The focus of our laboratory is the structure and function of pulmonary surfactant proteins. We are particularly interested in the antimicrobial, antioxidant, and immunomodulatory roles of surfactant proteins A and D in the alveolar space.
Young LR, Franz DN, Nagarkatte P, Fletcher CD, Wikenheiser-Brokamp KA, Galsky MD, Corbridge TC, Lam AP, Gelfand MJ, McCormack FX. Utility of FDG-PET inSporadic and Tuberous Sclerosis Associated Lymphangioleiomyomatosis. Chest. 2009 Apr 6. [Epub ahead of print] PubMed PMID: 19349386.
Schmithorst VJ, Altes TA, Young LR, Franz DN, Bissler JJ, McCormack FX,Dardzinski BJ, Brody AS. Automated algorithm for quantifying the extent of cysticchange on volumetric chest CT: initial results in Lymphangioleiomyomatosis. AJRAm J Roentgenol. 2009 Apr;192(4):1037-44. PubMed PMID: 19304711.
Kinder BW, Brown KK, McCormack FX, Ix JH, Kervitsky A, Schwarz MI, King TE Jr.Serum surfactant protein-A is a strong predictor of early mortality in idiopathicpulmonary fibrosis. Chest. 2009 Jun;135(6):1557-63. Epub 2009 Mar 2. PubMed PMID:19255294; PubMed Central PMCID: PMC2716710.
McCormack FX. Lymphangioleiomyomatosis: a clinical update. Chest. 2008Feb;133(2):507-16. Review. PubMed PMID: 18252917.
Young LR, Pasula R, Gulleman PM, Deutsch GH, McCormack FX. Susceptibility ofHermansky-Pudlak mice to bleomycin-induced type II cell apoptosis and fibrosis.Am J Respir Cell Mol Biol. 2007 Jul;37(1):67-74. Epub 2007 Mar 15. PubMed PMID:17363777; PubMed Central PMCID: PMC1899346.