2018

Glenn Foundation for Medical Research and AFAR Grants for Junior Faculty


Deborah Winter, PhD

Assistant Professor, Northwestern University

Uncovering the role of epigenomic reprogramming on monocyte development in aging

The body becomes increasingly susceptible to infection and chronic inflammatory conditions as it ages. This is attributed to the over-production and age-related reprogramming of circulating white blood cells, known as monocytes, that contribute to low-grade inflammation. In the proposed research, Dr. Deborah Winter will determine how monocyte development is altered in aging. Using a functional genomics approach to map the key factors involved in aging, Dr. Winter’s research will provide potential targets for therapies that can alleviate the negative effects on the immune system caused by aging and enable us to remain healthy as we age.

More 2018 Recipients of this Grant

Daniel Berry, PhD

Age-dependent decline of beige adipocyte induction and its metabolic consequences

Benjamin Cosgrove, PhD

Single-cell dissociation of muscle stem cell dysfunction in human aging

Isha Jain, PhD

Hypoxia as a therapy for age-associated proteotoxic stress and neurodegeneration

Kishore Kuchibhotla, PhD

Improving cognitive flexibility in aging by modulating context-dependent neural circuits

Kishore Kuchibhotla
Po-Ru Loh, PhD

Understanding the etiology and effects of age-related clonal hematopoiesis

Andreas Pfenning, PhD

Cell type-specific epigenetic decay underlying brain aging

Andrew Pickering, PhD

Determine if genetic and pharmacologic proteasome manipulation can prevent age-related cognitive deficits in mice and flies

Vivek Venkatachalam, PhD

Whole brain dynamics in aging C. elegans

Kevin Wang, MD, PhD

Rebooting the nuclear architecture as an innovative cellular reprogramming strategy to reverse aging

Nilay Yapici, PhD

Deciphering changes in the structure and function of neural circuits that regulate homeostatic drives during aging

Joshua Baker, MD, MSCE

Age and obesity-related alterations in skeletal muscle mitochondrial activity and lipid distribution, and associations with joint inflammation and cartilage degeneration in osteoarthritis