-
1
-
-
0031952314
-
Mapping the gene for sex linked anemia: An inherited defect of intestinal iron absorption in the mouse
-
Anderson, G.J., Murphy, T.L., Cowley, L., Evans, B.A., Halliday, J.W. & McLaren, G.D. (1998) Mapping the gene for sex linked anemia: an inherited defect of intestinal iron absorption in the mouse. Genomics, 48, 34-59.
-
(1998)
Genomics
, vol.48
, pp. 34-59
-
-
Anderson, G.J.1
Murphy, T.L.2
Cowley, L.3
Evans, B.A.4
Halliday, J.W.5
McLaren, G.D.6
-
2
-
-
0022545796
-
Transferrin receptors in the human gastrointestinal tract: Relationship to body iron stores
-
Bannerjee, D., Flanagan, P.R., Cluett, J. & Valberg, L.S. (1986) Transferrin receptors in the human gastrointestinal tract: relationship to body iron stores. Gastroenterology, 91, 861-869.
-
(1986)
Gastroenterology
, vol.91
, pp. 861-869
-
-
Bannerjee, D.1
Flanagan, P.R.2
Cluett, J.3
Valberg, L.S.4
-
3
-
-
0029953753
-
Haemochromatosis: The genetic disorder of the twenty-first century
-
Barton, J.C. & Bertoli, L.F. (1996) Haemochromatosis: the genetic disorder of the twenty-first century. Nature Medicine, 2, 394-395.
-
(1996)
Nature Medicine
, vol.2
, pp. 394-395
-
-
Barton, J.C.1
Bertoli, L.F.2
-
4
-
-
0000702937
-
Hemochromatosis
-
ed. by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle, McGraw-Hill, New York
-
Bothwell, T.H., Charlton, R.W. & Motulky, A.G. (1995) Hemochromatosis. The Metabolic and Molecular Bases of Inherited Disease (ed. by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle), pp. 2237-2270. McGraw-Hill, New York.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 2237-2270
-
-
Bothwell, T.H.1
Charlton, R.W.2
Motulky, A.G.3
-
5
-
-
0018652557
-
Monoclonal antibodies for analysis of the HLA system
-
Brodsky, F.M., Parham, P., Barnstaple, C.J., Crumpton, M.J. & Bodmer, W.F. (1979) Monoclonal antibodies for analysis of the HLA system. Immunological Reviews, 47, 3-62.
-
(1979)
Immunological Reviews
, vol.47
, pp. 3-62
-
-
Brodsky, F.M.1
Parham, P.2
Barnstaple, C.J.3
Crumpton, M.J.4
Bodmer, W.F.5
-
6
-
-
0021331061
-
Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes)
-
Cordell, J.L., Falini, B., Erber, W.N., Ghosh, A.K., Abdulaziz, Z., MacDonald, S., Pulford, K.A.F., Stein, H. & Mason, D.Y. (1984) Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes). Journal of Histochemistry and Cytochemistry, 32, 219-229.
-
(1984)
Journal of Histochemistry and Cytochemistry
, vol.32
, pp. 219-229
-
-
Cordell, J.L.1
Falini, B.2
Erber, W.N.3
Ghosh, A.K.4
Abdulaziz, Z.5
MacDonald, S.6
Pulford, K.A.F.7
Stein, H.8
Mason, D.Y.9
-
7
-
-
0031969395
-
Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation
-
Crawford, D.H.G., Jawinska, E.C., Cullen, L.M. & Powell, L.W. (1998) Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation. Gastroenterology, 114, 1003-1008.
-
(1998)
Gastroenterology
, vol.114
, pp. 1003-1008
-
-
Crawford, D.H.G.1
Jawinska, E.C.2
Cullen, L.M.3
Powell, L.W.4
-
8
-
-
0028176811
-
Iron overload in β-2 microglobulin deficient mice
-
de Sousa, M., Reimao, R., Lacerda, R., Hugo, P., Kaufmann, S.H.E. & Porto, G. (1994) Iron overload in β-2 microglobulin deficient mice. Immunological Letters, 39, 105-111.
-
(1994)
Immunological Letters
, 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
-
10
-
-
0026055969
-
A new monoclonal antibody (JC159) that detects glycophorin A for the diagnosis of erythroleukaemia
-
Erber, W.N., Mclachlan, J., Cordell, J.L., Turley, H., Reid, M. & Mason, D.Y. (1991) A new monoclonal antibody (JC159) that detects glycophorin A for the diagnosis of erythroleukaemia. Hematology Reviews, 5, 113-120.
-
(1991)
Hematology Reviews
, vol.5
, pp. 113-120
-
-
Erber, W.N.1
Mclachlan, J.2
Cordell, J.L.3
Turley, H.4
Reid, M.5
Mason, D.Y.6
-
11
-
-
0017990368
-
Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-sepharose
-
Ey, P.L., Prowse, S.J. & Jenkin, C.R. (1978) Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-sepharose. Immunochemistry, 15, 429-436.
-
(1978)
Immunochemistry
, vol.15
, pp. 429-436
-
-
Ey, P.L.1
Prowse, S.J.2
Jenkin, C.R.3
-
12
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder, J.N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D.A., Basava, A., Dormishian, F., Domingo, R., Ellis, M.C., Fullan, A., Hinton, L.M., Jones, N.L., Kimmel, B.E., Kronmal, G.S., Lauer, P., Lee, V.K., Loeb, D.B., Mapa, F.A., McLelland, E., Meyer, N.C., Mintier, G.A., Moeller, N., Moore, T., Morikang, E., Prass, C.E., Quintana, L., Starnes, S.M., Schatzman, R.C., Brunke, K.J., Prass, C.E., Quintana, L., Starnes, S.M., Schatzman, R.C., Brunke, K.J., Drayna, D.T., Risch, N.J., Bacon, B.R. & Wolff, R.K. (1996) A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics, 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
Dormishian, F.7
Domingo, R.8
Ellis, M.C.9
Fullan, A.10
Hinton, L.M.11
Jones, N.L.12
Kimmel, B.E.13
Kronmal, G.S.14
Lauer, P.15
Lee, V.K.16
Loeb, D.B.17
Mapa, F.A.18
McLelland, E.19
Meyer, N.C.20
Mintier, G.A.21
Moeller, N.22
Moore, T.23
Morikang, E.24
Prass, C.E.25
Quintana, L.26
Starnes, S.M.27
Schatzman, R.C.28
Brunke, K.J.29
Prass, C.E.30
Quintana, L.31
Starnes, S.M.32
Schatzman, R.C.33
Brunke, K.J.34
Drayna, D.T.35
Risch, N.J.36
Bacon, B.R.37
Wolff, R.K.38
more..
-
13
-
-
13144282684
-
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
-
Feder, J.N., Penny, D.M., Irrinki, A., Lee, V.K., Lebron, J.A., Watson, N. Tsuchihashi, Z., Sigal, E., Bjorkman, P.J. & Schatzman, R.C (1998) The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proceedings of the National Academy of Sciences of the United States of America, 95, 1472-1477.
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, pp. 1472-1477
-
-
Feder, J.N.1
Penny, D.M.2
Irrinki, A.3
Lee, V.K.4
Lebron, J.A.5
Watson, N.6
Tsuchihashi, Z.7
Sigal, E.8
Bjorkman, P.J.9
Schatzman, R.C.10
-
14
-
-
17644434333
-
The hemochromatosis founder mutation in HLA-H disrupts β2-microglobulin interaction and cell surface expression
-
Feder, J.N., Tsuchihashi, Z., Irrinki, A., Lee, V.K., Mapa, F.A., Morikang, E., Prass, C.E., Starnes, S.M., Wolff, R.K. Parkilla, S., Sly, W.S. & Schatzman, R.C. (1997) The hemochromatosis founder mutation in HLA-H disrupts β2-microglobulin interaction and cell surface expression. Journal of Biological Chemistry, 271, 14025-14028.
-
(1997)
Journal of Biological Chemistry
, vol.271
, 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
Parkilla, S.10
Sly, W.S.11
Schatzman, R.C.12
-
15
-
-
0029117908
-
Direct-rapid (DR) mutagenesis of large plasmids using PCR
-
Gatlin, J., Campbell, L.H., Schmidt, M.G. & Arrigo, S.J. (1995) Direct-rapid (DR) mutagenesis of large plasmids using PCR. Biotechniques, 19, 559-564.
-
(1995)
Biotechniques
, vol.19
, pp. 559-564
-
-
Gatlin, J.1
Campbell, L.H.2
Schmidt, M.G.3
Arrigo, S.J.4
-
16
-
-
0031888618
-
Hereditary haemochromatosis as an immunological disease
-
Gerhard, G.S., Ten Elshof, A.E. &. Chorney, M.J. (1998) Hereditary haemochromatosis as an immunological disease. British Journal of Haematology, 100, 247-255.
-
(1998)
British Journal of Haematology
, vol.100
, pp. 247-255
-
-
Gerhard, G.S.1
Ten Elshof, A.E.2
Chorney, M.J.3
-
17
-
-
0031550247
-
Identification of a mouse homologue for the hereditary haemochromatosis candidate gene
-
Hashimoto, K., Hirai, M. & Kurosawa, Y. (1997) Identification of a mouse homologue for the hereditary haemochromatosis candidate gene. Biochemical and Biophysical Research Communications, 250, 35-39.
-
(1997)
Biochemical and Biophysical Research Communications
, vol.250
, pp. 35-39
-
-
Hashimoto, K.1
Hirai, M.2
Kurosawa, Y.3
-
18
-
-
0021130764
-
Transferrin receptor on endothelium of brain capillaries
-
Jefferies, W.A., Brandon, M.R., Hunt, S.V. Williams, A.F., Gatter, K.C. & Mason, D.Y. (1984) Transferrin receptor on endothelium of brain capillaries. Nature, 312, 162-163.
-
(1984)
Nature
, vol.312
, pp. 162-163
-
-
Jefferies, W.A.1
Brandon, M.R.2
Hunt, S.V.3
Williams, A.F.4
Gatter, K.C.5
Mason, D.Y.6
-
19
-
-
0016756272
-
Continuous cultures of fused cells secreting antibody of predefined specificity
-
Kohler, G. & Milstein, C. (1975) Continuous cultures of fused cells secreting antibody of predefined specificity. Nature, 256, 495-498.
-
(1975)
Nature
, vol.256
, pp. 495-498
-
-
Kohler, G.1
Milstein, C.2
-
20
-
-
0026776394
-
An 'ironic' case of mistaken identity?
-
Kowdley, K.V. & Tavill, A.S. (1992) An 'ironic' case of mistaken identity? Hepatology, 16, 500-501.
-
(1992)
Hepatology
, vol.16
, pp. 500-501
-
-
Kowdley, K.V.1
Tavill, A.S.2
-
21
-
-
0032478524
-
Crystal structure of the hemochromatosis protein HFE and characterisation of its interaction with transferrin receptor
-
Lebron, J.A., Bennett, M.J., Vaughn, D. E., Chirino, A.J., Snow, P.M., Mintier, G.A., Feder, J.N. & Bjorkman, P.J. (1998) Crystal structure of the hemochromatosis protein HFE and characterisation of its interaction with transferrin receptor. Cell, 93, 111-123.
-
(1998)
Cell
, vol.93
, pp. 111-123
-
-
Lebron, J.A.1
Bennett, M.J.2
Vaughn, D.E.3
Chirino, A.J.4
Snow, P.M.5
Mintier, G.A.6
Feder, J.N.7
Bjorkman, P.J.8
-
22
-
-
0025233620
-
Differential expression of transferrin receptor in duodenal mucosa in iron overload: Evidence for a site-specific defect in genetic hemochromatosis
-
Lombard, M., Bomford, A.B., Polson, R.J., Bellingham, A.J. & Williams, R. (1990) Differential expression of transferrin receptor in duodenal mucosa in iron overload: evidence for a site-specific defect in genetic hemochromatosis. Gastroenterology, 98, 976-984.
-
(1990)
Gastroenterology
, vol.98
, pp. 976-984
-
-
Lombard, M.1
Bomford, A.B.2
Polson, R.J.3
Bellingham, A.J.4
Williams, R.5
-
23
-
-
0021770787
-
High level transient expression of a chloramphenicol acetyl transferase gene by DEAE dextran mediated DNA transfection coupled with a dimethyl sulphoxide or glycerol shock treatment
-
Lopata, M.A., Cleveland, D.W. & Sollner-Webb, B. (1984) High level transient expression of a chloramphenicol acetyl transferase gene by DEAE dextran mediated DNA transfection coupled with a dimethyl sulphoxide or glycerol shock treatment. Nucleic Acids Research, 12, 5707-5717.
-
(1984)
Nucleic Acids Research
, vol.12
, pp. 5707-5717
-
-
Lopata, M.A.1
Cleveland, D.W.2
Sollner-Webb, B.3
-
24
-
-
0021100710
-
High efficiency polyoma DNA transfection of chloroquine treated cells
-
Luthman, H. & Magnusson, G. (1983) High efficiency polyoma DNA transfection of chloroquine treated cells. Nucleic Acids Research, 11, 1295-1308.
-
(1983)
Nucleic Acids Research
, vol.11
, pp. 1295-1308
-
-
Luthman, H.1
Magnusson, G.2
-
25
-
-
0030923653
-
Global prevalence of putative haemochromatosis mutations
-
Merryweather-Clarke, A.T., Pointon, J.J., Shearman, J.D. & Robson, K.J. (1997) Global prevalence of putative haemochromatosis mutations. Journal of Medical Genetics, 34, 275-278.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 275-278
-
-
Merryweather-Clarke, A.T.1
Pointon, J.J.2
Shearman, J.D.3
Robson, K.J.4
-
26
-
-
0024427157
-
A human macrophage-associated antigen (CD68) detected by six different monoclonal antibodies
-
Micklem, K., Rigney, E., Cordell, J., Simmons, D., Stross, P., Turley, H., Seed, B. & Mason, D. (1989) A human macrophage-associated antigen (CD68) detected by six different monoclonal antibodies. British Journal of Haematology, 73, 6-11.
-
(1989)
British Journal of Haematology
, vol.73
, pp. 6-11
-
-
Micklem, K.1
Rigney, E.2
Cordell, J.3
Simmons, D.4
Stross, P.5
Turley, H.6
Seed, B.7
Mason, D.8
-
27
-
-
0345172216
-
Intracellular transport blockade caused by disruption of the disulfide bridge in the third external domain of the major histocompatibility complex class I antigen
-
Miyazaki, J-I., Apella, E. & Ozato, K. (1986) Intracellular transport blockade caused by disruption of the disulfide bridge in the third external domain of the major histocompatibility complex class I antigen. Proceedings of the National Academy of Sciences of the United States of America, 83, 757-761.
-
(1986)
Proceedings of the National Academy of Sciences of the United States of America
, vol.83
, pp. 757-761
-
-
Miyazaki, J.-I.1
Apella, E.2
Ozato, K.3
-
28
-
-
0031836060
-
Production, crystallization and preliminary X-ray analysis of the human MHC class Ib molecule HLA-E
-
O'Callaghan, C.A., Tormo, J., Willcox, B., Blundell, C.D., Jakobsen, B.K., Stuart, D.I., McMichael, A.J., Bell, J.I. & Jones, E.Y. (1998) Production, crystallization and preliminary X-ray analysis of the human MHC class Ib molecule HLA-E. Protein Science, 7, 1264-1266.
-
(1998)
Protein Science
, vol.7
, pp. 1264-1266
-
-
O'Callaghan, C.A.1
Tormo, J.2
Willcox, B.3
Blundell, C.D.4
Jakobsen, B.K.5
Stuart, D.I.6
McMichael, A.J.7
Bell, J.I.8
Jones, E.Y.9
-
29
-
-
0025195567
-
Restoration of H-2b expression and processing of endogenous antigens in the MHC class I pathway by fusion of a lymphoma mutant to L cells of the H-2k haplotype
-
Ohlen, C., Bastin, J.M., Ljunggren, H-G., Townsend, A.R.M. & Karre, K. (1990) Restoration of H-2b expression and processing of endogenous antigens in the MHC class I pathway by fusion of a lymphoma mutant to L cells of the H-2k haplotype. European Journal of Immunology, 20, 1873-1876.
-
(1990)
European Journal of Immunology
, vol.20
, pp. 1873-1876
-
-
Ohlen, C.1
Bastin, J.M.2
Ljunggren, H.-G.3
Townsend, A.R.M.4
Karre, K.5
-
30
-
-
0030712463
-
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
-
Parkilla, S., Waheed, A., Britton, R.S., Bacon, B.R., Zhou, X.Y., Tomatsu, S., Fleming, R.E. & Sly, W.S. (1997a) Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis. Proceedings of the National Academy of Sciences of the United States of America, 94, 13198-13202.
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, pp. 13198-13202
-
-
Parkilla, S.1
Waheed, A.2
Britton, R.S.3
Bacon, B.R.4
Zhou, X.Y.5
Tomatsu, S.6
Fleming, R.E.7
Sly, W.S.8
-
31
-
-
0031002910
-
Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals a unique pattern of expression in the gastrointestinal tract
-
Parkilla, S., Waheed, A., Britton, R.S., Feder, J.N., Tsuchihashi, Z., Schatzman, R.C., Bacon, B.R. & Sly, W.S. (1997b) Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals a unique pattern of expression in the gastrointestinal tract. Proceedings of the National Academy of Sciences of the United States of America, 94, 2534-2539.
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, pp. 2534-2539
-
-
Parkilla, 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
-
32
-
-
0029809511
-
Defective iron homeostasis in β2-microglobulin knockout mice recapitulates hereditary haemochromatosis in man
-
Santos, M., Schilham, M.W., Rademakers, L., Marx, J.J.M., de Sousa, M. & Clevers, H. (1996) Defective iron homeostasis in β2-microglobulin knockout mice recapitulates hereditary haemochromatosis in man. Journal of Experimental Medicine, 184, 1975-1985.
-
(1996)
Journal of Experimental Medicine
, vol.184
, pp. 1975-1985
-
-
Santos, M.1
Schilham, M.W.2
Rademakers, L.3
Marx, J.J.M.4
De Sousa, M.5
Clevers, H.6
-
33
-
-
0031202039
-
CD94/NKG2 is the predominant inhibitory receptor involved in recognition of HLA-G by decidual and peripheral blood NK cells
-
Soderstrom, K., Corliss, B., Lanier, L. & Philips, J.H. (1997) CD94/NKG2 is the predominant inhibitory receptor involved in recognition of HLA-G by decidual and peripheral blood NK cells. Journal of Immunology, 159, 1072-1075.
-
(1997)
Journal of Immunology
, vol.159
, pp. 1072-1075
-
-
Soderstrom, K.1
Corliss, B.2
Lanier, L.3
Philips, J.H.4
-
35
-
-
0017155490
-
Establishment and characterisation of a human histiocytic lymphoma cell line (U-937)
-
Sundstrom, C. & Nilsson, K. (1976) Establishment and characterisation of a human histiocytic lymphoma cell line (U-937). International Journal of Cancer, 17, 565-577.
-
(1976)
International Journal of Cancer
, vol.17
, pp. 565-577
-
-
Sundstrom, C.1
Nilsson, K.2
-
36
-
-
0024324442
-
Association of class I major histocompatibility heavy and light chains induced by viral peptides
-
Townsend, A.R.M., Ohlen, C., Bastin, J., Ljunggren, H-G., Foster, L. & Karre, K. (1989) Association of class I major histocompatibility heavy and light chains induced by viral peptides. Nature, 340, 443-448.
-
(1989)
Nature
, vol.340
, pp. 443-448
-
-
Townsend, A.R.M.1
Ohlen, C.2
Bastin, J.3
Ljunggren, H.-G.4
Foster, L.5
Karre, K.6
-
39
-
-
0030732164
-
Hereditary hemochromatosis: Effects of C282Y and H6 3D mutations on association with β2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells
-
Waheed, A., Parkilla, S., Zhou, X.Y., Tomatsu, S., Tsuchihashi, Z., Feder, J.N., Schatzman, R.C., Britton, R.S., Bacon, B.R. & Sly, W.S. (1997) Hereditary hemochromatosis: effects of C282Y and H6 3D mutations on association with β2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proceedings of the National Academy of Sciences of the United States of America, 94, 12384-12389.
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, pp. 12384-12389
-
-
Waheed, A.1
Parkilla, 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
-
40
-
-
0025616496
-
HLA class I transgenic mice as a model system to study MHC-restricted antigen recognition in man
-
Weiss, E.H., Schliesser, G., Botterton, C., McMichael, A.J., Reithmuller, G., Kievits, F., Ivanyi, P. & Brem, G. (1990) HLA class I transgenic mice as a model system to study MHC-restricted antigen recognition in man. Scandinavian Journal of Rheumatology, 87, (Suppl.), 91-96.
-
(1990)
Scandinavian Journal of Rheumatology
, vol.87
, Issue.SUPPL.
, pp. 91-96
-
-
Weiss, E.H.1
Schliesser, G.2
Botterton, C.3
McMichael, A.J.4
Reithmuller, G.5
Kievits, F.6
Ivanyi, P.7
Brem, G.8
-
41
-
-
0001376313
-
HFE gene knockout produces mouse model of hereditary hemochromatosis
-
Zhou, X.Y., Tomatsu, S., Fleming, R.E., Parkkila, S., Waheed, A., Jiang, J., Fei, Y., Brunt, E.M., Ruddy, D.A., Prass, C.E., Schatzman, R.C., O'Neill, R., Britton, R.S., Bacon, B.R. & Sly, W.S. (1998) HFE gene knockout produces mouse model of hereditary hemochromatosis. Proceedings of the National Academy of Sciences of the United States of America, 95, 2492-2497.
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, pp. 2492-2497
-
-
Zhou, X.Y.1
Tomatsu, S.2
Fleming, R.E.3
Parkkila, S.4
Waheed, A.5
Jiang, 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
|