-
1
-
-
12844260664
-
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
-
Mims MP, Guan Y, Pospisilova D, et al. Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload. Blood. 2005;105:1337-1342.
-
(2005)
Blood
, vol.105
, pp. 1337-1342
-
-
Mims, M.P.1
Guan, Y.2
Pospisilova, D.3
-
3
-
-
28444482404
-
Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake
-
Priwitzerova M, Nie G, Sheftel AD, Pospisilova D, Divoky V, Ponka P. Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake. Blood. 2005;106:3985-3987.
-
(2005)
Blood
, vol.106
, pp. 3985-3987
-
-
Priwitzerova, M.1
Nie, G.2
Sheftel, A.D.3
Pospisilova, D.4
Divoky, V.5
Ponka, P.6
-
4
-
-
2342447226
-
Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells
-
Priwitzerova M, Pospisilova D, Prchal JT, et al. Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells. Blood. 2004;103:3991-3992.
-
(2004)
Blood
, vol.103
, pp. 3991-3992
-
-
Priwitzerova, M.1
Pospisilova, D.2
Prchal, J.T.3
-
5
-
-
0038662619
-
Hepcidin, a putative mediator of anemia of inflammation, is a type II acute phase protein
-
Nemeth E, Valore EV, Territo M, Schiller G, Lichtenstein A, Ganz T. Hepcidin, a putative mediator of anemia of inflammation, is a type II acute phase protein. Blood. 2003;101:2461-2463.
-
(2003)
Blood
, vol.101
, pp. 2461-2463
-
-
Nemeth, E.1
Valore, E.V.2
Territo, M.3
Schiller, G.4
Lichtenstein, A.5
Ganz, T.6
-
6
-
-
30144443274
-
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1
-
Iolascon A, d'Apolito M, Servedio V, Cimmino F, Piga A, Camaschella C. Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1. Blood. 2006;107:349-354.
-
(2006)
Blood
, vol.107
, pp. 349-354
-
-
Iolascon, A.1
D'Apolito, M.2
Servedio, V.3
Cimmino, F.4
Piga, A.5
Camaschella, C.6
-
7
-
-
33646537173
-
Two new human DMT1 mutations in a compound heterozygous patient with microcytic anemia and low iron stores
-
Prepublished on January 26, 2006, as DOI 10.1182/blood-2005-10-4269
-
Beaumont C, Delaunay J, Hetet G, De Montalembert M, Grandchamp B, Tchernia GJ. Two new human DMT1 mutations in a compound heterozygous patient with microcytic anemia and low iron stores. Blood. Prepublished on January 26, 2006, as DOI 10.1182/blood-2005-10-4269.
-
Blood
-
-
Beaumont, C.1
Delaunay, J.2
Hetet, G.3
De Montalembert, M.4
Grandchamp, B.5
Tchernia, G.J.6
-
8
-
-
24744458603
-
Synthetic hepcidin causes rapid dose-dependent hypoferremia and is concentrated in ferroportin-containing organs
-
Rivera S, Nemeth E, Gabayan V, Lopez MA, Farshidi D, Ganz T. Synthetic hepcidin causes rapid dose-dependent hypoferremia and is concentrated in ferroportin-containing organs. Blood. 2005;106:2196-2199.
-
(2005)
Blood
, vol.106
, pp. 2196-2199
-
-
Rivera, S.1
Nemeth, E.2
Gabayan, V.3
Lopez, M.A.4
Farshidi, D.5
Ganz, T.6
-
9
-
-
0036791486
-
The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation
-
Nicolas G, Chauvet C, Viatte, et al. The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation. J Clin Invest. 2002;110:1037-1044.
-
(2002)
J Clin Invest
, vol.110
, pp. 1037-1044
-
-
Nicolas, G.1
Chauvet, C.2
Viatte3
|