Evidence map›Paper›PMID 42046563›Full record

ArticleNPJ dementia2026

Multi-omic phenotyping of MAPT V337M neurons reveals early changes in axonogenesis and tau phosphorylation.

Gregory A Mohl, Gary Dixon, Emily Marzette, Justin McKetney, Avi J Samelson, Carlota Pereda Serras, Julianne Jin, Nabeela Ariqat, Andrea Keys, Cristian Chavira and 4 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in NPJ dementia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Gregory A Mohl *Institute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Gary Dixon *Institute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Emily MarzetteInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Justin McKetneyGladstone Data Science and Biotechnology Institute, The J. David Gladstone Institutes, San Francisco, CA USA.
Avi J SamelsonInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Carlota Pereda SerrasInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Julianne JinInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Nabeela AriqatInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Andrea KeysInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Cristian ChaviraInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Andrew LiInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Steven C BoggessInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.
Danielle L SwaneyGladstone Data Science and Biotechnology Institute, The J. David Gladstone Institutes, San Francisco, CA USA.
Martin KampmannInstitute for Neurodegenerative Diseases, University of California San Francisco, San Francisco, CA USA.

Funding

Post Baccalaureate Research Opportunity To Promote Equity In Learning (PROPEL).R25GM144250 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Ryan D. Hernandez, Todd Nystul · 2022 to 2026
$1.8M
Functional Characterization of Tau Mutation and Post-translational ModificationsK99AG080116 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SAMELSON, AVI JACOB · 2023 to 2024
$246k
Mechanisms of tau misfolding in neurons elucidated by deep mutational scanning and CRISPR screeningF32AG063487 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SAMELSON, AVI JACOB · 2019 to 2021
$195k
NIA NIH HHS F32 AG063487NIA NIH HHS K99 AG080116NIGMS NIH HHS R25 GM144250
6 · The paper itself

Abstract

Tau aggregation is a hallmark of several neurodegenerative diseases, including Alzheimer's disease and frontotemporal dementia. There are disease-causing variants of the tau-encoding gene,

Indexed as

Cell biologyMolecular biologyNeurologyNeuroscience

Identifiers

PMID42046563
PMCPMC13110130

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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.