Clifford G. Kentros

The paper shows that the mouse anterior cingulate cortex uses dynamic single-cell activity to maintain stable population codes for object locations across repeated experiences.

The paper shows that direct entorhinal input is crucial for CA1 remapping in novel environments, enabling spatial map reorganization.

The paper shows that artificial remapping of place fields is reproducible and predictable based on grid subfield rate changes in the entorhinal-hippocampal system.

The paper investigates differential susceptibility of entorhinal neuronal subtypes to pathological tau species in Alzheimer's Disease, finding that ECLIII neurons show greater vulnerability than ECLII fan cells.

This study inhibits direct entorhinal inputs to CA1 and finds that theta phase precession is abolished but theta sequences are strengthened, suggesting entorhinal inputs drive learning rather than sequence generation.

This paper delineates four subregions within the mouse claustrum complex using fiber-architecture, genetic markers, and connectivity data, providing a reference framework for future studies.

This study identifies claustrum neurons and their connectivity patterns, showing they integrate inputs from multiple cortical regions and contribute to multimodal sensory processing.

The paper shows that layer Vb-to-Va connections are more effective in lateral entorhinal cortex than in medial entorhinal cortex, suggesting LEC plays a greater role in episodic memory consolidation.

The paper presents a microfluidic platform for creating functional neuromuscular junctions using human motor neurons and myotubes, validated by rabies virus tracing.

The paper develops viral vectors with brain region-specific gene expression using enhancer-driven gene expression (EDGE) to enable circuit-specific manipulations in any species.

The paper identifies unique cortical enhancers that enable cell-type-specific genetic tools through Enhancer-Driven Gene Expression.