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

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.

Advances in experimental medicine and biology - 1 Jan 2006

Ding Xi-Qin, Naash Muna I

Abstract excerpt

No abstract is available from the source.

Topics

Animals
Animals, Genetically Modified
Disease Models, Animal
Humans
Intermediate Filament Proteins
Membrane Glycoproteins
Mice
Mice, Transgenic
Mutation
Nerve Tissue Proteins
Peripherins
Protein Structure, Tertiary
Retinal Degeneration
Retinal Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Xenopus

Xenopus Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 17249567
DOI: 10.1007/0-387-32442-9_21
PMCID: PMC2793174

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.PMID 17249567Read ↗

Animal models of human retinal dystrophies.Semantic proximity Read ↗

Modulating Expression of Peripherin/<i>rds</i>in Transgenic Mice: Critical Levels and the Effect of OverexpressionSemantic proximity Read ↗

Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors.Semantic proximity Read ↗

The role of the peripherin/RDS gene in retinal dystrophies.Semantic proximity Read ↗

A novel peripherin/RDS mutation resulting in a retinal dystrophy with phenotypic variation.Semantic proximity Read ↗

The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic miceSemantic proximity Read ↗

A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophySemantic proximity Read ↗

The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies.Semantic proximity Read ↗

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

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

The use of canine models of inherited retinal degeneration to test novel therapeutic approaches.Semantic proximity Read ↗

Genetic animal models for retinal degeneration.Semantic proximity Read ↗

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