Gene mutation leads to epileptic encephalopathy symptoms, neuron death in mice

Mice with a genetic mutation that’s been observed in patients with epileptic encephalopathy, a severe form of congenital epilepsy, exhibit not only the seizure, developmental and behavioral symptoms of the disorder, but also neural degeneration and inflammation in the brain, University of Illinois...

Uncovering the Critical Function of Drg1 in Protein Synthesis

Biochemistry researchers at the University of Illinois Urbana-Champaign are conducting trailblazing work on a group of conserved proteins that are directly related to abnormal cell proliferation and developmental and neurological disorders. In a new article published in Cell Reports, biochemistry...

Study offers insight into underlying causes of seizure disorder in babies

Researchers report that infantile spasms, a rare but serious seizure disorder in babies, appear to be the result of a molecular pathway gone awry. In their study of a mouse model of the disorder, the researchers discovered that genetic mutations associated with the disease impair a pathway that is...

Welcome to Professor Xinzhu Yu

Professor Yu was one of ten new faculty hires made in the School of Molecular and Cellular Biology in the last three years. Yu is an assistant professor of molecular and integrative physiology and is an affiliate of the Beckman Institute.

New NIH grant to fund U of I research on Fragile X Syndrome

Recent clinical trials involving Fragile X Syndrome (FXS), a genetic disorder that causes mild to severe intellectual disability, indicate that potential drug treatments are not as effective as researchers initially hoped. This lack of therapeutic potential suggests there are some gaps in our...

Meet MCB: Professor Nien-Pei Tsai

Dr. Tsai’s lab focuses on understanding the molecular mechanisms underlying neuronal excitability imbalance in neurological and psychiatric disorders including epilepsy and autism.