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Oncogenes in B-Cell Neoplasia - Workshop at the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA, March 5-7, 1984 (Paperback, Softcover reprint of the original 1st ed. 1984)
Loot Price: R2,937
Discovery Miles 29 370
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Oncogenes in B-Cell Neoplasia - Workshop at the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA, March 5-7, 1984 (Paperback, Softcover reprint of the original 1st ed. 1984)
Series: Current Topics in Microbiology and Immunology, 113
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Michael Potter, Fritz Melchers, Martin Weigert The second workshop
on Mechanisms of B Cell Neoplasia was held in Bethesda, Maryland in
Wilson Hall at the National Institutes of Health on March 5, 6, and
7, 1984. It followed a workshop on the same topic that was held at
the Basel Institute for Immunology, March 15-17, 1983. That first
meeting attempted to bring together cell biologists, experimental
pathologists and molecular geneti- cists interested in B cells, to
discuss pathogenetic processes in the development and maintenance
of the neoplastic state. The impetus for this discussion emanated
from two important developments: first, the discovery of the viral
promoter insertion mechanism for acti- vating the myc oncogene in
bursal lymphomatosis by Hayward, Neil, and Astrin;-second, the
findings that the non-random chromosomal trans locations involving
the immunoglobulin gene chromosomes occur- red in very high
frequencies in murine plasmacytomas and human Burkitt's lymphomas.
During the planning stages of that meeting Shen-Ong et al.
discovered that non-random translocations activated the myc
oncogene. Promoter insertions and non-random trans locations
were-rwo mechanisms that caused transcription of the myc oncogene
messages in three different kinds of well defined experimental and
clinical B cell tumors. Unregulated myc gene transcription provided
the first evidence of a specific bioChemical lesion in B cell neo-
plasia.
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