Evidence map›Paper›PMID 38003438›Full record

ArticleInternational journal of molecular sciences2023

Adenosinergic System and BDNF Signaling Changes as a Cross-Sectional Feature of RTT: Characterization of

Catarina Miranda-Lourenço, Jéssica Rosa, Nádia Rei, Rita F Belo, Ana Luísa Lopes, Diogo Silva, Cátia Vieira, Teresa Magalhães-Cardoso, Ricardo Viais, Paulo Correia-de-Sá and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

12 authors at 2 institutions in 1 country.

Catarina Miranda-LourençoInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.ORCID 0000-0002-9633-7999
Jéssica RosaInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Nádia ReiInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.ORCID 0000-0003-0131-0126
Rita F BeloInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.ORCID 0000-0002-4553-3455
Ana Luísa LopesLaboratório de Farmacologia e Neurobiologia/MedInUP, Instituto de Ciências Biomédicas Abel Salazar-Universidade do Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Diogo SilvaLaboratório de Farmacologia e Neurobiologia/MedInUP, Instituto de Ciências Biomédicas Abel Salazar-Universidade do Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Cátia VieiraLaboratório de Farmacologia e Neurobiologia/MedInUP, Instituto de Ciências Biomédicas Abel Salazar-Universidade do Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Teresa Magalhães-CardosoLaboratório de Farmacologia e Neurobiologia/MedInUP, Instituto de Ciências Biomédicas Abel Salazar-Universidade do Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Ricardo ViaisInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Paulo Correia-de-SáLaboratório de Farmacologia e Neurobiologia/MedInUP, Instituto de Ciências Biomédicas Abel Salazar-Universidade do Porto (ICBAS-UP), 4050-313 Porto, Portugal.ORCID 0000-0002-6114-9189
Ana M SebastiãoInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Maria J DiógenesInstituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.
University of Lisbon · PTUniversidade do Porto · PT

Funding

Association Française du Syndrome de Rett N.AFaculdade de Medicina da Universidade de Lisboa/CHLN Gapic (project no. 20190017Fundação para a Ciência e Tecnologia 01-0145-FEDER-031929Fundação para a Ciência e Tecnologia FCT SFRH/BD/118238/2016Fundação para a Ciência e Tecnologia UID/BIM/4308/2019Fundação para a Ciência e Tecnologia UID/BIM/50005/2019Fundação para a Ciência e Tecnologia UIDP/04308/2020Twinnig action - Synanet N.AUniversity of Lisbon BD2015
6 · The paper itself

Abstract

Rett Syndrome is an X-linked neurodevelopmental disorder (RTT; OMIM#312750) associated to

Indexed as

Brain-Derived Neurotrophic FactorRett SyndromeAdenosineAnimalsCross-Sectional StudiesDisease Models, AnimalFemaleHumansMethyl-CpG-Binding Protein 2MiceMice, KnockoutAdenosineBrain-Derived Neurotrophic FactorMecp2 protein, mouseMethyl-CpG-Binding Protein 2adenosineBDNFMecp2 heterozygous femalesRett syndrome

Identifiers

PMID38003438
PMCPMC10671708
OpenAlexW4388636863

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.