(Q34559930)

3 August 2017

title

The human HYMAI/PLAGL1 differentially methylated region acts as an imprint control region in mice (English)

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3 August 2017

Rosalind M John

3

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Yusaku Nakabeppu

object named as

Yusaku Nakabeppu

6

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author name string

Takahiro Arima

1

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3 August 2017

Katsuhisa Yamasaki

2

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3 August 2017

Kiyoko Kato

4

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3 August 2017

Kunihiko Sakumi

5

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3 August 2017

Norio Wake

7

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3 August 2017

Tomohiro Kono

8

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3 August 2017

publication date

22 August 2006

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3 August 2017

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3 August 2017

volume

88

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3 August 2017

issue

5

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3 August 2017

page(s)

650-658

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

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

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Monoallelic expression: 'there can only be one'

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

7 January 2021

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

7 January 2021

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Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

7 January 2021

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

7 January 2021

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A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

7 January 2021

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Imprinting: focusing on the center

7 January 2021

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Chromatin modification and epigenetic reprogramming in mammalian development

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

The cell cycle control gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

7 January 2021

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Regulation of apoptosis and cell cycle arrest by Zac1, a novel zinc finger protein expressed in the pituitary gland and the brain

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

The mouse Zac1 locus: basis for imprinting and comparison with human ZAC.

7 January 2021

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Establishment of the primary imprint of the HYMAI/PLAGL1 imprint control region during oogenesis

7 January 2021

1 reference

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LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Epigenetic silencing of the imprinted gene ZAC by DNA methylation is an early event in the progression of human ovarian cancer

7 January 2021

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Transient neonatal diabetes, a disorder of imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Disruption of imprinting caused by deletion of the H19 gene region in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

An enhancer deletion affects both H19 and Igf2 expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Imprinting in Prader-Willi and Angelman syndromes

7 January 2021

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Towards a molecular understanding of Prader-Willi and Angelman syndromes

7 January 2021

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Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation

7 January 2021

1 reference

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Imprinting-mutation mechanisms in Prader-Willi syndrome

7 January 2021

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

7 January 2021

1 reference

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A mouse model for Prader-Willi syndrome imprinting-centre mutations

7 January 2021

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A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

7 January 2021

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Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

A human H19 transgene exhibits impaired paternal-specific imprint acquisition and maintenance in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

The imprinting box of the Prader-Willi/Angelman syndrome domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Shared role for differentially methylated domains of imprinted genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Maternal primary imprinting is established at a specific time for each gene throughout oocyte growth

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Methylation dynamics of imprinted genes in mouse germ cells.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Gene-specific timing and epigenetic memory in oocyte imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

A model system to study genomic imprinting of human genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2006.07.005

10.1016/J.YGENO.2006.07.005

7 January 2021

Identifiers

DOI

1 reference

3 August 2017

1 reference