Epigenetic modifications are processes that can cause heritable phenotypic changes without altering the genetic code. The Carless lab is interested in identifying such modifications that are associated with complex diseases.
Our goal is to understand how these might contribute to disease risk and be leveraged as potential novel therapies. To accomplish this, our lab combines human, animal, and cell-based systems. We investigate epigenetic mechanisms underlying neurological, neurodegenerative, and psychiatric disorders, such as epilepsy, bipolar disorder, and Alzheimer’s disease, as well as metabolism and metabolic disorders, such as obesity and diabetes.
The overarching goal of the Carless lab is to understand the role of epigenetic mechanisms in complex diseases.
Current projects in the Carless Lab focus on:
1. In vitro epigenetic editing to evaluate the impact of DNA methylation changes in complex diseases
2. Neurodevelopmental origins of neuropsychiatric disease
3. Development of “age-in-a-dish” models to study age- and disease-associated epigenetic signatures
4. DNA methylation changes associated with metabolic disease risk
5. The role of miRNAs in brain structure and function
We are part of the University of Texas at San Antonio, in the Department of Neuroscience, Developmental and Regenerative Biology.
Our group is also part of the UTSA Brain Health Consortium.
Our lab is located in:
Science and Engineering Building (SEB), Room 4.146
University of Texas at San Antonio
One UTSA Circle
San Antonio, TX 78249