Evidence map›Paper›PMID 35496917›Full record

ArticleFrontiers in cellular neuroscience2022

Cytoplasmic Polyadenylation Element-Binding Protein 1 Post-transcriptionally Regulates Fragile X Mental Retardation 1 Expression Through 3' Untranslated Region in Central Nervous System Neurons.

Souichi Oe, Shinichi Hayashi, Susumu Tanaka, Taro Koike, Yukie Hirahara, Ryohei Seki-Omura, Rio Kakizaki, Sumika Sakamoto, Yosuke Nakano, Yasuko Noda and 2 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in cellular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
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.

Souichi OeDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Shinichi HayashiDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Susumu TanakaDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Taro KoikeDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Yukie HiraharaDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Ryohei Seki-OmuraDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Rio KakizakiDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Sumika SakamotoDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Yosuke NakanoDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Yasuko NodaDepartment of Anatomy, Bio-Imaging and Neuro-Cell Science, Jichi Medical University, Shimotsuke, Japan.
Hisao YamadaBiwako Professional University of Rehabilitation, Higashiomi, Japan.
Masaaki KitadaDepartment of Anatomy, Kansai Medical University, Hirakata, Japan.
Kansai Medical University · JPJichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X syndrome (FXS) is an inherited intellectual disability caused by a deficiency in Fragile X mental retardation 1 (

Indexed as

cytoplasmic polyadenylation-binding protein 1fragile X mental retardation 1heat shock protein family A member 9mitochondriapost-transcriptional regulation

Identifiers

PMID35496917
PMCPMC9051318
OpenAlexW4223912142

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.