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

Genetic and genomic analyses of Drosophila melanogaster models of chromatin modification disorders.

Genetics - 9 Aug 2023

MacPherson Rebecca A, Shankar Vijay, Anholt Robert R H, Mackay Trudy F C

Abstract excerpt

Switch/sucrose nonfermentable (SWI/SNF)-related intellectual disability disorders (SSRIDDs) and Cornelia de Lange syndrome are rare syndromic neurodevelopmental disorders with overlapping clinical phenotypes. SSRIDDs are associated with the BAF (Brahma-Related Gene-1 associated factor) complex, whereas CdLS is a disorder of chromatin modification associated with the cohesin complex. Here, we used RNA interference...

Read the complete abstract on PubMed

Topics

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

Share to Cell Cycle Proteins
Share to Chromatin
Share to Chromosomal Proteins, Non-Histone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Drosophila

Share to Drosophila melanogaster

Share to Drosophila Proteins

Share to Genomics

Share to Sleep Apnea, Obstructive

Source

Open in PubMed Open full text

Identifiers

PMID: 37036413
DOI: 10.1093/genetics/iyad061
PMCID: PMC10411607

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Genetic and genomic analyses of Drosophila melanogaster models of chromatin modification disorders.PMID 37036413Read ↗

Genetic and Genomic Analyses of <i>Drosophila melanogaster</i> Models of Chromatin Modification DisordersSemantic proximity Read ↗

Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea.Semantic proximity Read ↗

The chromatin remodeler ISWI acts during <i>Drosophila</i> development to regulate adult sleepSemantic proximity Read ↗

Identification of <i>SMARCD1</i> as a syndromic intellectual disability gene that is required for memory and context-dependent regulation of neuronal genes in <i>Drosophila</i>Semantic proximity Read ↗

Phenotypic and Molecular Spectrum of Patients With Switch/sucrose Nonfermenting Complex-related Intellectual Disabilities in KoreaSemantic proximity Read ↗

BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms.Semantic proximity Read ↗

Chromatin remodellers as therapeutic targets.Semantic proximity Read ↗

Mammalian SWI/SNF Chromatin Remodeling Complexes: Emerging Mechanisms and Therapeutic StrategiesSemantic proximity Read ↗

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.Semantic proximity Read ↗

Mutational Landscapes and Phenotypic Spectrum of SWI/SNF-Related Intellectual Disability DisordersSemantic proximity Read ↗

Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.Semantic proximity Read ↗

Pathogenic variants in<i>SMARCA5</i>, a chromatin remodeler, cause a range of syndromic neurodevelopmental featuresSemantic proximity Read ↗

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