Evidence map›Paper›PMID 30338144›Full record

ArticleBiomedical optics express2018

Optical alignment device for two-photon microscopy.

Gregorio L Galiñanes, Paul J Marchand, Raphaël Turcotte, Sebastien Pellat, Na Ji, Daniel Huber

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Biomedical optics express, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Scanless two-photon voltage imaging.Nature communications · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. 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

6 authors at 2 institutions in 3 countries.

Gregorio L Galiñanes *Department of Basic Neurosciences, University of Geneva, Rue Michel Servet 1, 1206 Geneva, Switzerland.
Paul J Marchand *Department of Basic Neurosciences, University of Geneva, Rue Michel Servet 1, 1206 Geneva, Switzerland.
Raphaël TurcotteJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Sebastien PellatDepartment of Basic Neurosciences, University of Geneva, Rue Michel Servet 1, 1206 Geneva, Switzerland.
Na JiJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Daniel HuberDepartment of Basic Neurosciences, University of Geneva, Rue Michel Servet 1, 1206 Geneva, Switzerland.
University of Geneva · CHHoward Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two-photon excitation fluorescence microscopy has revolutionized our understanding of brain structure and function through the high resolution and large penetration depth it offers. Investigating neural structures

Indexed as

(170.0180) Microscopy(180.2520) Fluorescence microscopy(220.1000) Aberration compensation(220.1140) Alignment

Identifiers

PMID30338144
PMCPMC6191613
OpenAlexW2949995541

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.