Evidence map›Paper›PMID 16626699›Full record

ArticleExperimental eye research2006

Functional abnormalities in the retinal pigment epithelium of CFTR mutant mice.

Jiang Wu, Alan D Marmorstein, Neal S Peachey

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Ocular Changes in Cystic Fibrosis: A Review.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Bestrophins and retinopathies.Pflugers Archiv : European journal of physiology · 2010
    Review
  8. Article
  9. Article
  10. Functional roles of bestrophins in ocular epithelia.Progress in retinal and eye research · 2009
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Light and alcohol evoked electro-oculograms in cystic fibrosis.Documenta ophthalmologica. Advances in ophthalmology · 2006
    Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Jiang WuCole Eye Institute, Cole Eye Institute (I-31), Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Alan D Marmorstein
Neal S Peachey
Cleveland Clinic · USCleveland Eye Clinic · USUniversity of Arizona · US

Funding

BESTROPHIN AND RETINAL DISEASER01EY013160 · NEI · UNIVERSITY OF ARIZONA · PI MARMORSTEIN, ALAN D · 2000 to 2013
$5.0M
Vision Research Infrastructure Development GrantR24EY015638 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI HOLLYFIELD, JOE GILBERT · 2004 to 2008
$1.1M
The Mouse dc-ElectroretinogramR01EY014465 · NEI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI PEACHEY, NEAL S · 2003 to 2005
$683k
NEI NIH HHS R01 EY013160NEI NIH HHS R01 EY014465NEI NIH HHS R01EY13160NEI NIH HHS R01EY14465NEI NIH HHS R24 EY015638NEI NIH HHS R24EY15638
6 · The paper itself

Abstract

In response to light, the mouse retinal pigment epithelium (RPE) generates a series of slow changes in potential that are referred to as the c-wave, fast oscillation (FO) and light peak (LP) of the electroretinogram (ERG). While the FO is known to reflect a Cl(-) conductance generated at the basal membrane of the RPE, the specific channel (s) underlying this potential has not been identified. In the present study we examined two strains of mice with cftr mutations to define the contribution that cystic fibrosis transmembrane regulator (CFTR)-mediated Cl(-) conductance makes to the mouse ERG. Responses obtained from cftr(Delta508/Delta508) mice exhibited an overall reduction in all components generated by the RPE in response to light without alteration of the luminance response function. Responses obtained from cftr(-/-) mice were also reduced in amplitude. These results illustrate the usefulness of ERG analysis of mice deficient in ion channels that are expressed in the RPE, and indicate that CFTR contributes to the generation of RPE-driven ERG components, but that it is not the sole generator of any one of these components.

Indexed as

AnimalsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorElectric StimulationElectroretinographyMembrane PotentialsMiceMice, Inbred CFTRPigment Epithelium of EyeCystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID16626699
PMCPMC2871190
OpenAlexW2005883307

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.