Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome.

Acta geneticae medicae et gemellologiae - 1 Jan 1996

Wevrick R, Kerns J A, Francke U

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Base Sequence
Share to DNA
Share to Gene Expression

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genomic Imprinting

Share to Molecular Sequence Data

Share to Nucleic Acid Conformation

Share to Prader-Willi Syndrome

Source

Identifiers

PMID: 8872030
DOI: 10.1017/s000156600000129x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome.PMID 8872030Read ↗

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.Semantic proximity Read ↗

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.Semantic proximity Read ↗

Mosaic imprinting defect in a patient with an almost typical expression of the Prader–Willi syndromeSemantic proximity Read ↗

Imprinting in Angelman and Prader-Willi syndromesSemantic proximity Read ↗

[Genomic imprinting in Prader-Willi syndrome].Semantic proximity Read ↗

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.Semantic proximity Read ↗

Characterization of the imprinted IPW gene: allelic expression in normal and tumorigenic human tissues.Semantic proximity Read ↗

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

The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and ApoptosisSemantic proximity Read ↗

Disruption of the mouse necdin gene results in early post-natal lethality.Semantic proximity Read ↗

Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorderSemantic proximity Read ↗

Temporal and developmental requirements for the Prader-Willi imprinting center.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.