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Volumn 143, Issue 3, 2008, Pages 446-450

Purification and characterization of sideroblasts from patients with acquired and hereditary sideroblastic anaemia

Author keywords

Iron overload; Mitochondria; Myelodysplastic syndromes; Oxidative stress; Sideroblastic anaemia

Indexed keywords

GLYCOPHORIN A; MANGANESE SUPEROXIDE DISMUTASE; REACTIVE OXYGEN METABOLITE; TRANSFERRIN RECEPTOR;

EID: 54049135327     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2008.07358.x     Document Type: Letter
Times cited : (4)

References (10)
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    • 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. (1999) Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Human Molecular Genetics, 8, 743 749.
    • (1999) Human Molecular Genetics , vol.8 , pp. 743-749
    • Allikmets, R.1    Raskind, W.H.2    Hutchinson, A.3    Schueck, N.D.4    Dean, M.5    Koeller, D.M.6
  • 2
    • 2442691791 scopus 로고    scopus 로고
    • 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. (2004) Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA). American Journal of Human Genetics, 74, 1303 1308.
    • (2004) American Journal of Human Genetics , vol.74 , pp. 1303-1308
    • Bykhovskaya, Y.1    Casas, K.2    Mengesha, E.3    Inbal, A.4    Fischel-Ghodsian, N.5
  • 4
    • 0028148438 scopus 로고
    • X-linked sideroblastic anemia: Identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley
    • Cotter, P.D., Rucknagel, D.L. Bishop, D.F. (1994) X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley. Blood, 84, 3915 3924.
    • (1994) Blood , vol.84 , pp. 3915-3924
    • Cotter, P.D.1    Rucknagel, D.L.2    Bishop, D.F.3
  • 5
    • 0034142678 scopus 로고    scopus 로고
    • From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes
    • Gattermann, N. (2000) From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes. Leukemia Research, 24, 141 151.
    • (2000) Leukemia Research , vol.24 , pp. 141-151
    • Gattermann, N.1
  • 9
    • 0038281403 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in patients with myelodysplastic syndromes
    • Shin, M.G., Kajigaya, S., Levin, B.C. Young, N.S. (2003) Mitochondrial DNA mutations in patients with myelodysplastic syndromes. Blood, 101, 3118 3125.
    • (2003) Blood , vol.101 , pp. 3118-3125
    • Shin, M.G.1    Kajigaya, S.2    Levin, B.C.3    Young, N.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.