Evidence map›Paper›PMID 41975224›Full record

ArticleNature methods2026

Adaptive optical correction for in vivo two-photon fluorescence microscopy with neural fields.

Iksung Kang, Hyeonggeon Kim, Ryan Natan, Qinrong Zhang, Stella X Yu, Na Ji

Abstract read
In one paragraph

Article in Nature methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Recover Biological Structure from Sparse-View Diffraction Images with Neural Volumetric Prior.Proceedings. IEEE International Conference on Computer Vision · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Iksung KangDepartment of Neuroscience, University of California, Berkeley, Berkeley, CA, USA. iksung.kang@kaist.ac.kr.ORCID http://orcid.org/0000-0002-4009-6743
Hyeonggeon KimApplied Science and Technology Graduate Program, University of California, Berkeley, Berkeley, CA, USA.
Ryan NatanDepartment of Neuroscience, University of California, Berkeley, Berkeley, CA, USA.ORCID http://orcid.org/0000-0002-3123-4833
Qinrong ZhangDepartment of Neuroscience, University of California, Berkeley, Berkeley, CA, USA.ORCID http://orcid.org/0000-0001-8893-514X
Stella X YuDepartment of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI, USA.
Na JiDepartment of Neuroscience, University of California, Berkeley, Berkeley, CA, USA. jina@berkeley.edu.ORCID http://orcid.org/0000-0002-5527-1663

Funding

Integrated Biophysical and Neural Model of Electrical Stimulation EffectsR01NS109553 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BAZHENOV, MAKSIM V, HALGREN, ERIC · 2019 to 2023
$4.4M
Optimizing FACED for robust large-scale activity recordingU01NS137449 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI NA Ji · 2024 to 2026
$2.1M
Adaptive optical microscopy for high-accuracy recording of neural activity in vivoU01NS118300 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI JI, NA · 2021 to 2023
$1.7M
NINDS NIH HHS R01 NS109553NINDS NIH HHS U01 NS118300NINDS NIH HHS U01 NS137449U.S. Department of Energy (DOE) DE-SC0021986U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01NS109553U.S. Department of Health & Human Services | National Institutes of Health (NIH) U01NS118300U.S. Department of Health & Human Services | National Institutes of Health (NIH) U01NS137449
6 · The paper itself

Abstract

Adaptive optics restore ideal imaging performance in complex samples by measuring and correcting optical aberrations but often require custom-built microscopes with carefully aligned wavefront sensing/shaping devices and can be susceptible to sample motion. Here we describe NeAT, a computational framework using neural fields for adaptive optics two-photon fluorescence microscopy. NeAT estimates wavefront aberration and recovers sample structure from a 3D image stack without requiring external datasets for training. Incorporating motion correction in learning and correcting conjugation errors commonly found in commercial microscopes, NeAT is designed for deployment in biological laboratories for in vivo imaging. We validate NeAT's performance using a custom-built microscope with a wavefront sensor under varying signal-to-noise ratios, aberration and motion conditions. With a commercial microscope, we demonstrate real-time aberration correction for in vivo morphological and functional imaging in the living mouse brain, with NeAT improving the signal and accuracy of glutamate and calcium imaging of synapses and neurons.

Indexed as

Microscopy, Fluorescence, MultiphotonNeuronsAnimalsBrainImaging, Three-DimensionalMiceSignal-To-Noise RatioSynapses

Identifiers

PMID41975224
PMCPMC13446014

What OpenQuestion holds

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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.