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

An imprinted antisense transcript at the human GNAS1 locus

22 Mar 2000

Abstract excerpt

Recent studies of the GNAS1 gene have shown a highly complex imprinted expression pattern, with paternally, maternally and biallelically derived protein products, raising questions regarding how such transcriptional complexity is established and maintained. GNAS1 was originally identified as the gene encoding an important and widely expressed signal transduction protein, the alpha subunit of the stimulatory G...

Read the complete abstract on PubMed

Topics

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

Share to Blood groups and transfusion
Share to Genetic Syndromes and Imprinting
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10749992
DOI: 10.1093/hmg/9.5.835

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An imprinted antisense transcript at the human GNAS1 locusPMID 10749992Read ↗

Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins.Semantic proximity Read ↗

The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins.Semantic proximity Read ↗

Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology.Semantic proximity Read ↗

A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib.Semantic proximity Read ↗

GNAS -Related Loss-of-Function Disorders and the Role of Imprinting.Semantic proximity Read ↗

The gsalpha gene: predominant maternal origin of transcription in human thyroid gland and gonads.Semantic proximity Read ↗

Identification of a Methylation Imprint Mark within the Mouse <i>Gnas</i> LocusSemantic proximity Read ↗

Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly.Semantic proximity Read ↗

Imprinting on chromosome 20: tissue-specific imprinting and imprinting mutations in the GNAS locus.Semantic proximity Read ↗

The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene.Semantic proximity Read ↗

Control of imprinting at the Gnas cluster.Semantic proximity Read ↗

A cis-acting control region is required exclusively for the tissue-specific imprinting of Gnas.Semantic proximity Read ↗

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