Evidence map›Paper›PMID 28786980›Full record

ArticleTranslational psychiatry2017

Abolishing Tau cleavage by caspases at Aspartate

F Biundo, C d'Abramo, M D Tambini, H Zhang, D Del Prete, F Vitale, L Giliberto, O Arancio, L D'Adamio

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Targeting caspase-2 interactions with tau in Alzheimer's disease and related dementias.Translational research : the journal of laboratory and clinical medicine · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

F BiundoDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
C d'AbramoLitwin-Zucker Center for Research in Alzheimer's Disease, Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY, USA.
M D TambiniDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
H ZhangDepartment of Pathology and Cell Biology and Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.
D Del PreteDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
F VitaleLitwin-Zucker Center for Research in Alzheimer's Disease, Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY, USA.
L GilibertoLitwin-Zucker Center for Research in Alzheimer's Disease, Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY, USA.
O ArancioDepartment of Pathology and Cell Biology and Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.
L D'AdamioDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · USNorthwell Health · USColumbia University · US

Funding

BRI2 Familial British and Danish Dementias and Alzheimer's DiseaseR01AG033007 · NIA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI D'ADAMIO, LUCIANO · 2009 to 2019
$4.2M
Mechanisms of APP and APLP2 function at synapsesR01AG052286 · NIA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI D'ADAMIO, LUCIANO · 2016 to 2020
$3.5M
Characterization of a caspase-cleavage resistant tau knock-in mouseR21AG048971 · NIA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI D'ADAMIO, LUCIANO · 2015 to 2016
$459k
NIA NIH HHS R01 AG033007NIA NIH HHS R01 AG052286NIA NIH HHS R21 AG048971
6 · The paper itself

Abstract

TAU mutations are genetically linked to fronto-temporal dementia (FTD) and hyper-phosphorylated aggregates of Tau form neurofibrillary tangles (NFTs) that constitute a pathological hallmark of Alzheimer disease (AD) and FTD. These observations indicate that Tau has a pivotal role in the pathogenesis of neurodegenerative disorders. Tau is cleaved by caspases at Aspartate

Indexed as

AnimalsAspartic AcidBehavior, AnimalBrainCaspasesMemoryMemory DisordersMiceMice, TransgenicNeurofibrillary TanglesNeuronal PlasticityPhosphorylationtau ProteinsAspartic AcidCaspasestau Proteins

Identifiers

PMID28786980
PMCPMC5611732
OpenAlexW2742541652

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.