Evidence map›Paper›PMID 29046322›Full record

ArticleDisease models & mechanisms2017

Pumilio2-deficient mice show a predisposition for epilepsy.

Philipp Follwaczny, Rico Schieweck, Therese Riedemann, Antonia Demleitner, Tobias Straub, Anna H Klemm, Martin Bilban, Bernd Sutor, Bastian Popper, Michael A Kiebler

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Pumilio2 Promotes Growth of Mature Neurons.International journal of molecular sciences · 2021
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Local Translation in Nervous System Pathologies.Frontiers in integrative neuroscience · 2021
    Review
  20. 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

10 authors at 3 institutions in 3 countries.

Philipp FollwacznyBiomedical Center (BMC), Department for Cell Biology, Faculty of Medicine, LMU, Munich, 82152 Planegg-Martinsried, Germany.
Rico SchieweckBiomedical Center (BMC), Department for Cell Biology, Faculty of Medicine, LMU, Munich, 82152 Planegg-Martinsried, Germany.
Therese RiedemannBiomedical Center (BMC), Department of Physiological Genomics, Ludwig-Maximilians-University, Munich, 82152 Planegg-Martinsried, Germany.
Antonia DemleitnerBiomedical Center (BMC), Department for Cell Biology, Faculty of Medicine, LMU, Munich, 82152 Planegg-Martinsried, Germany.
Tobias StraubBiomedical Center (BMC), Core Facility Bioinformatics, Ludwig-Maximilians-University, Munich, 82152 Planegg-Martinsried, Germany.
Anna H KlemmBiomedical Center (BMC), Core Facility Bioimaging, Ludwig-Maximilians-University, Munich, 82152 Planegg-Martinsried, Germany.
Martin BilbanDepartment of Laboratory Medicine and Core Facility Genomics, Medical University of Vienna, 1090 Vienna, Austria.
Bernd SutorBiomedical Center (BMC), Department of Physiological Genomics, Ludwig-Maximilians-University, Munich, 82152 Planegg-Martinsried, Germany.
Bastian PopperBiomedical Center (BMC), Department for Cell Biology, Faculty of Medicine, LMU, Munich, 82152 Planegg-Martinsried, Germany bastian.popper@med.uni-muenchen.de mkiebler@lmu.de.ORCID 0000-0003-1517-695X
Michael A KieblerBiomedical Center (BMC), Department for Cell Biology, Faculty of Medicine, LMU, Munich, 82152 Planegg-Martinsried, Germany bastian.popper@med.uni-muenchen.de mkiebler@lmu.de.ORCID 0000-0002-8850-6297
Cell Medica (Switzerland) · CHLudwig-Maximilians-Universität München · DEMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is a neurological disease that is caused by abnormal hypersynchronous activities of neuronal ensembles leading to recurrent and spontaneous seizures in human patients. Enhanced neuronal excitability and a high level of synchrony between neurons seem to trigger these spontaneous seizures. The molecular mechanisms, however, regarding the development of neuronal hyperexcitability and maintenance of epilepsy are still poorly understood. Here, we show that pumilio RNA-binding family member 2 (Pumilio2; Pum2) plays a role in the regulation of excitability in hippocampal neurons of weaned and 5-month-old male mice. Almost complete deficiency of Pum2 in adult

Indexed as

Genetic Predisposition to DiseaseAction PotentialsAnimalsCA1 Region, HippocampalDendritesEpilepsyGene Expression RegulationGene Knockdown TechniquesMaleMice, Inbred C57BLPyramidal CellsReceptors, GABA-ARNA-Binding ProteinsRNA, MessengerSeizuresSodium ChannelsGabra2 protein, mousePum2 protein, mouseReceptors, GABA-ARNA-Binding ProteinsRNA, MessengerSodium ChannelsEpilepsyEpileptogenesisPUM2Pumilio2Risk factorRNA-binding protein

Identifiers

PMID29046322
PMCPMC5719250
OpenAlexW2766177296

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.