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Article

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

1 Dec 1992

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Share to Epigenetics and DNA Methylation
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1303276
DOI: 10.1038/ng1292-259

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome regionPMID 1303276Read ↗

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.Semantic proximity Read ↗

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchSemantic proximity Read ↗

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

Prader-Willi Syndrome Is Caused by Disruption of the SNRPN GeneSemantic proximity Read ↗

Structure and function correlations at the imprinted mouse Snrpn locus.Semantic proximity Read ↗

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain.Semantic proximity Read ↗

Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.Semantic proximity Read ↗

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.Semantic proximity Read ↗

Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene.Semantic proximity Read ↗

A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.Semantic proximity Read ↗

The imprinting box of the Prader-Willi/Angelman syndrome domain.Semantic proximity Read ↗

Genome Organization, Function, and Imprinting in Prader-Willi and Angelman SyndromesSemantic proximity Read ↗

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