Evidence map›Paper›PMID 15208716›Full record

ArticlePLoS biology2004

Functional fluorescent Ca2+ indicator proteins in transgenic mice under TET control.

Mazahir T Hasan, Rainer W Friedrich, Thomas Euler, Matthew E Larkum, Günter Giese, Matthias Both, Jens Duebel, Jack Waters, Hermann Bujard, Oliver Griesbeck and 4 more

Abstract readComparative Study
In one paragraph

Article in PLoS biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing 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

90 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Calcium imaging: a technique to monitor calcium dynamics in biological systems.Physiology and molecular biology of plants : an international journal of functional plant biology · 2023
    Review
  5. Imaging of Endoplasmic Reticulum CaFrontiers in endocrinology · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Inducible and combinatorial gene manipulation in mouse brain.Frontiers in cellular neuroscience · 2015
    Article
  16. Article
  17. Article
  18. Optical neural interfaces.Annual review of biomedical engineering · 2014
    Review
  19. Review
  20. Review

30 more citing papers are in PubMed but not listed here.

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

14 authors.

Mazahir T HasanMax Planck Institute for Medical Research, Heidelberg, Germany. mhasan@mpimf-heidelberg.mpg.de
Rainer W Friedrich
Thomas Euler
Matthew E Larkum
Günter Giese
Matthias Both
Jens Duebel
Jack Waters
Hermann Bujard
Oliver Griesbeck
Roger Y Tsien
Takeharu Nagai
Atsushi Miyawaki
Winfried Denk

Funding

DYNAMICS OF SIGNAL TRANSDUCTION IN NEURONSR01NS027177 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ADAMS, STEPHEN ROY, ELLISMAN, MARK H · 1989 to 2017
$5.8M
DYNAMICS OF SIGNAL TRANSDUCTION IN NEURONSR37NS027177 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TSIEN, ROGER Y · 2007 to 2013
$4.8M
NINDS NIH HHS NS27177NINDS NIH HHS R01 NS027177NINDS NIH HHS R37 NS027177
6 · The paper itself

Abstract

Genetically encoded fluorescent calcium indicator proteins (FCIPs) are promising tools to study calcium dynamics in many activity-dependent molecular and cellular processes. Great hopes-for the measurement of population activity, in particular-have therefore been placed on calcium indicators derived from the green fluorescent protein and their expression in (selected) neuronal populations. Calcium transients can rise within milliseconds, making them suitable as reporters of fast neuronal activity. We here report the production of stable transgenic mouse lines with two different functional calcium indicators, inverse pericam and camgaroo-2, under the control of the tetracycline-inducible promoter. Using a variety of in vitro and in vivo assays, we find that stimuli known to increase intracellular calcium concentration (somatically triggered action potentials (APs) and synaptic and sensory stimulation) can cause substantial and rapid changes in FCIP fluorescence of inverse pericam and camgaroo-2.

Indexed as

AnimalsBrainBrain MappingCalciumCalcium ChannelsDoxycyclineFluorescence Recovery After PhotobleachingGene ExpressionHeLa CellsHumansLuminescent ProteinsMiceMice, TransgenicMicroscopy, FluorescenceOlfactory BulbPhotic StimulationCalciumCalcium ChannelsDoxycyclineLuminescent Proteins

Identifiers

PMID15208716
PMCPMC423138

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.