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

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.

Proceedings of the National Academy of Sciences of the United States of America - 23 Nov 2004

Nishimura Darryl Y, Fath Melissa, Mullins Robert F, Searby Charles, Andrews Michael, Davis Roger, Andorf Jeaneen L, Mykytyn Kirk, Swiderski Ruth E, Yang Baoli, Carmi Rivka, Stone Edwin M, Sheffield Val C

Abstract excerpt

Bardet-Biedl syndrome (BBS) is a heterogeneous, pleiotropic human disorder characterized by obesity, retinopathy, polydactyly, renal and cardiac malformations, learning disabilities, hypogenitalism, and an increased incidence of diabetes and hypertension. No information is available regarding the...

Read the complete abstract on PubMed

Topics

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

Share to Bardet-Biedl Syndrome
Share to Cilia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Diseases, Cystic

Share to Photoreceptor Cells, Vertebrate

Share to Rhodopsin

Share to Sensation Disorders

Share to Social Dominance

Share to Spermatogenesis

Source

Open in PubMed Open full text

Identifiers

PMID: 15539463
DOI: 10.1073/pnas.0405496101
PMCID: PMC534519

Genes

BBS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15539463-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.PMID 15539463Read ↗

Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly.Semantic proximity Read ↗

A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity.Semantic proximity Read ↗

Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome.Semantic proximity Read ↗

BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment.Semantic proximity Read ↗

Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes.Semantic proximity Read ↗

Phenotypic variability of Bardet-Biedl syndrome: focusing on the kidney.Semantic proximity Read ↗

Bardet-Biedl syndrome: A rare genetic diseaseSemantic proximity Read ↗

Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management.Semantic proximity Read ↗

Bardet-Biedl syndrome.Semantic proximity Read ↗

Ectopic expression of BBS1 rescues male infertility, but not retinal degeneration, in a BBS1 mouse model.Semantic proximity Read ↗

Cone Photoreceptor Degeneration and Neuroinflammation in the Zebrafish Bardet-Biedl Syndrome 2 (bbs2) Mutant Does Not Lead to Retinal RegenerationSemantic proximity Read ↗

Bardet-Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene.Semantic proximity Read ↗

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