-
1
-
-
0034733635
-
A novel mammalian iron-regulated protein involved in intracellular iron metabolism
-
Abboud, S. & Haile, D.J. (2000) A novel mammalian iron-regulated protein involved in intracellular iron metabolism. Journal of Biological Chemistry, 275, 19906-19912.
-
(2000)
Journal of Biological Chemistry
, vol.275
, pp. 19906-19912
-
-
Abboud, S.1
Haile, D.J.2
-
2
-
-
0037622887
-
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient
-
Arden, K.E., Wallace, D.F., Dixon, J.L., Summerville, L., Searle, J.W., Anderson, G.J., Ramm, G.A., Powell, L.W. & Subramaniam, V.N. (2003) A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient. Gut, 52, 1215-1217.
-
(2003)
Gut
, vol.52
, pp. 1215-1217
-
-
Arden, K.E.1
Wallace, D.F.2
Dixon, J.L.3
Summerville, L.4
Searle, J.W.5
Anderson, G.J.6
Ramm, G.A.7
Powell, L.W.8
Subramaniam, V.N.9
-
3
-
-
0027819719
-
Erythrophagocytosis increases the expression of erythroid potentiating activity mRNA in human monocyte-macrophages
-
Bergamaschi, G., Recalde, H.H., Ponchio, L., Rosti, V. & Cazzola, M. (1993) Erythrophagocytosis increases the expression of erythroid potentiating activity mRNA in human monocyte-macrophages. Experimental Hematology, 21, 70-73.
-
(1993)
Experimental Hematology
, vol.21
, pp. 70-73
-
-
Bergamaschi, G.1
Recalde, H.H.2
Ponchio, L.3
Rosti, V.4
Cazzola, M.5
-
4
-
-
18744400781
-
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
-
Cazzola, M., Cremonesi, L., Papaioannou, M., Soriani, N., Kioumi, A., Charalambidou, A., Paroni, R., Romtsou, K., Levi, S., Ferrari, M., Arosio, P. & Christakis, J. (2002) Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3). British Journal of Haematology, 119, 539-546.
-
(2002)
British Journal of Haematology
, vol.119
, pp. 539-546
-
-
Cazzola, M.1
Cremonesi, L.2
Papaioannou, M.3
Soriani, N.4
Kioumi, A.5
Charalambidou, A.6
Paroni, R.7
Romtsou, K.8
Levi, S.9
Ferrari, M.10
Arosio, P.11
Christakis, J.12
-
5
-
-
0024429683
-
Development of an immunoassay for all human isoferritins, and its application to serum ferritin evaluation
-
Cozzi, A., Levi, S., Bazzigaluppi, E., Ruggeri, G. & Arosio, P. (1989) Development of an immunoassay for all human isoferritins, and its application to serum ferritin evaluation. Clinica Chimica Acta, 184, 197-206.
-
(1989)
Clinica Chimica Acta
, vol.184
, pp. 197-206
-
-
Cozzi, A.1
Levi, S.2
Bazzigaluppi, E.3
Ruggeri, G.4
Arosio, P.5
-
6
-
-
1542373640
-
Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs evidence for a proliferative role of L-ferritin
-
Cozzi, A., Corsi, B., Levi, S., Santambrogio, P., Biasiotto, G. & Arosio, P. (2004) Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs evidence for a proliferative role of L-ferritin. Blood, 103, 2377-2383.
-
(2004)
Blood
, vol.103
, pp. 2377-2383
-
-
Cozzi, A.1
Corsi, B.2
Levi, S.3
Santambrogio, P.4
Biasiotto, G.5
Arosio, P.6
-
7
-
-
0037100382
-
Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)
-
Devalia, V., Carter, K., Walker, A.P., Perkins, S.J., Worwood, M., May, A. & Dooley, J.S. (2002) Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). Blood, 100, 695-697.
-
(2002)
Blood
, vol.100
, pp. 695-697
-
-
Devalia, V.1
Carter, K.2
Walker, A.P.3
Perkins, S.J.4
Worwood, M.5
May, A.6
Dooley, J.S.7
-
8
-
-
0034677467
-
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
-
Donovan, A., Brownlie, A., Zhou, Y., Shepard, J., Pratt, S.J., Moynihan, J., Paw, B.H., Drejer, A., Barut, B., Zapata, A., Law, T.C., Brugnara, C., Lux, S.E., Pinkus, G.S., Pinkus, J.L., Kingsley, P.D., Palis, J., Fleming, M.D., Andrews, N.C. & Zon, L.I. (2000) Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter. Nature, 403, 776-781.
-
(2000)
Nature
, vol.403
, pp. 776-781
-
-
Donovan, A.1
Brownlie, A.2
Zhou, Y.3
Shepard, J.4
Pratt, S.J.5
Moynihan, J.6
Paw, B.H.7
Drejer, A.8
Barut, B.9
Zapata, A.10
Law, T.C.11
Brugnara, C.12
Lux, S.E.13
Pinkus, G.S.14
Pinkus, J.L.15
Kingsley, P.D.16
Palis, J.17
Fleming, M.D.18
Andrews, N.C.19
Zon, L.I.20
more..
-
9
-
-
0012756249
-
RNA interference in mammalian cells using siRNAs synthesized with T7 RNA polymerase
-
Donze, O. & Picard, D. (2002) RNA interference in mammalian cells using siRNAs synthesized with T7 RNA polymerase. Nucleic Acids Research, 30, e46.
-
(2002)
Nucleic Acids Research
, vol.30
-
-
Donze, O.1
Picard, D.2
-
10
-
-
0024348472
-
Model of reticuloendothelial iron metabolism in humans: Abnormal behavior in idiopathic hemochromatosis and in inflammation
-
Fillet, G., Beguin, Y. & Baldelli, L. (1989) Model of reticuloendothelial iron metabolism in humans: abnormal behavior in idiopathic hemochromatosis and in inflammation. Blood, 74, 844-851.
-
(1989)
Blood
, vol.74
, pp. 844-851
-
-
Fillet, G.1
Beguin, Y.2
Baldelli, L.3
-
12
-
-
10744219904
-
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload
-
Jouanolle, A.M., Douabin-Gicquel, V., Halimi, C, Loreal, O., Fergelot, P., Delacour, T., de Lajarte-Thirouard, A.S., Turlin, B., Le Gall, J.Y., Cadet, E., Rochette, J., David, V. & Brissot, P. (2003) Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload. Journal of Hepatology, 39, 286-289.
-
(2003)
Journal of Hepatology
, vol.39
, pp. 286-289
-
-
Jouanolle, A.M.1
Douabin-Gicquel, V.2
Halimi, C.3
Loreal, O.4
Fergelot, P.5
Delacour, T.6
De Lajarte-Thirouard, A.S.7
Turlin, B.8
Le Gall, J.Y.9
Cadet, E.10
Rochette, J.11
David, V.12
Brissot, P.13
-
13
-
-
0345688910
-
Iron loading and erythrophagocytosis increase ferroportin 1 (FPN1) expression in J774 macrophages
-
Knutson, M.D., Vafa, M.R., Haile, D.J. & Wessling-Resnick, M. (2003) Iron loading and erythrophagocytosis increase ferroportin 1 (FPN1) expression in J774 macrophages. Blood, 102, 4191-4197.
-
(2003)
Blood
, vol.102
, pp. 4191-4197
-
-
Knutson, M.D.1
Vafa, M.R.2
Haile, D.J.3
Wessling-Resnick, M.4
-
14
-
-
0037926880
-
Cytokine-mediated regulation of iron transport in human monocytic cells
-
Ludwiczek, S., Aigner, E., Theurl, I. & Weiss, G. (2003) Cytokine-mediated regulation of iron transport in human monocytic cells. Blood, 101, 4148-4154.
-
(2003)
Blood
, vol.101
, pp. 4148-4154
-
-
Ludwiczek, S.1
Aigner, E.2
Theurl, I.3
Weiss, G.4
-
15
-
-
0033861745
-
A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation
-
McKie, A.T., Marciani, P., Rolfs, A., Brennan, K., Wehr, K., Barrow, D., Miret, S., Bomford, A., Peters, T.J., Farzaneh, F., Hediger, M.A., Hentze, M.W. & Simpson, R.J. (2000) A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation. Molecular Cell, 5, 299-309.
-
(2000)
Molecular Cell
, vol.5
, pp. 299-309
-
-
McKie, A.T.1
Marciani, P.2
Rolfs, A.3
Brennan, K.4
Wehr, K.5
Barrow, D.6
Miret, S.7
Bomford, A.8
Peters, T.J.9
Farzaneh, F.10
Hediger, M.A.11
Hentze, M.W.12
Simpson, R.J.13
-
16
-
-
0036788304
-
Gene silencing in mammals by small interfering RNAs
-
McManus, M.T. & Sharp, P.A. (2002) Gene silencing in mammals by small interfering RNAs. Nature Reviews Genetics, 3, 737-747.
-
(2002)
Nature Reviews Genetics
, vol.3
, pp. 737-747
-
-
McManus, M.T.1
Sharp, P.A.2
-
17
-
-
17944380796
-
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene
-
Montosi, G., Donovan, A., Totaro, A., Garuti, C., Pignatti, E., Cassanelli, S., Trenor, C.C., Gasparini, P., Andrews, N.C. & Pietrangelo, A. (2001) Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. Journal of Clinical Investigation, 108, 619-623.
-
(2001)
Journal of Clinical Investigation
, vol.108
, pp. 619-623
-
-
Montosi, G.1
Donovan, A.2
Totaro, A.3
Garuti, C.4
Pignatti, E.5
Cassanelli, S.6
Trenor, C.C.7
Gasparini, P.8
Andrews, N.C.9
Pietrangelo, A.10
-
18
-
-
0034930197
-
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
-
Njajou, O.T., Vaessen, N., Joosse, M., Berghuis, B., van Dongen, J.W., Breuning, M.H., Snijders, P.J., Rutten, W.P., Sandkuijl, L.A., Oostra, B.A., van Duijn, CM. & Heutink, P. (2001) A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. Nature Genetics, 28, 213-214.
-
(2001)
Nature Genetics
, vol.28
, pp. 213-214
-
-
Njajou, O.T.1
Vaessen, N.2
Joosse, M.3
Berghuis, B.4
Van Dongen, J.W.5
Breuning, M.H.6
Snijders, P.J.7
Rutten, W.P.8
Sandkuijl, L.A.9
Oostra, B.A.10
Van Duijn, C.M.11
Heutink, P.12
-
19
-
-
0742272103
-
The ferroportin disease
-
Pietrangelo, A. (2004) The ferroportin disease. Blood Cells, Molecules, and Diseases, 32, 131-138.
-
(2004)
Blood Cells, Molecules, and Diseases
, vol.32
, pp. 131-138
-
-
Pietrangelo, A.1
-
20
-
-
0033517341
-
Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene
-
Pietrangelo, A., Montosi, G., Totaro, A., Garuti, C., Conte, D., Cassanelli, S., Fraquelli, M., Sardini, C, Vasta, F. & Gasparini, P. (1999) Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene. New England Journal of Medicine, 341, 725-732.
-
(1999)
New England Journal of Medicine
, vol.341
, pp. 725-732
-
-
Pietrangelo, A.1
Montosi, G.2
Totaro, A.3
Garuti, C.4
Conte, D.5
Cassanelli, S.6
Fraquelli, M.7
Sardini, C.8
Vasta, F.9
Gasparini, P.10
-
21
-
-
0021334141
-
A simple method of obtaining monocytes in suspension
-
Recalde, H.R. (1984) A simple method of obtaining monocytes in suspension. Journal of Immunological Methods, 69, 71-77.
-
(1984)
Journal of Immunological Methods
, vol.69
, pp. 71-77
-
-
Recalde, H.R.1
-
22
-
-
0038536855
-
Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the ferroportin1 gene (SLC11A3) in a large French-Canadian family
-
Rivard, S.R., Lanzara, C., Grimard, D., Carella, M., Simard, H., Ficarella, R., Simard, R., D'Adamo, A.P., De Braekeleer, M. & Gasparini, P. (2003) Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the ferroportin1 gene (SLC11A3) in a large French-Canadian family. Haematologica, 88, 824-826.
-
(2003)
Haematologica
, vol.88
, pp. 824-826
-
-
Rivard, S.R.1
Lanzara, C.2
Grimard, D.3
Carella, M.4
Simard, H.5
Ficarella, R.6
Simard, R.7
D'Adamo, A.P.8
De Braekeleer, M.9
Gasparini, P.10
-
23
-
-
0037100383
-
A valine deletion of ferroportin 1: A common mutation in hemochromastosis type 4
-
Roetto, A., Merryweather-Clarke, A.T., Daraio, F., Livesey, K., Pointon, J.J., Barbabietola, G., Piga, A., Mackie, P.H., Robson, K.J. & Camaschella, C. (2002) A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. Blood, 100, 733-734.
-
(2002)
Blood
, vol.100
, pp. 733-734
-
-
Roetto, A.1
Merryweather-Clarke, A.T.2
Daraio, F.3
Livesey, K.4
Pointon, J.J.5
Barbabietola, G.6
Piga, A.7
Mackie, P.H.8
Robson, K.J.9
Camaschella, C.10
-
24
-
-
0037100517
-
Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis
-
Wallace, D.F., Pedersen, P., Dixon, J.L., Stephenson, P., Searle, J.W., Powell, L.W. & Subramaniam, V.N. (2002) Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis. Blood, 100, 692-694.
-
(2002)
Blood
, vol.100
, pp. 692-694
-
-
Wallace, D.F.1
Pedersen, P.2
Dixon, J.L.3
Stephenson, P.4
Searle, J.W.5
Powell, L.W.6
Subramaniam, V.N.7
-
25
-
-
0037131264
-
Regulation of reticuloendothelial iron transporter MTP1 (Slc11a3) by inflammation
-
Yang, F., Liu, X.B., Quinones, M., Melby, P.C., Ghio, A. & Haile, D.J. (2002) Regulation of reticuloendothelial iron transporter MTP1 (Slc11a3) by inflammation. Journal of Biological Chemistry, 277, 39786-39791.
-
(2002)
Journal of Biological Chemistry
, vol.277
, pp. 39786-39791
-
-
Yang, F.1
Liu, X.B.2
Quinones, M.3
Melby, P.C.4
Ghio, A.5
Haile, D.J.6
|