-
1
-
-
0019952842
-
Hereditary Hemochromatosis analysis of laboratory expression of the disease by genotype in 18 pedigrees
-
1 Dadone MM, Kushner JP, Edwards CQ. Bishop DT, Skolnick MH: Hereditary Hemochromatosis analysis of laboratory expression of the disease by genotype in 18 pedigrees. Am J Clin Pathol 1982;78:196-207.
-
(1982)
Am J Clin Pathol
, vol.78
, pp. 196-207
-
-
Dadone, M.M.1
Kushner, J.P.2
Edwards, C.Q.3
Bishop, D.T.4
Skolnick, M.H.5
-
2
-
-
0023901798
-
Prevalence of hemochromatosis among 11,065 presumably healthy donors
-
2 Edwards CQ, Griffen LM, Goldgar D, Drummond C, Skolnick MH, Kushner JP: Prevalence of hemochromatosis among 11,065 presumably healthy donors. N Engl J Med 1988;318:1355-1362,.
-
(1988)
N Engl J Med
, vol.318
, pp. 1355-1362
-
-
Edwards, C.Q.1
Griffen, L.M.2
Goldgar, D.3
Drummond, C.4
Skolnick, M.H.5
Kushner, J.P.6
-
3
-
-
0029156301
-
Prevalence of heterozygotes for hemochromatosis in the white population of the United States
-
3 McLaren CE, Gordeuk VR, Looker AC, Hasselblad V, Edward CQ, Griffen LM, Kushner JP, Brittenham GM: Prevalence of heterozygotes for hemochromatosis in the white population of the United States. Blood 1995;86:2021-2027.
-
(1995)
Blood
, vol.86
, pp. 2021-2027
-
-
McLaren, C.E.1
Gordeuk, V.R.2
Looker, A.C.3
Hasselblad, V.4
Edward, C.Q.5
Griffen, L.M.6
Kushner, J.P.7
Brittenham, G.M.8
-
4
-
-
0000702937
-
Hemochromatosis
-
in Scriver CR, Beaudet AL, Sly WS, Valle D (eds): New York, McGraw-Hill
-
4 Bothwell TH, Charlton RW, Motulsky AG: Hemochromatosis, in Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The metabolic and molecular basis of inherited disease. New York, McGraw-Hill, 1995, pp. 2237-2269.
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 2237-2269
-
-
Bothwell, T.H.1
Charlton, R.W.2
Motulsky, A.G.3
-
5
-
-
0002106459
-
Hemochromatosis and the iron overload syndromes
-
in Zakim D, Boyer TD (eds): Philadelphia, W.B. Saunders
-
5 Bacon BR, Tavill AS: Hemochromatosis and the iron overload syndromes, in Zakim D, Boyer TD (eds): Hepatology. A textbook of liver disease. Philadelphia, W.B. Saunders, 1996. pp. 1439-1472.
-
(1996)
Hepatology. A Textbook of Liver Disease
, pp. 1439-1472
-
-
Bacon, B.R.1
Tavill, A.S.2
-
6
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
6 Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, et al.: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics 1996;13:399-408.
-
(1996)
Nature Genetics
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
Tsuchihashi, Z.4
Ruddy, D.A.5
Basava, A.6
-
7
-
-
0017158302
-
Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis
-
7 Simon M, Bourel M, Fauchet R, Genetet B: Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis. Gut 1976;17:332-334.
-
(1976)
Gut
, vol.17
, pp. 332-334
-
-
Simon, M.1
Bourel, M.2
Fauchet, R.3
Genetet, B.4
-
8
-
-
0027491809
-
Localization of the hemochromatosis gene close to D6S105
-
8 Jazwinska EC, Lee SC, Webb SI, Halliday JW, Powell LW: Localization of the hemochromatosis gene close to D6S105. Am J Hum Genet 1993;53:347-352.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 347-352
-
-
Jazwinska, E.C.1
Lee, S.C.2
Webb, S.I.3
Halliday, J.W.4
Powell, L.W.5
-
9
-
-
0032530484
-
Construction and validation of yeast artifical chromosome contig maps by RecA-assisted restriction endonuclease cleavage
-
9 Lauer P, Schneider SS, Gnirke A: Construction and validation of yeast artifical chromosome contig maps by RecA-assisted restriction endonuclease cleavage. Proc Natl Acad Sci USA 1998;95:11318-11323.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 11318-11323
-
-
Lauer, P.1
Schneider, S.S.2
Gnirke, A.3
-
10
-
-
0031744492
-
A haplotype and linkage disequilibrium analysis of the hemochromatosis gene region
-
10 Thomas W, Fullan A, Loeb DB, McClelland EE, Bacon BR, Wolff RK: A haplotype and linkage disequilibrium analysis of the hemochromatosis gene region. Hum Genet 1998;102:517-525.
-
(1998)
Hum Genet
, vol.102
, pp. 517-525
-
-
Thomas, W.1
Fullan, A.2
Loeb, D.B.3
McClelland, E.E.4
Bacon, B.R.5
Wolff, R.K.6
-
11
-
-
0030906761
-
Clone-Contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22
-
11 Lauer P, Meyer MC, Prass CE, Stranes SS, Wolff RK, Gnirke A: Clone-Contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22. Genome Research 1997;7:457-470.
-
(1997)
Genome Research
, vol.7
, pp. 457-470
-
-
Lauer, P.1
Meyer, M.C.2
Prass, C.E.3
Stranes, S.S.4
Wolff, R.K.5
Gnirke, A.6
-
12
-
-
0030130997
-
Localization of the hemochromatosis disease gene: Linkage disequlibrium analysis using an american patient collection
-
12 Sesse NK, Venditti CP, Chorney KA, Gerhard GS, Ma J, Hudson TJ, Phatak P, Chorney MJ: Localization of the hemochromatosis disease gene: Linkage disequlibrium analysis using an american patient collection. Boold Cells, Molecules, and Diseases 1996;22:36-46.
-
(1996)
Boold Cells, Molecules, and Diseases
, vol.22
, pp. 36-46
-
-
Sesse, N.K.1
Venditti, C.P.2
Chorney, K.A.3
Gerhard, G.S.4
Ma, J.5
Hudson, T.J.6
Phatak, P.7
Chorney, M.J.8
-
13
-
-
15444340362
-
A. 1.1-Mb transcript map of the hereditary hemochromatosis locus
-
13 Ruddy DA, Kronmal GS, Lee VK, Mintier GA, Quintana L, Domingo RJ, et al.: A. 1.1-Mb transcript map of the hereditary hemochromatosis locus. Genome Research 1997;7:441-456.
-
(1997)
Genome Research
, vol.7
, pp. 441-456
-
-
Ruddy, D.A.1
Kronmal, G.S.2
Lee, V.K.3
Mintier, G.A.4
Quintana, L.5
Domingo, R.J.6
-
14
-
-
0028176811
-
Iron overload in β2-microglobulin-deficient mice
-
14 De Sousa M, Reimao R, Lacerda R, Hugo P, Kaufmann SHE, Porto G: Iron overload in β2-microglobulin-deficient mice. Immunol. Lett. 1994 ;39:105-111.
-
(1994)
Immunol. Lett.
, vol.39
, pp. 105-111
-
-
De Sousa, M.1
Reimao, R.2
Lacerda, R.3
Hugo, P.4
Kaufmann, S.H.E.5
Porto, G.6
-
15
-
-
0030294028
-
Haemochromatosis and HLA-H
-
15 Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP: Haemochromatosis and HLA-H. Nature Genetics 1996;14:250-251.
-
(1996)
Nature Genetics
, vol.14
, pp. 250-251
-
-
Jazwinska, E.C.1
Cullen, L.M.2
Busfield, F.3
Pyper, W.R.4
Webb, S.I.5
Powell, L.W.6
Morris, C.P.7
Walsh, T.P.8
-
16
-
-
16144368650
-
Haemochromatosis and HLA-H
-
16 Jouanolle AM, Gandon G, Jezequel P, M. B, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bourie P, Carn G, Andrieux N, Giequel I, LeGall J, David V: Haemochromatosis and HLA-H. Nature Genetics 1996;14:251-252.
-
(1996)
Nature Genetics
, vol.14
, pp. 251-252
-
-
Jouanolle, A.M.1
Gandon, G.2
Jezequel, P.B.M.3
Campion, M.L.4
Yaouanq, J.5
Mosser, J.6
Fergelot, P.7
Chauvel, B.8
Bourie, P.9
Carn, G.10
Andrieux, N.11
Giequel, I.12
LeGall, J.13
David, V.14
-
18
-
-
0031047769
-
Mutations in the MHC class I-like candidate gene of hemochromatosis in French patients
-
18 Borot N, Roth M, Malfory L, Demangel C, Vinel J, Pascal J, Coppin H: Mutations in the MHC class I-like candidate gene of hemochromatosis in French patients. Immunogenetics 1997;45: 320-324.
-
(1997)
Immunogenetics
, vol.45
, pp. 320-324
-
-
Borot, N.1
Roth, M.2
Malfory, L.3
Demangel, C.4
Vinel, J.5
Pascal, J.6
Coppin, H.7
-
19
-
-
0030221927
-
Mutation analysis in hereditary hemochromatosis
-
19 Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Elshof AET, Gerhard GS, Chomey M: Mutation analysis in hereditary hemochromatosis. Blood Cells, Molecules, and Diseases 1996;31:187-194.
-
(1996)
Blood Cells, Molecules, and Diseases
, vol.31
, pp. 187-194
-
-
Beutler, E.1
Gelbart, T.2
West, C.3
Lee, P.4
Adams, M.5
Blackstone, R.6
Pockros, P.7
Kosty, M.8
Venditti, C.P.9
Phatak, P.D.10
Seese, N.K.11
Chorney, K.A.12
Elshof, A.E.T.13
Gerhard, G.S.14
Chomey, M.15
-
20
-
-
16944363480
-
Mutation analysis of the HLA-H gene in Italian hemochromatosis patients
-
20 Carella M, D'Ambrosio L, Totaro A, Grifa A, Valentino MA, Piperno A, Girelli D, Roetto A, Franco B, Gasparini P, Camaschella C: Mutation analysis of the HLA-H gene in Italian hemochromatosis patients. Am. J. Hum. Genet. 1997;60:828-832.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 828-832
-
-
Carella, M.1
Ambrosio, L.2
Totaro, A.3
Grifa, A.4
Valentino, M.A.5
Piperno, A.6
Girelli, D.7
Roetto, A.8
Franco, B.9
Gasparini, P.10
Camaschella, C.11
-
21
-
-
0023176346
-
Structure of the human class I histocompatibility antigen, HLA-A2
-
21 Bjorkman PJ, Saper MA, Samraoui B, Bennett WS, Strominger JL, Wiley DC: Structure of the human class I histocompatibility antigen, HLA-A2. Nature 1987;329:506-512.
-
(1987)
Nature
, vol.329
, pp. 506-512
-
-
Bjorkman, P.J.1
Saper, M.A.2
Samraoui, B.3
Bennett, W.S.4
Strominger, J.L.5
Wiley, D.C.6
-
22
-
-
0030827084
-
The significance of the 187G (H63D) mutation in hemochromatosis
-
22 Beutler E: The significance of the 187G (H63D) mutation in hemochromatosis. Am J Hum Genet 1997;61:762-764.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 762-764
-
-
Beutler, E.1
-
23
-
-
0031450438
-
Haemochromatosis, Hfc and genetic complexity
-
23 Risch N: Haemochromatosis, Hfc and genetic complexity. Nat Genet 1997;17:375-376.
-
(1997)
Nat Genet
, vol.17
, pp. 375-376
-
-
Risch, N.1
-
24
-
-
0031132040
-
Rapid diagnosis of the HLA-H gene Cys282Tyr mutation in hemochromatosis by polymerase chain reaction-a very rare mutation in the Chinese population
-
24 Chang J-G, Liu T-C, Lin S-F: Rapid diagnosis of the HLA-H gene Cys282Tyr mutation in hemochromatosis by polymerase chain reaction-a very rare mutation in the Chinese population. Blood 1997;89:3492-3493.
-
(1997)
Blood
, vol.89
, pp. 3492-3493
-
-
Chang, J.-G.1
Liu, T.-C.2
Lin, S.-F.3
-
25
-
-
0031778690
-
The hemochromatosis 845 G to A and 187 C to G mutations: Prevalence in non-caucasian populations
-
25 Cullen LM, Gao X, Easteal S, Jazwinska EC: The hemochromatosis 845 G to A and 187 C to G mutations: Prevalence in non-caucasian populations. Am J Hum Genet 1998;62:1403-1407.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1403-1407
-
-
Cullen, L.M.1
Gao, X.2
Easteal, S.3
Jazwinska, E.C.4
-
26
-
-
0030878126
-
HLA-H and associated proteins in patients with hemochromatosis
-
26 Beutler E, West C, Gelbart T: HLA-H and associated proteins in patients with hemochromatosis. Mol Med 1997;3:397-402.
-
(1997)
Mol Med
, vol.3
, pp. 397-402
-
-
Beutler, E.1
West, C.2
Gelbart, T.3
-
27
-
-
0032171048
-
Transferrin receptor mutation analysis in hereditary hemochromatosis patients
-
27 Tsuchihashi Z, Hansen SL, Quintana L, Kronmal GS, Mapa FA, Feder JN, Wolff RK: Transferrin receptor mutation analysis in hereditary hemochromatosis patients. Blood Cells, Molecules, and Diseases 1998;31:317-321.
-
(1998)
Blood Cells, Molecules, and Diseases
, vol.31
, pp. 317-321
-
-
Tsuchihashi, Z.1
Hansen, S.L.2
Quintana, L.3
Kronmal, G.S.4
Mapa, F.A.5
Feder, J.N.6
Wolff, R.K.7
-
28
-
-
0020095112
-
Exon/intron organization and complete nucleotide sequence of an HLA gene
-
28 Malissen M, Malissen B, Jordan BR: Exon/intron organization and complete nucleotide sequence of an HLA gene. Proc Natl Acad Sci USA 1982;79:893-897.
-
(1982)
Proc Natl Acad Sci USA
, vol.79
, pp. 893-897
-
-
Malissen, M.1
Malissen, B.2
Jordan, B.R.3
-
30
-
-
0000558870
-
The hereditary hemochromatosis gene and iron homeostasis
-
30 Feder JN, Penny DM, Irrinki A, Mintier GA, Lebron JA, Gross CN, Lee L, Tsuchihashi Z, Enns CA, Bjorkman PJ, Schatzman RC: The hereditary hemochromatosis gene and iron homeostasis: Molecular Biology of Hematopoiesis 1999;6.
-
(1999)
Molecular Biology of Hematopoiesis
, vol.6
-
-
Feder, J.N.1
Penny, D.M.2
Irrinki, A.3
Mintier, G.A.4
Lebron, J.A.5
Gross, C.N.6
Lee, L.7
Tsuchihashi, Z.8
Enns, C.A.9
Bjorkman, P.J.10
Schatzman, R.C.11
-
31
-
-
0025373363
-
β2Microglobulin deficient mice lack CD4-8+ cytolytic T cells
-
31 Zijlstra M, Bix M, Simister NE, Loring JM, Raulet DH, Jaenisch R: β2Microglobulin deficient mice lack CD4-8+ cytolytic T cells. Nature 1990;344:742-746.
-
(1990)
Nature
, vol.344
, pp. 742-746
-
-
Zijlstra, M.1
Bix, M.2
Simister, N.E.3
Loring, J.M.4
Raulet, D.H.5
Jaenisch, R.6
-
32
-
-
17644434333
-
The hemochromatosis founder mutation in HLA-H disrupts b2-microglobulin interaction and cell surface expression
-
32 Feder JN, Tsuchihashi Z, Irrinki A, Lee VK, Mapa FA, Morikang E, Prass CE, Starnes SM, Wolff RK, Parkkila S, Sly WS, Schatzman RC: The hemochromatosis founder mutation in HLA-H disrupts b2-microglobulin interaction and cell surface expression. J Biol Chem 1997;272:14025-14028.
-
(1997)
J Biol Chem
, vol.272
, pp. 14025-14028
-
-
Feder, J.N.1
Tsuchihashi, Z.2
Irrinki, A.3
Lee, V.K.4
Mapa, F.A.5
Morikang, E.6
Prass, C.E.7
Starnes, S.M.8
Wolff, R.K.9
Parkkila, S.10
Sly, W.S.11
Schatzman, R.C.12
-
33
-
-
0030732164
-
Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with b2-microglobulin,intracellular processing, and cell surface expression of the HFE protein in COS-7 cells
-
33 Waheed A, Parkkila S, Zhou XY, Tomatsu S, Tsuchihashi Z, Feder JN, Schatzman RC, Britton RS, Bacon BR, Sly WS: Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with b2-microglobulin,intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proc Natl Acad Sci USA 1997;94:12384-12389.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 12384-12389
-
-
Waheed, A.1
Parkkila, S.2
Zhou, X.Y.3
Tomatsu, S.4
Tsuchihashi, Z.5
Feder, J.N.6
Schatzman, R.C.7
Britton, R.S.8
Bacon, B.R.9
Sly, W.S.10
-
34
-
-
0031002910
-
Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract
-
34 Parkkila S, Waheed A, Britton RS, Feder JN, Tsuchihashi Z, Schatzman RC, Bacon BR, Sly WS: Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract. Proc Natl Acad Sci USA 1997; 94:2534-2539.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2534-2539
-
-
Parkkila, S.1
Waheed, A.2
Britton, R.S.3
Feder, J.N.4
Tsuchihashi, Z.5
Schatzman, R.C.6
Bacon, B.R.7
Sly, W.S.8
-
35
-
-
13144282684
-
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
-
35 Feder JN, Penny DM, Irrinke A, Lee VK, Lebron JA, Waston N, Tsuchihashi Z, Sigal E, Bjorkman PJ, Schatzman RC: The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proc Natl Acad Sci USA 1988;95:1472-1477.
-
(1988)
Proc Natl Acad Sci USA
, vol.95
, pp. 1472-1477
-
-
Feder, J.N.1
Penny, D.M.2
Irrinke, A.3
Lee, V.K.4
Lebron, J.A.5
Waston, N.6
Tsuchihashi, Z.7
Sigal, E.8
Bjorkman, P.J.9
Schatzman, R.C.10
-
36
-
-
0030712463
-
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
-
36 Parkkila S, Waheed A, Britton RS, R. BB, Zhou XY, Tomatsu S, Fleming RH, Sly WS: Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis. Proc Natl Acad Sci USA 1997;94:13198-13202.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13198-13202
-
-
Parkkila, S.1
Waheed, A.2
Britton, R.S.3
BB, R.4
Zhou, X.Y.5
Tomatsu, S.6
Fleming, R.H.7
Sly, W.S.8
-
37
-
-
0032555601
-
Co-trafficking of HFE with transferrin receptor implies role in intracellular iron regulation
-
37 Gross CN, Irrinki A, Feder JN, Enns CA: Co-trafficking of HFE with transferrin receptor implies role in intracellular iron regulation. J Biol Chem 1998;273:22068-22074.
-
(1998)
J Biol Chem
, vol.273
, pp. 22068-22074
-
-
Gross, C.N.1
Irrinki, A.2
Feder, J.N.3
Enns, C.A.4
-
38
-
-
0022550401
-
Comparative studies of the binding and growth-supportive ability of mammalian transferrins in human cells, 1986
-
38 Penhallow RC, Brown-Mason A, Woodworth RC: Comparative studies of the binding and growth-supportive ability of mammalian transferrins in human cells, 1986;J Cell Physiol 1986;128:251-260.
-
(1986)
J Cell Physiol
, vol.128
, pp. 251-260
-
-
Penhallow, R.C.1
Brown-Mason, A.2
Woodworth, R.C.3
-
39
-
-
0032478524
-
Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor
-
39 Lebron JA, Bennett MJ, Chirino AJ, Snow PM, Mintier GA, Feder JN, Bjorkman PJ: Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor. Cell 1998;93:111-123.
-
(1998)
Cell
, vol.93
, pp. 111-123
-
-
Lebron, J.A.1
Bennett, M.J.2
Chirino, A.J.3
Snow, P.M.4
Mintier, G.A.5
Feder, J.N.6
Bjorkman, P.J.7
-
40
-
-
0026794581
-
The three-dimensional structure of HLA-B27 at 2.1 Å resolution suggests a general mechanism for tight peptide binding to MHC
-
40 Madden DR, Gorga JC, Strominger JL, Wiley DC: The three-dimensional structure of HLA-B27 at 2.1 Å resolution suggests a general mechanism for tight peptide binding to MHC. Cell 1992;70:1035-1048.
-
(1992)
Cell
, vol.70
, pp. 1035-1048
-
-
Madden, D.R.1
Gorga, J.C.2
Strominger, J.L.3
Wiley, D.C.4
-
42
-
-
0001376313
-
HFE gene knockout produces mouse model of hereditary hemochromatosis
-
42 Zhou XY, Tomatsu S, Fleming RE, Parkkila S, Waheed A, Jinxing J, Fei Y, Brunt EM, Ruddy DA, Prass CE, Schatzman RC, O'Neill R, Britton RS, Bacon BR, Sly WS: HFE gene knockout produces mouse model of hereditary hemochromatosis. Proc Natl Acad Sci USA 1998;95:2492-2497.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 2492-2497
-
-
Zhou, X.Y.1
Tomatsu, S.2
Fleming, R.E.3
Parkkila, S.4
Waheed, A.5
Jinxing, J.6
Fei, Y.7
Brunt, E.M.8
Ruddy, D.A.9
Prass, C.E.10
Schatzman, R.C.11
O'Neill, R.12
Britton, R.S.13
Bacon, B.R.14
Sly, W.S.15
-
43
-
-
0025824547
-
Regulation of intestinal iron absroption and mucosal iron kinetics in hereditary hemochromatosis
-
43 McLaren GD, Nathanson MH, Jacobs A, Trevett D, Thomson W: Regulation of intestinal iron absroption and mucosal iron kinetics in hereditary hemochromatosis. 1991;J Lab Clin Med 117:390-401.
-
(1991)
J Lab Clin Med
, vol.117
, pp. 390-401
-
-
McLaren, G.D.1
Nathanson, M.H.2
Jacobs, A.3
Trevett, D.4
Thomson, W.5
-
44
-
-
0030755366
-
-
44 Gunshin H., Mackenzie B, Bergor UV, Gunshin Y, Romero MF, Boron WF, Nussberger S, Gollan JL, Matthias AH: Cloning and characterization of a mammalian proton-coupled metal-iron transporter. 1997;388:482-488.
-
(1997)
Cloning and Characterization of a Mammalian Proton-coupled Metal-iron Transporter
, vol.388
, pp. 482-488
-
-
Gunshin, H.1
Mackenzie, B.2
Bergor, U.V.3
Gunshin, Y.4
Romero, M.F.5
Boron, W.F.6
Nussberger, S.7
Gollan, J.L.8
Matthias, A.H.9
-
45
-
-
0030763856
-
Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transport gene
-
45 Fleming MD, Trenor CC, Su MA, Foernzler D, Beier DR, Dietrich WF, Andrews NC: Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transport gene. Nat Genet 1997;16:383-386.
-
(1997)
Nat Genet
, vol.16
, pp. 383-386
-
-
Fleming, M.D.1
Trenor, C.C.2
Su, M.A.3
Foernzler, D.4
Beier, D.R.5
Dietrich, W.F.6
Andrews, N.C.7
-
47
-
-
0020700570
-
The significance of transferrin for intestinal iron absorption
-
47 Huebers HA, Huebers E, Csiba E, Rummel W, Finch CA: The significance of transferrin for intestinal iron absorption. Blood 1983; 61:283-290.
-
(1983)
Blood
, vol.61
, pp. 283-290
-
-
Huebers, H.A.1
Huebers, E.2
Csiba, E.3
Rummel, W.4
Finch, C.A.5
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