Evidence map›Paper›PMID 39337400›Full record

ArticleInternational journal of molecular sciences2024

Quintessential Synergy: Concurrent Transient Administration of Integrated Stress Response Inhibitors and BACE1 and/or BACE2 Activators as the Optimal Therapeutic Strategy for Alzheimer's Disease.

Vladimir Volloch, Sophia Rits-Volloch

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

2 authors.

Vladimir VollochDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, MA 02115, USA.
Sophia Rits-VollochDivision of Molecular Medicine, Children's Hospital, Boston, MA 02115, USA.

Funding

NIH HHS NIH R21 GM056179; NIH RO1 AR036819.
6 · The paper itself

Abstract

The present study analyzes two potential therapeutic approaches for Alzheimer's disease (AD). One is the suppression of the neuronal integrated stress response (ISR). Another is the targeted degradation of intraneuronal amyloid-beta (

Indexed as

Alzheimer DiseaseAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesAmyloid beta-PeptidesAnimalsHumansStress, PhysiologicalAmyloid beta-PeptidesAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBACE1 protein, humanBACE2 protein, humanamyloid cascade hypothesis 2.0 (ACH2.0)AβPP-independent generation of iAβconventional and unconventional Alzheimer’s diseasedepletion of iAβ via the activation of BACE1 and/or BACE2initiation of translation from the AUG codon encoding Met671 of the intact or 5′-truncated human AβPP mRNAintraneuronal Aβ (iAβ)neuronal integrated stress response (ISR)RNA-dependent asymmetric amplification of human AβPP mRNAsuppression of the neuronal ISRtherapeutic strategies for conventional and unconventional Alzheimer’s disease

Identifiers

PMID39337400
PMCPMC11432332

What OpenQuestion holds

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Registered trials

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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.