Mapping the gene for sex-linked anemia: An inherited defect of intestinal iron absorption in the mouse

Genomics

Volumn 48, Issue 1, 1998, Pages 34-39

  Anderson, Gregory J ^a,b   Murphy, Therese L ^a,b   Cowley, Lex ^a,b   Evans, Betty A ^a,b   Halliday, June W ^a,b   McLaren, Gordon D ^a,b  

^a ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

^b UNIVERSITY OF NORTH DAKOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ANEMIA; ANIMAL MODEL; ARTICLE; GENE LOCUS; GENE MAPPING; GENETIC DISORDER; GENETIC LINKAGE; INTESTINE ABSORPTION; IRON ABSORPTION; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER; X CHROMOSOME RECESSIVE DISORDER;

EID: 0031952314     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5138     Document Type: Article

References (22)

1. Bannerman R. M., Cooper R. G. Sex-linked anemia: A hypochromic anemia of mice. Science. 151:1966;581-582.
2. Bannerman R. M., Edwards J. A., Pinkerton P. H. Hereditary disorders of the red cell in animals. Prog. Hematol. 8:1973;131-179.
3. Bannerman R. M., Pinkerton P. H. X-linked hypochromic anemia of mice. Br.J.Haematol. 13:1967;1000-1013.
4. Bothwell T. H., Charlton R. W., Cook J. D., Finch C. A. Iron Metabolism in Man. 1979;. p. 256-283.
5. Copeland N. G., Gilbert D. J., Jenkins N. A., Nadeau J. H., Eppig J. T., Maltais L. J., Miller J. C., Dietrich W. F., Steen R. G., Lincoln S. E., Weaver A., Joyce D. C., Merchant M., Wessel M., Katz H., Stein L. D., Reeve M. P., Daly M. J., Dregde R. D., Marquis A., Goodman N., Lander E. S. Genome maps IV. Science. 262:1993;67.
6. Davis L. G., Dibner M. D., Battey J. F. Basic Methods in Molecular Biology. 1986;Elsevier, New York. p. 42-43.
7. Dietrich W. F., Katz H., Lincoln S., Shin H.-S., Friedman J., Dracopoli N. C., Lander E. A genetic map of the mouse suitable for typing intraspecific crosses. Genetics. 131:1992;423-447.
8. Dietrich W. F., Miller J. C., Steen R. G., Merchant M., Damron D., Nahf R., Gross A., Joyce D. C., Wessel M., Dredge R. D., Marquis A., Stein L., Goodman N., Page D. C., Lander E. S. A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nat. Genet. 7:1994;220-245.
9. Edwards J. A., Bannerman R. M. Hereditary defect of intestinal iron transport in mice with sex-linked anemia. J. Clin. Invest. 49:1970;1869-1871.
10. Falconer D. S., Isaacson J. H. The genetics of sex-linked anaemia in the mouse. Genet.Res. 3:1962;248-250.
11. Farcich E. A., Morgan E. H. Diminished iron acquisition by cells and tissues of Belgrade laboratory rats. Am. J. Physiol. 262:1992;R220-R224.
12. Feder J. N., Gnirke A., Thomas W., Tsuchihashi Z., Ruddy D. A., Basava A., Dormishian F., Domingo R., Ellis M. C., Fullan A., Hinton L. M., Jones N. L., Kimmel B. E., Kronmal G. S., Lauer P., Lee P. K., Loeb D. B., Mapa F. A., McLelland E., Meyer N. C., Mintier G. A., Moeller N., Moore N., Morikang E., Prass C. E., Quintana L., Starnes S. M., Schatzman R. C., Brunke K. J., Drayna D. T., Risch N. J., Bacon B. R., Wolff R. K. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat. Genet. 13:1996;399-408.
13. Fleming M. D., Trenor C. C., Su M. A., Foernzler D., Beier D. R., Dietrich W. F., Andrews N. C. Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transport gene. Nat. Genet. 16:1997;383-386.
14. Green M. C. Gene mapping. The Mouse in Biomedical Research. 1981;Academic Press, New York.
15. Grewal M. S. A sex-linked anemia in the mouse. Genet.Res. 3:1962;238-247.
16. Gunshin H., Mackenzie B., Berger U. V., Gunshin Y., Romero M. F., Boron W. F., Nussberger S., Gollan J. L., Hediger M. A. Cloning and characterization of a mammalian proton-coupled metal-ion transporter. Nature. 388:1997;482-488.
17. Halliday J. W., Powell L. W. Hemochromatosis and other diseases of iron overload. Lauffer R. B. Iron and Human Disease. 1992;CRC Press, Boca Raton.
18. Hartman K. R. Microcytic anaemia with iron malabsorption. Blood. 84:1994;19a.
19. Manis J. Intestinal iron transport defect in the mouse with sex-linked anemia. Am.J.Physiol. 220:1971;135-139.
20. Pinkerton P. H., Bannerman R. M. Hereditary defect in iron absorption in mice. Nature. 216:1967;482-483.
21. Russell E. S. Hereditary anemias of the mouse: A review for geneticists. Adv.Genet. 20:1979;357-459.
22. Skikne B. S., Baynes R. D. Iron absorption. Brock J. H., Halliday J. W., Pippard M. J., Powell L. W. Iron Metabolism in Health and Disease. 1994;Saunders, London.