-
1
-
-
0002341637
-
A series of cases of splenomegaly in children with anemia and peculiar bone changes
-
Cooley T.B., Lee P. A series of cases of splenomegaly in children with anemia and peculiar bone changes. Trans Am Pediatr Soc 1925, 37:29.
-
(1925)
Trans Am Pediatr Soc
, vol.37
, pp. 29
-
-
Cooley, T.B.1
Lee, P.2
-
2
-
-
0034605653
-
Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases
-
Weatherall D.J. Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases. BMJ 2000, 321(7269):1117-1120.
-
(2000)
BMJ
, vol.321
, Issue.7269
, pp. 1117-1120
-
-
Weatherall, D.J.1
-
3
-
-
0035320886
-
Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias
-
Weatherall D.J. Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias. Nat Rev Genet 2001, 2(4):245-255.
-
(2001)
Nat Rev Genet
, vol.2
, Issue.4
, pp. 245-255
-
-
Weatherall, D.J.1
-
4
-
-
0000844285
-
Molecular mechanisms of β thalassemia
-
Cambridge University Press, Cambridge (UK), M.H. Steinberg, B.G. Forget, D.R. Higgs (Eds.)
-
Forget B.G. Molecular mechanisms of β thalassemia. Disorders of hemoglobin: genetics, pathophysiology and clinical management 2001, 252-276. Cambridge University Press, Cambridge (UK). M.H. Steinberg, B.G. Forget, D.R. Higgs (Eds.).
-
(2001)
Disorders of hemoglobin: genetics, pathophysiology and clinical management
, pp. 252-276
-
-
Forget, B.G.1
-
5
-
-
84932616635
-
-
Cambridge University Press, Cambridge (UK)
-
Steinberg M.H., Forget B.G., Higgs D.R., et al. Disorders of hemoglobin: genetics, pathophysiology and clinical management 2009, Cambridge University Press, Cambridge (UK), p. 1-826. 2nd edition.
-
(2009)
Disorders of hemoglobin: genetics, pathophysiology and clinical management
, pp. 1-826
-
-
Steinberg, M.H.1
Forget, B.G.2
Higgs, D.R.3
-
6
-
-
0021257787
-
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinians
-
Cao A., Pintus L., Lecca U., et al. Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinians. Clin Genet 1984, 26(1):12-22.
-
(1984)
Clin Genet
, vol.26
, Issue.1
, pp. 12-22
-
-
Cao, A.1
Pintus, L.2
Lecca, U.3
-
7
-
-
0031851068
-
The morbidity of bone disease in thalassemia
-
Vichinsky E.P. The morbidity of bone disease in thalassemia. Ann N Y Acad Sci 1998, 850:344-348.
-
(1998)
Ann N Y Acad Sci
, vol.850
, pp. 344-348
-
-
Vichinsky, E.P.1
-
8
-
-
0034773091
-
Clinical management of beta-thalassemia major
-
Wonke B. Clinical management of beta-thalassemia major. Semin Hematol 2001, 38(4):350-359.
-
(2001)
Semin Hematol
, vol.38
, Issue.4
, pp. 350-359
-
-
Wonke, B.1
-
10
-
-
0028823093
-
The management of patients with Cooley's anemia: transfusions and splenectomy
-
Piomelli S. The management of patients with Cooley's anemia: transfusions and splenectomy. Semin Hematol 1995, 32(4):262-268.
-
(1995)
Semin Hematol
, vol.32
, Issue.4
, pp. 262-268
-
-
Piomelli, S.1
-
11
-
-
0034783438
-
Chelation therapy in beta-thalassemia: an optimistic update
-
Giardina P.J., Grady R.W. Chelation therapy in beta-thalassemia: an optimistic update. Semin Hematol 2001, 38(4):360-366.
-
(2001)
Semin Hematol
, vol.38
, Issue.4
, pp. 360-366
-
-
Giardina, P.J.1
Grady, R.W.2
-
12
-
-
70449468812
-
Vascular complications after splenectomy for hematologic disorders
-
Crary S.E., Buchanan G.R. Vascular complications after splenectomy for hematologic disorders. Blood 2009, 114(14):2861-2868.
-
(2009)
Blood
, vol.114
, Issue.14
, pp. 2861-2868
-
-
Crary, S.E.1
Buchanan, G.R.2
-
13
-
-
0036092892
-
The hypercoagulable state in thalassemia
-
Eldor A., Rachmilewitz E.A. The hypercoagulable state in thalassemia. Blood 2002, 99(1):36-43.
-
(2002)
Blood
, vol.99
, Issue.1
, pp. 36-43
-
-
Eldor, A.1
Rachmilewitz, E.A.2
-
14
-
-
41449094655
-
Stroke in thalassemia: a dilemma
-
Taher A., Mehio G., Isma'eel H., et al. Stroke in thalassemia: a dilemma. Am J Hematol 2008, 83(4):343.
-
(2008)
Am J Hematol
, vol.83
, Issue.4
, pp. 343
-
-
Taher, A.1
Mehio, G.2
Isma'eel, H.3
-
15
-
-
77953372767
-
Future alternative therapies for beta-thalassemia
-
Rivella S., Rachmilewitz E. Future alternative therapies for beta-thalassemia. Expert Rev Hematol 2009, 2(6):685.
-
(2009)
Expert Rev Hematol
, vol.2
, Issue.6
, pp. 685
-
-
Rivella, S.1
Rachmilewitz, E.2
-
17
-
-
0020564074
-
A mouse model for beta-thalassemia
-
Skow L.C., Burkhart B.A., Johnson F.M., et al. A mouse model for beta-thalassemia. Cell 1983, 34(3):1043-1052.
-
(1983)
Cell
, vol.34
, Issue.3
, pp. 1043-1052
-
-
Skow, L.C.1
Burkhart, B.A.2
Johnson, F.M.3
-
18
-
-
0023007966
-
Compensatory increase in levels of beta minor globin in murine beta-thalassemia is under translational control
-
Curcio M.J., Kantoff P., Schafer M.P., et al. Compensatory increase in levels of beta minor globin in murine beta-thalassemia is under translational control. J Biol Chem 1986, 261(34):16126-16132.
-
(1986)
J Biol Chem
, vol.261
, Issue.34
, pp. 16126-16132
-
-
Curcio, M.J.1
Kantoff, P.2
Schafer, M.P.3
-
19
-
-
33750033613
-
Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia
-
De Franceschi L., Daraio F., Filippini A., et al. Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia. Haematologica 2006, 91(10):1336-1342.
-
(2006)
Haematologica
, vol.91
, Issue.10
, pp. 1336-1342
-
-
De Franceschi, L.1
Daraio, F.2
Filippini, A.3
-
20
-
-
0029589914
-
A mouse model for beta 0-thalassemia
-
Yang B., Kirby S., Lewis J., et al. A mouse model for beta 0-thalassemia. Proc Natl Acad Sci U S A 1995, 92(25):11608-11612.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, Issue.25
, pp. 11608-11612
-
-
Yang, B.1
Kirby, S.2
Lewis, J.3
-
21
-
-
0029045603
-
Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells
-
Ciavatta D.J., Ryan T.M., Farmer S.C., et al. Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells. Proc Natl Acad Sci U S A 1995, 92(20):9259-9263.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, Issue.20
, pp. 9259-9263
-
-
Ciavatta, D.J.1
Ryan, T.M.2
Farmer, S.C.3
-
22
-
-
0037606048
-
A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human beta -globin gene transfer
-
Rivella S., May C., Chadburn A., et al. A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human beta -globin gene transfer. Blood 2003, 101(8):2932-2939.
-
(2003)
Blood
, vol.101
, Issue.8
, pp. 2932-2939
-
-
Rivella, S.1
May, C.2
Chadburn, A.3
-
23
-
-
0028880455
-
Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor
-
Wu H., Liu X., Jaenisch R., et al. Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor. Cell 1995, 83(1):59-67.
-
(1995)
Cell
, vol.83
, Issue.1
, pp. 59-67
-
-
Wu, H.1
Liu, X.2
Jaenisch, R.3
-
24
-
-
0025029837
-
Erythropoietin receptor: cloning strategy and structural features
-
D'Andrea A., Fasman G., Wong G., et al. Erythropoietin receptor: cloning strategy and structural features. Int J Cell Cloning 1990, 8(Suppl 1):173-180.
-
(1990)
Int J Cell Cloning
, vol.8
, Issue.SUPPL. 1
, pp. 173-180
-
-
D'Andrea, A.1
Fasman, G.2
Wong, G.3
-
25
-
-
0024563574
-
Expression cloning of the murine erythropoietin receptor
-
D'Andrea A.D., Lodish H.F., Wong G.G. Expression cloning of the murine erythropoietin receptor. Cell 1989, 57(2):277-285.
-
(1989)
Cell
, vol.57
, Issue.2
, pp. 277-285
-
-
D'Andrea, A.D.1
Lodish, H.F.2
Wong, G.G.3
-
26
-
-
0142135175
-
Roles for an Epo receptor Tyr-343 Stat5 pathway in proliferative co-signaling with kit
-
Li K., Miller C., Hegde S., et al. Roles for an Epo receptor Tyr-343 Stat5 pathway in proliferative co-signaling with kit. J Biol Chem 2003, 278(42):40702-40709.
-
(2003)
J Biol Chem
, vol.278
, Issue.42
, pp. 40702-40709
-
-
Li, K.1
Miller, C.2
Hegde, S.3
-
27
-
-
33645525963
-
Core erythropoietin receptor signals for late erythroblast development
-
Menon M.P., Fang J., Wojchowski D.M. Core erythropoietin receptor signals for late erythroblast development. Blood 2006, 107(7):2662-2672.
-
(2006)
Blood
, vol.107
, Issue.7
, pp. 2662-2672
-
-
Menon, M.P.1
Fang, J.2
Wojchowski, D.M.3
-
28
-
-
33644647514
-
Signals for stress erythropoiesis are integrated via an erythropoietin receptor-phosphotyrosine-343-Stat5 axis
-
Menon M.P., Karur V., Bogacheva O., et al. Signals for stress erythropoiesis are integrated via an erythropoietin receptor-phosphotyrosine-343-Stat5 axis. J Clin Invest 2006, 116(3):683-694.
-
(2006)
J Clin Invest
, vol.116
, Issue.3
, pp. 683-694
-
-
Menon, M.P.1
Karur, V.2
Bogacheva, O.3
-
29
-
-
0033566296
-
The glucocorticoid receptor cooperates with the erythropoietin receptor and c-Kit to enhance and sustain proliferation of erythroid progenitors in vitro
-
von Lindern M., Zauner W., Mellitzer G., et al. The glucocorticoid receptor cooperates with the erythropoietin receptor and c-Kit to enhance and sustain proliferation of erythroid progenitors in vitro. Blood 1999, 94(2):550-559.
-
(1999)
Blood
, vol.94
, Issue.2
, pp. 550-559
-
-
von Lindern, M.1
Zauner, W.2
Mellitzer, G.3
-
30
-
-
34948895031
-
EPO modulation of cell-cycle regulatory genes, and cell division, in primary bone marrow erythroblasts
-
Fang J., Menon M., Kapelle W., et al. EPO modulation of cell-cycle regulatory genes, and cell division, in primary bone marrow erythroblasts. Blood 2007, 110(7):2361-2370.
-
(2007)
Blood
, vol.110
, Issue.7
, pp. 2361-2370
-
-
Fang, J.1
Menon, M.2
Kapelle, W.3
-
31
-
-
35649000051
-
Negative autoregulation by FAS mediates robust fetal erythropoiesis
-
Socolovsky M., Murrell M., Liu Y., et al. Negative autoregulation by FAS mediates robust fetal erythropoiesis. PLoS Biol 2007, 5(10):e252.
-
(2007)
PLoS Biol
, vol.5
, Issue.10
-
-
Socolovsky, M.1
Murrell, M.2
Liu, Y.3
-
32
-
-
67649453787
-
The JAK2V617F mutation in polycythemia vera and other myeloproliferative disorders: one mutation for three diseases?
-
James C. The JAK2V617F mutation in polycythemia vera and other myeloproliferative disorders: one mutation for three diseases?. Hematology Am Soc Hematol Educ Program 2008, 69-75.
-
(2008)
Hematology Am Soc Hematol Educ Program
, pp. 69-75
-
-
James, C.1
-
33
-
-
71749114664
-
Mechanisms of mutations in myeloproliferative neoplasms
-
Levine R.L. Mechanisms of mutations in myeloproliferative neoplasms. Best Pract Res Clin Haematol 2009, 22(4):489-494.
-
(2009)
Best Pract Res Clin Haematol
, vol.22
, Issue.4
, pp. 489-494
-
-
Levine, R.L.1
-
34
-
-
33748206336
-
Constitutive activation of STAT5 and Bcl-xL overexpression can induce endogenous erythroid colony formation in human primary cells
-
Garcon L., Rivat C., James C., et al. Constitutive activation of STAT5 and Bcl-xL overexpression can induce endogenous erythroid colony formation in human primary cells. Blood 2006, 108(5):1551-1554.
-
(2006)
Blood
, vol.108
, Issue.5
, pp. 1551-1554
-
-
Garcon, L.1
Rivat, C.2
James, C.3
-
35
-
-
0035760889
-
Ineffective erythropoiesis in Stat5a(-/-)5b(-/-) mice due to decreased survival of early erythroblasts
-
Socolovsky M., Nam H., Fleming M.D., et al. Ineffective erythropoiesis in Stat5a(-/-)5b(-/-) mice due to decreased survival of early erythroblasts. Blood 2001, 98(12):3261-3273.
-
(2001)
Blood
, vol.98
, Issue.12
, pp. 3261-3273
-
-
Socolovsky, M.1
Nam, H.2
Fleming, M.D.3
-
36
-
-
0033597715
-
Fetal anemia and apoptosis of red cell progenitors in Stat5a-/-5b-/- mice: a direct role for Stat5 in Bcl-X(L) induction
-
Socolovsky M., Fallon A.E., Wang S., et al. Fetal anemia and apoptosis of red cell progenitors in Stat5a-/-5b-/- mice: a direct role for Stat5 in Bcl-X(L) induction. Cell 1999, 98(2):181-191.
-
(1999)
Cell
, vol.98
, Issue.2
, pp. 181-191
-
-
Socolovsky, M.1
Fallon, A.E.2
Wang, S.3
-
37
-
-
33646696616
-
Erythroid progenitor renewal versus differentiation: genetic evidence for cell autonomous, essential functions of EpoR, Stat5 and the GR
-
Dolznig H., Grebien F., Deiner E.M., et al. Erythroid progenitor renewal versus differentiation: genetic evidence for cell autonomous, essential functions of EpoR, Stat5 and the GR. Oncogene 2006, 25(20):2890-2900.
-
(2006)
Oncogene
, vol.25
, Issue.20
, pp. 2890-2900
-
-
Dolznig, H.1
Grebien, F.2
Deiner, E.M.3
-
38
-
-
55749096751
-
Stat5 regulates cellular iron uptake of erythroid cells via IRP-2 and TfR-1
-
Kerenyi M.A., Grebien F., Gehart H., et al. Stat5 regulates cellular iron uptake of erythroid cells via IRP-2 and TfR-1. Blood 2008, 112(9):3878-3888.
-
(2008)
Blood
, vol.112
, Issue.9
, pp. 3878-3888
-
-
Kerenyi, M.A.1
Grebien, F.2
Gehart, H.3
-
39
-
-
52649091181
-
Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression
-
Zhu B.M., McLaughlin S.K., Na R., et al. Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression. Blood 2008, 112(5):2071-2080.
-
(2008)
Blood
, vol.112
, Issue.5
, pp. 2071-2080
-
-
Zhu, B.M.1
McLaughlin, S.K.2
Na, R.3
-
40
-
-
0014728103
-
Ferrokinetics in man
-
Finch C.A., Deubelbeiss K., Cook J.D., et al. Ferrokinetics in man. Medicine 1970, 49(1):17-53.
-
(1970)
Medicine
, vol.49
, Issue.1
, pp. 17-53
-
-
Finch, C.A.1
Deubelbeiss, K.2
Cook, J.D.3
-
41
-
-
0034669951
-
The importance of erythroid expansion in determining the extent of apoptosis in erythroid precursors in patients with beta-thalassemia major
-
Centis F., Tabellini L., Lucarelli G., et al. The importance of erythroid expansion in determining the extent of apoptosis in erythroid precursors in patients with beta-thalassemia major. Blood 2000, 96(10):3624-3629.
-
(2000)
Blood
, vol.96
, Issue.10
, pp. 3624-3629
-
-
Centis, F.1
Tabellini, L.2
Lucarelli, G.3
-
42
-
-
0034538786
-
Ineffective erythropoiesis in beta-thalassemia major is due to apoptosis at the polychromatophilic normoblast stage
-
Mathias L.A., Fisher T.C., Zeng L., et al. Ineffective erythropoiesis in beta-thalassemia major is due to apoptosis at the polychromatophilic normoblast stage. Exp Hematol 2000, 28(12):1343-1353.
-
(2000)
Exp Hematol
, vol.28
, Issue.12
, pp. 1343-1353
-
-
Mathias, L.A.1
Fisher, T.C.2
Zeng, L.3
-
43
-
-
0027181636
-
Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe beta-thalassemia (Cooley's anemia)
-
Yuan J., Angelucci E., Lucarelli G., et al. Accelerated programmed cell death (apoptosis) in erythroid precursors of patients with severe beta-thalassemia (Cooley's anemia). Blood 1993, 82(2):374-377.
-
(1993)
Blood
, vol.82
, Issue.2
, pp. 374-377
-
-
Yuan, J.1
Angelucci, E.2
Lucarelli, G.3
-
44
-
-
50949133924
-
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in {beta}-thalassemia
-
Libani I.V., Guy E.C., Melchiori L., et al. Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in {beta}-thalassemia. Blood 2008, 112(3):875-885.
-
(2008)
Blood
, vol.112
, Issue.3
, pp. 875-885
-
-
Libani, I.V.1
Guy, E.C.2
Melchiori, L.3
-
45
-
-
67749103803
-
Ineffective erythropoiesis and thalassemias
-
Rivella S. Ineffective erythropoiesis and thalassemias. Curr Opin Hematol 2009, 16(3):187-194.
-
(2009)
Curr Opin Hematol
, vol.16
, Issue.3
, pp. 187-194
-
-
Rivella, S.1
-
46
-
-
45149113001
-
JAK2 mutations are present in all cases of polycythemia vera
-
Wang Y.L., Vandris K., Jones A., et al. JAK2 mutations are present in all cases of polycythemia vera. Leukemia 2008, 22(6):1289.
-
(2008)
Leukemia
, vol.22
, Issue.6
, pp. 1289
-
-
Wang, Y.L.1
Vandris, K.2
Jones, A.3
-
47
-
-
59249091317
-
The role of oxidative stress in hemolytic anemia
-
Fibach E., Rachmilewitz E. The role of oxidative stress in hemolytic anemia. Curr Mol Med 2008, 8(7):609-619.
-
(2008)
Curr Mol Med
, vol.8
, Issue.7
, pp. 609-619
-
-
Fibach, E.1
Rachmilewitz, E.2
-
48
-
-
34547699517
-
Foxo3 is required for the regulation of oxidative stress in erythropoiesis
-
Marinkovic D., Zhang X., Yalcin S., et al. Foxo3 is required for the regulation of oxidative stress in erythropoiesis. J Clin Invest 2007, 117(8):2133-2144.
-
(2007)
J Clin Invest
, vol.117
, Issue.8
, pp. 2133-2144
-
-
Marinkovic, D.1
Zhang, X.2
Yalcin, S.3
-
49
-
-
77951046942
-
Targeting iron homeostasis induces cellular differentiation and synergizes with differentiating agents in acute myeloid leukemia
-
Callens C., Coulon S., Naudin J., et al. Targeting iron homeostasis induces cellular differentiation and synergizes with differentiating agents in acute myeloid leukemia. J Exp Med 2010, 207(4):731-750.
-
(2010)
J Exp Med
, vol.207
, Issue.4
, pp. 731-750
-
-
Callens, C.1
Coulon, S.2
Naudin, J.3
-
50
-
-
77951040369
-
Metabolism and the leukemic stem cell
-
Abdel-Wahab O., Levine R.L. Metabolism and the leukemic stem cell. J Exp Med 2010, 207(4):677-680.
-
(2010)
J Exp Med
, vol.207
, Issue.4
, pp. 677-680
-
-
Abdel-Wahab, O.1
Levine, R.L.2
-
51
-
-
76349118307
-
Transferrin therapy ameliorates disease in beta-thalassemic mice
-
Li H., Rybicki A.C., Suzuka S.M., et al. Transferrin therapy ameliorates disease in beta-thalassemic mice. Nat Med 2010, 16(2):177-182.
-
(2010)
Nat Med
, vol.16
, Issue.2
, pp. 177-182
-
-
Li, H.1
Rybicki, A.C.2
Suzuka, S.M.3
-
52
-
-
0033599057
-
Disorders of iron metabolism
-
Andrews N.C. Disorders of iron metabolism. N Engl J Med 1999, 341(26):1986-1995.
-
(1999)
N Engl J Med
, vol.341
, Issue.26
, pp. 1986-1995
-
-
Andrews, N.C.1
-
53
-
-
0034284595
-
LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity
-
Krause A., Neitz S., Magert H.J., et al. LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity. FEBS Lett 2000, 480(2-3):147-150.
-
(2000)
FEBS Lett
, vol.480
, Issue.2-3
, pp. 147-150
-
-
Krause, A.1
Neitz, S.2
Magert, H.J.3
-
54
-
-
0035896642
-
Hepcidin, a urinary antimicrobial peptide synthesized in the liver
-
Park C.H., Valore E.V., Waring A.J., et al. Hepcidin, a urinary antimicrobial peptide synthesized in the liver. J Biol Chem 2001, 276(11):7806-7810.
-
(2001)
J Biol Chem
, vol.276
, Issue.11
, pp. 7806-7810
-
-
Park, C.H.1
Valore, E.V.2
Waring, A.J.3
-
55
-
-
10844258104
-
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
-
Nemeth E., Tuttle M.S., Powelson J., et al. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 2004, 306(5704):2090-2093.
-
(2004)
Science
, vol.306
, Issue.5704
, pp. 2090-2093
-
-
Nemeth, E.1
Tuttle, M.S.2
Powelson, J.3
-
56
-
-
30144432585
-
The N-terminus of hepcidin is essential for its interaction with ferroportin: structure-function study
-
Nemeth E., Preza G.C., Jung C.L., et al. The N-terminus of hepcidin is essential for its interaction with ferroportin: structure-function study. Blood 2006, 107(1):328-333.
-
(2006)
Blood
, vol.107
, Issue.1
, pp. 328-333
-
-
Nemeth, E.1
Preza, G.C.2
Jung, C.L.3
-
57
-
-
0035896581
-
A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload
-
Pigeon C., Ilyin G., Courselaud B., et al. A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload. J Biol Chem 2001, 276(11):7811-7819.
-
(2001)
J Biol Chem
, vol.276
, Issue.11
, pp. 7811-7819
-
-
Pigeon, C.1
Ilyin, G.2
Courselaud, B.3
-
58
-
-
0036791486
-
The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation
-
Nicolas G., Chauvet C., Viatte L., et al. The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation. J Clin Invest 2002, 110(7):1037-1044.
-
(2002)
J Clin Invest
, vol.110
, Issue.7
, pp. 1037-1044
-
-
Nicolas, G.1
Chauvet, C.2
Viatte, L.3
-
59
-
-
2342510407
-
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin
-
Nemeth E., Rivera S., Gabayan V., et al. IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin. J Clin Invest 2004, 113(9):1271-1276.
-
(2004)
J Clin Invest
, vol.113
, Issue.9
, pp. 1271-1276
-
-
Nemeth, E.1
Rivera, S.2
Gabayan, V.3
-
60
-
-
0038662619
-
Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein
-
Nemeth E., Valore E.V., Territo M., et al. Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein. Blood 2003, 101(7):2461-2463.
-
(2003)
Blood
, vol.101
, Issue.7
, pp. 2461-2463
-
-
Nemeth, E.1
Valore, E.V.2
Territo, M.3
-
61
-
-
33751175421
-
Interleukin-6 induces hepcidin expression through STAT3
-
Wrighting D.M., Andrews N.C. Interleukin-6 induces hepcidin expression through STAT3. Blood 2006, 108(9):3204-3209.
-
(2006)
Blood
, vol.108
, Issue.9
, pp. 3204-3209
-
-
Wrighting, D.M.1
Andrews, N.C.2
-
62
-
-
0012994611
-
Hepcidin, a new iron regulatory peptide
-
Nicolas G., Viatte L., Bennoun M., et al. Hepcidin, a new iron regulatory peptide. Blood Cells Mol Dis 2002, 29(3):327-335.
-
(2002)
Blood Cells Mol Dis
, vol.29
, Issue.3
, pp. 327-335
-
-
Nicolas, G.1
Viatte, L.2
Bennoun, M.3
-
63
-
-
33745742487
-
Hepcidin mRNA levels in mouse liver respond to inhibition of erythropoiesis
-
Vokurka M., Krijt J., Sulc K., et al. Hepcidin mRNA levels in mouse liver respond to inhibition of erythropoiesis. Physiol Res 2006, 55(6):667-674.
-
(2006)
Physiol Res
, vol.55
, Issue.6
, pp. 667-674
-
-
Vokurka, M.1
Krijt, J.2
Sulc, K.3
-
64
-
-
0033585129
-
The hemochromatosis protein HFE competes with transferrin for binding to the transferrin receptor
-
Lebron J.A., West A.P., Bjorkman P.J. The hemochromatosis protein HFE competes with transferrin for binding to the transferrin receptor. J Mol Biol 1999, 294(1):239-245.
-
(1999)
J Mol Biol
, vol.294
, Issue.1
, pp. 239-245
-
-
Lebron, J.A.1
West, A.P.2
Bjorkman, P.J.3
-
65
-
-
39649115776
-
The transferrin receptor modulates Hfe-dependent regulation of hepcidin expression
-
Schmidt P.J., Toran P.T., Giannetti A.M., et al. The transferrin receptor modulates Hfe-dependent regulation of hepcidin expression. Cell Metab 2008, 7(3):205-214.
-
(2008)
Cell Metab
, vol.7
, Issue.3
, pp. 205-214
-
-
Schmidt, P.J.1
Toran, P.T.2
Giannetti, A.M.3
-
66
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder J.N., Gnirke A., Thomas W., et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996, 13(4):399-408.
-
(1996)
Nat Genet
, vol.13
, Issue.4
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
-
67
-
-
0033597780
-
Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family
-
Kawabata H., Yang R., Hirama T., et al. Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family. J Biol Chem 1999, 274(30):20826-20832.
-
(1999)
J Biol Chem
, vol.274
, Issue.30
, pp. 20826-20832
-
-
Kawabata, H.1
Yang, R.2
Hirama, T.3
-
68
-
-
33749393565
-
Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing
-
Goswami T., Andrews N.C. Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing. J Biol Chem 2006, 281(39):28494-28498.
-
(2006)
J Biol Chem
, vol.281
, Issue.39
, pp. 28494-28498
-
-
Goswami, T.1
Andrews, N.C.2
-
69
-
-
60649103774
-
Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression
-
Gao J., Chen J., Kramer M., et al. Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression. Cell Metab 2009, 9(3):217-227.
-
(2009)
Cell Metab
, vol.9
, Issue.3
, pp. 217-227
-
-
Gao, J.1
Chen, J.2
Kramer, M.3
-
70
-
-
33644876815
-
A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression
-
Wang R.H., Li C., Xu X., et al. A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression. Cell Metab 2005, 2(6):399-409.
-
(2005)
Cell Metab
, vol.2
, Issue.6
, pp. 399-409
-
-
Wang, R.H.1
Li, C.2
Xu, X.3
-
71
-
-
33646370235
-
Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression
-
Babitt J.L., Huang F.W., Wrighting D.M., et al. Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression. Nat Genet 2006, 38(5):531-539.
-
(2006)
Nat Genet
, vol.38
, Issue.5
, pp. 531-539
-
-
Babitt, J.L.1
Huang, F.W.2
Wrighting, D.M.3
-
72
-
-
34447137331
-
Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance
-
Babitt J.L., Huang F.W., Xia Y., et al. Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance. J Clin Invest 2007, 117(7):1933-1939.
-
(2007)
J Clin Invest
, vol.117
, Issue.7
, pp. 1933-1939
-
-
Babitt, J.L.1
Huang, F.W.2
Xia, Y.3
-
73
-
-
51649096725
-
Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver
-
Kautz L., Meynard D., Monnier A., et al. Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver. Blood 2008, 112(4):1503-1509.
-
(2008)
Blood
, vol.112
, Issue.4
, pp. 1503-1509
-
-
Kautz, L.1
Meynard, D.2
Monnier, A.3
-
74
-
-
46749158788
-
Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin
-
Xia Y., Babitt J.L., Sidis Y., et al. Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin. Blood 2008, 111(10):5195-5204.
-
(2008)
Blood
, vol.111
, Issue.10
, pp. 5195-5204
-
-
Xia, Y.1
Babitt, J.L.2
Sidis, Y.3
-
75
-
-
63449122819
-
Lack of the bone morphogenetic protein BMP6 induces massive iron overload
-
Meynard D., Kautz L., Darnaud V., et al. Lack of the bone morphogenetic protein BMP6 induces massive iron overload. Nat Genet 2009, 41(4):478-481.
-
(2009)
Nat Genet
, vol.41
, Issue.4
, pp. 478-481
-
-
Meynard, D.1
Kautz, L.2
Darnaud, V.3
-
76
-
-
66749183353
-
Cross-talk between the mitogen activated protein kinase and bone morphogenetic protein/hemojuvelin pathways is required for the induction of hepcidin by holotransferrin in primary mouse hepatocytes
-
Ramey G., Deschemin J.C., Vaulont S. Cross-talk between the mitogen activated protein kinase and bone morphogenetic protein/hemojuvelin pathways is required for the induction of hepcidin by holotransferrin in primary mouse hepatocytes. Haematologica 2009, 94(6):765-772.
-
(2009)
Haematologica
, vol.94
, Issue.6
, pp. 765-772
-
-
Ramey, G.1
Deschemin, J.C.2
Vaulont, S.3
-
77
-
-
33751549663
-
TfR2 localizes in lipid raft domains and is released in exosomes to activate signal transduction along the MAPK pathway
-
Calzolari A., Raggi C., Deaglio S., et al. TfR2 localizes in lipid raft domains and is released in exosomes to activate signal transduction along the MAPK pathway. J Cell Sci 2006, 119(Pt 21):4486-4498.
-
(2006)
J Cell Sci
, vol.119
, Issue.PART 21
, pp. 4486-4498
-
-
Calzolari, A.1
Raggi, C.2
Deaglio, S.3
-
78
-
-
47649126246
-
Forging a field: the golden age of iron biology
-
Andrews N.C. Forging a field: the golden age of iron biology. Blood 2008, 112(2):219-230.
-
(2008)
Blood
, vol.112
, Issue.2
, pp. 219-230
-
-
Andrews, N.C.1
-
79
-
-
70450214396
-
The role of hepcidin in iron metabolism
-
Nemeth E., Ganz T. The role of hepcidin in iron metabolism. Acta Haematol 2009, 122(2-3):78-86.
-
(2009)
Acta Haematol
, vol.122
, Issue.2-3
, pp. 78-86
-
-
Nemeth, E.1
Ganz, T.2
-
80
-
-
42649118442
-
Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)
-
Finberg K.E., Heeney M.M., Campagna D.R., et al. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nat Genet 2008, 40(5):569-571.
-
(2008)
Nat Genet
, vol.40
, Issue.5
, pp. 569-571
-
-
Finberg, K.E.1
Heeney, M.M.2
Campagna, D.R.3
-
81
-
-
44449177930
-
The serine protease TMPRSS6 is required to sense iron deficiency
-
Du X., She E., Gelbart T., et al. The serine protease TMPRSS6 is required to sense iron deficiency. Science 2008, 320(5879):1088-1092.
-
(2008)
Science
, vol.320
, Issue.5879
, pp. 1088-1092
-
-
Du, X.1
She, E.2
Gelbart, T.3
-
82
-
-
56449096622
-
The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin
-
Silvestri L., Pagani A., Nai A., et al. The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin. Cell Metab 2008, 8(6):502-511.
-
(2008)
Cell Metab
, vol.8
, Issue.6
, pp. 502-511
-
-
Silvestri, L.1
Pagani, A.2
Nai, A.3
-
83
-
-
27144459908
-
Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin
-
Lin L., Goldberg Y.P., Ganz T. Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin. Blood 2005, 106(8):2884-2889.
-
(2005)
Blood
, vol.106
, Issue.8
, pp. 2884-2889
-
-
Lin, L.1
Goldberg, Y.P.2
Ganz, T.3
-
84
-
-
77952573858
-
Downregulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis
-
Finberg K.E., Whittlesey R.L., Fleming M.D., et al. Downregulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis. Blood 2010, 115(18):3817-3826.
-
(2010)
Blood
, vol.115
, Issue.18
, pp. 3817-3826
-
-
Finberg, K.E.1
Whittlesey, R.L.2
Fleming, M.D.3
-
85
-
-
23644460325
-
A mouse model of juvenile hemochromatosis
-
Huang F.W., Pinkus J.L., Pinkus G.S., et al. A mouse model of juvenile hemochromatosis. J Clin Invest 2005, 115(8):2187-2191.
-
(2005)
J Clin Invest
, vol.115
, Issue.8
, pp. 2187-2191
-
-
Huang, F.W.1
Pinkus, J.L.2
Pinkus, G.S.3
-
86
-
-
0346433908
-
Decreased hepcidin mRNA expression in thalassemic mice
-
Adamsky K, Weizer O, Amariglio N, et al. Decreased hepcidin mRNA expression in thalassemic mice. Br J Haematol 2004, 124(1):123-124.
-
(2004)
Br J Haematol
, vol.124
, Issue.1
, pp. 123-124
-
-
Adamsky, K.1
Weizer, O.2
Amariglio, N.3
-
87
-
-
33845245942
-
Suppression of hepcidin during anemia requires erythropoietic activity
-
Pak M., Lopez M.A., Gabayan V., et al. Suppression of hepcidin during anemia requires erythropoietic activity. Blood 2006, 108(12):3730-3735.
-
(2006)
Blood
, vol.108
, Issue.12
, pp. 3730-3735
-
-
Pak, M.1
Lopez, M.A.2
Gabayan, V.3
-
88
-
-
0025077835
-
Iron metabolism in thalassemia intermedia
-
Fiorelli G., Fargion S., Piperno A., et al. Iron metabolism in thalassemia intermedia. Haematologica 1990, 75(Suppl 5):89-95.
-
(1990)
Haematologica
, vol.75
, Issue.SUPPL. 5
, pp. 89-95
-
-
Fiorelli, G.1
Fargion, S.2
Piperno, A.3
-
89
-
-
34249658982
-
Ineffective erythropoiesis in {beta}-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
-
Gardenghi S., Marongiu M.F., Ramos P., et al. Ineffective erythropoiesis in {beta}-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin. Blood 2007, 109(11):5027-5035.
-
(2007)
Blood
, vol.109
, Issue.11
, pp. 5027-5035
-
-
Gardenghi, S.1
Marongiu, M.F.2
Ramos, P.3
-
90
-
-
33748370295
-
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera
-
Weizer-Stern O., Adamsky K., Amariglio N., et al. Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera. Br J Haematol 2006, 135(1):129-138.
-
(2006)
Br J Haematol
, vol.135
, Issue.1
, pp. 129-138
-
-
Weizer-Stern, O.1
Adamsky, K.2
Amariglio, N.3
-
91
-
-
33745684771
-
MRNA expression of iron regulatory genes in beta-thalassemia intermedia and beta-thalassemia major mouse models
-
Weizer-Stern O., Adamsky K., Amariglio N., et al. mRNA expression of iron regulatory genes in beta-thalassemia intermedia and beta-thalassemia major mouse models. Am J Hematol 2006, 81(7):479-483.
-
(2006)
Am J Hematol
, vol.81
, Issue.7
, pp. 479-483
-
-
Weizer-Stern, O.1
Adamsky, K.2
Amariglio, N.3
-
92
-
-
34447306076
-
Liver iron concentrations and urinary hepcidin in beta-thalassemia
-
Origa R., Galanello R., Ganz T., et al. Liver iron concentrations and urinary hepcidin in beta-thalassemia. Haematologica 2007, 92(5):583-588.
-
(2007)
Haematologica
, vol.92
, Issue.5
, pp. 583-588
-
-
Origa, R.1
Galanello, R.2
Ganz, T.3
-
93
-
-
33845342174
-
Urinary hepcidin in congenital chronic anemias
-
Kearney S.L., Nemeth E., Neufeld E.J., et al. Urinary hepcidin in congenital chronic anemias. Pediatr Blood Cancer 2007, 48(1):57-63.
-
(2007)
Pediatr Blood Cancer
, vol.48
, Issue.1
, pp. 57-63
-
-
Kearney, S.L.1
Nemeth, E.2
Neufeld, E.J.3
-
94
-
-
19544386871
-
Hepcidin in iron overload disorders
-
Papanikolaou G., Tzilianos M., Christakis J.I., et al. Hepcidin in iron overload disorders. Blood 2005, 105(10):4103-4105.
-
(2005)
Blood
, vol.105
, Issue.10
, pp. 4103-4105
-
-
Papanikolaou, G.1
Tzilianos, M.2
Christakis, J.I.3
-
95
-
-
33745755350
-
The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major
-
Kattamis A., Papassotiriou I., Palaiologou D., et al. The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major. Haematologica 2006, 91(6):809-812.
-
(2006)
Haematologica
, vol.91
, Issue.6
, pp. 809-812
-
-
Kattamis, A.1
Papassotiriou, I.2
Palaiologou, D.3
-
96
-
-
34347389655
-
Iron homeostasis during transfusional iron overload in beta-thalassemia and sickle cell disease: changes in iron regulatory protein, hepcidin, and ferritin expression
-
Jenkins Z.A., Hagar W., Bowlus C.L., et al. Iron homeostasis during transfusional iron overload in beta-thalassemia and sickle cell disease: changes in iron regulatory protein, hepcidin, and ferritin expression. Pediatr Hematol Oncol 2007, 24(4):237-243.
-
(2007)
Pediatr Hematol Oncol
, vol.24
, Issue.4
, pp. 237-243
-
-
Jenkins, Z.A.1
Hagar, W.2
Bowlus, C.L.3
-
97
-
-
0346433908
-
Decreased hepcidin mRNA expression in thalassemic mice
-
Adamsky K., Weizer O., Amariglio N., et al. Decreased hepcidin mRNA expression in thalassemic mice. Br J Haematol 2004, 124(1):123-124.
-
(2004)
Br J Haematol
, vol.124
, Issue.1
, pp. 123-124
-
-
Adamsky, K.1
Weizer, O.2
Amariglio, N.3
-
98
-
-
59249095557
-
Regulation of iron absorption in hemoglobinopathies
-
Rechavi G., Rivella S. Regulation of iron absorption in hemoglobinopathies. Curr Mol Med 2008, 8(7):646-662.
-
(2008)
Curr Mol Med
, vol.8
, Issue.7
, pp. 646-662
-
-
Rechavi, G.1
Rivella, S.2
-
99
-
-
9144261634
-
In vivo reduction of erythrocyte oxidant stress in a murine model of beta-thalassemia
-
de Franceschi L., Turrini F., Honczarenko M., et al. In vivo reduction of erythrocyte oxidant stress in a murine model of beta-thalassemia. Haematologica 2004, 89(11):1287-1298.
-
(2004)
Haematologica
, vol.89
, Issue.11
, pp. 1287-1298
-
-
de Franceschi, L.1
Turrini, F.2
Honczarenko, M.3
-
100
-
-
67651043722
-
Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells
-
Tanno T., Porayette P., Sripichai O., et al. Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells. Blood 2009, 114(1):181-186.
-
(2009)
Blood
, vol.114
, Issue.1
, pp. 181-186
-
-
Tanno, T.1
Porayette, P.2
Sripichai, O.3
-
101
-
-
34948904750
-
High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin
-
Tanno T., Bhanu N.V., Oneal P.A., et al. High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin. Nat Med 2007, 13(9):1096-1101.
-
(2007)
Nat Med
, vol.13
, Issue.9
, pp. 1096-1101
-
-
Tanno, T.1
Bhanu, N.V.2
Oneal, P.A.3
-
102
-
-
54349102037
-
Serum hepcidin level and erythropoietic activity after hematopoietic stem cell transplantation
-
Kanda J., Mizumoto C., Kawabata H., et al. Serum hepcidin level and erythropoietic activity after hematopoietic stem cell transplantation. Haematologica 2008, 93(10):1550-1554.
-
(2008)
Haematologica
, vol.93
, Issue.10
, pp. 1550-1554
-
-
Kanda, J.1
Mizumoto, C.2
Kawabata, H.3
-
103
-
-
77954335457
-
Expression of growth differentiation factor 15 is not elevated in individuals with iron deficiency secondary to volunteer blood donation
-
Tanno T., Rabel A., Lee Y.T., et al. Expression of growth differentiation factor 15 is not elevated in individuals with iron deficiency secondary to volunteer blood donation. Transfusion 2010, 50(7):1532-1535.
-
(2010)
Transfusion
, vol.50
, Issue.7
, pp. 1532-1535
-
-
Tanno, T.1
Rabel, A.2
Lee, Y.T.3
-
104
-
-
58149092194
-
Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblasts
-
Ramirez J.M., Schaad O., Durual S., et al. Growth differentiation factor 15 production is necessary for normal erythroid differentiation and is increased in refractory anaemia with ring-sideroblasts. Br J Haematol 2009, 144(2):251-262.
-
(2009)
Br J Haematol
, vol.144
, Issue.2
, pp. 251-262
-
-
Ramirez, J.M.1
Schaad, O.2
Durual, S.3
-
105
-
-
77955906936
-
Hepcidin and Hfe in iron overload in beta-thalassemia
-
Gardenghi S, Ramos P, Follenzi A, et al. Hepcidin and Hfe in iron overload in beta-thalassemia. Ann N Y Acad Sci 2010, 1202:221-225.
-
(2010)
Ann N Y Acad Sci
, vol.1202
, pp. 221-225
-
-
Gardenghi, S.1
Ramos, P.2
Follenzi, A.3
-
106
-
-
0037847496
-
Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis
-
Nicolas G., Viatte L., Lou D.Q., et al. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis. Nat Genet 2003, 34(1):97-101.
-
(2003)
Nat Genet
, vol.34
, Issue.1
, pp. 97-101
-
-
Nicolas, G.1
Viatte, L.2
Lou, D.Q.3
-
107
-
-
36248937215
-
Oxidative stress in red blood cells, platelets and polymorphonuclear leukocytes from patients with myelodysplastic syndrome
-
Ghoti H., Amer J., Winder A., et al. Oxidative stress in red blood cells, platelets and polymorphonuclear leukocytes from patients with myelodysplastic syndrome. Eur J Haematol 2007, 79(6):463-467.
-
(2007)
Eur J Haematol
, vol.79
, Issue.6
, pp. 463-467
-
-
Ghoti, H.1
Amer, J.2
Winder, A.3
-
108
-
-
0025060810
-
Oxidative denaturation of red blood cells in thalassemia
-
Shinar E., Rachmilewitz E.A. Oxidative denaturation of red blood cells in thalassemia. Semin Hematol 1990, 27(1):70-82.
-
(1990)
Semin Hematol
, vol.27
, Issue.1
, pp. 70-82
-
-
Shinar, E.1
Rachmilewitz, E.A.2
-
109
-
-
27844497945
-
FOXO transcription factors at the interface between longevity and tumor suppression
-
Greer E.L., Brunet A. FOXO transcription factors at the interface between longevity and tumor suppression. Oncogene 2005, 24(50):7410-7425.
-
(2005)
Oncogene
, vol.24
, Issue.50
, pp. 7410-7425
-
-
Greer, E.L.1
Brunet, A.2
|