Evidence map›Paper›PMID 40672178›Full record

ArticlebioRxiv : the preprint server for biology2025

Autophagy activators normalize aberrant Tau proteostasis and rescue synapses in human familial Alzheimer's disease iPSC-derived cortical organoids.

Sergio R Labra, Jadon Compher, Akhil Prabhavalkar, Mireya Almaraz, Claudia Cedeño Kwong, Christine Baal, Maria Talantova, Nima Dolatabadi, Julian Piña-Sanz, Yubo Wang and 14 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Sergio R LabraNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-4072-1131
Jadon CompherNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0009-0003-6080-1280
Akhil PrabhavalkarNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Mireya AlmarazNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Claudia Cedeño KwongNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0009-0003-7349-6596
Christine BaalNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0009-0004-8379-1318
Maria TalantovaNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-6460-1302
Nima DolatabadiNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Julian Piña-SanzNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-3049-9338
Yubo WangNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Leonard YoonNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-8663-5757
Swagata GhatakNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0001-5462-401X
Zi GaoNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Yuting ZhangNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Dorit TrudlerNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-5835-3322
Lynee MasseyNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.
Wei LinTranslational Genomics Research Institute, Phoenix, AZ, USA.ORCID 0000-0002-7506-3466
Anthony BalistreriNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-7409-7031
Michael BulaNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-2164-0619
Nicholas J SchorkTranslational Genomics Research Institute, Phoenix, AZ, USA.
Tony S MondalaGenomics Core, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-2809-3187
Steven R HeadGenomics Core, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-5490-2750
Jeffery W KellyNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0001-8943-3395
Stuart A LiptonNeurodegeneration New Medicines Center, The Scripps Research Institute, La Jolla, CA, USA.ORCID 0000-0002-3490-1259

Funding

Leadership in AD/ADRD Drug DiscoveryR35AG071734 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI LIPTON, STUART A · 2021 to 2025
$5.4M
S-Nitrosylation-Induced Posttranslational Modification and Aberrant Cell Signaling in Sporadic Alzheimer's DiseaseR01AG056259 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI LIPTON, STUART A · 2017 to 2021
$3.3M
Aberrant protein S-nitrosylation mediates Gene-Environment Interactions in AD/ADRDU01AG088679 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI STUART A LIPTON, Tomohiro Nakamura · 2024 to 2026
$2.7M
Pharmacologic Lysosomal Flux Activators to Ameliorate Alzheimer's Disease and Related DementiasR01AG073418 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI JEFFERY W KELLY · 2024 to 2026
$2.5M
NRSA Training CoreTL1TR002551 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TEYTON, LUC · 2018 to 2022
$1.2M
NCATS NIH HHS TL1 TR002551NIA NIH HHS R01 AG056259NIA NIH HHS R01 AG073418NIA NIH HHS R35 AG071734NIA NIH HHS U01 AG088679
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common form of dementia worldwide. Despite extensive progress, the cellular and molecular mechanisms of AD remain incompletely understood, partially due to inadequate disease models. To illuminate the earliest changes in hereditary (familial) Alzheimer's disease, we developed an isogenic AD cerebrocortical organoid (CO) model. Our refined methodology produces COs containing excitatory and inhibitory neurons alongside glial cells, utilizing established isogenic wild-type and diseased human induced pluripotent stem cells (hiPSCs) carrying heterozygous familial AD mutations, namely PSEN1

Indexed as

Alzheimer’s diseaseAmyloid Beta Precursor ProteinAutophagychronic treatmentCortical organoidshuman modeliPSC-derivedoligomersPresenilin 1pTauTau

Identifiers

PMID40672178
PMCPMC12265565

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.