Evidence map›Paper›PMID 38563493›Full record

ReviewBiochemical Society transactions2024

The molecular mechanisms driving Plasmodium cell division.

David S Guttery, Mohammad Zeeshan, Anthony A Holder, Rita Tewari

Open access · hybridAbstract readReview
In one paragraph

Review in Biochemical Society transactions, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Life science alliance · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. mBio · 2025
    Article
  7. DivergentLife science alliance · 2025
    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.

David S GutterySchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, U.K.ORCID 0000-0003-0418-580X
Mohammad ZeeshanSchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, U.K.
Anthony A HolderMalaria Parasitology Laboratory, The Francis Crick Institute, London, U.K.
Rita TewariSchool of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, U.K.ORCID 0000-0003-3943-1847
Queen's Medical Centre · GBThe Francis Crick Institute · GBUniversity of Leicester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria, a vector borne disease, is a major global health and socioeconomic problem caused by the apicomplexan protozoan parasite Plasmodium. The parasite alternates between mosquito vector and vertebrate host, with meiosis in the mosquito and proliferative mitotic cell division in both hosts. In the canonical eukaryotic model, cell division is either by open or closed mitosis and karyokinesis is followed by cytokinesis; whereas in Plasmodium closed mitosis is not directly accompanied by concomitant cell division. Key molecular players and regulatory mechanisms of this process have been identified, but the pivotal role of certain protein complexes and the post-translational modifications that modulate their actions are still to be deciphered. Here, we discuss recent evidence for the function of known proteins in Plasmodium cell division and processes that are potential novel targets for therapeutic intervention. We also identify key questions to open new and exciting research to understand divergent Plasmodium cell division.

Indexed as

Cell DivisionMalariaPlasmodiumProtozoan ProteinsAnimalsCytokinesisHost-Parasite InteractionsHumansMeiosisMitosisProtein Processing, Post-TranslationalProtozoan Proteinscell divisionclosed mitosiscrystalloidsDNA replicationPlasmodiumreversible protein phosphorylation

Identifiers

PMID38563493
PMCPMC11088906
OpenAlexW4393425853

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.