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

OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the Polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR

18 Jul 2020

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 Cleft Lip and Palate Research
Share to Ocular Disorders and Treatments
Share to Urological Disorders and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32692983
DOI: 10.1016/j.ydbio.2020.06.013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the Polycomb-group repressive complex 1.1 (PRC1.1) gene BCORPMID 32692983Read ↗

Role of the Transcriptional Corepressor Bcor in Embryonic Stem Cell Differentiation and Early Embryonic DevelopmentSemantic proximity Read ↗

BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.Semantic proximity Read ↗

Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome.Semantic proximity Read ↗

A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS.Semantic proximity Read ↗

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.Semantic proximity Read ↗

Expanding the phenotype of the X-linked BCOR microphthalmia syndromes.Semantic proximity Read ↗

BCOR regulates mesenchymal stem cell function by epigenetic mechanisms.Semantic proximity Read ↗

Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features.Semantic proximity Read ↗

A rare genotype of biallelic mosaic variants in BCOR gene causing a bilateral ocular anterior segment dysgenesis and cataracts.Semantic proximity Read ↗

Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndromeSemantic proximity Read ↗

Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination.Semantic proximity Read ↗

Knockdown of PR-DUB subunit calypso in the developing Drosophila eye and wing results in mis-patterned tissues with altered size and shape.Semantic proximity Read ↗

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