Evidence map›Paper›PMID 20090204›Full record

ReviewJournal of genetics2009

Channelrhodopsins provide a breakthrough insight into strategies for curing blindness.

Hiroshi Tomita, Eriko Sugano, Hitomi Isago, Makoto Tamai

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Control of Brain State Transitions with a Photoswitchable Muscarinic Agonist.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Restoration of the majority of the visual spectrum by using modified Volvox channelrhodopsin-1.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  8. Article
  9. Review
  10. Review
  11. Diversity of Chlamydomonas channelrhodopsins.Photochemistry and photobiology
    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

4 authors.

Hiroshi TomitaTohoku University Institute for International Advanced Interdisciplinary Research, Seiryo Aoba Sendai Miyagi, Japan. hiroshi-tomita@iiare.tohoku.ac.jp
Eriko Sugano
Hitomi Isago
Makoto Tamai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photoreceptor cells are the only retinal neurons that can absorb photons. Their degeneration due to some diseases or injuries leads to blindness. Retinal prostheses electrically stimulating surviving retinal cells and evoking a pseudo light sensation have been investigated over the past decade for restoring vision. Currently, a gene therapy approach is under development. Channelrhodopsin-2 derived from the green alga Chlamydomonas reinhardtii, is a microbial-type rhodopsin. Its specific characteristic is that it functions as a light-driven cation-selective channel. It has been reported that the channelrhodopsin-2 transforms inner light-insensitive retinal neurons to light-sensitive neurons. Herein, we introduce new strategies for restoring vision by using channelrhodopsins and discuss the properties of adeno-associated virus vectors widely used in gene therapy.

Indexed as

Algal ProteinsAnimalsBlindnessChlamydomonas reinhardtiiGenetic TherapyHumansIon PumpsLight Signal TransductionModels, BiologicalRhodopsinSignal TransductionAlgal ProteinsIon PumpsRhodopsin

Identifiers

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.