Evidence map›Paper›PMID 32757160›Full record

ArticleMolecular neurobiology2020

Decreased Myocyte Enhancer Factor 2 Levels in the Hippocampus of Huntington's Disease Mice Are Related to Cognitive Dysfunction.

Laura Vidal-Sancho, Sara Fernández-García, Irene Solés-Tarrés, Jordi Alberch, Xavier Xifró

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Mild cognitive impairment in Huntington's disease: challenges and outlooks.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

5 authors at 2 institutions in 1 country.

Laura Vidal-SanchoNew Therapeutic Targets Group, Department of Medical Science, Faculty of Medicine, University of Girona, 17003, Girona, Spain.
Sara Fernández-GarcíaDepartament de Biomedicina, Institut de Neurociències, Facultat de Medicina, Universitat de Barcelona, 08036, Barcelona, Spain.
Irene Solés-TarrésNew Therapeutic Targets Group, Department of Medical Science, Faculty of Medicine, University of Girona, 17003, Girona, Spain.
Jordi AlberchDepartament de Biomedicina, Institut de Neurociències, Facultat de Medicina, Universitat de Barcelona, 08036, Barcelona, Spain.
Xavier XifróNew Therapeutic Targets Group, Department of Medical Science, Faculty of Medicine, University of Girona, 17003, Girona, Spain. xavier.xifro@udg.edu.ORCID http://orcid.org/0000-0002-7417-9475
Universitat de Girona · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ES

Funding

Ministerio de Ciencia, Innovación y Universidades RD06/0010/0006Ministerio de Ciencia, Innovación y Universidades SAF2017-88076-RUniversitat de Girona MPCUdG2016/036
6 · The paper itself

Abstract

People suffering from Huntington's disease (HD) present cognitive deficits. Hippocampal dysfunction has been involved in the HD learning and memory impairment, but proteins leading this dysregulation are not fully characterized. Here, we studied the contribution of the family of transcription factors myocyte enhancer factor 2 (MEF2) to the HD cognitive deficits. To this aim, we first analyzed MEF2 protein levels and found that they are reduced in the hippocampus of exon-1 (R6/1) and full-length (Hdh

Indexed as

AnilidesAnimalsBiomarkersCaspase 3Cells, CulturedCognitive DysfunctionDisease Models, AnimalHippocampusHuntingtin ProteinHuntington DiseaseMaleMEF2 Transcription FactorsMemoryMice, TransgenicMutant ProteinsNeuritesAnilidesBiomarkersCaspase 3Huntingtin ProteinMEF2 Transcription FactorsMutant ProteinsN1-(2-aminophenyl)-N8-phenyloctanediamideRNA, MessengerCaspase-3Cognitive dysfunctionHippocampusHuntington’s diseaseMEF-2

Identifiers

PMID32757160
OpenAlexW3047566062

What OpenQuestion holds

Textmetadata
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.