-
1
-
-
0017158302
-
Association of HLA-B14 antigens with idiopathic hemochromatosis
-
Simon M, Bourel M, Fauchet R, Genetet B: Association of HLA-B14 antigens with idiopathic hemochromatosis. Gut 1976;17:332-334.
-
(1976)
Gut
, vol.17
, pp. 332-334
-
-
Simon, M.1
Bourel, M.2
Fauchet, R.3
Genetet, B.4
-
2
-
-
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, Ellis MC Jr, 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, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;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.8
Ellis M.C., Jr.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
Prass, C.E.25
Quintana, L.26
Starnes, S.M.27
Schatzman, R.C.28
Brunke, K.J.29
Drayna, D.T.30
Risch, N.J.31
Bacon, B.R.32
Wolff, R.K.33
more..
-
3
-
-
16944363480
-
Mutations analysis of HLA-H gene in Italian hemochromatosis patients
-
Carella M, D'Ambrosio L, Totaro A, Valentine MA, Piperno A, Girelli D, Roetto A, Franco B, Gasparini P, Camaschella C: Mutations analysis of 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
D'Ambrosio, L.2
Totaro, A.3
Valentine, M.A.4
Piperno, A.5
Girelli, D.6
Roetto, A.7
Franco, B.8
Gasparini, P.9
Camaschella, C.10
-
4
-
-
0031047769
-
Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients
-
Borot N, Roth JP, Malfroy L, Demangel C, Vinel JP, Pascal JP, Coppin H: Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients. Immunogenetics 1997;45:320-324.
-
(1997)
Immunogenetics
, vol.45
, pp. 320-324
-
-
Borot, N.1
Roth, J.P.2
Malfroy, L.3
Demangel, C.4
Vinel, J.P.5
Pascal, J.P.6
Coppin, H.7
-
5
-
-
16144368650
-
Haemochromatosis and HLA-H
-
Jouanolle AM, Gandon G, Jezequel P, Blayau M, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn G, Andrieux N, Gicquel I, Le Gall JY, David V: Haemochromatosis and HLA-H. Nat Genet 1996;14:251-252.
-
(1996)
Nat Genet
, vol.14
, pp. 251-252
-
-
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, G.11
Andrieux, N.12
Gicquel, I.13
Le Gall, J.Y.14
David, V.15
-
6
-
-
0030294028
-
Haemochromatosis and HLA-H
-
Jazwinska EC, Mac Cullen L, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP: Haemochromatosis and HLA-H. Nat Genet 1996;14:249-251.
-
(1996)
Nat Genet
, vol.14
, pp. 249-251
-
-
Jazwinska, E.C.1
Mac Cullen, L.2
Busfield, F.3
Pyper, W.R.4
Webb, S.I.5
Powell, L.W.6
Morris, C.P.7
Walsh, T.P.8
-
7
-
-
17644434333
-
2-microglobulin interaction and cell surface expression
-
2-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
Parkkilas, S.10
Sly, W.S.11
Schatzman, R.C.12
-
8
-
-
0029670047
-
2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism
-
2 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 1996;93:1529-1534.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 1529-1534
-
-
Rothenberg, B.E.1
Voland, J.R.2
-
9
-
-
0029809511
-
Defective iron homeostasis in β2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man
-
Santos M, Schilham MW, Rademakers LHPM, Marx JJM, De Sousa M, Clevers H: Defective iron homeostasis in β2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man. J Exp Med 1996;184:19765-1985.
-
(1996)
J Exp Med
, vol.184
, pp. 19765-21985
-
-
Santos, M.1
Schilham, M.W.2
Rademakers, L.H.P.M.3
Marx, J.J.M.4
De Sousa, M.5
Clevers, H.6
-
10
-
-
0030814039
-
Genetic and clinical description of hemochromatosis probands and heterozygotes: Evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis
-
Barton JC, Shih WWH, Sawada-Hirai R, Acton RT. Harmon L, Rivers C, Rothenberg BE: Genetic and clinical description of hemochromatosis probands and heterozygotes: Evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis. Blood Cells Mol Dis 1997;23:135-145.
-
(1997)
Blood Cells Mol Dis
, vol.23
, pp. 135-145
-
-
Barton, J.C.1
Shih, W.W.H.2
Sawada-Hirai, R.3
Acton, R.T.4
Harmon, L.5
Rivers, C.6
Rothenberg, B.E.7
-
11
-
-
0030827084
-
The significance of the 187G (H63D) mutation in hemochromatosis
-
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
-
12
-
-
0031028026
-
A new syndrome of iron overload with normal transferrin saturation
-
Moirand R, Mortaji AM, Loreal O, Paillard F, Brissot P, Deugnier Y: A new syndrome of iron overload with normal transferrin saturation. Lancet 1997;349:95-97.
-
(1997)
Lancet
, vol.349
, pp. 95-97
-
-
Moirand, R.1
Mortaji, A.M.2
Loreal, O.3
Paillard, F.4
Brissot, P.5
Deugnier, Y.6
-
13
-
-
0344696059
-
HLA-H mutations in patients with iron overload and normal transferrin saturation
-
Saint-Malo, June
-
Deugnier Y, Moirand R, Jouanolle AM, Le Gall JY, Brissot P, David V: HLA-H mutations in patients with iron overload and normal transferrin saturation. International Symposium Iron in Biology and Medicine, Saint-Malo, June 1997.
-
(1997)
International Symposium Iron in Biology and Medicine
-
-
Deugnier, Y.1
Moirand, R.2
Jouanolle, A.M.3
Le Gall, J.Y.4
Brissot, P.5
David, V.6
-
14
-
-
0344696057
-
HLA-H gene mutations and haemochromatosis: The likely association of H63D with mild pheno-type and the detection of S65C, a novel variant in exon 2
-
April
-
Henz S, Reichen J, Liechti-Gallati S: HLA-H gene mutations and haemochromatosis: The likely association of H63D with mild pheno-type and the detection of S65C, a novel variant in exon 2. European Association for Study of the Liver Meeting, April 1997.
-
(1997)
European Association for Study of the Liver Meeting
-
-
Henz, S.1
Reichen, J.2
Liechti-Gallati, S.3
-
15
-
-
0030213227
-
Interpreting cDNA sequences: Some insights from studies on translation
-
Kosak M: Interpreting cDNA sequences: Some insights from studies on translation. Mamm Genome 1996;7:563-574.
-
(1996)
Mamm Genome
, vol.7
, pp. 563-574
-
-
Kosak, M.1
-
17
-
-
0030691970
-
Gene HLA-G: Le plus classique des non classiques
-
Le Bouteiller P, Lenfant F: Gene HLA-G: Le plus classique des non classiques. Med Sci 1997;13:1436-1444.
-
(1997)
Med Sci
, vol.13
, pp. 1436-1444
-
-
Le Bouteiller, P.1
Lenfant, F.2
-
18
-
-
0002414681
-
A single nucleotide deletion in the putative hemochromatosis gene in a patient who is negative for both the C282Y and H63D mutations
-
Saint-Malo, June
-
Pointon JJ, Shearman JD, Merryweather-Clarke AT, Robson KJH: A single nucleotide deletion in the putative hemochromatosis gene in a patient who is negative for both the C282Y and H63D mutations. International Symposium Iron in Biology and Medicine, Saint-Malo, June 1997.
-
(1997)
International Symposium Iron in Biology and Medicine
-
-
Pointon, J.J.1
Shearman, J.D.2
Merryweather-Clarke, A.T.3
Robson, K.J.H.4
-
19
-
-
13144259692
-
Juvenile and adult hemochromatosis are distinct genetic disorders
-
Camaschella C, Roetto A, Cicilano M, Pasquero P. Bosio S, Gubetta L, Di Vito F, Girelli D. Totaro A, Carella M, Grifa A, Gasparini P: Juvenile and adult hemochromatosis are distinct genetic disorders. Eur J Hum Genet 1997;5:371-375.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 371-375
-
-
Camaschella, C.1
Roetto, A.2
Cicilano, M.3
Pasquero, P.4
Bosio, S.5
Gubetta, L.6
Di Vito, F.7
Girelli, D.8
Totaro, A.9
Carella, M.10
Grifa, A.11
Gasparini, P.12
|