Evidence map›Paper›PMID 35022326›Full record

ReviewGenes & development2022

Coupling crossover and synaptonemal complex in meiosis.

Corinne Grey, Bernard de Massy

Abstract readReview
In one paragraph

Review in Genes & development, 2022. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Abnormalities of Oocyte Maturation: Mechanisms and Implications.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Variations of wheat (Frontiers in plant science · 2022
    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.

Corinne GreyInstitut de Génétique Humaine (IGH), Centre National de la Recherche Scientifique, Université Montpellier, Montpellier 34396, France.
Bernard de MassyInstitut de Génétique Humaine (IGH), Centre National de la Recherche Scientifique, Université Montpellier, Montpellier 34396, France.ORCID 0000-0002-0950-2758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During meiosis, a molecular program induces DNA double-strand breaks (DSBs) and their repair by homologous recombination. DSBs can be repaired with or without crossovers. ZMM proteins promote the repair toward crossover. The sites of DSB repair are also sites where the axes of homologous chromosomes are juxtaposed and stabilized, and where a structure called the synaptonemal complex initiates, providing further regulation of both DSB formation and repair. How crossover formation and synapsis initiation are linked has remained unknown. The study by Pyatnitskaya and colleagues (pp. 53-69) in this issue of

Indexed as

Crossing Over, GeneticSynaptonemal ComplexChromosome PairingDNA Breaks, Double-StrandedDNA RepairMeiosisaneuploidychromosome segregationcrossing overDSB repairhomologous recombinationhomologous synapsismeiosisprotein–protein interactions

Identifiers

PMID35022326
PMCPMC8763052

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.