(Q52128313)

22 April 2018

title

Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype? (English)

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22 April 2018

author

Constantin Polychronakos

series ordinal

2

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22 April 2018

Anna Naumova

series ordinal

3

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22 April 2018

author name string

Croteau S

series ordinal

1

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22 April 2018

publication date

1 September 2001

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22 April 2018

published in

Genesis

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22 April 2018

volume

31

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22 April 2018

issue

1

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22 April 2018

page(s)

11-16

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22 April 2018

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

cites work

1 reference

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

21 January 2018

1 reference

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain.

21 January 2018

1 reference

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

21 January 2018

1 reference

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Imprinted expression and methylation of the mouse H19 gene are conserved in extraembryonic lineages.

21 January 2018

1 reference

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

21 January 2018

1 reference

H19 and Igf2 are expressed and differentially imprinted in neuroectoderm-derived cells in the mouse brain.

21 January 2018

1 reference

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

21 January 2018

1 reference

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

Mosaic and polymorphic imprinting of the WT1 gene in humans.

21 January 2018

1 reference

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.

21 January 2018

1 reference

Role for DNA methylation in genomic imprinting

21 January 2018

1 reference

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

21 January 2018

1 reference

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome

21 January 2018

1 reference

Relaxation of imprinted genes in human cancer.

21 January 2018

1 reference

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

21 January 2018

1 reference

Site of action of imprinted genes revealed by phenotypic analysis of parthenogenetic embryos.

21 January 2018

1 reference

Genomic imprinting is disrupted in interspecific Peromyscus hybrids.

21 January 2018

1 reference

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

An imprinted locus associated with transient neonatal diabetes mellitus

21 January 2018

1 reference

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

21 January 2018

1 reference

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

21 January 2018

1 reference

Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

21 January 2018

1 reference

Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo

21 January 2018

1 reference

DNA methylation, genomic imprinting and cancer.

21 January 2018

1 reference

Parental genomic imprinting of the human IGF2 gene

21 January 2018

1 reference

Xist-deficient mice are defective in dosage compensation but not spermatogenesis

21 January 2018

1 reference

Epigenetic heterogeneity at imprinted loci in normal populations

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/GENE.1077

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22 April 2018

PubMed ID

11668673

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22 April 2018