Evidence map›Paper›PMID 40568154›Full record

ArticlebioRxiv : the preprint server for biology2025

Targeted gene transfer into developmentally defined cell populations of the primate brain.

Ana Rita Ribeiro Gomes, Natalie Hamel, Surjeet Mastwal, Naim Wright, David C Ide, Christopher T Richie, Ted B Usdin, Kuan Hong Wang, David A Leopold

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. 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

9 authors.

Ana Rita Ribeiro GomesSection on Cognitive Neurophysiology and Imaging, Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.
Natalie HamelSection on Cognitive Neurophysiology and Imaging, Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.
Surjeet MastwalSection on Cognitive Neurophysiology and Imaging, Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.
Naim WrightSection on Cognitive Neurophysiology and Imaging, Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.
David C IdeSection on Instrumentation, National Institute of Mental Health, National Institutes of Health, Bethesda MD.
Christopher T RichieGenetic Engineering and Viral Vector Core, National Institute of Drug Abuse, National Institutes of Health, Baltimore, MD.
Ted B UsdinSystems Neuroscience Imaging Resource, National Institute of Mental Health, National Institutes of Health, Bethesda MD.
Kuan Hong WangDepartment of Neuroscience, Del Monte Institute for Neuroscience, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0002-2249-5417
David A LeopoldSection on Cognitive Neurophysiology and Imaging, Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.

Funding

Visual Adaptation and Neuronal SelectivityZIAMH002898 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEOPOLD, DAVID A · 2009 to 2025
$13.6M
University of Rochester Intellectual and Developmental Disabilities Research CenterP50HD103536 · NICHD · UNIVERSITY OF ROCHESTER · PI JOHN J FOXE, Anna K Majewska · 2020 to 2026
$9.8M
Intramural NIH HHS ZIA MH002898NICHD NIH HHS P50 HD103536
6 · The paper itself

Abstract

The primate brain possesses unique physiological and developmental features whose systematic investigation is hampered by a paucity of transgenic germline models and tools. Here, we present a minimally invasive method to introduce transgenes widely across the primate cerebral cortex using ultrasound-guided fetal intracerebroventricular viral injections (FIVI). This technique enables rapid-onset and long-lasting transgene expression following the delivery of recombinant adeno-associated viruses (rAAVs). By adjusting the gestational timing of injections, viral serotypes, and transcriptional regulatory elements, rAAV FIVI allows for systematic targeting of specific cell populations. We demonstrate the versatility of this method through restricted laminar expression in the cortex, Cre-dependent targeting of neurons, CRISPR-based gene editing, and labeling of peripheral somatosensory and retinal pathways. By mimicking key desirable features of germline transgenic models, this efficient and targeted method for gene transfer into the fetal primate brain opens new avenues for experimental and translational neuroscience across the lifespan.

Identifiers

PMID40568154
PMCPMC12190174

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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.