Evidence map›Paper›PMID 38003227›Full record

ReviewInternational journal of molecular sciences2023

Animal Models for the Study of Gaucher Disease.

Or Cabasso, Aparna Kuppuramalingam, Lindsey Lelieveld, Martijn Van der Lienden, Rolf Boot, Johannes M Aerts, Mia Horowitz

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

Review 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. 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

7 authors at 2 institutions in 2 countries.

Or CabassoShmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel.
Aparna KuppuramalingamShmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel.
Lindsey LelieveldLeiden Institute of Chemistry, Leiden University, 9502 Leiden, The Netherlands.
Martijn Van der LiendenLeiden Institute of Chemistry, Leiden University, 9502 Leiden, The Netherlands.ORCID 0000-0002-6458-1479
Rolf BootLeiden Institute of Chemistry, Leiden University, 9502 Leiden, The Netherlands.
Johannes M AertsLeiden Institute of Chemistry, Leiden University, 9502 Leiden, The Netherlands.ORCID 0000-0001-8168-2565
Mia HorowitzShmunis School of Biomedicine and Cancer Research, Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel.
Leiden University · NLTel Aviv University · IL

Funding

ICI I00029NWO-BBOL 737.016.002Pfizer Ltd. 56288973
6 · The paper itself

Abstract

In Gaucher disease (GD), a relatively common sphingolipidosis, the mutant lysosomal enzyme acid β-glucocerebrosidase (GCase), encoded by the

Indexed as

Gaucher DiseaseAnimalsModels, AnimalMutationPsychosineUnfolded Protein ResponsePsychosinesphingosyl beta-glucosideER stressGBA1glucocerebrosidase (GCase)glucosylceramide (GlcCer)inflammationknockin animalsknockout animalsmisfoldingunfolded protein response (UPR)

Identifiers

PMID38003227
PMCPMC10671165
OpenAlexW4388445740

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.