-
1
-
-
0001439691
-
The control of cellular iron homeostasis
-
J.H. Brock, J.W. Halliday, M.M. Pippard, and L.W. Powell (eds). London: W. B. Saunders
-
Harford JB, Rouault TA, Klausner RD (1994) The control of cellular iron homeostasis. In J.H. Brock, J.W. Halliday, M.M. Pippard, and L.W. Powell (eds): Iron Metabolism in Health and Disease. London: W. B. Saunders, pp. 123-149.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 123-149
-
-
Harford, J.B.1
Rouault, T.A.2
Klausner, R.D.3
-
2
-
-
0030762909
-
Ironing out anaemia
-
Vulpe C, Gitschier J (1997) Ironing out anaemia. Nat Genet 16: 319-320.
-
(1997)
Nat Genet
, vol.16
, pp. 319-320
-
-
Vulpe, C.1
Gitschier, J.2
-
3
-
-
0030763856
-
Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene
-
Fleming MD, Trenor CC III, Su MA, Foernzler D, Beier DR, Dietrich W, Frews NC (1997) Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nat Genet 16:383-386.
-
(1997)
Nat Genet
, vol.16
, pp. 383-386
-
-
Fleming, M.D.1
Trenor C.C. III2
Su, M.A.3
Foernzler, D.4
Beier, D.R.5
Dietrich, W.6
Frews, N.C.7
-
4
-
-
0030755366
-
Cloning and characterization of a mammalian proton-coupled metal-ion transporter
-
Gunshin H, Mackenzie B, Berger UV, Gunshin Y, Romero MF, Boron WF, Nussberger S, Gollan JL, Hediger MA (1997) Cloning and characterization of a mammalian proton-coupled metal-ion transporter. Nature 388:82-488.
-
(1997)
Nature
, vol.388
, pp. 82-488
-
-
Gunshin, H.1
Mackenzie, B.2
Berger, U.V.3
Gunshin, Y.4
Romero, M.F.5
Boron, W.F.6
Nussberger, S.7
Gollan, J.L.8
Hediger, M.A.9
-
5
-
-
0002159387
-
Iron transport
-
J.H. Brock, J.W. Halliday, M.M. Pippard, and L.W. Powell (eds). London: W. B. Saunders
-
Baker E, Morgan EH (1994) Iron transport. In J.H. Brock, J.W. Halliday, M.M. Pippard, and L.W. Powell (eds): Iron Metabolism in Health and Disease. London: W. B. Saunders, pp. 63-95.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 63-95
-
-
Baker, E.1
Morgan, E.H.2
-
6
-
-
0003179404
-
Iron metabolism: An evolutionary perspective
-
J.H. Brock, J. W. Halliday, M.M. Pippard, and L.W. Powell (eds). London: W. B. Saunders
-
Aisen P (1994) Iron metabolism: An evolutionary perspective. In J.H. Brock, J. W. Halliday, M.M. Pippard, and L.W. Powell (eds): Iron Metabolism in Health and Disease. London: W. B. Saunders, pp. 1-30.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 1-30
-
-
Aisen, P.1
-
7
-
-
0026229290
-
mRNA-protein interactions regulate critical pathways in cellular iron metabolism
-
Kuhn LC (1991) mRNA-protein interactions regulate critical pathways in cellular iron metabolism. Br J Haematol 79:1-5.
-
(1991)
Br J Haematol
, vol.79
, pp. 1-5
-
-
Kuhn, L.C.1
-
8
-
-
0024516594
-
Oxidation- Reduction and the molecular mechanism of a regulatory RNA-protein interaction
-
Hentze MW, Rouault RA, Harford JB, Klausner RD (1989) Oxidation-reduction and the molecular mechanism of a regulatory RNA-protein interaction. Science 244:357-359.
-
(1989)
Science
, vol.244
, pp. 357-359
-
-
Hentze, M.W.1
Rouault, R.A.2
Harford, J.B.3
Klausner, R.D.4
-
9
-
-
0001019873
-
Primary iron overload
-
J. H. Brock, J. W. Halliday, M. J. Pippard, and L. W. Powell (eds). London: W. B. Saunders
-
Powell LW, Jazwinska EC, Halliday JW (1994) Primary iron overload. In J. H. Brock, J. W. Halliday, M. J. Pippard, and L. W. Powell (eds): Iron Metabolism in Health and Disease. London: W. B. Saunders, pp. 228-270.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 228-270
-
-
Powell, L.W.1
Jazwinska, E.C.2
Halliday, J.W.3
-
12
-
-
0001898140
-
Secondary iron overload
-
J. H. Brock, J. W. Halliday, M. J. Pippard and L. W. Powell (eds): London: W. B. Saunders
-
Pippard MJ (1994) Secondary iron overload. In J. H. Brock, J. W. Halliday, M. J. Pippard and L. W. Powell (eds): Iron Metabolism in Health and Disease London: W. B. Saunders, pp. 271-309.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 271-309
-
-
Pippard, M.J.1
-
13
-
-
0016588364
-
The pathology of the liver in hemochromatosis
-
J. Joachim (ed). New York: Appleton-Century-Crofts
-
Powell LW, Kerr JFR (1975) The pathology of the liver in hemochromatosis. In J. Joachim (ed): Pathology Annual. New York: Appleton-Century-Crofts, pp. 317.
-
(1975)
Pathology Annual
, pp. 317
-
-
Powell, L.W.1
Kerr, J.F.R.2
-
14
-
-
0022656390
-
Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis
-
Bassett ML, Halliday JW, Powell LW (1986) Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis. Hepatology 6:24-29.
-
(1986)
Hepatology
, vol.6
, pp. 24-29
-
-
Bassett, M.L.1
Halliday, J.W.2
Powell, L.W.3
-
16
-
-
0025975437
-
A history of phlebotomy therapy for hemochromatosis
-
Crosby WH (1991) A history of phlebotomy therapy for hemochromatosis. Am J Med Sci 301:28-31.
-
(1991)
Am J Med Sci
, vol.301
, pp. 28-31
-
-
Crosby, W.H.1
-
17
-
-
0022368621
-
Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis
-
Neiderau C, Fischer R, Sonnenberg A, Stremmel W, Trampisch HJ, Stromeyer G (1985) Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis. N Engl J Med 313: 1256-1262.
-
(1985)
N Engl J Med
, vol.313
, pp. 1256-1262
-
-
Neiderau, C.1
Fischer, R.2
Sonnenberg, A.3
Stremmel, W.4
Trampisch, H.J.5
Stromeyer, G.6
-
18
-
-
0004241915
-
-
London: Oxford University Press
-
Sheldon JH (1935) Haemochromatosis. London: Oxford University Press.
-
(1935)
Haemochromatosis
-
-
Sheldon, J.H.1
-
19
-
-
0016848003
-
Hémochromatosse idiopathique. Maladie associée à l'antigène tissulaire HL-A3?
-
Simon M, Pawlotsky Y, Bourel M, Fauchet R, Genetet B (1975) Hémochromatosse idiopathique. Maladie associée à l'antigène tissulaire HL-A3? Nouv Presse Med 4:1432.
-
(1975)
Nouv Presse Med
, vol.4
, pp. 1432
-
-
Simon, M.1
Pawlotsky, Y.2
Bourel, M.3
Fauchet, R.4
Genetet, B.5
-
20
-
-
0028878293
-
Haplotype analysis in Australian hemochromatosis patients: Evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis
-
Jazwinska EC, Pyper WR, Burt MJ, Francis JL, Goldwurm S, Webb SI, Lee SC, Halliday JW, Powell LW (1995) Haplotype analysis in Australian hemochromatosis patients: Evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis. Am J Hum Genet 56:428-433.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 428-433
-
-
Jazwinska, E.C.1
Pyper, W.R.2
Burt, M.J.3
Francis, J.L.4
Goldwurm, S.5
Webb, S.I.6
Lee, S.C.7
Halliday, J.W.8
Powell, L.W.9
-
21
-
-
15844397210
-
The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients
-
Piperno A, Arosio C, Fargion S, Roetto A, Nicoli C, Girelli D, Sbaiz L, Gasparini P Boari G, Sampietro M, Camaschella C (1996) The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients. Hepatology 24:43-46.
-
(1996)
Hepatology
, vol.24
, pp. 43-46
-
-
Piperno, A.1
Arosio, C.2
Fargion, S.3
Roetto, A.4
Nicoli, C.5
Girelli, D.6
Sbaiz, L.7
Gasparini, P.8
Boari, G.9
Sampietro, M.10
Camaschella, C.11
-
22
-
-
0030045484
-
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: Implications for mapping the haemochromatosis gene (HFE)
-
Gandon G, Jouanolle AM, Chauvel B, Mauvieux V, le Treut A, Feingold J, Le Gall JY, David V, Yaouang J (1996) Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: Implications for mapping the haemochromatosis gene (HFE) Hum Genet 97:103-113.
-
(1996)
Hum Genet
, vol.97
, pp. 103-113
-
-
Gandon, G.1
Jouanolle, A.M.2
Chauvel, B.3
Mauvieux, V.4
Le Treut, A.5
Feingold, J.6
Le Gall, J.Y.7
David, V.8
Yaouang, J.9
-
23
-
-
0028805511
-
New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105
-
Raha-Chowdhury R, Bowen DJ, Stone C, Pointon JJ, Terwilliger JD, Shearman JD, Robson KJ, Bomford A, Worwood M (1995) New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105. Hum Mol Genet 4:1869-1874.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1869-1874
-
-
Raha-Chowdhury, R.1
Bowen, D.J.2
Stone, C.3
Pointon, J.J.4
Terwilliger, J.D.5
Shearman, J.D.6
Robson, K.J.7
Bomford, A.8
Worwood, M.9
-
24
-
-
0030130997
-
Localization of the hemochromatosis disease gene: Linkage disequilibrium analysis using an American patient collection
-
Seese NK, Venditti CP, Chorney KA, Gerhard GS, Ma J, Hudson TJ, Phatak PD, Chorney MJ (1996) Localization of the hemochromatosis disease gene: Linkage disequilibrium analysis using an American patient collection. Blood Cells Mol Dis 22:36-46.
-
(1996)
Blood Cells Mol Dis
, vol.22
, pp. 36-46
-
-
Seese, N.K.1
Venditti, C.P.2
Chorney, K.A.3
Gerhard, G.S.4
Ma, J.5
Hudson, T.J.6
Phatak, P.D.7
Chorney, M.J.8
-
25
-
-
0027232739
-
Concordance of iron storage in siblings with genetic haemochromatosis: Evidence for a predominantly genetic effect on iron storage
-
Crawford DHG, Halliday JW, Summers KM, Burke M, Powell LW (1993) Concordance of iron storage in siblings with genetic haemochromatosis: Evidence for a predominantly genetic effect on iron storage. Hepatology 17:833-837.
-
(1993)
Hepatology
, vol.17
, pp. 833-837
-
-
Crawford, D.H.G.1
Halliday, J.W.2
Summers, K.M.3
Burke, M.4
Powell, L.W.5
-
26
-
-
0029078117
-
Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene
-
Crawford DHG, Powell LW, Leggett BA, Francis JS, Fletcher LM, Webb SI, Halliday JW, Jazwinska EC (1995) Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene. Am J Hum Genet 57:362-367.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 362-367
-
-
Crawford, D.H.G.1
Powell, L.W.2
Leggett, B.A.3
Francis, J.S.4
Fletcher, L.M.5
Webb, S.I.6
Halliday, J.W.7
Jazwinska, E.C.8
-
27
-
-
16944362620
-
Haplotype analysis of haemochromatosis: Evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes
-
Ajioka RS, Jorde LB, Gruen JR, Yu P, Dimitrova D, Barrow J, Radisky E, Edwards CQ, Griffen LM, Kushner JP (1997) Haplotype analysis of haemochromatosis: Evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes. Am J Hum Genet 60: 1439-1447.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1439-1447
-
-
Ajioka, R.S.1
Jorde, L.B.2
Gruen, J.R.3
Yu, P.4
Dimitrova, D.5
Barrow, J.6
Radisky, E.7
Edwards, C.Q.8
Griffen, L.M.9
Kushner, J.P.10
-
28
-
-
0029985519
-
A 4.5- Megabase YAC contig and physical map over the hemochromatosis gene region
-
Burt MJ, Smit DJ, Pyper WR, Powell LW, Jazwinska EC (1996) A 4.5-Megabase YAC contig and physical map over the hemochromatosis gene region Genomics 33:153-158.
-
(1996)
Genomics
, vol.33
, pp. 153-158
-
-
Burt, M.J.1
Smit, D.J.2
Pyper, W.R.3
Powell, L.W.4
Jazwinska, E.C.5
-
29
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Wolff RK (1996) A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 13:399-408.
-
(1996)
Nat Genet
, 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., Jr.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
McClelland, E.19
Meyer, N.C.20
Mintier, G.A.21
Moeller, N.22
Moore, T.23
Morikang, E.24
Wolff, R.K.25
more..
-
30
-
-
0030294028
-
Haemochromatotis and HLA-H
-
Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP (1996) Haemochromatotis and HLA-H. Nat Genet 14:249-251.
-
(1996)
Nat Genet
, vol.14
, pp. 249-251
-
-
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
-
31
-
-
0030294028
-
Haemochromatotis and HLA-H
-
Jouanolle AM, Gandon G, Jezequel P, Blayau M, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn Grieux N, Gicquel I, Le Gall J-Y, David V (1996) Haemochromatotis and HLA-H. Nat Genet 14:249-251.
-
(1996)
Nat Genet
, vol.14
, pp. 249-251
-
-
Jouanolle, A.M.1
Gandon, G.2
Jezequel, P.3
Blayau, M.4
Campion, M.L.5
Yaouanq, J.6
Mosser, J.7
Fergelot, P.8
Chauvel, B.9
Bouric, P.10
Carn Grieux, N.11
Gicquel, I.12
Le Gall, J.-Y.13
David, V.14
-
34
-
-
0025324091
-
Structure, function, and diversity of class I major histocompatibility complex molecules
-
Bjorkman PJ, Parham P (1990) Structure, function, and diversity of class I major histocompatibility complex molecules. Annu Rev Biochem 59: 253-288.
-
(1990)
Annu Rev Biochem
, vol.59
, pp. 253-288
-
-
Bjorkman, P.J.1
Parham, P.2
-
35
-
-
0028019409
-
New tricks for old molecules
-
Ravetch JV, Margulies DH (1994) New tricks for old molecules. Nature 372:323-324.
-
(1994)
Nature
, vol.372
, pp. 323-324
-
-
Ravetch, J.V.1
Margulies, D.H.2
-
36
-
-
0028061347
-
A major histocompatibility complex class I-like fe receptor cloned from human placenta
-
Story CM, Mikulska J, Simister NE (1994) A major histocompatibility complex class I-like fe receptor cloned from human placenta. J Exp Med 180:2377-2381.
-
(1994)
J Exp Med
, vol.180
, pp. 2377-2381
-
-
Story, C.M.1
Mikulska, J.2
Simister, N.E.3
-
37
-
-
0030221927
-
Mutational analysis in hereditary hemochromatosis
-
Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Ten Elshof AE, Gerhard GS, Chorney M (1996) Mutational analysis in hereditary hemochromatosis. Blood Cells Mol Dis 22:187-194.
-
(1996)
Blood Cells Mol Dis
, vol.22
, 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
Ten Elshof, A.E.13
Gerhard, G.S.14
Chorney, M.15
-
38
-
-
16944363480
-
Mutation analysis of the HLA-H gene in Italian haemochromatosis patients
-
Carella M, D'Ambrosio L, Totaro A, Grifa A, Valentino MA, Piperno A, Girelli D, Roetto A, Franco B, Gasparini P, Camaschella C (1997) Mutation analysis of the HLA-H gene in Italian haemochromatosis patients. Am J Hum Genet 60:828-832.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 828-832
-
-
Carella, M.1
D'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
-
39
-
-
0005600868
-
The UK Haemochromatosis Consortium: A simple genetic test identifies 90% of UK patients with haemochromatosis
-
The UK Haemochromatosis Consortium: A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut 41:841, 1997
-
(1997)
Gut
, vol.41
, pp. 841
-
-
-
40
-
-
17644434333
-
2-microglobulin interaction and cell surface expression
-
2-microglobulin interaction and cell surface expression. J Biol Chem 272: 14025-14028.
-
(1997)
J Biol Chem
, vol.272
, pp. 14025-14028
-
-
Feder, J.N.1
Tsuchihasi, 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
-
41
-
-
0031037009
-
Genetic irony beyond haemochromatosis: Clinical effects of HLA-H mutations
-
Beutler E (1997) Genetic irony beyond haemochromatosis: Clinical effects of HLA-H mutations. Lancet 349:296-297.
-
(1997)
Lancet
, vol.349
, pp. 296-297
-
-
Beutler, E.1
-
42
-
-
0004371140
-
Polymorphisms in the haemochromatosis gene
-
St Malo
-
Douabin V, Deugnier Y, Jouanolle AM, Moirand R, Macqueron G, Gireau A, Le Gall JY, David V (1997) Polymorphisms in the haemochromatosis gene. Proceedings of the International Symposium: Iron in Biology and Medicine. p267. St Malo.
-
(1997)
Proceedings of the International Symposium: Iron in Biology and Medicine
, pp. 267
-
-
Douabin, V.1
Deugnier, Y.2
Jouanolle, A.M.3
Moirand, R.4
Macqueron, G.5
Gireau, A.6
Le Gall, J.Y.7
David, V.8
-
44
-
-
0023714951
-
Is all genetic (hereditary) hemochromatosis HLA-associated?
-
Powell LW, Bassett ML, Axelsen E, Ferluga J, Halliday JW (1988) Is all genetic (hereditary) hemochromatosis HLA-associated? Ann NY Acad Sci 526:23-33.
-
(1988)
Ann NY Acad Sci
, vol.526
, pp. 23-33
-
-
Powell, L.W.1
Bassett, M.L.2
Axelsen, E.3
Ferluga, J.4
Halliday, J.W.5
-
46
-
-
0019290540
-
The genetics of haemochromatosis
-
Simon M, Alexandre JL, Fauchet R, Genetet B, Bourel M (1980) The genetics of haemochromatosis. Prog Med Genet 4:135-138.
-
(1980)
Prog Med Genet
, vol.4
, pp. 135-138
-
-
Simon, M.1
Alexandre, J.L.2
Fauchet, R.3
Genetet, B.4
Bourel, M.5
-
47
-
-
0030963287
-
Prevalence of hereditary haemochromatosis in a Massachusetts corporation: Is Celtic origin a risk factor?
-
Smith BN, Kantrowitz W, Grace ND, Greenberg MS, Patton TJ, Ookubo R, Sorger K, Semeraro JG, Doyle JR, Cooper AG, Kamat BR, Maregni LM R, WM (1997) Prevalence of hereditary haemochromatosis in a Massachusetts corporation: Is Celtic origin a risk factor? Hepatology 25:1439-1446.
-
(1997)
Hepatology
, vol.25
, pp. 1439-1446
-
-
Smith, B.N.1
Kantrowitz, W.2
Grace, N.D.3
Greenberg, M.S.4
Patton, T.J.5
Ookubo, R.6
Sorger, K.7
Semeraro, J.G.8
Doyle, J.R.9
Cooper, A.G.10
Kamat, B.R.11
Maregni, L.M.R.12
M, W.13
-
50
-
-
0001417410
-
Iron Deficiency
-
J. H. Brock, J. W. Halliday, M. J. Pippard, and L. W. Powell (eds). London: W. B. Saunders
-
Baynes RD (1994) Iron Deficiency. In J. H. Brock, J. W. Halliday, M. J. Pippard, and L. W. Powell (eds): Iron Metabolism in Health and Disease. London: W. B. Saunders, pp. 190-225.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 190-225
-
-
Baynes, R.D.1
-
51
-
-
0029670047
-
2inf2 Knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism
-
2inf2 Knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism. Proc Natl Acad Sci USA 93: 1529-1534.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 1529-1534
-
-
Rothenberg, B.E.1
Voland, J.R.2
-
53
-
-
0031002910
-
Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract
-
Parkkila S, Waheed A, Britton RS, Feder JN, Tsuchihashi Z, Schatzman RC, Bacon BR, Sly WS (1994) 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 94:2534-2539.
-
(1994)
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
-
54
-
-
0017874765
-
The genetic control of HLA-A and B antigens in somatic cell hybrids: Requirement for beta2 microglobulin
-
Arce-Gomez B, Jones EA, Barnstable CJ, Solomon E, Bodmer WF (1978) The genetic control of HLA-A and B antigens in somatic cell hybrids: Requirement for beta2 microglobulin. Tissue Antigens 11: 96-112.
-
(1978)
Tissue Antigens
, vol.11
, pp. 96-112
-
-
Arce-Gomez, B.1
Jones, E.A.2
Barnstable, C.J.3
Solomon, E.4
Bodmer, W.F.5
-
55
-
-
0023851808
-
Rescue of Daudi cell HLA expression by transfection of the mouse beta 2-microglobulin
-
Seong RH, Clayberger CA, Krensky AM, Parnes JR (1988) Rescue of Daudi cell HLA expression by transfection of the mouse beta 2-microglobulin. J Exp Med 167:288-299.
-
(1988)
J Exp Med
, vol.167
, pp. 288-299
-
-
Seong, R.H.1
Clayberger, C.A.2
Krensky, A.M.3
Parnes, J.R.4
-
56
-
-
0025775723
-
A recycling pathway between the endoplasmic reticulum and the Golgi apparatus for retention of unassembled MHC class I molecules
-
Hsu VW, Yuan LC, Nuchtern JG, Lippincott-Schwartz J, Hammerling GJ, Klausner RD (1991) A recycling pathway between the endoplasmic reticulum and the Golgi apparatus for retention of unassembled MHC class I molecules. Nature 352:441-444.
-
(1991)
Nature
, vol.352
, pp. 441-444
-
-
Hsu, V.W.1
Yuan, L.C.2
Nuchtern, J.G.3
Lippincott-Schwartz, J.4
Hammerling, G.J.5
Klausner, R.D.6
-
57
-
-
0031024211
-
Hemochromatosis and "HLA-H": Definite!
-
Jazwinska EC, Powell LW (1997) Hemochromatosis and "HLA-H": Definite! Hepatology 25:495-496.
-
(1997)
Hepatology
, vol.25
, pp. 495-496
-
-
Jazwinska, E.C.1
Powell, L.W.2
-
58
-
-
0029051968
-
Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older
-
Baer DM, Simons JL, Staples RL, Rumore GJ, Morton CJ (1995) Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older. Am J Med 98:464-468.
-
(1995)
Am J Med
, vol.98
, pp. 464-468
-
-
Baer, D.M.1
Simons, J.L.2
Staples, R.L.3
Rumore, G.J.4
Morton, C.J.5
-
59
-
-
0029029626
-
Screening blood donors for hereditary hemochromatosis: Decision analysis model based on a 30-year database
-
Adams PC, Gregor JC, Kertesz AE, Valberg LS, (1995) Screening blood donors for hereditary hemochromatosis: Decision analysis model based on a 30-year database. Gastroenterology 109:177-188.
-
(1995)
Gastroenterology
, vol.109
, pp. 177-188
-
-
Adams, P.C.1
Gregor, J.C.2
Kertesz, A.E.3
Valberg, L.S.4
|