top of page
two astrocytes.tif

Welcome to the Galvan Lab

Identifying molecular and biochemical alterations that cause Alzheimer's disease and other dementias

We seek to understand the processes that drive Alzheimer's disease (AD) with a focus on those that link aging to AD and other dementias, and to define the therapeutic potential of drug candidate molecules in AD.  We use  genetic manipulations in rodents, in vivo optical and MRI- and PET-based brain imaging, tissue and single-cell -omics, biochemical, physiological, and behavioral tools, as well as cellular and molecular biology approaches.  Our goal is to advance our understanding of age-associated neurological disease mechanisms and identify interventions to prevent or treat AD and other age-associated dementias.  


Brain vascular dysfunction in Alzheimer's disease

PS19 NTg DAF-FM vessel overlay - doctored cropped and doctored more - for artwork 8 bit ch

Vascular tau in Alzheimer's and other tauopathies

Dots 1.png
PS19 tau o.tau and lectin image.tif
Home: Project

Brain vascular endothelial cell senescence in Alzheimer's disease


Regulation of peripheral metabolism and lifespan

by neuronal mTOR

More information
RxA tam-cre female.jpg
Dots 2.png

Astrocyte senescence

in Alzheimer's disease


Mailing Address


Department of Biochemistry and Molecular Biology
University of Oklahoma Health Sciences Center
940 Stanton L. Young Blvd, BMSB 810
Oklahoma City, OK 73104

Contact us

Phone: (405) 271-2227 ext 32778

bottom of page