Aura Perez

Assistant Professor
School of Medicine
Research Scientist
Drumm Lab
Department of Genetics and Genome Sciences
School of Medicine

Research Information

Research Interests

My research revolves around two main topics: excessive inflammation observed in the lungs of cystic fibrosis (CF) patients and the malnutrition and malabsorption seen in these patients. 

Publications

  • Gupta S, Heacock M, Perez A, and Davis PB. Antibodies to the polymeric immunoglobulin receptor with different binding and trafficking Patterns. Am. J. Respir. Cell. Mol. Biol. 33(4):363-370, 2005. 
  • Perez A, Issler AC, Cotton CU, Kelley TJ, Verkman AS, and Davis PB. CFTR inhibition mimics the cystic fibrosis inflammatory profile. Am. J. Physiol. Lung Cell. Mol. Physiol. 292(2):L383-L395, 2007
  • Perez A, van Heeckeren AM, Nichols D, Gupta S, Eastman JF, and Davis PB. Peroxisome proliferators-activated receptor gamma in cystic fibrosis lung epithelium. Am. J. Physiol. Lung Cell. Mol. Physiol. 295(2):L303-L313, 2008. PMC2519842.
  • Perez A, and Davis PB. Gene profile changes after pseudomonas aeruginosa exposure in immortalized airway epithelial cells. JSFG 5:179-194, 2004.
  • Bryan R, Kube D, Perez A, Davis PB, and Prince A. Overproduction of the CFTR R domain leads to increased levels of asialoGM1 and increased Pseudomonas aeruginosa binding by epithelial cells. Am J Respir Cell Mol Biol. 19(2):269-277, 1998.
  • Kube D, Adams L, Perez A, and Davis PB. Terminal sialylation is altered in airway cells with impaired CFTR-mediated chloride transport. Am. J. Physiol. Lung Cell. Mol. Physiol. 280(3):L482-L492, 2001.