Evidence map›Paper›PMID 33606241›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

In Vivo Imaging of Protein Interactions in the Germplasm with Bimolecular Fluorescent Complementation.

Roshan Priyarangana Perera, Roland Dosch

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.3field-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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

2 authors at 1 institution in 1 country.

Roshan Priyarangana PereraInstitute of Developmental Biochemistry, University Medical Center, Göttingen, Germany. vetrosh@gmail.com.
Roland DoschInstitute for Developmental Biochemistry, University of Göttingen Medical Center, Georg-August-Universität, Göttingen, Germany. roland.dosch@med.uni-goettingen.de.
University of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-protein interactions (PPIs) play a central role in all cellular processes. The discovery of green fluorescent protein (GFP) and split varieties, which are functionally reconstituted by complementation, led to the development of the bimolecular fluorescence complementation (BiFC) assay for the investigation of PPI in vivo. BiFC became a popular tool, as it is a convenient and quick technology to directly visualize PPI in a wide variety of living cells. In combination with the transparency of the early zebrafish embryo, it also permits detection of PPI in the context of an entire living organism, which performs all spatial and temporal regulations missing in in vitro systems like tissue culture. However, the application of BiFC in some research areas including the study of zebrafish is limited due to the lack of efficient and convenient BiFC expression vectors. Here, we describe the engineering of a novel set of Gateway

Indexed as

AnimalsBiological AssayEmbryo, NonmammalianFluorescenceGenetic VectorsGreen Fluorescent ProteinsLuminescent ProteinsMicroscopy, FluorescenceProtein Interaction MappingRNA HelicasesZebrafishZebrafish ProteinsGreen Fluorescent ProteinsLuminescent ProteinsRNA HelicasesZebrafish ProteinsBimolecular fluorescence complementation (BiFC) assayBucky ballGateway vectorsProtein–protein interactionVasaZebrafish

Identifiers

PMID33606241
OpenAlexW3133148176

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.