This Program Project is a multi-disciplinary research effort focused on understanding the genetics, expression, and function of human immune receptor genes and proteins. Major emphasis is on how immunoreceptor genes and lymphoid-specific oncogenes are regulated, mutated, and function. In some instances the studies are on deliberately produced hybridomas, in others, on spontaneous transformations which occur during human malignancies such as acute and chronic lymphatic leukemia, in others, viral transformants are used. Three projects are proposed, bringing together three independent investigators around three core components. One core laboratory provides cell culture facilities for all members of the Program Project. A second core provides molecular biology expertise, while a third core is an administrative unit.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA044016-05
Application #
3094110
Study Section
Special Emphasis Panel (SRC (A2))
Project Start
1987-09-01
Project End
1996-11-30
Budget Start
1992-12-01
Budget End
1993-11-30
Support Year
5
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
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Andris, J S; Brodeur, B R; Capra, J D (1993) Molecular characterization of human antibodies to bacterial antigens: utilization of the less frequently expressed VH2 and VH6 heavy chain variable region gene families. Mol Immunol 30:1601-16
Baer, R (1993) TAL1, TAL2 and LYL1: a family of basic helix-loop-helix proteins implicated in T cell acute leukaemia. Semin Cancer Biol 4:341-7
Potter, K N; Li, Y; Pascual, V et al. (1993) Molecular characterization of a cross-reactive idiotope on human immunoglobulins utilizing the VH4-21 gene segment. J Exp Med 178:1419-28
Cai, J; Humphries, C; Lutz, C et al. (1992) Analysis of VH251 gene mutation in chronic lymphocytic leukemia (CLL) and normal B-cell subsets. Ann N Y Acad Sci 651:384-92

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