(Q33523010)

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Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function

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scholarly article

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Europe PubMed Central

PubMed publication ID

27 July 2017

Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function (English)

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Europe PubMed Central

PubMed publication ID

27 July 2017

maternal health

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Piroska E Szabó

object named as

Piroska E Szabó

2

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author name string

Li Han

1

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Europe PubMed Central

PubMed publication ID

27 July 2017

Jeffrey R Mann

3

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Europe PubMed Central

PubMed publication ID

27 July 2017

publication date

8 January 2010

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Europe PubMed Central

PubMed publication ID

27 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

e1000803

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

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Creative Commons Attribution 4.0 International

8 January 2010

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April 2022 Public Data File from Crossref

copyright status

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H19 acts as a trans regulator of the imprinted gene network controlling growth in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Epigenetic regulation of growth: lessons from Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Control of imprinting at the Gnas cluster.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

The genetic aetiology of Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Two distinct mechanisms of silencing by the KvDMR1 imprinting control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

High-frequency generation of viable mice from engineered bi-maternal embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

A mammalian microRNA expression atlas based on small RNA library sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

The imprinted H19 noncoding RNA is a primary microRNA precursor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Genomic imprinting in mammals: emerging themes and established theories

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Chromosome-wide identification of novel imprinted genes using microarrays and uniparental disomies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

The expression profile of microRNAs in mouse embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Genome-wide prediction of imprinted murine genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Imprinted genes in the placenta--a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Interactions between imprinting effects in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Role of CTCF binding sites in the Igf2/H19 imprinting control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

What good is genomic imprinting: the function of parent-specific gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Igf2 imprinting does not require its own DNA methylation or H19 RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Phenotypic alterations in insulin-deficient mutant mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

The structural H19 gene is required for transgene imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Inviability of parthenogenones is determined by pronuclei, not egg cytoplasm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Role of paternal and maternal genomes in mouse development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Two maternally derived X chromosomes contribute to parthenogenetic inviability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Parental imprinting of the mouse H19 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

14 July 2018

Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Appropriate expression of imprinted genes on mouse chromosome 12 extends development of bi-maternal embryos to term.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Igf2 deficiency results in delayed lung development at the end of gestation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Unbalanced placental expression of imprinted genes in human intrauterine growth restriction.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

The chicken beta-globin insulator element conveys chromatin boundary activity but not imprinting at the mouse Igf2/H19 domain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

31 October 2018

Imprinting of Igf2 and H19 from a 130 kb YAC transgene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794364

31 October 2018

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Normal postimplantation development of mouse parthenogenetic embryos to the forelimb bud stage

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000803

21 January 2018

Placental growth retardation due to loss of imprinting of Phlda2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Do we understand the evolution of genomic imprinting?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of a modified H19 RNA does not cause embryonic lethality in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20062522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1000803

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

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