Funded Projects

Browse wide-ranging research at the frontiers of neuroscience supported by Wu Tsai Neurosciences Institute grants, awards, and training fellowships.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2016
A principled investigation into the heterogeneous coding properties of medial entorhinal cortex that support accurate spatial navigation

Navigation through an environment to a remembered location is a critical skill we use every day. How does our brain accomplish such a task? Over the last few decades, several lines of evidence have suggested that a brain region called medial entorhinal cortex (MEC) supports navigation by encoding information our location and movement within an environment.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2016
Understanding why neurons die in disease

Many neurological diseases feature the death of neurons, but the mechanisms that mediate cell death in these disorders are unknown. Astrogliosis, the response of a cell-type called “astrocytes” to injury, is common to most diseases of the central nervous system (CNS), and recent studies in our lab suggest that some reactive astrocytes may release a protein that is potently toxic to neurons.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2020
How do Schwann cells sort and myelinate axons in the developing peripheral nervous system?

Schwann cells (SCs) sort and myelinate peripheral axons, and impairments in either process can cause long-term disability. There are no therapeutic strategies for targeting SC dysfunction, underscoring the need to investigate mechanisms of sorting and myelination. Both processes require highly motile SC cytoplasmic protrusions, but the basis of this motility is unclear.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2020
Magnetic Resonance Imaging of Epileptogenesis

Absence epilepsy is a form of pediatric epilepsy which causes seizures with brief lapses in awareness. Electron microscopy results in a murine model of absence epilepsy support the hypothesis that maladaptive myelination plays a role in disease progression.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2021
Elucidating mechanisms of microglial tiling

In a process called tiling, homeostatic microglia homogenously organize in a grid-like fashion to achieve efficient surveillance of the brain. The molecular mechanisms underlying tiling are unknown. I hypothesize that microglia use cell-surface proteins to sense density of neighboring microglia, thereby contributing to constant cell-to-cell distances.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2021
Design and development of a high-performance intra-cortical speech BCI

Many neurological injuries and diseases such as brainstem stroke and Amyotrophic Lateral Sclerosis (ALS) result in severe speech impairment, drastically reducing quality of life. Recent progress in brain-computer interfaces (BCI) has allowed these individuals to communicate, but performance is still far lower than typical spoken conversation speeds.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2022
Leveraging screenomics to identify mental illness: Detecting bipolar disorder through computational analysis of smartphone screen data

Mental illnesses like bipolar disorder affect millions of people around the world, but early symptoms are often difficult to detect. Working across the disciplines of clinical psychology, communication, and computer science, my research will develop a novel computational tool to identify signals of mania and depression in real-time.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2022
Mechanistic insights into glycerophospholipid metabolism in the lysosome

Phospholipid dysregulation is implicated in the pathogenesis of lysosomal storage disorders (LSDs). We found that glycerophosphodiesters (GPDs) accumulate in lysosomes derived from Batten disease models, a life-limiting LSD whose pathological mechanism remains elusive. GPDs are the degradation products of glycerophospholipid catabolism by phospholipases.