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the claim
The synaptic cleft is maintained through specific structural cell adhesion molecules
the verdict
SUPPORTED
the evidence backs this
refutedsupported
the weight of evidence
6 sources for · 0 against

The synaptic cleft and the structural integrity between pre- and postsynaptic terminals are maintained through specific trans-synaptic cell adhesion molecules.

Evidence for · 6
2022 · cited by 20
Paper 1 demonstrates that the presynaptic adhesion protein neurexin stabilizes postsynaptic structures and circuit connectivity.
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The analysis

The retrieved literature consistently supports the claim that synaptic adhesion molecules (such as neurexins, LRR-containing proteins, and dystroglycan) are responsible for establishing, bridging, and maintaining the structural architecture of the synaptic cleft. Multiple papers detail how these specific molecular interactions link pre- and postsynaptic compartments. Therefore, the verdict is SUPPORTED.

More for · 5
2019 · cited by 18
Paper 2 discusses how presynaptic membrane proteins like neurexins and LAR-RPTPs act as hubs that orchestrate synaptic adhesion pathways.
2019 · cited by 5
Paper 6 reviews how membrane receptor-like cell adhesion molecules and secreted proteins in the synaptic cleft mediate structural linkages between pre- and postsynaptic terminals.
2025 · cited by 3
Paper 7 highlights that cell adhesion molecules and associated secreted factors play pivotal roles in establishing and maintaining synaptic connectivity across the cleft.
2025 · cited by 3
Paper 8 shows that the cell adhesion molecule Dystroglycan is required for the formation and maintenance of synapses through specific extracellular and intracellular interactions.
2026 · cited by 1
Paper 10 notes that synaptic cell adhesion molecules are essential for synapse development and maintenance by physically linking presynaptic terminals to postsynaptic structures.
The paper trail · every fact has a biography
first checked04 Aug 2026
judged → SUPPORTED · 8304 Aug 2026
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