Evidence map›Paper›PMID 32221932›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2020

Light Microscopy in Trypanosomes: Use of Fluorescent Proteins and Tags.

Samuel Dean, Jack Sunter

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
11.1field-weighted citation impact, top 2% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Mesolens imaging in microbiology.Essays in biochemistry · 2026
    Review
  2. Identification of a conserved gene family with an essential role inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Cytological profiling of trypanocidal principles fromPhytomedicine plus : international journal of phytotherapy and phytopharmacology · 2025
    Article
  7. Article
  8. Article
  9. Subcellular protein localisation ofWellcome open research · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. 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

2 authors at 2 institutions in 1 country.

Samuel DeanWarwick Medical School, University of Warwick, Coventry, UK. Samuel.Dean@warwick.ac.uk.
Jack SunterDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, UK. jsunter@brookes.ac.uk.
Oxford Brookes University · GBUniversity of Warwick · GB

Funding

Wellcome Trust 104627/Z/14/ZWellcome Trust 108445/Z/15/Z
6 · The paper itself

Abstract

Fluorescence microscopy enables the localization of proteins to specific structures within a cell which have either been fused to a fluorescence protein or detected by immunofluorescence. Here, we describe the various procedures that can be used to prepare both the procyclic form and bloodstream form of the human pathogen Trypanosoma brucei for fluorescence microscopy. The choice of procedure to be used is determined by various parameters, including protein characteristics and the scientific question being investigated.

Indexed as

Cell NucleolusCell NucleusDNA, KinetoplastIntravital MicroscopyLife Cycle StagesLuminescent ProteinsMicroscopy, FluorescenceParasitologyTrypanosoma brucei bruceiDNA, KinetoplastLuminescent ProteinsCytoskeletonsFluorescent proteinsLight microscopyLive cellTrypanosomes

Identifiers

PMID32221932
OpenAlexW3013687877

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.