Evidence map›Paper›PMID 41895449›Full record

ReviewMolecules and cells2026

Molecular continuity between axon guidance and synaptic function.

Seongjun Kim, Hye Jin Cho, I-Hao Wang, Sung Jin Park

Abstract readReview
In one paragraph

Review in Molecules and cells, 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

4 authors.

Seongjun KimDepartment of Physiology, Sungkyunkwan University School of Medicine, Suwon, Korea.
Hye Jin ChoDepartment of Physiology, Sungkyunkwan University School of Medicine, Suwon, Korea.
I-Hao WangBroad Institute of Harvard and MIT, Cambridge, MA, USA.
Sung Jin ParkDepartment of Physiology, Sungkyunkwan University School of Medicine, Suwon, Korea. Electronic address: parksj1126@skku.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The precise assembly of neural circuits is a marvel of cellular engineering, requiring the seamless coordination of long-range axon navigation and short-range synapse formation. Traditionally, these 2 processes were thought to be governed by distinct sets of molecular cues. However, emerging evidence challenges this dichotomy, revealing that proteins canonically associated with mature synaptic transmission are "repurposed" early in development to instruct selective neuronal pairing, including axon guidance and target recognition. In this mini-review, we discuss the molecular versatility of key synaptic proteins, including latrophilins, N-methyl-D-aspartate receptors, cerebellins, neurexins, and other complementary adhesion systems. We highlight how these molecules utilize non-canonical mechanisms, such as ion flux-independent signaling and trans-neuronal adhesion, to couple initial wiring decisions with later synaptic specialization. This functional duality suggests a "molecular continuum" in brain development, offering broader insights into how cells maximize their proteomic toolkit to build complex biological systems.

Indexed as

Axon GuidanceAxonsSynapsesAnimalsHumansNeurexinsNeurodevelopmentReceptors, N-Methyl-D-AspartateSynaptic TransmissionNeurexinsReceptors, N-Methyl-D-AspartateCerebellinCircuit assemblyLatrophilinNeurexinN-methyl-D-aspartate receptors

Identifiers

PMID41895449
PMCPMC13094498

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.