Evidence map›Paper›PMID 28912154›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia.

Jinsoo Seo, Oleg Kritskiy, L Ashley Watson, Scarlett J Barker, Dilip Dey, Waseem K Raja, Yuan-Ta Lin, Tak Ko, Sukhee Cho, Jay Penney and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 4 pooled it
11.4field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 4 syntheses or guidelines pooled it, 161 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Using Brain Organoids to Explore Human Neurobiology.Cellular and molecular neurobiology · 2026
    Review
  7. International journal of molecular sciences · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Advances in the treatment of Alzheimer's disease.Frontiers in pharmacology · 2026
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. CRISPR-engineered deletion ofbioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Article
  20. Article

47 more citing papers are in PubMed but not listed here.

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

17 authors at 3 institutions in 1 country.

Jinsoo SeoPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Oleg KritskiyPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
L Ashley WatsonPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Scarlett J BarkerPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Dilip DeyPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Waseem K RajaPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Yuan-Ta LinPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Tak KoPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Sukhee ChoPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
Jay PenneyPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.
M Catarina SilvaCenter for Genomic Medicine, Chemical Neurobiology Laboratory, Departments of Neurology and Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.ORCID 0000-0001-5421-6673
Steven D SheridanCenter for Genomic Medicine, Chemical Neurobiology Laboratory, Departments of Neurology and Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.ORCID 0000-0003-1045-1158
Diane LucenteMolecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.
James F GusellaMolecular Neurogenetics Unit, Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.
Bradford C DickersonMassachusetts General Hospital Frontotemporal Disorders Unit, Gerontology Research Unit, and Alzheimer's Disease Research Center, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129, and.ORCID 0000-0002-5958-3445
Stephen J HaggartyCenter for Genomic Medicine, Chemical Neurobiology Laboratory, Departments of Neurology and Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114.ORCID 0000-0002-7872-168X
Li-Huei TsaiPicower Institute for Learning and Memory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, lhtsai@mit.edu.ORCID 0000-0003-1262-0592
Massachusetts Institute of Technology · USHarvard University · USBroad Institute · US

Funding

RAPID GENE DISCOVERYP01GM061354 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI MORTON, CYNTHIA CASSON · 2001 to 2019
$24.3M
The Cdk5/35 KinaseR37NS051874 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI TSAI, LI-HUEI · 2016 to 2022
$3.2M
Autosomal Dominant FTLD Tauopathy Patient-Specific Stem Cell ModelsR21NS085487 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI DICKERSON, BRADFORD C, HAGGARTY, STEPHEN J · 2014 to 2015
$479k
NIGMS NIH HHS P01 GM061354NINDS NIH HHS R21 NS085487NINDS NIH HHS R37 NS051874
6 · The paper itself

Abstract

Increased p25, a proteolytic fragment of the regulatory subunit p35, is known to induce aberrant activity of cyclin-dependent kinase 5 (Cdk5), which is associated with neurodegenerative disorders, including Alzheimer's disease. Previously, we showed that replacing endogenous p35 with the noncleavable mutant p35 (Δp35) attenuated amyloidosis and improved cognitive function in a familial Alzheimer's disease mouse model. Here, to address the role of p25/Cdk5 in tauopathy, we generated double-transgenic mice by crossing mice overexpressing mutant human tau (P301S) with Δ

Indexed as

Pluripotent Stem CellsAnimalsCA3 Region, HippocampalCyclin-Dependent Kinase 5Frontotemporal DementiaHumansLong-Term PotentiationMiceMice, TransgenicMossy Fibers, HippocampalPhosphorylationPhosphotransferasesStem Cell TransplantationSynapsesSynaptophysinTauopathiesCdk5 protein, mouseCdk5r1 protein, mouseCyclin-Dependent Kinase 5PhosphotransferasesSynaptophysinAlzheimer's diseasecerebral organoidscyclin-dependent kinase 5iPSCsisogenictauopathy

Identifiers

PMID28912154
PMCPMC5637118
OpenAlexW2754798875

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.