메뉴 건너뛰기




Volumn 3, Issue 4, 2008, Pages

The role of the iron transporter ABCB7 in Refractory Anemia with Ring Sideroblasts

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABCB7 TRANSPORTER; ABCB7 PROTEIN, HUMAN; CD34 ANTIGEN;

EID: 44849143798     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0001970     Document Type: Article
Times cited : (107)

References (26)
  • 3
    • 0037372442 scopus 로고    scopus 로고
    • Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
    • Cazzola M, Invernizzi R, Bergamaschi G, Levi S, Corsi B, et al. (2003) Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia. Blood 101: 1996-2000.
    • (2003) Blood , vol.101 , pp. 1996-2000
    • Cazzola, M.1    Invernizzi, R.2    Bergamaschi, G.3    Levi, S.4    Corsi, B.5
  • 4
    • 28844463547 scopus 로고    scopus 로고
    • Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodyplastic syndromes
    • Breccia M, Carmosino I, Biondo F, Mancini M, Russo E, et al. (2006) Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodyplastic syndromes. Leuk Res 30: 178-182.
    • (2006) Leuk Res , vol.30 , pp. 178-182
    • Breccia, M.1    Carmosino, I.2    Biondo, F.3    Mancini, M.4    Russo, E.5
  • 6
    • 0014940544 scopus 로고
    • Familial sideroblastic anaemia: Problem of Xg and X chromosome inactivation
    • Weatherall DJ, Pembrey ME, Hall EG, Sanger R, Tippett P, et al. (1970) Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation. Lancet 2: 744-748.
    • (1970) Lancet , vol.2 , pp. 744-748
    • Weatherall, D.J.1    Pembrey, M.E.2    Hall, E.G.3    Sanger, R.4    Tippett, P.5
  • 7
    • 0036483546 scopus 로고    scopus 로고
    • Multiple mechanisms for hereditary sideroblastic anemia
    • Furuyama K, Sassa S (2002) Multiple mechanisms for hereditary sideroblastic anemia. Cell Mol Biol (Noisy-le-grand) 48: 5-10.
    • (2002) Cell Mol Biol (Noisy-le-grand) , vol.48 , pp. 5-10
    • Furuyama, K.1    Sassa, S.2
  • 8
    • 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 PD, Rucknagel DL, Bishop DF (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
  • 9
    • 0034329310 scopus 로고    scopus 로고
    • 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, et al. (2000) Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation. Blood 96: 3256-3264.
    • (2000) Blood , vol.96 , pp. 3256-3264
    • Bekri, S.1    Kispal, G.2    Lange, H.3    Fitzsimons, E.4    Tolmie, J.5
  • 10
    • 0032920837 scopus 로고    scopus 로고
    • Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)
    • Allikmets R, Raskind WH, Hutchinson A, Schueck ND, Dean M, et al. (1999) Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Hum Mol Genet 8: 743-749.
    • (1999) Hum Mol Genet , vol.8 , pp. 743-749
    • Allikmets, R.1    Raskind, W.H.2    Hutchinson, A.3    Schueck, N.D.4    Dean, M.5
  • 11
    • 0031616020 scopus 로고    scopus 로고
    • Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia
    • Shimada Y, Okuno S, Kawai A, Shinomiya H, Saito A, et al. (1998) Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia. J Hum Genet 43: 115-122.
    • (1998) J Hum Genet , vol.43 , pp. 115-122
    • Shimada, Y.1    Okuno, S.2    Kawai, A.3    Shinomiya, H.4    Saito, A.5
  • 12
    • 0030608677 scopus 로고    scopus 로고
    • The ABC transporter Atm1p is required for mitochondrial iron homeostasis
    • Kispal G, Csere P, Guiard B, Lill R (1997) The ABC transporter Atm1p is required for mitochondrial iron homeostasis. FEBS Lett 418: 346-350.
    • (1997) FEBS Lett , vol.418 , pp. 346-350
    • Kispal, G.1    Csere, P.2    Guiard, B.3    Lill, R.4
  • 13
    • 34147158934 scopus 로고    scopus 로고
    • Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis
    • Pondarre C, Campagna DR, Antiochos B, Sikorskii L, Mulhern H, et al. (2007) Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis. Blood 109: 3567-3569.
    • (2007) Blood , vol.109 , pp. 3567-3569
    • Pondarre, C.1    Campagna, D.R.2    Antiochos, B.3    Sikorskii, L.4    Mulhern, H.5
  • 14
    • 34147165135 scopus 로고    scopus 로고
    • RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload
    • Cavadini P, Biasiotto G, Poli M, Levi S, Verudi R, et al. (2007) RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload. Blood 109: 3552-3559.
    • (2007) Blood , vol.109 , pp. 3552-3559
    • Cavadini, P.1    Biasiotto, G.2    Poli, M.3    Levi, S.4    Verudi, R.5
  • 16
    • 34547474047 scopus 로고    scopus 로고
    • Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q- syndrome patients
    • Pellagatti A, Jadersten M, Forsblom AM, Cattan H, Christensson B, et al. (2007) Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q- syndrome patients. Proc Natl Acad Sci U S A 104: 11406-11411.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 11406-11411
    • Pellagatti, A.1    Jadersten, M.2    Forsblom, A.M.3    Cattan, H.4    Christensson, B.5
  • 17
    • 0037307728 scopus 로고    scopus 로고
    • Granulocyte colony-stimulating factor inhibits spontaneous cytochrome c release and mitochandria-dependent apoptosis of myelodysplastic syndrome hematopoietic progenitors
    • Tehranchi R, Fadeel B, Forsblom AM, Christensson B, Samuelsson J, et al. (2003) Granulocyte colony-stimulating factor inhibits spontaneous cytochrome c release and mitochandria-dependent apoptosis of myelodysplastic syndrome hematopoietic progenitors. Blood 101: 1080-1086.
    • (2003) Blood , vol.101 , pp. 1080-1086
    • Tehranchi, R.1    Fadeel, B.2    Forsblom, A.M.3    Christensson, B.4    Samuelsson, J.5
  • 18
    • 33745615399 scopus 로고    scopus 로고
    • Gene expression profiles of CD346+ cells in myelodysplastic syndromes: Involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype
    • Pellagatti A, Cazzola M, Giagounidis AA, Malcovati L, Porta MG, et al. (2006) Gene expression profiles of CD346+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype. Blood 108: 337-345.
    • (2006) Blood , vol.108 , pp. 337-345
    • Pellagatti, A.1    Cazzola, M.2    Giagounidis, A.A.3    Malcovati, L.4    Porta, M.G.5
  • 19
    • 0035710746 scopus 로고    scopus 로고
    • Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta CM) Method
    • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta CM) Method. Methods 25: 402-408.
    • (2001) Methods , vol.25 , pp. 402-408
    • Livak, K.J.1    Schmittgen, T.D.2
  • 20
    • 34147171967 scopus 로고    scopus 로고
    • Candidate gene mutation analysis in idiopathic acquired sideroblastic anemia (refractory anemia with ringed sideroblasts)
    • Steensma DP, Hecksel KA, Porcher JC, Lasho TL (2007) Candidate gene mutation analysis in idiopathic acquired sideroblastic anemia (refractory anemia with ringed sideroblasts). Leek Res 31: 623-628.
    • (2007) Leek Res , vol.31 , pp. 623-628
    • Steensma, D.P.1    Hecksel, K.A.2    Porcher, J.C.3    Lasho, T.L.4
  • 21
    • 34047116826 scopus 로고    scopus 로고
    • Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
    • Weber M, Hellmann I, Stadler MB, Ramos L, Paabo S, et al. (2007) Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat Genet 39: 457-466.
    • (2007) Nat Genet , vol.39 , pp. 457-466
    • Weber, M.1    Hellmann, I.2    Stadler, M.B.3    Ramos, L.4    Paabo, S.5
  • 22
    • 20244389965 scopus 로고    scopus 로고
    • Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS)
    • Gibbons RJ, Pellagatti A, Garrick D, Wood WG, Malik N, et al. (2003) Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS). Nat Genet 34: 446-449.
    • (2003) Nat Genet , vol.34 , pp. 446-449
    • Gibbons, R.J.1    Pellagatti, A.2    Garrick, D.3    Wood, W.G.4    Malik, N.5
  • 23
    • 34548221891 scopus 로고    scopus 로고
    • Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional historic modification
    • Warner MH, Roinick KL, Arndt KM (2007) Rtf1 is a multifunctional component of the Paf1 complex that regulates gene expression by directing cotranscriptional historic modification. Mol Cell Biol 27: 6103-6115.
    • (2007) Mol Cell Biol , vol.27 , pp. 6103-6115
    • Warner, M.H.1    Roinick, K.L.2    Arndt, K.M.3
  • 24
    • 0035171624 scopus 로고    scopus 로고
    • Characterization of a six-subunit holoelongator complex required for the regulated expression of a group of genes in Saccharomyces cerevisiae
    • Krogan NJ, Greenblatt JF (2001) Characterization of a six-subunit holoelongator complex required for the regulated expression of a group of genes in Saccharomyces cerevisiae. Mol Cell Biol 21: 8203-8212.
    • (2001) Mol Cell Biol , vol.21 , pp. 8203-8212
    • Krogan, N.J.1    Greenblatt, J.F.2
  • 25
    • 0037022226 scopus 로고    scopus 로고
    • Human Elongator facilitates RNA polymerase II transcription through chromatin
    • Kim JH, Lane WS, Reinberg D (2002) Human Elongator facilitates RNA polymerase II transcription through chromatin. Proc Natl Acad Sci U S A 99: 1241-1246.
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 1241-1246
    • Kim, J.H.1    Lane, W.S.2    Reinberg, D.3
  • 26
    • 33751092279 scopus 로고    scopus 로고
    • Transcriptional profiling of genes induced in the livers of patients treated with carbamazepine
    • Oscarson M, Zanger UM, Rifki OF, Klein K, Eichelbaum M, et al. (2006) Transcriptional profiling of genes induced in the livers of patients treated with carbamazepine. Clin Pharmacol Ther 80: 440-456.
    • (2006) Clin Pharmacol Ther , vol.80 , pp. 440-456
    • Oscarson, M.1    Zanger, U.M.2    Rifki, O.F.3    Klein, K.4    Eichelbaum, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.