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MeSH Review

Anemia, Sideroblastic

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  1. Iron overload complicating sideroblastic anemia--is the gene for hemochromatosis responsible? Barron, R., Grace, N.D., Sherwood, G., Powell, L.W. Gastroenterology (1989) [Pubmed]
  2. Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA). Bykhovskaya, Y., Casas, K., Mengesha, E., Inbal, A., Fischel-Ghodsian, N. Am. J. Hum. Genet. (2004) [Pubmed]
  3. Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Allikmets, R., Raskind, W.H., Hutchinson, A., Schueck, N.D., Dean, M., Koeller, D.M. Hum. Mol. Genet. (1999) [Pubmed]
  4. Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation. Bekri, S., Kispal, G., Lange, H., Fitzsimons, E., Tolmie, J., Lill, R., Bishop, D.F. Blood (2000) [Pubmed]
  5. SOD2-deficiency anemia: protein oxidation and altered protein expression reveal targets of damage, stress response, and antioxidant responsiveness. Friedman, J.S., Lopez, M.F., Fleming, M.D., Rivera, A., Martin, F.M., Welsh, M.L., Boyd, A., Doctrow, S.R., Burakoff, S.J. Blood (2004) [Pubmed]
  6. Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: an autosomal recessive syndrome in Persian Jews caused by a mutation in the PUS1 gene. Zeharia, A., Fischel-Ghodsian, N., Casas, K., Bykhocskaya, Y., Tamari, H., Lev, D., Mimouni, M., Lerman-Sagie, T. J. Child Neurol. (2005) [Pubmed]
  7. Treatment of sideroblastic anemia with chloroquine. Drénou, B., Guyader, D., Turlin, B., Fauchet, R. N. Engl. J. Med. (1995) [Pubmed]
  8. X-linked, pyridoxine-responsive sideroblastic anemia. Harris, J.W. N. Engl. J. Med. (1994) [Pubmed]
  9. X-linked pyridoxine-responsive sideroblastic anemia due to a Thr388-to-Ser substitution in erythroid 5-aminolevulinate synthase. Cox, T.C., Bottomley, S.S., Wiley, J.S., Bawden, M.J., Matthews, C.S., May, B.K. N. Engl. J. Med. (1994) [Pubmed]
  10. Erythrocyte pyridoxine kinase levels in patients with sideroblastic anemia. Chillar, R.K., Johnson, C.S., Beutler, E. N. Engl. J. Med. (1976) [Pubmed]
  11. Interaction between succinyl CoA synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia. Furuyama, K., Sassa, S. J. Clin. Invest. (2000) [Pubmed]
  12. The response of a child with primary sideroblastic anemia to cyclophosphamide. Sieff, C.A., Chessells, J.M. Blood (1980) [Pubmed]
  13. Sideroblastic anemia associated with penicillamine therapy. Sullivan, A.L., Burakoff, R., Weintraub, L.R. Arch. Intern. Med. (1981) [Pubmed]
  14. Nutritional anemia in alcoholism. Lindenbaum, J., Roman, M.J. Am. J. Clin. Nutr. (1980) [Pubmed]
  15. Erythroid 5-aminolevulinate synthase is located on the X chromosome. Cox, T.C., Bawden, M.J., Abraham, N.G., Bottomley, S.S., May, B.K., Baker, E., Chen, L.Z., Sutherland, G.R. Am. J. Hum. Genet. (1990) [Pubmed]
  16. Granulocyte colony-stimulating factor inhibits spontaneous cytochrome c release and mitochondria-dependent apoptosis of myelodysplastic syndrome hematopoietic progenitors. Tehranchi, R., Fadeel, B., Forsblom, A.M., Christensson, B., Samuelsson, J., Zhivotovsky, B., Hellstrom-Lindberg, E. Blood (2003) [Pubmed]
  17. Cytogenetic and cytochemical studies on progenitor cells of primary acquired sideroblastic anemia (PASA): involvement of multipotent myeloid stem cells in PASA clone and mosaicism with normal clone. Amenomori, T., Tomonaga, M., Jinnai, I., Soda, H., Nonaka, H., Matsuo, T., Yoshida, Y., Kuriyama, K., Ichimaru, M., Suematsu, T. Blood (1987) [Pubmed]
  18. Sideroblastic anemia recurring during two pregnancies. Jackson, N., Hamizah, I. Int. J. Hematol. (1996) [Pubmed]
  19. Familial sideroblastic anemia with emergence of monosomy 5 and myelodysplastic syndrome. Kardos, G., Veerman, A.J., de Waal, F.C., van Oudheusden, L.J., Slater, R. Med. Pediatr. Oncol. (1996) [Pubmed]
  20. Crystal structure of 5-aminolevulinate synthase, the first enzyme of heme biosynthesis, and its link to XLSA in humans. Astner, I., Schulze, J.O., van den Heuvel, J., Jahn, D., Schubert, W.D., Heinz, D.W. EMBO J. (2005) [Pubmed]
  21. Chloramphenicol-induced mitochondrial dysfunction is associated with decreased transferrin receptor expression and ferritin synthesis in K562 cells and is unrelated to IRE-IRP interactions. Leiter, L.M., Thatte, H.S., Okafor, C., Marks, P.W., Golan, D.E., Bridges, K.R. J. Cell. Physiol. (1999) [Pubmed]
  22. A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia. Bekri, S., May, A., Cotter, P.D., Al-Sabah, A.I., Guo, X., Masters, G.S., Bishop, D.F. Blood (2003) [Pubmed]
  23. Absence of mitochondrial superoxide dismutase results in a murine hemolytic anemia responsive to therapy with a catalytic antioxidant. Friedman, J.S., Rebel, V.I., Derby, R., Bell, K., Huang, T.T., Kuypers, F.A., Epstein, C.J., Burakoff, S.J. J. Exp. Med. (2001) [Pubmed]
  24. Heme deficiency in erythroid lineage causes differentiation arrest and cytoplasmic iron overload. Nakajima, O., Takahashi, S., Harigae, H., Furuyama, K., Hayashi, N., Sassa, S., Yamamoto, M. EMBO J. (1999) [Pubmed]
  25. Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia. Cazzola, M., Invernizzi, R., Bergamaschi, G., Levi, S., Corsi, B., Travaglino, E., Rolandi, V., Biasiotto, G., Drysdale, J., Arosio, P. Blood (2003) [Pubmed]
  26. Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis. Cotter, P.D., May, A., Li, L., Al-Sabah, A.I., Fitzsimons, E.J., Cazzola, M., Bishop, D.F. Blood (1999) [Pubmed]
  27. Nonmyeloablative allogeneic hematopoietic stem cell transplantation for congenital sideroblastic anemia. Medeiros, B.C., Kolhouse, J.F., Cagnoni, P.J., Ryder, J., Nieto, Y., Rabinovitch, R., Shpall, E.J., Bearman, S.I., Jones, R.B., McSweeney, P.A. Bone Marrow Transplant. (2003) [Pubmed]
  28. Vitamin B6 deficiency on hemodialysis causing sideroblastic anemia. Nankivell, B.J. Nephron (1991) [Pubmed]
  29. Histological changes in cardiac hemochromatosis improved by an iron-chelating agent. A biopsy case. Tashiro, A., Satodate, R., Segawa, I. Acta Pathol. Jpn. (1990) [Pubmed]
  30. Molecular cloning and characterization of a novel human putative transmembrane protein homologous to mouse sideroflexin associated with sideroblastic anemia. Zheng, H., Ji, C., Zou, X., Wu, M., Jin, Z., Yin, G., Li, J., Feng, C., Cheng, H., Gu, S., Xie, Y., Mao, Y. DNA Seq. (2003) [Pubmed]
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