Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL054658-01A1
Application #
2233061
Study Section
Lung Biology and Pathology Study Section (LBPA)
Project Start
1996-05-01
Project End
2001-04-30
Budget Start
1996-05-01
Budget End
1997-04-30
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Moller, David R (2007) Potential etiologic agents in sarcoidosis. Proc Am Thorac Soc 4:465-8
Song, Zhimin; Marzilli, Lisa; Greenlee, Brian M et al. (2005) Mycobacterial catalase-peroxidase is a tissue antigen and target of the adaptive immune response in systemic sarcoidosis. J Exp Med 201:755-67
Moller, D R (2003) Treatment of sarcoidosis -- from a basic science point of view. J Intern Med 253:31-40
Moller, David R; Chen, Edward S (2002) What causes sarcoidosis? Curr Opin Pulm Med 8:429-34
Chen, E S; Greenlee, B M; Wills-Karp, M et al. (2001) Attenuation of lung inflammation and fibrosis in interferon-gamma-deficient mice after intratracheal bleomycin. Am J Respir Cell Mol Biol 24:545-55
Moller, D R (1999) Cells and cytokines involved in the pathogenesis of sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 16:24-31
Moller, D R (1998) Involvement of T cells and alterations in T cell receptors in sarcoidosis. Semin Respir Infect 13:174-83
Moller, D R (1998) T-cell receptor genes in sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 15:158-64
Moller, D R (1997) Etiology of sarcoidosis. Clin Chest Med 18:695-706