Pathobiology and Molecular Medicine  http://www.gbs.uab.edu  http://www.uab.edu/graduate  Back to Main

Faculty Detail    
Name JARROD BARNES
PhD
 
Campus Address BMR2 434 Zip 0006
Phone  (205) 975-5300
E-mail  barnesj5@uab.edu
Other websites
     

Education
Undergraduate  University of Georgia      B.S. 
Graduate  University of Georgia      PhD 
Fellowship  Cleveland Clinic      Postdoctoral Fellow 


Faculty Appointment(s)
Appointment Type Department Division Rank
Primary  Med - Pulmonary/Allergy/Critical Care  Med - Pulmonary/Allergy/Critical Care Associate Professor
Center  Ctr for Clinical & Translational Sci  Ctr for Clinical & Translational Sci Associate Professor
Center  Cystic Fibrosis Research Center  Cystic Fibrosis Research Center Associate Professor

Graduate Biomedical Sciences Affiliations
Pathobiology and Molecular Medicine 

Biographical Sketch 
Dr. Barnes is an Assistant Professor of Medicine at the University of Alabama at Birmingham (UAB). Following his training in Glycobiology at the Complex Carbohydrate Research Center at the University of Georgia, he was recruited to the Cleveland Clinic Lerner College of Medicine, where he combined his basic research experiences with more translational approaches in the Department of Pathobiology within the Lerner Research Institute. Dr. Barnes’ research has focused on dysregulated glucose metabolism and its role in aberrant glycosylation in pulmonary vascular disease. Specifically, his work has demonstrated that glucose dysregulation impacts glycosylation and glycosyltransferases that drive cell proliferation in idiopathic pulmonary arterial hypertension (IPAH). His research will continue to explore the molecular mechanisms that regulate metabolism and glycosylation in IPAH as well as other pulmonary diseases including COPD and Cystic Fibrosis.



Research/Clinical Interest
Title
Mechanisms of metabolic dysregulation and aberrant glycosylation in pulmonary disease
Description
Glycobiology Pulmonary Vascular Disease Metabolism and aging

Keywords
glycosylation, pulmonary vascular disease, metabolism