Neuroscience explores the intricate machinery of the brain and nervous system, seeking to understand how we think, feel, and move. From the microscopic dance of individual neurons to the complex networks that shape our memories and behaviors, this field peels back the layers of our biological selves to reveal the origins of consciousness and disease.

At Gist.Science, we bring these discoveries directly from bioRxiv, the leading preprint server for biological sciences, to a broader audience. We process every new neuroscience preprint as it is uploaded, transforming dense academic manuscripts into clear, plain-language explanations alongside detailed technical summaries. This ensures that both curious readers and specialists can stay current with the latest breakthroughs before they are formally published.

Below are the latest neuroscience papers we have processed from bioRxiv, offering fresh insights into the workings of the mind.

🧠 neuroscience

Dynamic construction of subjective time through statistical learning of event structure

This study demonstrates that subjective time is dynamically constructed through statistical learning of event structure, where hierarchical representations and semantic meaning actively warp the perception of duration by compressing time within events and dilating it at boundaries, independent of dedicated internal clocks or physiological arousal.

Zeng, Q., Trübutschek, D., Turk-Browne, N. B., Melloni, L.2026-04-23
🧠 neuroscience

Visual cortical dynamics supporting predictable attentional capture

Using laminar neurophysiology in macaques, this study demonstrates that predictable visual contexts optimize attentional selection by streamlining feedforward cortical processing to enhance target responses through reduced variability and suppress distractors via adapted dynamics, thereby revealing independent mechanisms for target enhancement and distractor suppression.

Groot, J. J., Schall, J. D., Westerberg, J. A.2026-04-23
🧠 neuroscience

CXCL10 drives female-specific tau pathology progression and defines sex-dependent vulnerability in tauopathy model mice

This study identifies CXCL10 as a key female-specific driver of tau pathology progression in mouse models, demonstrating that its genetic ablation significantly reduces tau burden and extends survival through a sex-dependent mechanism that operates independently of T cell infiltration or general glial activation.

Uenishi, R., Kawata, R., Manabe, T., Matsuba, Y., Mihira, N., Takeo, T., Sado, T. C., Hijioka, M., Saito, T.2026-04-22