Evidence map›Paper›PMID 31570707›Full record

ArticleNature communications2019

Constitutive XBP-1s-mediated activation of the endoplasmic reticulum unfolded protein response protects against pathological tau.

Sarah M Waldherr, Timothy J Strovas, Taylor A Vadset, Nicole F Liachko, Brian C Kraemer

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
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  5. Glutamatergic neuron degeneration inmicroPublication biology · 2026
    Article
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  7. Review
  8. Article
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  17. Review
  18. Dual roles of UPRJournal of molecular medicine (Berlin, Germany) · 2023
    Review
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Sarah M WaldherrMolecular and Cellular Biology Interdisciplinary Program, University of Washington, Seattle, WA, 98195, USA.
Timothy J StrovasGeriatrics Research Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, 98108, USA.ORCID http://orcid.org/0000-0002-0176-0293
Taylor A VadsetDivision of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington, Seattle, WA, 98104, USA.
Nicole F LiachkoDivision of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington, Seattle, WA, 98104, USA.
Brian C KraemerMolecular and Cellular Biology Interdisciplinary Program, University of Washington, Seattle, WA, 98195, USA. kraemerb@u.washington.edu.ORCID http://orcid.org/0000-0002-2252-7634
University of Washington · USUniversity of Puget Sound · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
Transgenic Mouse Models of Tau PathologiesP01AG017586 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LEE, VIRGINIA M · 2000 to 2021
$37.3M
Neurobehavior, Neuropathology, and Risk Factors in Alzheimer's DiseaseT32AG052354 · NIA · UNIVERSITY OF WASHINGTON · PI Brian C. Kraemer, ELAINE R. PESKIND · 2016 to 2026
$6.7M
Protection from pathological tau by activation of the ER unfolded protein responseR01AG066211 · NIA · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI KRAEMER, BRIAN C. · 2020 to 2024
$2.7M
BLRD VA I01 BX002619BLRD VA I01 BX004044NIA NIH HHS P01 AG017586NIA NIH HHS R01 AG066211NIA NIH HHS T32 AG052354NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

To endure over the organismal lifespan, neurons utilize multiple strategies to achieve protein homeostasis (proteostasis). Some homeostatic mechanisms act in a subcellular compartment-specific manner, but others exhibit trans-compartmental mechanisms of proteostasis. To identify pathways protecting neurons from pathological tau protein, we employed a transgenic Caenorhabditis elegans model of human tauopathy exhibiting proteostatic disruption. We show normal functioning of the endoplasmic reticulum unfolded protein response (UPR

Indexed as

AnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinseIF-2 KinaseEndoplasmic ReticulumEndoplasmic Reticulum-Associated DegradationHomeostasisHumansModels, AnimalNeurodegenerative DiseasesNeuronsPhenotypeTauopathiestau ProteinsATF-6 protein, C elegansCaenorhabditis elegans ProteinsCarrier ProteinseIF-2 Kinasetau ProteinsTranscription FactorsX-Box Binding Protein 1XBP-1 protein, C elegansXBP1 protein, human

Identifiers

PMID31570707
PMCPMC6768869
OpenAlexW2975503857

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.