Evidence map›Paper›PMID 39912399›Full record

ReviewJournal of biosciences2025

Glutamate metabolism disruption in Johanson-Blizzard syndrome: Insights from

Yi Li, Shangbang Gao

Abstract readReview
PubMed
In one paragraph

Review in Journal of biosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

2 authors.

Yi LiKey Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.
Shangbang Gao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Johanson-Blizzard syndrome (JBS) is a complex autosomal recessive disorder that manifests through a spectrum of symptoms, with deficiencies in the ubiquitin-protein ligase E3 component N-recognin 1 (UBR-1) at its genetic core. Despite its clinical significance, the molecular intricacies of UBR-1's role in JBS remain largely elusive, presenting a formidable challenge in devising targeted treatments. The nematode

Indexed as

Caenorhabditis elegans ProteinsCataractEctodermal DysplasiaEpilepsyExocrine Pancreatic InsufficiencyGlutamic AcidIchthyosisIntellectual DisabilityRetinal DegenerationScalp DermatosesUbiquitin-Protein LigasesAnimalsAnus, ImperforateCaenorhabditis elegansDisease Models, AnimalGrowth DisordersCaenorhabditis elegans ProteinsGlutamic AcidUbiquitin-Protein Ligases

Identifiers

PMID39912399

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.