Evidence map›Paper›PMID 25414670›Full record

ReviewFrontiers in physiology2014

Optogenetic sensors and effectors: CHROMus-the Cornell Heart Lung Blood Institute Resource for Optogenetic Mouse Signaling.

Bo Shui, Jane C Lee, Shaun Reining, Frank K Lee, Michael I Kotlikoff

Abstract readReview
In one paragraph

Review in Frontiers in physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. IPbioRxiv : the preprint server for biology · 2026
    Article
  2. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  3. Article
  4. Article
  5. Light Control in Microbial Systems.International journal of molecular sciences · 2024
    Review
  6. Molecular and cellular basis of praziquantel action in the cardiovascular system.American journal of physiology. Cell physiology · 2023
    Article
  7. Article
  8. Fluorescent protein transgenic mice for the study of CaFree radical biology & medicine · 2022
    Review
  9. Brighten the Future: Photobiomodulation and Optogenetics.Focus (American Psychiatric Publishing) · 2022
    Review
  10. Article
  11. Cardiac optogenetics: a decade of enlightenment.Nature reviews. Cardiology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Contractile pericytes determine the direction of blood flow at capillary junctions.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review
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

5 authors.

Bo ShuiDepartment of Biomedical Sciences, College of Veteirnary Medicine, Cornell University Ithaca, NY, USA.
Jane C LeeDepartment of Biomedical Sciences, College of Veteirnary Medicine, Cornell University Ithaca, NY, USA.
Shaun ReiningDepartment of Biomedical Sciences, College of Veteirnary Medicine, Cornell University Ithaca, NY, USA.
Frank K LeeDepartment of Biomedical Sciences, College of Veteirnary Medicine, Cornell University Ithaca, NY, USA.
Michael I KotlikoffDepartment of Biomedical Sciences, College of Veteirnary Medicine, Cornell University Ithaca, NY, USA.

Funding

Genetic Resource for Optical SignalingR24HL120847 · NHLBI · CORNELL UNIVERSITY · PI KOTLIKOFF, MICHAEL I. · 2014 to 2018
$3.1M
NHLBI NIH HHS R24 HL120847
6 · The paper itself

Abstract

Significant progress has been made in the last decade in the development of optogenetic effectors and sensors that can be deployed to understand complex biological signaling in mammals at a molecular level, without disrupting the distributed, lineage specific signaling circuits that comprise nuanced physiological responses. A major barrier to the widespread exploitation of these imaging tools, however, is the lack of readily available genetic reagents that can be easily combined to probe complex biological processes. Ideally, one could envision purpose-produced mouse lines expressing optically compatible sensors and effectors, sensor pairs in distinct lineages, or sensor pairs in discrete subcellular compartments, such that they could be crossed to enable in vivo imaging studies of unprecedented scientific power. Such lines could also be combined with mice to determine the alteration in signaling accompanying targeted gene deletion or addition. In order to address this lack, the National Heart Lung and Blood Institute has recently funded an optogenetic resource designed to create optically compatible, combinatorial mouse lines that will advance NHLBI research. Here we review recent advances in optogenetic sensor and effectors and describe the rationale and goals for the establishment of the Cornell/National Heart Lung Blood Resource for Optogenetic Mouse Signaling (CHROMus).

Indexed as

Ca2+ sensorsfluorescent imaginggenetically encoded Ca2+ indicatorsgreen fluorescent proteinsrhodopsintransgenic mice

Identifiers

PMID25414670
PMCPMC4222331

What OpenQuestion holds

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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.