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Lab affiliation

Department of Ophthalmology, University of California, Irvine, CA 92697 (1)
Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Prague, Czech Republic ORCID logohttp://orcid.org/0000-0001-6976-8446 (1)
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Medical Bioanalytics Institute for Ophthalmic Research Eberhard-Karls-University Tuebingen (1)
Michelle Heck, USDA-ARS, Emerging Pests and Pathogens Research Unit, Holly Center, Ithaca, NY, USA (1)
Scripps Research (1)
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The Bardet-Biedl protein Bbs1 controls photoreceptor outer segment protein and lipid composition

Summary

Primary cilia are key sensory organelles whose dysfunction leads to ciliopathy disorders such as Bardet-Biedl syndrome (BBS). Retinal degeneration is common in ciliopathies, since the outer segments (OSs) of photoreceptors are highly specialized primary cilia. BBS...

2022-02-18 | MTBLS4013 | MetaboLights

Thiocapsa bogorovii strain:BBS

Thiocapsa bogorovii strain:BBS Genome sequencing

PRJNA787410 | ENA

Pediococcus pentosaceus strain:BBS 1

Pediococcus pentosaceus strain:BBS 1 Raw sequence reads

PRJNA937182 | ENA

Lactiplantibacillus plantarum strain:BBS 13 | isolate:Bamboo shoot fermentation

Lactiplantibacillus plantarum BBS 13 isolated from for Lao Traditional Bamboo Shoot Fermentation (Nor mai som),

PRJNA937409 | ENA

Usher syndrome proteins ADGRV1 (USH2C) and CIB2 (USH1J) interact and share a common interactome containing TRiC/CCT-BBS chaperonins

The human Usher syndrome (USH) is the most common form of a sensory hereditary ciliopathy characterized by progressive vision and hearing loss. Mutations in the genes ADGRV1 and CIB2 have been associated with two distinct sub-types of USH, namely USH2C and USH1J. The proteins encoded by the two gene...

ORGANISM(S): Homo sapiens (Human)

2023-10-24 | PXD042629 | Pride