Evidence map›Paper›PMID 32761777›Full record

ArticleEMBO reports2020

Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin-deficient mice.

Xiaolai Zhou, Mieu Brooks, Peizhou Jiang, Shunsuke Koga, Aamir R Zuberi, Matthew C Baker, Tammee M Parsons, Monica Castanedes-Casey, Virginia Phillips, Ariston L Librero and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Analyses of plasma multi-omic data across ancestries identify novel pathways implicated in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Challenges of modelling TDP-43 pathology in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
  12. Article
  13. Review
  14. Cortex-SpecificThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The endolysosomal pathway and ALS/FTD.Trends in neurosciences · 2023
    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

16 authors at 2 institutions in 2 countries.

Xiaolai ZhouDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.ORCID 0000-0002-4531-4658
Mieu BrooksDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Peizhou JiangDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Shunsuke KogaDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Aamir R ZuberiThe Rare and Orphan Disease Center, JAX Center for Precision Genetics, Bar Harbor, ME, USA.
Matthew C BakerDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Tammee M ParsonsDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Monica Castanedes-CaseyDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Virginia PhillipsDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Ariston L LibreroDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Aishe KurtiDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
John D FryerDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Guojun BuDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Cathleen LutzThe Rare and Orphan Disease Center, JAX Center for Precision Genetics, Bar Harbor, ME, USA.
Dennis W DicksonDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.ORCID 0000-0001-7189-7917
Rosa RademakersDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.ORCID 0000-0002-4049-0863
Jacksonville College · USUniversity of Antwerp · BE

Funding

Research Education ComponentP30AG062677 · NIA · MAYO CLINIC ROCHESTER · PI NILUFER ERTEKIN-TANER · 2019 to 2026
$33.5M
The Jackson Laboratory Center for Precision Genetics: From New Models to Novel TherapeuticsU54OD020351 · OD · JACKSON LABORATORY · PI KORSTANJE, RONNY · 2015 to 2019
$10.2M
Genetic Discovery and Pathobiology of Frontotemporal Lobar Degeneration and Related TDP-43 ProteinopathiesR35NS097261 · NINDS · MAYO CLINIC JACKSONVILLE · PI RADEMAKERS, ROSA · 2017 to 2019
$2.9M
NIA NIH HHS P30 AG062677NIH HHS U54 OD020351NINDS NIH HHS R35 NS097261The Bluefield Project to Cure FTDthe Jackson Laboratory's Genetic Engineering Technologies Scientific Service
6 · The paper itself

Abstract

Progranulin (PGRN) and transmembrane protein 106B (TMEM106B) are important lysosomal proteins implicated in frontotemporal lobar degeneration (FTLD) and other neurodegenerative disorders. Loss-of-function mutations in progranulin (GRN) are a common cause of FTLD, while TMEM106B variants have been shown to act as disease modifiers in FTLD. Overexpression of TMEM106B leads to lysosomal dysfunction, while loss of Tmem106b ameliorates lysosomal and FTLD-related pathologies in young Grn

Indexed as

Frontotemporal DementiaFrontotemporal Lobar DegenerationAnimalsIntercellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, KnockoutMutationNerve Tissue ProteinsProgranulinsIntercellular Signaling Peptides and ProteinsMembrane ProteinsNerve Tissue ProteinsProgranulinsTmem106b protein, mousefrontotemporal lobar degenerationlysosomesprogranulinTdp-43Tmem106b

Identifiers

PMID32761777
PMCPMC7534638
OpenAlexW3047087218

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.