(Q51026043)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23636699%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

title

No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generations (English)

1 reference

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29 February 2020

12

1 reference

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29 February 2020

Neil A Youngson

1

1 reference

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29 February 2020

Lucia Daxinger

4

1 reference

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29 February 2020

Jacqueline M Matthews

11

1 reference

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29 February 2020

3

Amity R Roberts

1 reference

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29 February 2020

author name string

Trevor Epp

2

1 reference

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29 February 2020

Alyson Ashe

5

1 reference

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29 February 2020

Edward Huang

6

1 reference

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29 February 2020

Krystal L Lester

7

1 reference

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29 February 2020

Sarah K Harten

8

1 reference

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29 February 2020

Graham F Kay

9

1 reference

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29 February 2020

Timothy Cox

10

1 reference

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29 February 2020

Emma Whitelaw

13

1 reference

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29 February 2020

publication date

1 May 2013

1 reference

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29 February 2020

number of pages

12

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

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29 February 2020

volume

24

1 reference

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29 February 2020

issue

5-6

1 reference

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29 February 2020

page(s)

206-217

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00335-013-9451-5

29 February 2020

exact match

0 references

cites work

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Transgenerational epigenetic effects on brain functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Modifiers of epigenetic reprogramming show paternal effects in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Beyond DNA: integrating inclusive inheritance into an extended theory of evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Chromatin replication and epigenome maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

A forward genetic screen identifies eukaryotic translation initiation factor 3, subunit H (eIF3h), as an enhancer of variegation in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Smchd1-dependent and -independent pathways determine developmental dynamics of CpG island methylation on the inactive X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Mouse centric and pericentric satellite repeats form distinct functional heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Environmentally induced epigenetic transgenerational inheritance of phenotype and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Epigenetic transgenerational actions of vinclozolin on promoter regions of the sperm epigenome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Global profiling of DNA methylation erasure in mouse primordial germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Mouse telocentric sequences reveal a high rate of homogenization and possible role in Robertsonian translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Timing of establishment of paternal methylation imprints in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Sperm-borne microRNA-34c is required for the first cleavage division in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Epigenetic inheritance at the agouti locus in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Transgenerational genetic effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Efficient localization of mutations by interval haplotype analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Structural basis for recognition of H3K4 methylation status by the DNA methyltransferase 3A ATRX-DNMT3-DNMT3L domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Sensitive flow cytometric analysis reveals a novel type of parent-of-origin effect in the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

RNA-mediated non-mendelian inheritance of an epigenetic change in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Role for piRNAs and noncoding RNA in de novo DNA methylation of the imprinted mouse Rasgrf1 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Reduced levels of two modifiers of epigenetic gene silencing, Dnmt3a and Trim28, cause increased phenotypic noise

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Transgenerational epigenetic effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

A missense mutation in the transcription factor Foxo3a causes teratomas and oocyte abnormalities in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Chromatin methylation activity of Dnmt3a and Dnmt3a/3L is guided by interaction of the ADD domain with the histone H3 tail

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-013-9451-5

Abnormal methylation does not prevent X inactivation in ICF patients.

21 January 2018

1 reference

12 December 2020

The miR-124-Sox9 paramutation: RNA-mediated epigenetic control of embryonic and adult growth

1 reference

12 December 2020

Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome

1 reference

12 December 2020

Reactivation of heritably silenced gene expression in mice

1 reference

12 December 2020

Understanding transgenerational epigenetic inheritance via the gametes in mammals

1 reference

12 December 2020

Distinctive chromatin in human sperm packages genes for embryo development

1 reference

12 December 2020