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[7] In a 2026 neuropathic-pain study, photoaffinity-probe experiments identified LanCL1 as a binding target of LAT8881-derived probe material in nervous-system models, and LanCL1 knockdown blocked the reported LAT8881 activity in those models

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doi:10.1590/abd1806-4841.20175481 Poljak, Borut, and Raja Dahmane

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