(Q36436597)

14 August 2017

1 reference

title

Imprinting defects on human chromosome 15. (English)

1 reference

14 August 2017

Horsthemke B

1

1 reference

PubMed ID

16575192

14 August 2017

Buiting K

series ordinal

2

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14 August 2017

1 January 2006

1 reference

Cytogenetics and Genome Research

14 August 2017

1 reference

14 August 2017

113

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14 August 2017

292-299

1 reference

14 August 2017

1-4

1 reference

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

14 August 2017

1 reference

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

21 January 2018

1 reference

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

21 January 2018

1 reference

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

1 reference

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect

21 January 2018

1 reference

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

21 January 2018

1 reference

Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos.

21 January 2018

1 reference

Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia.

21 January 2018

1 reference

Reactivation of the paternal X chromosome in early mouse embryos

21 January 2018

1 reference

Epigenetic inheritance at the agouti locus in the mouse

21 January 2018

1 reference

An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.

21 January 2018

1 reference

Imprinting-mutation mechanisms in Prader-Willi syndrome

21 January 2018

1 reference

Epigenetic dynamics of imprinted X inactivation during early mouse development

21 January 2018

1 reference

The imprinting mechanism of the Prader-Willi/Angelman regional control center

21 January 2018

1 reference

Epigenetic reprogramming in mammalian development

21 January 2018

1 reference

In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000090844

1 reference

14 August 2017

1 reference

PubMed ID

16575192