-
1
-
-
0033759823
-
Haemochromatosis: Novel gene discovery and the molecular pathophysiology of iron metabolism
-
Griffiths W, Cox T. Haemochromatosis: novel gene discovery and the molecular pathophysiology of iron metabolism. Hum Mol Genet 2000;9:2377-2382.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2377-2382
-
-
Griffiths, W.1
Cox, T.2
-
2
-
-
0028903259
-
Aceruloplasminemia: Molecular characterization of this disorder of iron metabolism
-
Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc Natl Acad Sci USA 1995;92:2539-2543.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2539-2543
-
-
Harris, Z.L.1
Takahashi, Y.2
Miyajima, H.3
Serizawa, M.4
MacGillivray, R.T.5
Gitlin, J.D.6
-
3
-
-
0028895749
-
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans
-
Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, Morita H, et al. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nat Genet 1995;9:267-272.
-
(1995)
Nat Genet
, vol.9
, pp. 267-272
-
-
Yoshida, K.1
Furihata, K.2
Takeda, S.3
Nakamura, A.4
Yamamoto, K.5
Morita, H.6
-
4
-
-
0023240051
-
Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration
-
Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration. Neurology 1987;37:761- 767.
-
(1987)
Neurology
, vol.37
, pp. 761-767
-
-
Miyajima, H.1
Nishimura, Y.2
Mizoguchi, K.3
Sakamoto, M.4
Shimizu, T.5
Honda, N.6
-
5
-
-
0028090209
-
Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus
-
Logan JI, Harveyson KB, Wisdom GB, Hughes AE, Archbold GP. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus. Q J Med 1994;87:663-670.
-
(1994)
Q J Med
, vol.87
, pp. 663-670
-
-
Logan, J.I.1
Harveyson, K.B.2
Wisdom, G.B.3
Hughes, A.E.4
Archbold, G.P.5
-
6
-
-
0029007765
-
Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a Japanese family
-
Morita H, Ikeda S, Yamamoto K, Morita S, Yoshida K, Nomoto S, et al. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family. Ann Neurol 1995;37:646-656.
-
(1995)
Ann Neurol
, vol.37
, pp. 646-656
-
-
Morita, H.1
Ikeda, S.2
Yamamoto, K.3
Morita, S.4
Yoshida, K.5
Nomoto, S.6
-
7
-
-
0032579397
-
Role of ceruloplasmin in cellular iron uptake
-
Mukhopadhyay CK, Attieh ZK, Fox PL. Role of ceruloplasmin in cellular iron uptake. Science 1998;279:714-717.
-
(1998)
Science
, vol.279
, pp. 714-717
-
-
Mukhopadhyay, C.K.1
Attieh, Z.K.2
Fox, P.L.3
-
8
-
-
0030584404
-
Iron metabolism in eukaryotes: Mars and Venus at it again
-
Kaplan J, O'Halloran TV. Iron metabolism in eukaryotes: Mars and Venus at it again. Science 1996;271:1510-1512.
-
(1996)
Science
, vol.271
, pp. 1510-1512
-
-
Kaplan, J.1
O'Halloran, T.V.2
-
9
-
-
0032875387
-
Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux
-
Harris ZL, Durley AP, Man TK, Gitlin JD. Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proc Natl Acad Sci USA 1999;96:10812-10817.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 10812-10817
-
-
Harris, Z.L.1
Durley, A.P.2
Man, T.K.3
Gitlin, J.D.4
-
10
-
-
0014027719
-
The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum
-
Osaki S, Johnson DEF. The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum. J Biol Chem 1996;241:2746-2751.
-
(1996)
J Biol Chem
, vol.241
, pp. 2746-2751
-
-
Osaki, S.1
Johnson, D.E.F.2
-
11
-
-
0033543720
-
Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin
-
Gosriwatana I, Loréal O, Lu S, Brissot P, Porter J, Hider RC. Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin. Anal Biochem 1999;273:212-220.
-
(1999)
Anal Biochem
, vol.273
, pp. 212-220
-
-
Gosriwatana, I.1
Loréal, O.2
Lu, S.3
Brissot, P.4
Porter, J.5
Hider, R.C.6
-
12
-
-
0031760199
-
Automated measurement of serum ferroxidase activity
-
Erel O. Automated measurement of serum ferroxidase activity. Clin Chem 1998;44:2313-2319.
-
(1998)
Clin Chem
, vol.44
, pp. 2313-2319
-
-
Erel, O.1
-
13
-
-
2542474997
-
Plasma clearance studies
-
Lewis SM, Bayly RJ, editors. Churchill Livingstone and London: Saunders
-
Cavill I. Plasma clearance studies. Lewis SM, Bayly RJ, editors. Radioisotopes in haematology. Churchill Livingstone and London: Saunders, 1977. vol. 14. pp. 214-244.
-
(1977)
Radioisotopes in haematology
, vol.14
, pp. 214-244
-
-
Cavill, I.1
-
14
-
-
2542425696
-
Radionucleide blood cell survival studies
-
Lewis SM, Bayly RJ, editors. Churchill Livingstone and London: Saunders
-
Stuart A, Bentley A, Miller D. Radionucleide blood cell survival studies. Lewis SM, Bayly RJ, editors. Radioisotopes in haematology. Churchill Livingstone and London: Saunders, 1977. pp. 245-262.
-
(1977)
Radioisotopes in haematology
, pp. 245-262
-
-
Stuart, A.1
Bentley, A.2
Miller, D.3
-
15
-
-
0027945442
-
Hemochromatosis: Diagnosis and quantification of liver iron with gradient-echo MR imaging
-
Gandon Y, Guyader D, Heautot JF, Reda MI, Yaouanq J, Buhe T, et al. Hemochromatosis: diagnosis and quantification of liver iron with gradient-echo MR imaging. Radiology 1994;193:533-538.
-
(1994)
Radiology
, vol.193
, pp. 533-538
-
-
Gandon, Y.1
Guyader, D.2
Heautot, J.F.3
Reda, M.I.4
Yaouanq, J.5
Buhe, T.6
-
17
-
-
0019352109
-
Assessment of liver iron content in 271 patients: A reevaluation of direct and indirect methods
-
Brissot P, Bourel M, Herry D, Verger JP, Messner M, Beaumont C, et al. Assessment of liver iron content in 271 patients: a reevaluation of direct and indirect methods. Gastroenterology 1981;80:557-565.
-
(1981)
Gastroenterology
, vol.80
, pp. 557-565
-
-
Brissot, P.1
Bourel, M.2
Herry, D.3
Verger, J.P.4
Messner, M.5
Beaumont, C.6
-
18
-
-
0018126828
-
Ascorbic acid status in idiopathic hemochromatosis
-
Brissot P, Deugnier Y, Le Treut A, Regnouard F, Simon M, Bourel M. Ascorbic acid status in idiopathic hemochromatosis. Digestion 1978;17:479-487.
-
(1978)
Digestion
, vol.17
, pp. 479-487
-
-
Brissot, P.1
Deugnier, Y.2
Le Treut, A.3
Regnouard, F.4
Simon, M.5
Bourel, M.6
-
19
-
-
0001338684
-
Ceruloplasmin: A multifunctional metalloprotein of vertebrate plasma
-
Sigel H, editor. New York, NY: Marcel Dekker
-
Frieden E. Ceruloplasmin: a multifunctional metalloprotein of vertebrate plasma. Sigel H, editor. Metal ions in biological systems. New York, NY: Marcel Dekker, 1981. pp. 117-142.
-
(1981)
Metal ions in biological systems
, pp. 117-142
-
-
Frieden, E.1
-
20
-
-
0029618814
-
A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus
-
Daimon M, Kato T, Kawanami T, Tominaga M, Igarashi M, Yamatani K, et al. A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus. Biochem Biophys Res Commun 1995;217:89-95.
-
(1995)
Biochem Biophys Res Commun
, vol.217
, pp. 89-95
-
-
Daimon, M.1
Kato, T.2
Kawanami, T.3
Tominaga, M.4
Igarashi, M.5
Yamatani, K.6
-
21
-
-
0033546624
-
Estimation of the gene frequency of aceruloplasminemia in Japan
-
Miyajima H, Kohno S, Takahashi Y, Yonekawa O, Kanno T. Estimation of the gene frequency of aceruloplasminemia in Japan. Neurology 1999;53:617-619.
-
(1999)
Neurology
, vol.53
, pp. 617-619
-
-
Miyajima, H.1
Kohno, S.2
Takahashi, Y.3
Yonekawa, O.4
Kanno, T.5
-
22
-
-
0029800745
-
Expression of the ceruloplasmin gene in the human retina and brain: Implications for a pathogenic model in aceruloplasminemia
-
Klomp LW, Gitlin JD. Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia. Hum Mol Genet 1996;5:1989-1996.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1989-1996
-
-
Klomp, L.W.1
Gitlin, J.D.2
-
23
-
-
0030856558
-
A novel glycosylphosphatidylinositol-anchored form of ceruloplasmin is expressed by mammalian astrocytes
-
Patel BN, David S. A novel glycosylphosphatidylinositol-anchored form of ceruloplasmin is expressed by mammalian astrocytes. J Biol Chem 1997;272:20185-20190.
-
(1997)
J Biol Chem
, vol.272
, pp. 20185-20190
-
-
Patel, B.N.1
David, S.2
-
24
-
-
0034635402
-
Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain
-
Patel BN, Dunn RJ, David S. Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain. J Biol Chem 2000;275:4305-4310.
-
(2000)
J Biol Chem
, vol.275
, pp. 4305-4310
-
-
Patel, B.N.1
Dunn, R.J.2
David, S.3
-
25
-
-
0030913415
-
Intestinal absorption and enterohepatic cycling of biliary iron originating from plasma non-transferrin-bound iron in rats
-
Brissot P, Bolder U, Schteingart CD, Arnaud J, Hofmann AF. Intestinal absorption and enterohepatic cycling of biliary iron originating from plasma non-transferrin-bound iron in rats. Hepatology 1997;25:1457-1461.
-
(1997)
Hepatology
, vol.25
, pp. 1457-1461
-
-
Brissot, P.1
Bolder, U.2
Schteingart, C.D.3
Arnaud, J.4
Hofmann, A.F.5
-
26
-
-
0034062537
-
Genes that modify the hemochromatosis phenotype in mice
-
Levy JE, Montross LK, Andrews NC. Genes that modify the hemochromatosis phenotype in mice. J Clin Invest 2000;105:1209-1216.
-
(2000)
J Clin Invest
, vol.105
, pp. 1209-1216
-
-
Levy, J.E.1
Montross, L.K.2
Andrews, N.C.3
-
27
-
-
0031907553
-
Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia
-
Miyajima H, Adachi J, Tatsuno Y, Takahashi Y, Fujimoto M, Kaneko E, et al. Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia. Neurology 1998;50:130-136.
-
(1998)
Neurology
, vol.50
, pp. 130-136
-
-
Miyajima, H.1
Adachi, J.2
Tatsuno, Y.3
Takahashi, Y.4
Fujimoto, M.5
Kaneko, E.6
-
28
-
-
0030003830
-
Increased plasma lipid peroxidation in patients with aceruloplasminemia
-
Miyajima H, Takahashi Y, Serizawa M, Kaneko E, Gitlin JD. Increased plasma lipid peroxidation in patients with aceruloplasminemia. Free Radic Biol Med 1996;20:757-760.
-
(1996)
Free Radic Biol Med
, vol.20
, pp. 757-760
-
-
Miyajima, H.1
Takahashi, Y.2
Serizawa, M.3
Kaneko, E.4
Gitlin, J.D.5
-
29
-
-
0026601599
-
Liver pathology in genetic hemochromatosis: A review of 135 homozygous cases and their bioclinical correlations
-
Deugnier YM, Loréal O, Turlin B, Guyader D, Jouanolle H, Moirand R, et al. Liver pathology in genetic hemochromatosis: a review of 135 homozygous cases and their bioclinical correlations. Gastroenterology 1992;102:2050-2059.
-
(1992)
Gastroenterology
, vol.102
, pp. 2050-2059
-
-
Deugnier, Y.M.1
Loréal, O.2
Turlin, B.3
Guyader, D.4
Jouanolle, H.5
Moirand, R.6
-
30
-
-
0027500840
-
Preneoplastic significance of hepatic iron-free foci in genetic hemochromatosis: A study of 185 patients
-
Deugnier YM, Charalambous P, Le Quilleuc D, Turlin B, Searle J, Brissot P, et al. Preneoplastic significance of hepatic iron-free foci in genetic hemochromatosis: a study of 185 patients. Hepatology 1993;18:1363-1369.
-
(1993)
Hepatology
, vol.18
, pp. 1363-1369
-
-
Deugnier, Y.M.1
Charalambous, P.2
Le Quilleuc, D.3
Turlin, B.4
Searle, J.5
Brissot, P.6
-
31
-
-
0031028026
-
A new syndrome of liver iron overload with normal transferrin saturation
-
Moirand R, Mortaji AM, Loréal O, Paillard F, Brissot P, Deugnier Y. A new syndrome of liver 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
Loréal, O.3
Paillard, F.4
Brissot, P.5
Deugnier, Y.6
-
32
-
-
0034767941
-
Histologic features of the liver in insulin resistance-associated iron overload. A study of 139 patients
-
Turlin B, Mendler MH, Moirand R, Guyader D, Guillygomarc'h A, Deugnier Y. Histologic features of the liver in insulin resistance-associated iron overload. A study of 139 patients. Am J Clin Pathol 2001;116:263-270.
-
(2001)
Am J Clin Pathol
, vol.116
, pp. 263-270
-
-
Turlin, B.1
Mendler, M.H.2
Moirand, R.3
Guyader, D.4
Guillygomarc'h, A.5
Deugnier, Y.6
-
33
-
-
0029913626
-
Long term survival in patients with hereditary hemochromatosis
-
Niederau C, Fischer R, Pürschel A, Stremmel W, Häussinger D, Strohmeyer G. Long term survival in patients with hereditary hemochromatosis. Gastroenterology 1996;110:1107-1119.
-
(1996)
Gastroenterology
, vol.110
, pp. 1107-1119
-
-
Niederau, C.1
Fischer, R.2
Pürschel, A.3
Stremmel, W.4
Häussinger, D.5
Strohmeyer, G.6
-
34
-
-
0029618814
-
-
Daimon M, Kato T, Kawanami T, Tominaga M, Igarashi M, Yamanati K, et al. Biochem Biophys Res Commun 1995;217:89-95.
-
(1995)
Biochem Biophys Res Commun
, vol.217
, pp. 89-95
-
-
Daimon, M.1
Kato, T.2
Kawanami, T.3
Tominaga, M.4
Igarashi, M.5
Yamanati, K.6
-
35
-
-
0035156262
-
Obesity, body fat distribution, insulin sensitivity and islet b-cell function as explanations for metabolic diversity
-
Kahn SE, Prigeon RL, Schwartz RS, Fujimoto WY, Knopp RH, Brunzell JD, et al. Obesity, body fat distribution, insulin sensitivity and islet b-cell function as explanations for metabolic diversity. J Nutr 2001;131:354S-360S.
-
(2001)
J Nutr
, vol.131
-
-
Kahn, S.E.1
Prigeon, R.L.2
Schwartz, R.S.3
Fujimoto, W.Y.4
Knopp, R.H.5
Brunzell, J.D.6
-
36
-
-
0031058837
-
Use of desferrioxamine in the treatment of aceruloplasminemia
-
Miyajima H, Takahashi Y, Kamata T, Shimizu H, Sakai N, Gitlin JD. Use of desferrioxamine in the treatment of aceruloplasminemia. Ann Neurol 1997;41:404-407.
-
(1997)
Ann Neurol
, vol.41
, pp. 404-407
-
-
Miyajima, H.1
Takahashi, Y.2
Kamata, T.3
Shimizu, H.4
Sakai, N.5
Gitlin, J.D.6
-
37
-
-
0033152287
-
Investigation into the correlation between the structure of hydroxypyridinones and blood-brain barrier permeability
-
Habgood MD, Liu ZD, Dehkordi LS, Khodr HH, Abbott J, Hider RC. Investigation into the correlation between the structure of hydroxypyridinones and blood-brain barrier permeability. Biochem Pharmacol 1999;57:1305-1310.
-
(1999)
Biochem Pharmacol
, vol.57
, pp. 1305-1310
-
-
Habgood, M.D.1
Liu, Z.D.2
Dehkordi, L.S.3
Khodr, H.H.4
Abbott, J.5
Hider, R.C.6
|