inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

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

Ends Xist, but where are the beginnings?

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7 January 2021

Imprinting and the initiation of gene silencing in the germ line.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-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%2FS0092-8674%2800%2900101-X

7 January 2021

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

The sins of the fathers and mothers: genomic imprinting in mammalian development.

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

X chromosome inactivation, XIST, and pursuit of the X-inactivation center

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2900101-X

7 January 2021

10.1016/S0092-8674(00)00101-X

Identifiers

DOI

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25 April 2018

PubMed ID

11051544

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25 April 2018