Evidence map›Paper›PMID 34299143›Full record

ReviewInternational journal of molecular sciences2021

Emerging Opportunities in Human Pluripotent Stem-Cells Based Assays to Explore the Diversity of Botulinum Neurotoxins as Future Therapeutics.

Juliette Duchesne de Lamotte, Anselme Perrier, Cécile Martinat, Camille Nicoleau

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

4 authors at 3 institutions in 1 country.

Juliette Duchesne de LamotteIPSEN Innovation, 91940 Les Ulis, France.ORCID 0000-0002-0546-3886
Anselme PerrierI-STEM, INSERM UMR861, Université Evry-Paris Saclay, 91100 Corbeil-Essonne, France.
Cécile MartinatI-STEM, INSERM UMR861, Université Evry-Paris Saclay, 91100 Corbeil-Essonne, France.ORCID 0000-0002-5234-1064
Camille NicoleauIPSEN Innovation, 91940 Les Ulis, France.
Inserm · FRCentre National de la Recherche Scientifique · FRIpsen (France) · FR

Funding

Association Nationale de la Recherche et de la Technologie 2017/0859
6 · The paper itself

Abstract

Botulinum neurotoxins (BoNTs) are produced by Clostridium botulinum and are responsible for botulism, a fatal disorder of the nervous system mostly induced by food poisoning. Despite being one of the most potent families of poisonous substances, BoNTs are used for both aesthetic and therapeutic indications from cosmetic reduction of wrinkles to treatment of movement disorders. The increasing understanding of the biology of BoNTs and the availability of distinct toxin serotypes and subtypes offer the prospect of expanding the range of indications for these toxins. Engineering of BoNTs is considered to provide a new avenue for improving safety and clinical benefit from these neurotoxins. Robust, high-throughput, and cost-effective assays for BoNTs activity, yet highly relevant to the human physiology, have become indispensable for a successful translation of engineered BoNTs to the clinic. This review presents an emerging family of cell-based assays that take advantage of newly developed human pluripotent stem cells and neuronal function analyses technologies.

Indexed as

AnimalsBiological AssayBotulinum ToxinsHumansNeuronsNeurotoxinsPluripotent Stem CellsBotulinum ToxinsNeurotoxinsBoNT-based therapeuticsbotulinum neurotoxinscell-based assayshigh-throughputhuman pluripotent stem cells

Identifiers

PMID34299143
PMCPMC8308099
OpenAlexW3179645528

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.