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Title: Inborn anemias in mice. Progress report, 1 August 1979-15 July 1980

Technical Report ·
DOI:https://doi.org/10.2172/6638920· OSTI ID:6638920

Four macrocytic anemias, four hemolytic anemias, nonhemolytic microcytic anemia, transitory siderocytic anemia, sex-linked iron-transport anemia, an ..cap alpha..-thalassemia, and a new target-cell anemia are under investigation in mice. Each of these blood dyscrasias is caused by the action of a unique mutant gene, which determines the structure of different intracellular molecules, and thus controls a different metabolic process. Thus the wide range of different hereditary anemias has considerable potential for uncovering many different aspects of hemopoietic homeostatic mechanisms in the mouse. Each anemia is studied through: (a) characterization of peripheral blood values; (b) determinations of radiosensitivity under a variety of conditions; (c) measurements of iron metabolism and heme synthesis; (d) histological and biochemical study of blood-forming tissue; (e) functional tests of the stem cell component; (f) examination of responses to erythroid stimuli; and (g) transplantation of tissue between individuals of differently affected genotypes.

Research Organization:
Jackson Lab., Bar Harbor, ME (USA)
DOE Contract Number:
AS02-76EV03264
OSTI ID:
6638920
Report Number(s):
DOE/EV/03264-19
Country of Publication:
United States
Language:
English