(Q52552714)

3 May 2018

title

Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells. (English)

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3 May 2018

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Ting-Fen Tsai

1

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3 May 2018

Jan Bressler

series ordinal

2

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3 May 2018

Yong-Hui Jiang

series ordinal

3

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3 May 2018

Arthur L Beaudet

series ordinal

4

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3 May 2018

publication date

1 December 2003

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3 May 2018

published in

Genesis

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3 May 2018

volume

37

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3 May 2018

issue

4

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3 May 2018

page(s)

151-161

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3 May 2018

Gametic imprinting in mammals

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Genomic imprinting in mammals.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

A mammalian protein with specific demethylase activity for mCpG DNA.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Dnmt3L and the establishment of maternal genomic imprints.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Factors affecting ectopic gene conversion in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Promoter-specific activation and demethylation by MBD2/demethylase

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Structure and function correlations at the imprinted mouse Snrpn locus.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

An imprinted, mammalian bicistronic transcript encodes two independent proteins

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Aberrant methylation of an imprinted gene U2af1-rs1(SP2) caused by its own transgene

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Trans allele methylation and paramutation-like effects in mice.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Xist has properties of the X-chromosome inactivation centre

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Paramutation and related allelic interactions

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Structure and function of the human chromosome 15 imprinting center

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Imprinting in Angelman and Prader-Willi syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Homologous association of oppositely imprinted chromosomal domains

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Efficient Cre-loxP-induced mitotic recombination in mouse embryonic stem cells

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Release of epigenetic gene silencing by trans-acting mutations in Arabidopsis

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Core promoter elements can regulate transcription on a separate chromosome in trans

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Imprinting in Prader-Willi and Angelman syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

The imprinting mechanism of the Prader-Willi/Angelman regional control center

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Transgenic and mutational analyses of meiotic recombination in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Chromosome engineering in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Transvection effects involving DNA methylation during meiosis in the mouse

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Epigenetic reprogramming in mammalian development

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Genomic imprinting: parental influence on the genome

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Preferential S-phase pairing of the imprinted region on distal mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Gene inactivation triggered by recognition between DNA repeats

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

A CpG-rich RNA and an RNA helicase tightly associated with the DNA demethylation complex are present mainly in dividing chick embryo cells.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

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/10.1002%2FGENE.10237

7 January 2021

A histone H3 methyltransferase controls DNA methylation in Neurospora crassa

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

https://api.crossref.org/works/10.1002%2FGENE.10237

1 reference

7 January 2021

Transvection and other homology effects

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10237

7 January 2021

Identifiers

DOI

10.1002/GENE.10237

1 reference

3 May 2018

PubMed ID

14666508

1 reference

3 May 2018