Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia.
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M. Cazzola | P. Arosio | E. Travaglino | G. Bergamaschi | S. Levi | R. Invernizzi | J. Drysdale | B. Corsi | V. Rolandi | G. Biasiotto
[1] M. Cazzola,et al. Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation. , 2002, Blood.
[2] P. Arosio,et al. Human Mitochondrial Ferritin Expressed in HeLa Cells Incorporates Iron and Affects Cellular Iron Metabolism* , 2002, The Journal of Biological Chemistry.
[3] D. Richardson,et al. Erythroid differentiation and protoporphyrin IX down-regulate frataxin expression in Friend cells: characterization of frataxin expression compared to molecules involved in iron metabolism and hemoglobinization. , 2002, Blood.
[4] F. Torti,et al. Regulation of ferritin genes and protein. , 2002, Blood.
[5] N. Andrews,et al. Recent advances in disorders of iron metabolism: mutations, mechanisms and modifiers. , 2001, Human molecular genetics.
[6] P. Arosio,et al. A Human Mitochondrial Ferritin Encoded by an Intronless Gene* , 2001, The Journal of Biological Chemistry.
[7] M Cazzola,et al. Myelodysplastic syndromes: recent advances. , 2001, Haematologica.
[8] M. Cazzola,et al. Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females. , 2000, Blood.
[9] G Flandrin,et al. The World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues. Report of the Clinical Advisory Committee meeting, Airlie House, Virginia, November, 1997. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.
[10] Miyuki Kobayashi,et al. Significance of electron‐dense deposits in the mitochondrial matrix of erythroid precursors in aplastic anaemia and myelodysplastic syndrome , 1999, British journal of haematology.
[11] M. Cazzola,et al. 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. , 1999, Blood.
[12] B. Schlegelberger,et al. Assignment1 of human putative tumor suppressor genes ST13 (alias SNC6) and ST14 (alias SNC19) to human chromosome bands 22q13 and 11q24→q25 by in situ hybridization , 1999, Cytogenetic and Genome Research.
[13] D. Bishop,et al. The molecular biology and pyridoxine responsiveness of X-linked sideroblastic anaemia. , 1998, Haematologica.
[14] P. Ponka. Tissue-specific regulation of iron metabolism and heme synthesis: distinct control mechanisms in erythroid cells. , 1997, Blood.
[15] P. Harrison,et al. The ferritins: molecular properties, iron storage function and cellular regulation. , 1996, Biochimica et biophysica acta.
[16] A. May,et al. The molecular basis of the sideroblastic anemias , 1996, Current opinion in hematology.
[17] A. May,et al. 6 Sideroblastic anaemia , 1994 .
[18] R. Klausner,et al. Regulating the fate of mRNA: The control of cellular iron metabolism , 1993, Cell.
[19] P. Harrison,et al. Evidence of H- and L-chains have co-operative roles in the iron-uptake mechanism of human ferritin. , 1992, The Biochemical journal.
[20] M. Hentze,et al. Coordination of cellular iron metabolism by post-transcriptional gene regulation. , 1992, Journal of inorganic biochemistry.
[21] M. Cazzola,et al. Immunocytochemical detection of ferritin in human bone marrow and peripheral blood cells using monoclonal antibodies specific for the H and L subunit , 1990, British journal of haematology.
[22] N. Gattermann,et al. Two types of acquired idiopathic sideroblastic anaemia (AISA) , 1990, British journal of haematology.
[23] M. Cazzola,et al. Natural history of idiopathic refractory sideroblastic anemia. , 1988, Blood.
[24] P. D. Souza,et al. Erythroblast iron metabolism in sideroblastic marrows , 1982, British journal of haematology.
[25] M. Goossens,et al. DNA analysis in the diagnosis of hemoglobin disorders. , 1981, Methods in enzymology.
[26] Y. Ueda,et al. delta-Aminolevulinic acid synthetase in erythroblasts of patients with pyridoxine-responsive anemia. Hypercatabolism caused by the increased susceptibility to the controlling protease. , 1979, The Journal of clinical investigation.
[27] R. Hillman,et al. Red cell manual , 1974 .
[28] A. Goldberg,et al. The Sideroblastic Anaemias , 1965, Postgraduate medical journal.