-
1
-
-
33646337674
-
Iron metabolism meets signal transduction
-
Anderson GJ, Frazer DM (2006) Iron metabolism meets signal transduction. Nature Genetics 38: 503-4.
-
(2006)
Nature Genetics
, vol.38
, pp. 503-504
-
-
Anderson, G.J.1
Frazer, D.M.2
-
2
-
-
47649126246
-
Forging a field: the golden age of iron biology
-
Andrews NC (2008) Forging a field: the golden age of iron biology Blood 112: 219-30.
-
(2008)
Blood
, vol.112
, pp. 219-230
-
-
Andrews, N.C.1
-
3
-
-
63449103712
-
BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism
-
Andriopoulos B Jr (2009) BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism. Nature Genetics 41: 482-7.
-
(2009)
Nature Genetics
, vol.41
, pp. 482-487
-
-
Andriopoulos Jr., B.1
-
4
-
-
72449156527
-
Ferric carboxymaltose in patients with heart failure and iron deficiency
-
Anker SD, Colet JC, Filippatos G et al. (2009) Ferric carboxymaltose in patients with heart failure and iron deficiency. New England Journal of Medicine 361: 2436-48.
-
(2009)
New England Journal of Medicine
, vol.361
, pp. 2436-2448
-
-
Anker, S.D.1
Colet, J.C.2
Filippatos, G.3
-
5
-
-
34447137331
-
Modulation of bone morphogenetic protein signalling in vivo regulates systemic iron balance
-
Babitt JL, Huang FW, Xia Y et al. (2007) Modulation of bone morphogenetic protein signalling in vivo regulates systemic iron balance. Journal of Clinical Investigation 117: 1933-9.
-
(2007)
Journal of Clinical Investigation
, vol.117
, pp. 1933-1939
-
-
Babitt, J.L.1
Huang, F.W.2
Xia, Y.3
-
6
-
-
0028808309
-
Neurodegeneration and diabetes: UK nationwide study of Weifrom (DIDMOAD) syndrome
-
Barrett TG, Bundey S, Macleod AF (1995) Neurodegeneration and diabetes: UK nationwide study of Weifrom (DIDMOAD) syndrome. Lancet 346: 1458-63.
-
(1995)
Lancet
, vol.346
, pp. 1458-1463
-
-
Barrett, T.G.1
Bundey, S.2
Macleod, A.F.3
-
7
-
-
0037362778
-
Soluble transferrin receptor for the evaluation of erythropoiesis and iron status
-
Beguin Y (2003) Soluble transferrin receptor for the evaluation of erythropoiesis and iron status. Clinica Chimica Acta 329: 9-22.
-
(2003)
Clinica Chimica Acta
, vol.329
, pp. 9-22
-
-
Beguin, Y.1
-
8
-
-
33748754872
-
Congenital sideroblastic anemias
-
Bottomley, S (2006) Congenital sideroblastic anemias. Current Hematology Reports 5: 41-49.
-
(2006)
Current Hematology Reports
, vol.5
, pp. 41-49
-
-
Bottomley, S.1
-
9
-
-
51249119361
-
Recent advances in the understanding of inherited sideroblastic anaemia
-
Camaschella, C (2008) Recent advances in the understanding of inherited sideroblastic anaemia. British Journal of Haematology 143: 27-38.
-
(2008)
British Journal of Haematology
, vol.143
, pp. 27-38
-
-
Camaschella, C.1
-
10
-
-
0036430202
-
Hereditary hyperferritinaemia/cataract syndrome Best Practice and Research
-
Cazzola M (2002) Hereditary hyperferritinaemia/cataract syndrome. Best Practice and Research. Clinical Haematology 15: 385-98.
-
(2002)
Clinical Haematology
, vol.15
, pp. 385-398
-
-
Cazzola, M.1
-
13
-
-
44449177930
-
The serine protease TMPRSS6 is required to sense iron deficiency
-
Du X, She E, Gelbart T (2008) The serine protease TMPRSS6 is required to sense iron deficiency. Science 320: 1088-92.
-
(2008)
Science
, vol.320
, pp. 1088-1092
-
-
Du, X.1
She, E.2
Gelbart, T.3
-
14
-
-
42649118442
-
Mutations in TMPRSS6 cause iron - refractory iron deficiency anaemia (IRIDA)
-
Finberg KE, Heeney MM, Campagna DR et al. (2008) Mutations in TMPRSS6 cause iron - refractory iron deficiency anaemia (IRIDA). Nature Genetics 40: 569-71.
-
(2008)
Nature Genetics
, vol.40
, pp. 569-571
-
-
Finberg, K.E.1
Heeney, M.M.2
Campagna, D.R.3
-
15
-
-
33749393565
-
Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing
-
Goswami T, Andrews NC (2006) Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing. Journal of Biological Chemistry 281: 28494-8.
-
(2006)
Journal of Biological Chemistry
, vol.281
, pp. 28494-8
-
-
Goswami, T.1
Andrews, N.C.2
-
16
-
-
20344403788
-
Role of autoimmune gastritis, Helicobacter pylori and coeliac disease in refractory or unexplained iron deficiency anaemia
-
Hershko C, Hoffbrand AV, Keret D (2005) Role of autoimmune gastritis, Helicobacter pylori and coeliac disease in refractory or unexplained iron deficiency anaemia. Haematologica 90: 585-95.
-
(2005)
Haematologica
, vol.90
, pp. 585-595
-
-
Hershko, C.1
Hoffbrand, A.V.2
Keret, D.3
-
17
-
-
70450211327
-
Recent advances in the understanding of iron metabolism and iron - related diseases
-
12 articles covering all aspects of iron metabolism and related diseases
-
Hoffbrand AV (ed.) (2009) Recent advances in the understanding of iron metabolism and iron - related diseases. Acta Haematologica 122: 75-184, 12 articles covering all aspects of iron metabolism and related diseases.
-
(2009)
Acta Haematologica
, vol.122
, pp. 75-184
-
-
Hoffbrand, A.V.1
-
18
-
-
63149128149
-
Molecular basis of inherited microcytic anaemia due to defects in iron acquisitions or haem synthesis
-
Iolascon A, De Falco L, Beaumont C (2009) Molecular basis of inherited microcytic anaemia due to defects in iron acquisitions or haem synthesis. Haematologica 94: 395-408.
-
(2009)
Haematologica
, vol.94
, pp. 395-408
-
-
Iolascon, A.1
De Falco, L.2
Beaumont, C.3
-
19
-
-
61849088361
-
Regulation of growth differentiation factor 15 expression by intracellular iron
-
Lakhal S, Talbot NP, Crosby A et al. (2009) Regulation of growth differentiation factor 15 expression by intracellular iron. Blood 113: 1555-63.
-
(2009)
Blood
, vol.113
, pp. 1555-1563
-
-
Lakhal, S.1
Talbot, N.P.2
Crosby, A.3
-
20
-
-
0032990411
-
Mutations in SCL19AZ cause thiamine - responsive megaloblastic anaemia associated with diabetes mellitus and deafness
-
Lebay V, Ras T, Baran D et al. (1999) Mutations in SCL19AZ cause thiamine - responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nature Genetics 22: 300-4.
-
(1999)
Nature Genetics
, vol.22
, pp. 300-304
-
-
Lebay, V.1
Ras, T.2
Baran, D.3
-
21
-
-
4344581912
-
Revised European best practice guidelines for the management of anaemia in patients with chronic renal failure
-
Locatelli F, Aljama P, Bárány P et al. (2004) Revised European best practice guidelines for the management of anaemia in patients with chronic renal failure. Nephrology, Dialysis, Transplantation 19 (Suppl. 2): 1-47.
-
(2004)
Nephrology, Dialysis, Transplantation
, vol.19
, Issue.SUPPL. 2
, pp. 1-47
-
-
Locatelli, F.1
Aljama, P.2
Bárány, P.3
-
22
-
-
0141890065
-
Behavioural and developmental effects of preventing iron - deficiency anaemia in healthy full - term infants
-
Lozoff B, De Andraca I, Castillo M et al. (2003) Behavioural and developmental effects of preventing iron - deficiency anaemia in healthy full - term infants. Pediatrics 112: 846-54.
-
(2003)
Pediatrics
, vol.112
, pp. 846-854
-
-
Lozoff, B.1
De Andraca, I.2
Castillo, M.3
-
24
-
-
63449122819
-
Lack of the bone morphogenetic protein BMP6 induces massive iron overload
-
Meynard D, Kautz L, Darnaud V et al. (2009) Lack of the bone morphogenetic protein BMP6 induces massive iron overload. Nature Genetics 41: 478-81.
-
(2009)
Nature Genetics
, vol.41
, pp. 478-481
-
-
Meynard, D.1
Kautz, L.2
Darnaud, V.3
-
25
-
-
84885776758
-
-
Online Mendelian Inheritance in Man (OMIM) Knowledge base of human genes and genetic disorders
-
Online Mendelian Inheritance in Man (OMIM) Available at www.ncbi.nlm.nih.gov/OMIM/. Knowledge base of human genes and genetic disorders.
-
-
-
-
27
-
-
66749138982
-
Matriptase - 2 (TMPRSS6): a proteolytic regulator of iron homeostasis
-
Ramsay AJ, Hooper JD, Folgueras AR et al. (2009) Matriptase - 2 (TMPRSS6): a proteolytic regulator of iron homeostasis. Haematologica 94: 840-9.
-
(2009)
Haematologica
, vol.94
, pp. 840-849
-
-
Ramsay, A.J.1
Hooper, J.D.2
Folgueras, A.R.3
-
28
-
-
56449096622
-
The serine protease matriptase - 2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin
-
Silvestri L, Pagani A, Nai A et al. (2008) The serine protease matriptase - 2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin. Cell Metabolism 6: 502-11.
-
(2008)
Cell Metabolism
, vol.6
, pp. 502-511
-
-
Silvestri, L.1
Pagani, A.2
Nai, A.3
-
29
-
-
0036428760
-
Iron transport across cell membranes: molecular understanding of duodenal and placental iron transport
-
Srai SK, Bomford A, McArdle HJ (2002) Iron transport across cell membranes: molecular understanding of duodenal and placental iron transport. Best Practice and Research. Clinical Haematology 15: 243-59.
-
(2002)
Best Practice and Research. Clinical Haematology
, vol.15
, pp. 243-259
-
-
Srai, S.K.1
Bomford, A.2
McArdle, H.J.3
-
30
-
-
34948904750
-
High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin
-
Tanno T, Bhanu NV, Oneal PA et al. (2007) High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin. Nature Medicine 13: 1096-101.
-
(2007)
Nature Medicine
, vol.13
, pp. 1096-1101
-
-
Tanno, T.1
Bhanu, N.V.2
Oneal, P.A.3
-
32
-
-
33751175421
-
Interleukin - 6 induces hepcidin expression through STAT3
-
Wrighting DM, Andrews NC (2006) Interleukin - 6 induces hepcidin expression through STAT3. Blood 108: 3204-9.
-
(2006)
Blood
, vol.108
, pp. 3204-3209
-
-
Wrighting, D.M.1
Andrews, N.C.2
-
33
-
-
59449109182
-
Iron homeostasis: recently identified proteins provide insight into novel control mechanisms
-
Zhang AS, Enns CA (2009) Iron homeostasis: recently identified proteins provide insight into novel control mechanisms. Journal of Biological Chemistry 284: 711-15.
-
(2009)
Journal of Biological Chemistry
, vol.284
, pp. 711-715
-
-
Zhang, A.S.1
Enns, C.A.2
|