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

Use of a novel system for defining a gene imprinting region.

Biochemical and biophysical research communications - 29 Oct 1993

Rachmilewitz J, Gonik B, Goshen R, Ariel I, Schneider T, de Groot N, Hochberg A

Abstract excerpt

Gene imprinting involves the expression of a single allele, depending on its parental origin. In this report, we describe the use of a novel system, implementing human tissues exclusively endowed with either maternally or paternally inherited chromosomes, to better define a known gene imprinting region. Specific RNA transcripts for Placental Ribonuclease Inhibitor (PRI) and Cathepsin D were analysed by northern...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Blotting, Northern
Share to Chromosomes, Human, Pair 11

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

Share to Gene Expression

Share to Placenta

Share to Pregnancy

Share to RNA, Neoplasm

Source

Identifiers

PMID: 7694575
DOI: 10.1006/bbrc.1993.2300

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Use of a novel system for defining a gene imprinting region.PMID 7694575Read ↗

Parental imprinting of the human H19 geneSemantic proximity Read ↗

Altered imprinting, promoter usage, and expression of insulin-like growth factor-II gene in gestational trophoblastic diseases.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 ↗

Relaxation of imprinted genes in human cancer.Semantic proximity Read ↗

Dissociation of IGF2 and H19 imprinting in human brain.Semantic proximity Read ↗

The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans.Semantic proximity Read ↗

The product of the imprinted H19 gene is an oncofetal RNA.Semantic proximity Read ↗

Imprinted H19 gene expression in embryogenesis and human cancer: the oncofetal connection.Semantic proximity Read ↗

Promoter-specific imprinting of the human insulin-like growth factor-II gene.Semantic proximity Read ↗

Random monoallelic expression of the imprinted IGF2 and H19 genes in the absence of discriminative parental marks.Semantic proximity Read ↗

Altered gene expression in human placentas after IVF/ICSISemantic proximity Read ↗

Genomic imprinting in ruminants: allele-specific gene expression in parthenogenetic sheep.Semantic proximity Read ↗

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