Evidence map›Paper›PMID 35955854›Full record

ArticleInternational journal of molecular sciences2022

Luteolin Treatment Ameliorates Brain Development and Behavioral Performance in a Mouse Model of CDKL5 Deficiency Disorder.

Marianna Tassinari, Nicola Mottolese, Giuseppe Galvani, Domenico Ferrara, Laura Gennaccaro, Manuela Loi, Giorgio Medici, Giulia Candini, Roberto Rimondini, Elisabetta Ciani and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Safety and efficacy of Igk-TATk-CDKL5 gene therapy in mosaic CDKL5 deficiency.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Rett and Rett-related disorders: Common mechanisms for shared symptoms?Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. TRRAP-mediated acetylation on Sp1 regulates adult neurogenesis.Computational and structural biotechnology journal · 2023
    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

11 authors at 1 institution in 1 country.

Marianna TassinariDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-2078-9638
Nicola MottoleseDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0002-3066-0945
Giuseppe GalvaniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Domenico FerraraDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Laura GennaccaroDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0002-0438-2152
Manuela LoiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Giorgio MediciDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Giulia CandiniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Roberto RimondiniDepartment of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-4099-513X
Elisabetta CianiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.
Stefania TrazziDepartment of Biomedical and Neuromotor Sciences, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-2623-2769
University of Bologna · IT

Funding

CARISBO foundation 2020.0400
6 · The paper itself

Abstract

CDKL5 deficiency disorder (CDD), a rare and severe neurodevelopmental disease caused by mutations in the X-linked

Indexed as

LuteolinProtein Serine-Threonine KinasesAnimalsBrainDisease Models, AnimalEpileptic SyndromesFemaleMiceMice, KnockoutSpasms, InfantileCDKL5 protein, mouseLuteolinProtein Serine-Threonine KinasesCDKL5 deficiency disorderdendritic spinesluteolinmicroglianeurogenesisneuronal plasticity

Identifiers

PMID35955854
PMCPMC9369425
OpenAlexW4290498593

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.