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

Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies.

Advances in experimental medicine and biology - 1 Jan 2010

Fischer M Dominik, Tanimoto Naoyuki, Beck Susanne C, Huber Gesine, Schaeferhoff Karin, Michalakis Stylianos, Riess Olaf, Wissinger Bernd, Biel Martin, Bonin Michael, Seeliger Mathias W

Abstract excerpt

PURPOSE: We performed a comprehensive in vivo assessment of retinal morphology and function in cpfl1 (cone photoreceptor function loss 1) mice to better define the disease process in this model of cone dystrophies. METHODS: Mice were examined using electroretinography (ERG), confocal scanning laser ophthalmoscopy (cSLO), and spectral domain optical coherence tomography (SD-OCT). Cross-breeding cpfl1 mutants with...

Read the complete abstract on PubMed

Topics

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

Share to Electroretinography
Share to Eye Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Green Fluorescent Proteins

Share to Imaging, Three-Dimensional

Share to Mice, Mutant Strains

Share to Retina

Share to Retinitis Pigmentosa

Share to Structure-Activity Relationship

Source

Identifiers

PMID: 20238063
DOI: 10.1007/978-1-4419-1399-9_68

Genes

ERG

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

Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies.PMID 20238063Read ↗

Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy.Semantic proximity Read ↗

Retinal network dysfunction precedes structural degeneration in severe <i>GUCA1A</i> cone-rod dystrophySemantic proximity Read ↗

Validating Fluorescent Chrnb4.EGFP Mouse Models for the Study of Cone Photoreceptor DegenerationSemantic proximity Read ↗

Zebrafish and inherited photoreceptor disease: Models and insightsSemantic proximity Read ↗

Cone Opsins and Inherited Retinal Disease.Semantic proximity Read ↗

In vivo assessment of photoreceptor function in human diseases caused by photoreceptor-specific gene mutations.Semantic proximity Read ↗

Visual Cone Arrestin 4 Contributes to Visual Function and Cone Health.Semantic proximity Read ↗

Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutations.Semantic proximity Read ↗

Diminished Cone Sensitivity in cpfl3 Mice Is Caused by Defective Transducin Signaling.Semantic proximity Read ↗

Preservation of Cone Photoreceptors after a Rapid yet Transient Degeneration and Remodeling in Cone-Only<i>Nrl</i><sup>−/−</sup>Mouse RetinaSemantic proximity Read ↗

Impairment of Vision in a Mouse Model of Usher Syndrome Type III.Semantic proximity Read ↗

Deep phenotyping of the Cdhr1-/- mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degeneration.Semantic proximity Read ↗

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