-
1
-
-
0036439058
-
A review of the molecular diagnosis of thalassemia
-
GU, X. & Y. ZENG. 2002. A review of the molecular diagnosis of thalassemia. Hematology 7: 203-209.
-
(2002)
Hematology
, vol.7
, pp. 203-209
-
-
Gu, X.1
Zeng, Y.2
-
2
-
-
0019450469
-
Molecular basis for mild forms of homozygous beta-thalassaemia
-
WEATHERALL, D.J., L. PRESSLEY, W.G. WOOD, et al. 1981. Molecular basis for mild forms of homozygous beta-thalassaemia. Lancet 1: 527-529.
-
(1981)
Lancet
, vol.1
, pp. 527-529
-
-
Weatherall, D.J.1
Pressley, L.2
Wood, W.G.3
-
3
-
-
0035215117
-
Diagnosing myocardial iron overload
-
HOFFBRAND, A.V. 2001. Diagnosing myocardial iron overload. Eur. Heart J. 22: 2140-2141.
-
(2001)
Eur. Heart J.
, vol.22
, pp. 2140-2141
-
-
Hoffbrand, A.V.1
-
5
-
-
2142773321
-
The pathophysiology of β-thalassemia
-
M.H. Steinberg, B.G. Forget, D.R. Higgs, and R.L. Nagel, Eds.: Cambridge University Press. Cambridge, MA
-
RACHMILEWITZ, E.A. & S. SCHRIER. 2001. The pathophysiology of β-thalassemia. In Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management. M.H. Steinberg, B.G. Forget, D.R. Higgs, and R.L. Nagel, Eds.: 223-251. Cambridge University Press. Cambridge, MA.
-
(2001)
Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management.
, pp. 223-251
-
-
Rachmilewitz, E.A.1
Schrier, S.2
-
6
-
-
0022021390
-
Auto-oxidation and a membrane associated "Fenton Reagent": A possible explanation for development of membrane lesions in sickle erythrocytes
-
HEBBEL, R.P. 1985. Auto-oxidation and a membrane associated "Fenton Reagent": a possible explanation for development of membrane lesions in sickle erythrocytes. Clin. Hematol. 14: 129-140.
-
(1985)
Clin. Hematol.
, vol.14
, pp. 129-140
-
-
Hebbel, R.P.1
-
7
-
-
0018164919
-
Non-specific serum iron in thalassaemia: An abnormal serum iron fraction of potential toxicity
-
HERSHKO, C., G. GRAHAMK, G.W. BATES, et al. 1978. Non-specific serum iron in thalassaemia: an abnormal serum iron fraction of potential toxicity. Br. J. Haematol. 40: 255-263.
-
(1978)
Br. J. Haematol.
, vol.40
, pp. 255-263
-
-
Hershko, C.1
Grahamk, G.2
Bates, G.W.3
-
8
-
-
0033677772
-
The importance of non-transferrin bound iron in disorders of iron metabolism
-
BREUER, W., C. HERSHKO & Z.I. CABANTCHIK. 2000. The importance of non-transferrin bound iron in disorders of iron metabolism. Transfus. Sci. 23: 185-192.
-
(2000)
Transfus. Sci.
, vol.23
, pp. 185-192
-
-
Breuer, W.1
Hershko, C.2
Cabantchik, Z.I.3
-
9
-
-
0033543720
-
Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin
-
GOSRIWATANA, I., O. LOREAL, S. LU, et al. 1999. Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin. Anal. Biochem. 273: 212-220.
-
(1999)
Anal. Biochem.
, vol.273
, pp. 212-220
-
-
Gosriwatana, I.1
Loreal, O.2
Lu, S.3
-
10
-
-
0141705304
-
Labile plasma iron in iron overload: Redox activity and susceptibility to chelation
-
ESPOSITO, B.P., W. BREUER, P. SIRANKAPRACHA, et al. 2003. Labile plasma iron in iron overload: redox activity and susceptibility to chelation. Blood 102: 2670-2677.
-
(2003)
Blood
, vol.102
, pp. 2670-2677
-
-
Esposito, B.P.1
Breuer, W.2
Sirankapracha, P.3
-
12
-
-
0036570964
-
A review of fluorescence methods for assessing labile iron in cells and biological fluids
-
ESPOSITO, B.P., S. EPSZTEJN, W. BREUER, et al. 2002. A review of fluorescence methods for assessing labile iron in cells and biological fluids. Anal. Biochem. 304: 1-18.
-
(2002)
Anal. Biochem.
, vol.304
, pp. 1-18
-
-
Esposito, B.P.1
Epsztejn, S.2
Breuer, W.3
-
13
-
-
0037108199
-
The labile iron pool: Characterization, measurement, and participation in cellular processes
-
KAKHLON, O. & Z.I. CABANTCHIK. 2002. The labile iron pool: characterization, measurement, and participation in cellular processes. Free Radic. Biol. Med. 33: 1037-1046.
-
(2002)
Free Radic. Biol. Med.
, vol.33
, pp. 1037-1046
-
-
Kakhlon, O.1
Cabantchik, Z.I.2
-
14
-
-
0033826764
-
Iron regulatory proteins and the molecular control of mammalian iron metabolism
-
EISENSTEIN, R.S. 2001. Iron regulatory proteins and the molecular control of mammalian iron metabolism. Annu. Rev. Nutr. 20: 627-662.
-
(2001)
Annu. Rev. Nutr.
, vol.20
, pp. 627-662
-
-
Eisenstein, R.S.1
-
15
-
-
14944387002
-
Iron trafficking in the mitochondrion: Novel pathways revealed by disease
-
NAPIER, I., P. PONKA & D.R. RICHARDSON. 2005. Iron trafficking in the mitochondrion: novel pathways revealed by disease. Blood 105: 1867-1874.
-
(2005)
Blood
, vol.105
, pp. 1867-1874
-
-
Napier, I.1
Ponka, P.2
Richardson, D.R.3
-
16
-
-
11144226961
-
Intracellular kinetics of iron in reticulocytes: Evidence for endosome involvement in iron targeting to mitochondria
-
ZHANG, A.S., A.D. SHEFTEL & P. PONKA. 2005. Intracellular kinetics of iron in reticulocytes: evidence for endosome involvement in iron targeting to mitochondria. Blood 105: 368-375.
-
(2005)
Blood
, vol.105
, pp. 368-375
-
-
Zhang, A.S.1
Sheftel, A.D.2
Ponka, P.3
-
17
-
-
0035896642
-
Hepcidin, a urinary antimicrobial peptide synthesized in the liver
-
PARK, C.H., E.V. VALORE, A.J. WARING, et al. 2001. Hepcidin, a urinary antimicrobial peptide synthesized in the liver. J. Biol. Chem. 276: 7806-7810.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 7806-7810
-
-
Park, C.H.1
Valore, E.V.2
Waring, A.J.3
-
18
-
-
0034284595
-
LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity
-
KRAUSE, A., S. NEITZ, H.J. MAGERT, et al. 2000. LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity. FEBS Lett. 480: 147-150.
-
(2000)
FEBS Lett.
, vol.480
, pp. 147-150
-
-
Krause, A.1
Neitz, S.2
Magert, H.J.3
-
19
-
-
0041672570
-
Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation
-
GANZ, T. 2003. Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation. Blood 102: 783-788.
-
(2003)
Blood
, vol.102
, pp. 783-788
-
-
Ganz, T.1
-
20
-
-
10844258104
-
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
-
NEMETH, E., M.S. TUTTLE, J. POWELSON, et al. 2004. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 306: 2090-2093.
-
(2004)
Science
, vol.306
, pp. 2090-2093
-
-
Nemeth, E.1
Tuttle, M.S.2
Powelson, J.3
-
21
-
-
0035896581
-
A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload
-
PIGEON, C., G. ILYIN, B. COURSELAUD, et al. 2001. A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload. J. Biol. Chem. 276: 7811-7819.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 7811-7819
-
-
Pigeon, C.1
Ilyin, G.2
Courselaud, B.3
-
22
-
-
0038662619
-
Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein
-
NEMETH, E., E.V. VALORE, M. TERRITO, et al. 2003. Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein. Blood 101: 2461-2463.
-
(2003)
Blood
, vol.101
, pp. 2461-2463
-
-
Nemeth, E.1
Valore, E.V.2
Territo, M.3
-
23
-
-
0012994611
-
Hepcidin, a new iron regulatory peptide
-
NICOLAS, G., L. VIATTE, M. BENNOUN, et al. 2002. Hepcidin, a new iron regulatory peptide. Blood Cells Mol. Dis. 29: 327-335.
-
(2002)
Blood Cells Mol. Dis.
, vol.29
, pp. 327-335
-
-
Nicolas, G.1
Viatte, L.2
Bennoun, M.3
-
24
-
-
0037606048
-
A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human beta-globin gene transfer
-
RIVELLA, S., C. MAY, A. CHADBURN, et al. 2003. A novel murine model of Cooley anemia and its rescue by lentiviral-mediated human beta-globin gene transfer. Blood 101: 2932-2939.
-
(2003)
Blood
, vol.101
, pp. 2932-2939
-
-
Rivella, S.1
May, C.2
Chadburn, A.3
-
25
-
-
0346433908
-
Decreased hepcidin mRNA expression in thalassemic mice
-
ADAMSKY, K., O. WEIZER, N. AMARIGLIO, et al. 2004. Decreased hepcidin mRNA expression in thalassemic mice. Br. J. Haematol. 124: 123-124.
-
(2004)
Br. J. Haematol.
, vol.124
, pp. 123-124
-
-
Adamsky, K.1
Weizer, O.2
Amariglio, N.3
-
26
-
-
29744470665
-
mRNA expression of iron regulatory genes in thalassemia intermedia and thalassemia major mice models
-
In press
-
WEIZER, O., K. ADAMSKY, N. AMARIGLIO, et al. mRNA expression of iron regulatory genes in thalassemia intermedia and thalassemia major mice models. Am. J. Hematol. In press.
-
Am. J. Hematol.
-
-
Weizer, O.1
Adamsky, K.2
Amariglio, N.3
-
28
-
-
4644309964
-
Tissue-specific changes in iron metabolism genes in mice following phenylhydrazine-induced haemolysis
-
LATUNDE-DADA, G.O., C.D. VULPE, G.J. ANDERSON, et al. 2004. Tissue-specific changes in iron metabolism genes in mice following phenylhydrazine-induced haemolysis. Biochim. Biophys. Acta 1690: 169-176.
-
(2004)
Biochim. Biophys. Acta
, vol.1690
, pp. 169-176
-
-
Latunde-Dada, G.O.1
Vulpe, C.D.2
Anderson, G.J.3
-
29
-
-
0029097965
-
Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo
-
SHALEV, O., T. REPKA, A. GOLDFARB, et al. 1995. Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo. Blood 86: 2008-2013.
-
(1995)
Blood
, vol.86
, pp. 2008-2013
-
-
Shalev, O.1
Repka, T.2
Goldfarb, A.3
-
30
-
-
0032896230
-
Deferiprone therapy in homozygous human -thalassemia removes erythrocyte membrane free iron and reduces KCl co-transport activity
-
DE FRANCESCHI, L., O. SHALEV, A. PIGA, et al. 1999. Deferiprone therapy in homozygous human -thalassemia removes erythrocyte membrane free iron and reduces KCl co-transport activity. J. Lab. Clin. Med. 133: 64-69.
-
(1999)
J. Lab. Clin. Med.
, vol.133
, pp. 64-69
-
-
De Franceschi, L.1
Shalev, O.2
Piga, A.3
-
31
-
-
4444274916
-
Labile plasma iron (LPI) as an indicator of chelatable plasma redox activity in iron-overloaded beta-thalassaemia/HbE partients treated with an oral chelator
-
POOTRAKUL, P., W. BREUER, M. SAMETBAND, et al. 2004. Labile plasma iron (LPI) as an indicator of chelatable plasma redox activity in iron-overloaded beta-thalassaemia/HbE partients treated with an oral chelator. Blood 104: 1504-1510.
-
(2004)
Blood
, vol.104
, pp. 1504-1510
-
-
Pootrakul, P.1
Breuer, W.2
Sametband, M.3
-
32
-
-
3242780446
-
Oxidative status and malondialdehyde in β-thalassemia patients
-
CIGHETTI, G., L. DUCA, L. BORTONE, et al. 2002. Oxidative status and malondialdehyde in β-thalassemia patients. Eur. J. Clin. Invest. 32: 55-60.
-
(2002)
Eur. J. Clin. Invest.
, vol.32
, pp. 55-60
-
-
Cighetti, G.1
Duca, L.2
Bortone, L.3
-
33
-
-
0035007589
-
Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in β-thalassemia intermedia patients
-
TESORIERE, L., D. D'ARPA, D. BUTERA, et al. 2001. Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in β-thalassemia intermedia patients. Free Radical Res. 34: 529-540.
-
(2001)
Free Radical Res.
, vol.34
, pp. 529-540
-
-
Tesoriere, L.1
D'Arpa, D.2
Butera, D.3
-
34
-
-
0018728292
-
Vitamin E deficiency in β-thalassemia major: Changes in hematological and biochemical parameters after a therapeutic trial with α-tocopherol
-
RACHMILEWITZ, E.A., A. SHIFTER & I. KAHANE. 1979. Vitamin E deficiency in β-thalassemia major: changes in hematological and biochemical parameters after a therapeutic trial with α-tocopherol. Am. J. Clin. Nutr. 32: 1850-1858.
-
(1979)
Am. J. Clin. Nutr.
, vol.32
, pp. 1850-1858
-
-
Rachmilewitz, E.A.1
Shifter, A.2
Kahane, I.3
-
35
-
-
0242600642
-
Effects of N-acetylcysteine on dense cell formation in sickle cell disease
-
PACE, B.S., A. SHARTAVA, A. PACK-MABIEN, et al. 2003. Effects of N-acetylcysteine on dense cell formation in sickle cell disease. Am. J. Hematol. 73: 26-32.
-
(2003)
Am. J. Hematol.
, vol.73
, pp. 26-32
-
-
Pace, B.S.1
Shartava, A.2
Pack-Mabien, A.3
|