Yu Mu

The paper creates a comprehensive atlas of larval zebrafish neuron morphology, including excitatory and inhibitory identities and connectivity patterns.

The paper introduces a far-red dopamine sensor, HaloDA1.0, enabling multiplex imaging of neurochemical networks in vivo with high sensitivity and versatility.

This paper introduces a new class of fluorophores with enhanced photostability, solubility, and tunable properties for advanced biological imaging applications.

The paper introduces NEMOer, a set of genetically encoded calcium indicators that enhance the detection of ER/SR calcium dynamics, enabling sensitive and dynamic imaging in both excitable and non-excitable cells.

This paper develops a red fluorescent calcium indicator, SomaFRCaMPi, which improves neuronal activity imaging accuracy and scale in vivo by reducing neuropil contamination and enhancing signal-to-noise ratio.

This study uses GRIT to measure tryptophan dynamics across species and scales, revealing links between tryptophan metabolism, inflammation, and behavior.

This study shows how chemosensory cues affect eye-body coordination in larval zebrafish, with aversive cues enhancing coordination and food cues promoting forward movement.

The paper introduces an all-optical technique for brain-wide calcium imaging and optogenetic stimulation in larval zebrafish, showing it can trigger behavior and neural activity changes.

This study evaluates dimensionality reduction methods for calcium imaging data and introduces CILDS, which outperforms existing methods in recovering low-dimensional neural activity.

The paper analyzes whole-brain neuronal activity in larval zebrafish during visual stimuli and motor output, revealing functional brain nuclei and convergent sensorimotor transformations.

The paper introduces multi-scale approaches to improve imaging and analysis of large neuronal populations by decimating spatial and temporal resolution to enable faster imaging or larger field of view with minimal accuracy loss.