(Q33632372)

28 July 2017

1 reference

title

Mechanisms of genomic imprinting (English)

1 reference

28 July 2017

2

Bartolomei MS

1 reference

28 July 2017

Brannan CI

1

1 reference

28 July 2017

1 April 1999

1 reference

Current Opinion in Genetics & Development

28 July 2017

1 reference

28 July 2017

9

1 reference

28 July 2017

2

1 reference

28 July 2017

164-170

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Competition--a common motif for the imprinting mechanism?

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Genomic imprinting in mammals.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Imprinting mechanisms in mammals.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Imprinting mechanisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

DNA (cytosine-5)-methyltransferases in mouse cells and tissues. Studies with a mechanism-based probe.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

A candidate mammalian DNA methyltransferase related to pmt1p of fission yeast

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Factors affecting meiotic and developmental competence of primary spermatocyte nuclei injected into mouse oocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

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%2899%2980025-2

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%2899%2980025-2

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%2FS0959-437X%2899%2980025-2

7 January 2021

Chromatin conformation of the H19 epigenetic mark.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Location of enhancers is essential for the imprinting of H19 and Igf2 genes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

A group of scs elements function as domain boundaries in an enhancer-blocking assay

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Imprinting in Angelman and Prader-Willi syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Imprinting in Prader-Willi and Angelman syndromes.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

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%2899%2980025-2

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/10.1016%2FS0959-437X%2899%2980025-2

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%2899%2980025-2

7 January 2021

Structure and function correlations at the imprinted mouse Snrpn locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Methylation analysis of the PWS/AS region does not support an enhancer-competition model

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

Competitive edge at the imprinted Prader-Willi/Angelman region?

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2899%2980025-2

7 January 2021

10.1016/S0959-437X(99)80025-2

Identifiers

DOI

1 reference

28 July 2017

1 reference

PubMed ID

10322141