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
EPFL-Stanford Exchange
2017
High-speed force probes for deconstructing the biophysics of mechanotransduction

The purpose of this collaborative project is to study neuronal mechanisms associated with social stress. In particular we will test whether the energy producing systems, known as mitochondria, in a specific set of brain cells are important to confer resilience to stressful stimuli. This research may lead to treatments of stress and anxiety disorders. 

 

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2015
Understanding cellular responses induced by chronic implantation of electrodes using a novel human neural differentiation platform

Electrodes implanted in the brain have great potential, with applications in neurodegenerative disease, brain-computer interfaces, and more. However, the presence of electrodes in brain tissue causes a response known as gliosis, in which a scar forms around the electrode, reducing its effectiveness and access to neurons.

Wu Tsai Neurosciences Institute
EPFL-Stanford Exchange
2017
High-speed nanomechanical probing of auditory mechano-sensitive cells

Our ability to detect and interpret sounds relies on specialized sensory cells within the snail-shaped hearing organ of the inner ear—the cochlea. These hair cells sense physical movement and then convert that mechanical stimulus into a biological signal that we perceive as sound. These mechano-sensory cells perform this task within microseconds and can do so for sub-nanomechanical stimuli.

Wu Tsai Neurosciences Institute
EPFL-Stanford Exchange
2017
Quantitative imaging for multi-scale modeling of neurological diseases

My proposed visit to the Van De Ville lab is centered on the idea to expand our methods beyond brain tumors to other neurological diseases using the Van De Ville lab’s expertise in neuro-imaging. Imaging genomics has been focused mainly on oncology; however, other neurological diseases can be studied in the same way.

Wu Tsai Neurosciences Institute
EPFL-Stanford Exchange
2017
Biologically plausible neural algorithms for learning structured sequences

Humans naturally learn to generate and process complicated sequential patterns. For example, a concert pianist can learn an enormous repertoire of memorized music. In neuroscience, it is widely thought that synaptic plasticity – the process by which the connections between neurons change response to experience – underlies such remarkable behavior.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2017
Engineering versatile deep neural networks that model cortical flexibility

In the course of everyday functioning, animals (including humans) are constantly faced with real-world environments in which they are required to shift unpredictably between multiple, sometimes unfamiliar, tasks. But how brains support this rapid adaptation of decision making schema, and how they allocate resources towards learning novel tasks is largely unknown both neuroscientifically and algorithmically.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2018
Deep brain microstimulation for memory recovery

Yi Lui's project aims to use deep brain microstimulation (DBMS), which causes even less brain damage and has higher spatial resolution than DBS, for memory recovery.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2018
Synaptic rules and circuit architectures for learning from feedback

Dr. Brandon Jay Bhasin will use engineering principles from modern control theory, experimental neuroscience and computational neuroscience to significantly advance understanding of how feedback driven plasticity in a tractable neural circuit is orchestrated across multiple synaptic sites and over various timescales so that circuit dynamics are changed to improve performance.

Wu Tsai Neurosciences Institute
EPFL-Stanford Exchange
Modelling the Pupil Light Reflex for Non-Image Forming Vision

Although you’re aware of the light that you see, light also affects us in ways that you might not appreciate. These so called “non-image forming” (NIF) pathways were recently discovered, they start in the human eye before projecting to over a dozen brain regions. They modulate aspects of human function including our daily rhythms, our sleep patterns, the way we feel and the way we think.

Wu Tsai Neurosciences Institute
SIGF - Graduate Fellowship
2019
Weak supervision in medical multi-modal time series

The project aims to alleviate this bottleneck by developing a weak supervision system that optimally deals with time-series data and takes advantage of multiple data modalities.

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.