Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Institutional National Research Service Award (T32)
Project #
5T32AI007238-04
Application #
3530997
Study Section
Microbiology and Infectious Diseases Research Committee (MID)
Project Start
1982-08-01
Project End
1987-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Langkamp-Henken, B; Geller, A M; LeGros Jr, H L et al. (1994) Characterization of distinct forms of methionine adenosyltransferase in nucleated, and mature human erythrocytes and erythroleukemic cells. Biochim Biophys Acta 1201:397-404
Marion, T N; Tillman, D M; Krishnan, M K et al. (1994) Immunoglobulin variable-region structures in immunity and autoimmunity to DNA. Tohoku J Exp Med 173:43-63
Kaufman, M R; Shaw, C E; Jones, I D et al. (1993) Biogenesis and regulation of the Vibrio cholerae toxin-coregulated pilus: analogies to other virulence factor secretory systems. Gene 126:43-9
Majumdar, G; Ohnishi, H; Tomai, M A et al. (1993) Role of antigen-presenting cells in activation of human T cells by the streptococcal M protein superantigen: requirement for secreted and membrane-associated costimulatory factors. Infect Immun 61:785-90
Desai, D D; Krishnan, M R; Swindle, J T et al. (1993) Antigen-specific induction of antibodies against native mammalian DNA in nonautoimmune mice. J Immunol 151:1614-26
Krishnan, M R; Marion, T N (1993) Structural similarity of antibody variable regions from immune and autoimmune anti-DNA antibodies. J Immunol 150:4948-57
Peek, J A; Taylor, R K (1992) Characterization of a periplasmic thiol:disulfide interchange protein required for the functional maturation of secreted virulence factors of Vibrio cholerae. Proc Natl Acad Sci U S A 89:6210-4
Tomai, M A; Beachey, E H; Majumdar, G et al. (1992) Metabolically active antigen presenting cells are required for human T cell proliferation in response to the superantigen streptococcal M protein. FEMS Microbiol Immunol 4:155-64
Tomai, M A; Aelion, J A; Dockter, M E et al. (1991) T cell receptor V gene usage by human T cells stimulated with the superantigen streptococcal M protein. J Exp Med 174:285-8
Kaufman, M R; Seyer, J M; Taylor, R K (1991) Processing of TCP pilin by TcpJ typifies a common step intrinsic to a newly recognized pathway of extracellular protein secretion by gram-negative bacteria. Genes Dev 5:1834-46

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