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

Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration.

International journal of molecular sciences - 29 Oct 2020

Genc Ayse M, Makia Mustafa S, Sinha Tirthankar, Conley Shannon M, Al-Ubaidi Muayyad R, Naash Muna I

Abstract excerpt

The large number of inherited retinal disease genes (IRD), including the photopigment rhodopsin and the photoreceptor outer segment (OS) structural component peripherin 2 (PRPH2), has prompted interest in identifying common cellular mechanisms involved in degeneration. Although metabolic dysregulation has been shown to play an important role in the progression of the disease etiology, identifying a common...

Read the complete abstract on PubMed

Topics

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

Share to Eye Proteins
Share to Homeostasis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mice, Knockout

Share to Peripherins

Share to Photoreceptor Cells, Vertebrate

Share to Retina

Share to Retinal Degeneration

Share to rho GTP-Binding Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 33138244
DOI: 10.3390/ijms21218083
PMCID: PMC7662319

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration.PMID 33138244Read ↗

PRPH2/RDS and ROM-1: Historical context, current views and future considerations.Semantic proximity Read ↗

RDH12 retinopathy: clinical features, biology, genetics and future directionsSemantic proximity Read ↗

Retinitis pigmentosa: defined from a molecular point of view.Semantic proximity Read ↗

Retinal Pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 -Related Phenotype.Semantic proximity Read ↗

Dominant <i>RDH12</i> -retinitis pigmentosa impairs photoreceptor development and cone function in retinal organoidsSemantic proximity Read ↗

New insights into the nutritional genomics of adult-onset riboflavin-responsive diseasesSemantic proximity Read ↗

Retinol Dehydrogenases Regulate Vitamin A Metabolism for Visual Function.Semantic proximity Read ↗

Rhodopsin as a Molecular Target to Mitigate Retinitis Pigmentosa.Semantic proximity Read ↗

Retinitis pigmentosa and related disorders: phenotypes of rhodopsin and peripherin/RDS mutations.Semantic proximity Read ↗

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene.Semantic proximity Read ↗

Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2.Semantic proximity Read ↗

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.Semantic proximity Read ↗

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