(Q52187194)

26 April 2018

review article

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title

Imprinting mechanisms in mammals. (English)

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26 April 2018

author

Wolf Reik

series ordinal

1

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26 April 2018

author name string

Walter J

series ordinal

2

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26 April 2018

publication date

1 April 1998

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26 April 2018

Current Opinion in Genetics & Development

published in

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26 April 2018

volume

8

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26 April 2018

page(s)

154-164

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26 April 2018

issue

2

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26 April 2018

Imprinted genes and regulation of gene expression by epigenetic inheritance.

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Competition--a common motif for the imprinting mechanism?

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Parental imprinting and human disease

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Parental imprinting of autosomal mammalian genes

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The Wellcome Prize Lecture. Genetic imprinting: the battle of the sexes rages on.

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Genomic imprinting in mice: its function and mechanism

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Multiple roles for DNA methylation in gametic imprinting

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DNA methylation in genomic imprinting

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Formation of methylation patterns in the mammalian genome

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Genomic imprinting of chromatin in Drosophila melanogaster

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Role for DNA methylation in genomic imprinting

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

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7 January 2021

Parental-origin-specific epigenetic modification of the mouse H19 gene

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7 January 2021

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

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7 January 2021

Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus.

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7 January 2021

Evidence that random and imprinted Xist expression is controlled by preemptive methylation.

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7 January 2021

A new imprinted gene cloned by a methylation-sensitive genome scanning method

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7 January 2021

Conservation of a maternal-specific methylation signal at the human IGF2R locus

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7 January 2021

Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method.

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7 January 2021

Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse.

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7 January 2021

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

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7 January 2021

Genomic structure and parent-of-origin-specific methylation of Peg1.

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7 January 2021

Human PEG1/MEST, an imprinted gene on chromosome 7

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7 January 2021

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

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7 January 2021

Genomic imprinting and chromosomal localization of the human MEST gene

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7 January 2021

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

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

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

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7 January 2021

Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Characteristics of imprinted genes

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Dynamic methylation adjustment and counting as part of imprinting mechanisms

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

The pre-implantation ontogeny of the H19 methylation imprint.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

An oocyte-specific methylation imprint center in the mouse U2afbp-rs/U2af1-rs1 gene marks the establishment of allele-specific methylation during preimplantation development.

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7 January 2021

Methylation of the mouse Xist gene in sperm and eggs correlates with imprinted Xist expression and paternal X-inactivation.

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7 January 2021

Gamete-specific methylation correlates with imprinting of the murine Xist gene.

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7 January 2021

An imprinting element from the mouse H19 locus functions as a silencer in Drosophila.

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7 January 2021

Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes.

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7 January 2021

Regulation of genomic imprinting by gametic and embryonic processes.

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7 January 2021

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

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7 January 2021

Parental imprinting of an Igf-2 transgene

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7 January 2021

The structural H19 gene is required for transgene imprinting

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7 January 2021

A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting

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7 January 2021

Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element

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7 January 2021

Panning for gold at the K stream

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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%2FS0959-437X%2898%2980136-6

7 January 2021

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinting moves to the centre

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

An enhancer deletion affects both H19 and Igf2 expression

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

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/10.1016%2FS0959-437X%2898%2980136-6

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/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

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7 January 2021

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Developmental regulation of genomic imprinting during gametogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

DNA demethylation in vitro: involvement of RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

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%2FS0959-437X%2898%2980136-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Xist has properties of the X-chromosome inactivation centre

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinting at the mouse Ins2 locus: evidence for cis- and trans-allelic interactions.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Homologous association of oppositely imprinted chromosomal domains

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

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/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

A chromatin model of IGF2/H19 imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Polymorphic functional imprinting of the human IGF2 gene among individuals, in blood cells, is associated with H19 expression

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

How does DNA methylation repress transcription?

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Genomic imprinting: a chromatin connection

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinted genes have few and small introns

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinted genes are up-regulated by growth arrest in embryonic fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Genomic regions regulating imprinting and insulin-like growth factor-II promoter 3 activity in transgenics: novel enhancer and silencer elements.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980136-6

7 January 2021

10.1016/S0959-437X(98)80136-6

Identifiers

DOI

1 reference

26 April 2018

PubMed ID

9610405

1 reference

26 April 2018