Evidence map›Paper›PMID 41569488›Full record

ReviewAdvances in neurobiology2026

Optical Approaches to Dissect the Structure and Dynamics of the Synapse at Nanoscale Resolution.

Jongyun Myeong, Vitaly A Klyachko

Abstract readReview
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In one paragraph

Review in Advances in neurobiology, 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

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

2 authors.

Jongyun MyeongDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Vitaly A KlyachkoDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA. klyachko@wustl.edu.ORCID https://orcid.org/0000-0003-3449-243X

Funding

Mechanisms of Synaptic Transmission in Healthy and Disease StatesR35NS111596 · NINDS · WASHINGTON UNIVERSITY · PI Vitaly A Klyachko · 2019 to 2026
$6.3M
NINDS NIH HHS R35 NS111596
6 · The paper itself

Abstract

The complex nanostructure and spatiotemporal dynamics of central synapses remain among the fundamental mysteries of neurobiology. The resolution of traditional microscopy techniques-constrained by the intrinsic limits of light diffraction-is largely insufficient to study central synapses effectively. Conventional imaging can resolve areas roughly the size of a synapse's active zone, that is, severalfold larger than the size of synaptic vesicles. Recent advances have generated several super-resolution imaging modalities that overcome or bypass the light diffraction limit to support studies of synaptic nanostructure. In this chapter, we present the principles, features, and limitations of the most common super-resolution imaging tools. Though these advancements have greatly improved our understanding of synaptic architecture and dynamics, significant challenges remain. Difficulties of translating the existing tools to in vivo applications, and the inherent trade-off between spatial and temporal resolution, continue to limit studies of the function of central synapses in native tissue.

Indexed as

Optical ImagingSynapsesAnimalsHumansSingle-particle trackingStimulated emission depletion microscopyStochastic optical reconstruction microscopyStructured illumination microscopySuper-resolution imagingSynaptic nanostructure

Identifiers

What OpenQuestion holds

Textmetadata
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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.