The Role of the Iron Transporter ABCB7 in Refractory Anemia with Ring Sideroblasts
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Luca Malcovati | Eva Hellström-Lindberg | Mario Cazzola | James S. Wainscoat | Maryam Nikpour | M. Cazzola | M. Jädersten | E. Hellström-Lindberg | J. Boultwood | D. Bowen | L. Malcovati | A. Pellagatti | A. Giagounidis | S. Killick | J. Wainscoat | M. D. Della Porta | T. Littlewood | Beena Pushkaran | Andrea Pellagatti | Jacqueline Boultwood | Martin Jädersten | Beena Pushkaran | Carrie Fidler | Helen Cattan | Tim J. Littlewood | Matteo G. Della Porta | Sally Killick | Aristoteles Giagounidis | David Bowen | C. Fidler | H. Cattan | M. Nikpour | Helen Cattan
[1] M. Eichelbaum,et al. Transcriptional profiling of genes induced in the livers of patients treated with carbamazepine , 2006, Clinical pharmacology and therapeutics.
[2] D. Reinberg,et al. Human Elongator facilitates RNA polymerase II transcription through chromatin , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[3] B. Sander,et al. Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q− syndrome patients , 2007, Proceedings of the National Academy of Sciences.
[4] P. Arosio,et al. causes an iron-deficient phenotype with mitochondrial iron overload RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells , 2009 .
[5] B. Guiard,et al. The ABC transporter Atm1p is required for mitochondrial iron homeostasis , 1997, FEBS letters.
[6] B. Zhivotovsky,et al. Granulocyte colony-stimulating factor inhibits spontaneous cytochrome c release and mitochondria-dependent apoptosis of myelodysplastic syndrome hematopoietic progenitors. , 2003, Blood.
[7] Michael B. Stadler,et al. Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome , 2007, Nature Genetics.
[8] K. Furuyama,et al. Multiple mechanisms for hereditary sideroblastic anemia. , 2002, Cellular and molecular biology.
[9] M. Cazzola,et al. Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia. , 2003, Blood.
[10] Li Wang,et al. Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype. , 2006, Blood.
[11] M. Fleming,et al. Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis. , 2007, Blood.
[12] P. Nguyen,et al. Myelodysplastic syndromes , 2009, Nature Reviews Disease Primers.
[13] M. Pembrey,et al. Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation. , 1970, Lancet.
[14] Nevan J. Krogan,et al. Characterization of a Six-Subunit Holo-Elongator Complex Required for the Regulated Expression of a Group of Genes in Saccharomyces cerevisiae , 2001, Molecular and Cellular Biology.
[15] C. Langford,et al. Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS) , 2003, Nature Genetics.
[16] A. Hutchinson,et al. Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) , 1999, Human molecular genetics.
[17] Hines Jd,et al. The sideroblastic anemias. , 1970 .
[18] I. Bernát Sándor,et al. [Sideroblastic anemias]. , 1991, Orvosi hetilap.
[19] T. Fujiwara,et al. Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia , 1998, Journal of Human Genetics.
[20] D. Bishop,et al. X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley. , 1994, Blood.
[21] H. Gralnick,et al. Proposals for the classification of the myelodysplastic syndromes , 1982, British journal of haematology.
[22] Kelli L. Roinick,et al. Rtf1 Is a Multifunctional Component of the Paf1 Complex That Regulates Gene Expression by Directing Cotranscriptional Histone Modification , 2007, Molecular and Cellular Biology.
[23] J. Tolmie,et al. Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation. , 2000, Blood.
[24] Thomas D. Schmittgen,et al. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.
[25] D. Steensma,et al. Candidate gene mutation analysis in idiopathic acquired sideroblastic anemia (refractory anemia with ringed sideroblasts). , 2007, Leukemia research.
[26] R. Latagliata,et al. Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodyplastic syndromes. , 2006, Leukemia research.