Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene (Q48371609)

11 February 2018

title

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene (English)

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11 February 2018

author name string

Howell CY

1

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11 February 2018

Bestor TH

2

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11 February 2018

Ding F

3

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11 February 2018

Latham KE

4

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11 February 2018

Mertineit C

5

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11 February 2018

Trasler JM

6

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11 February 2018

Chaillet JR

7

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11 February 2018

language of work or name

English

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publication date

1 March 2001

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11 February 2018

published in

Cell

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11 February 2018

volume

104

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11 February 2018

issue

6

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11 February 2018

page(s)

829-838

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11 February 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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Epigenetic modifications necessary for normal development are established during oocyte growth in mice

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Subcellular localization of annexin V in human foreskin fibroblasts: nuclear localization depends on growth state.

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

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The DNA methyltransferases of mammals

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DNA methyltransferase is actively retained in the cytoplasm during early development

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Properties and localization of DNA methyltransferase in preimplantation mouse embryos: implications for genomic imprinting

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Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis

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7 January 2021

High sensitivity mapping of methylated cytosines

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7 January 2021

Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs

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7 January 2021

Structure of human DNMT2, an enigmatic DNA methyltransferase homolog that displays denaturant-resistant binding to DNA

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7 January 2021

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

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7 January 2021

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

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7 January 2021

Parthenogenetic activation of oocytes in c-mos-deficient mice

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Preimplantation development of mouse embryos in KSOM: Augmentation by amino acids and analysis of gene expression

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An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

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

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A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei

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Maternal rescue of transforming growth factor-beta 1 null mice

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Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

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7 January 2021

Role for DNA methylation in genomic imprinting

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Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7.

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Mammalian (cytosine-5) methyltransferases cause genomic DNA methylation and lethality in Drosophila.

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Nuclear transplantation in mouse embryos.

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7 January 2021

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

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7 January 2021

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

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7 January 2021

Molecular cloning and characterization of annexin V-binding proteins with highly hydrophilic peptide structure

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7 January 2021

The influence of demethylating agents on preimplantation development of mice

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7 January 2021

Chromosome methylation patterns during mammalian preimplantation development

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7 January 2021

DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci

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7 January 2021

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

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7 January 2021

Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms

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7 January 2021

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

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7 January 2021

Mater, a maternal effect gene required for early embryonic development in mice

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7 January 2021

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

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7 January 2021

A 5′ 2-Kilobase-Pair Region of the Imprinted Mouse H19 Gene Exhibits Exclusive Paternal Methylation throughout Development

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7 January 2021

The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development

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7 January 2021

Cytosine methylation and mammalian development

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7 January 2021

Transcription of IAP endogenous retroviruses is constrained by cytosine methylation

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7 January 2021

Growing Y-junction carbon nanotubes

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7 January 2021

A candidate mammalian DNA methyltransferase related to pmt1p of fission yeast

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7 January 2021

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

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7 January 2021

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Identifiers

DOI

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11 February 2018

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11 February 2018