Evidence map›Paper›PMID 39438652›Full record

ArticleCommunications biology2024

Loss of CLN3 in microglia leads to impaired lipid metabolism and myelin turnover.

Seda Yasa, Elisabeth S Butz, Alessio Colombo, Uma Chandrachud, Luca Montore, Sarah Tschirner, Matthias Prestel, Steven D Sheridan, Stephan A Müller, Janos Groh and 3 more

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Yeast as a Model for Human Disease.International journal of molecular sciences · 2026
    Review
  8. Article
  9. Review
  10. Gene therapy ameliorates neuromuscular pathology in CLN3 disease.Acta neuropathologica communications · 2025
    Article
  11. 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

13 authors.

Seda YasaCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Elisabeth S ButzCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Alessio ColomboGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
Uma ChandrachudCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Luca MontoreCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA.
Sarah TschirnerGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
Matthias PrestelGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
Steven D SheridanCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA.ORCID 0000-0003-1045-1158
Stephan A MüllerGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.ORCID 0000-0003-3414-307X
Janos GrohInstitute of Neuronal Cell Biology, Technical University Munich, Munich, Germany.ORCID 0000-0002-7628-0163
Stefan F LichtenthalerGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.ORCID 0000-0003-2211-2575
Sabina TahirovicGerman Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.ORCID 0000-0003-4403-9559
Susan L CotmanCenter for Genomic Medicine, Massachusetts General Hospital Research Institute, Boston, MA, USA. scotman@mgh.harvard.edu.ORCID 0000-0003-3114-0543

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BROWN, DENNIS · 2000 to 2019
$31.4M
P&F programP30DK135043 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Deborah J Wexler · 2023 to 2026
$5.4M
NIDDK NIH HHS P30 DK043351NIDDK NIH HHS P30 DK057521NIDDK NIH HHS P30 DK135043
6 · The paper itself

Abstract

Loss-of-function mutations in CLN3 cause juvenile Batten disease, featuring neurodegeneration and early-stage neuroinflammation. How loss of CLN3 function leads to early neuroinflammation is not yet understood. Here, we have comprehensively studied microglia from Cln3

Indexed as

Lipid MetabolismMembrane GlycoproteinsMicrogliaMolecular ChaperonesMyelin SheathAnimalsAutophagyLysosomesMiceMice, Inbred C57BLMice, KnockoutNeuronal Ceroid-LipofuscinosesCLN3 protein, mouseMembrane GlycoproteinsMolecular Chaperones

Identifiers

PMID39438652
PMCPMC11496662

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.