Evidence map›Paper›PMID 39386710›Full record

ArticlebioRxiv : the preprint server for biology2024

Tau P301S Transgenic Mice Develop Gait and Eye Movement Impairments That Mimic Progressive Supranuclear Palsy.

Rose B Creed, Scott C Harris, Sadhana Sridhar, Sascha du Lac, David S Zee, Felice A Dunn, Guy Bouvier, Alexandra B Nelson

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

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

8 authors.

Rose B CreedKavli Institute for Fundamental Neuroscience, UCSF, San Francisco, CA, 94158.ORCID 0000-0003-4893-2010
Scott C HarrisDepartment of Ophthalmology, UCSF, San Francisco, CA, 94158.ORCID 0000-0002-3567-4481
Sadhana SridharKavli Institute for Fundamental Neuroscience, UCSF, San Francisco, CA, 94158.ORCID 0000-0003-0041-3414
Sascha du LacDepartment of Otolaryngology-Head and Neck Surgery, Neurology, and Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0003-4669-3191
David S ZeeDepartments of Neurology, Ophthalmology, Otolaryngology-Head and Neck Surgery, and Neuroscience, The Johns Hopkins School of Medicine, Baltimore, USA.ORCID 0000-0003-3909-2494
Felice A DunnDepartment of Ophthalmology, UCSF, San Francisco, CA, 94158.ORCID 0000-0003-0784-0259
Guy BouvierUniversité Paris-Saclay, CNRS, Institut des Neurosciences Paris-Saclay, 91400 Saclay, France.ORCID 0000-0002-6160-7186
Alexandra B NelsonKavli Institute for Fundamental Neuroscience, UCSF, San Francisco, CA, 94158.ORCID 0000-0002-9305-5662

Funding

Striatal Mechanisms of Levodopa-Induced DyskinesiaR01NS101354 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alexandra Nelson · 2018 to 2026
$3.3M
Retinal mechanisms underlying the optokinetic reflexR01EY035028 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Felice A Dunn, ALEX L KOLODKIN · 2024 to 2026
$1.6M
Neural circuits underlying motor impairments in a rodent model of progressive supranuclear palsyK00NS108458 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CREED, ROSE BERTHE · 2020 to 2023
$320k
Central mechanisms for integrating distinct retinal inputs during the optokinetic reflex in miceF31EY033225 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HARRIS, SCOTT C · 2021 to 2023
$121k
NEI NIH HHS F31 EY033225NEI NIH HHS R01 EY035028NINDS NIH HHS K00 NS108458NINDS NIH HHS R01 NS101354
6 · The paper itself

Abstract

Progressive supranuclear palsy (PSP) is a neurodegenerative disorder with an estimated prevalence of 5-7 people in 100,000. Clinically characterized by impairments in gait, balance, and eye movements, as well as aggregated Tau pathology, PSP leads to death in approximately 5-8 years. No disease-modifying treatments are currently available. The contribution of Tau pathology to the symptoms of patients with PSP is poorly understood, in part due to lack of a rodent model that recapitulates characteristic aspects of PSP. Here, we assessed the hTau.P301S mouse for key clinical features of PSP, finding progressive impairments in balance and gait coordination. Additionally, we found impairments in fast vertical eye movements, one of the most distinctive features of PSP. Across animals, we found that Tau pathology in motor control regions correlated with motor deficits. These findings highlight the utility of the hP301S mouse in modeling key aspects of PSP.

Identifiers

PMID39386710
PMCPMC11463522

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.