-
1
-
-
0023664014
-
Rat ceruloplasmin: Molecular cloning and gene expression in liver, choroid plexus, yolk sac, placenta and testis
-
Aldred A.R., Grimes A., Schreiber G., Mercer J.F.B. Rat ceruloplasmin: Molecular cloning and gene expression in liver, choroid plexus, yolk sac, placenta and testis. J. Biol. Chem. 262:1987;2875-2878.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 2875-2878
-
-
Aldred, A.R.1
Grimes, A.2
Schreiber, G.3
Mercer, J.F.B.4
-
2
-
-
0343337650
-
Liver and biliary system development and function
-
R. Behrman, R. Kliegman, & A. Arvia. Philadelphia, PA: WB Saunders
-
Balistreri W.F. Liver and biliary system development and function. Behrman R., Kliegman R., Arvia A. Textbook of Pediatrics. 1996;1125-1127 WB Saunders, Philadelphia, PA.
-
(1996)
Textbook of Pediatrics
, pp. 1125-1127
-
-
Balistreri, W.F.1
-
3
-
-
0025752631
-
Hepatic caeruloplasmin-gene expression during development in the guinea pig. Correlation with changes in hepatic copper metabolism
-
Bingle C.D., Epstein O., Srai S.K., Gitlin J.D. Hepatic caeruloplasmin-gene expression during development in the guinea pig. Correlation with changes in hepatic copper metabolism. Biochem. J. 276:1991;771-775.
-
(1991)
Biochem. J.
, vol.276
, pp. 771-775
-
-
Bingle, C.D.1
Epstein, O.2
Srai, S.K.3
Gitlin, J.D.4
-
4
-
-
0023017420
-
Molecular mechanisms of protein secretion: The role of the signal sequence
-
Briggs M.S., Gierasch L.M. Molecular mechanisms of protein secretion: the role of the signal sequence. Adv. Prot. Chem. 38:1986;109-180.
-
(1986)
Adv. Prot. Chem.
, vol.38
, pp. 109-180
-
-
Briggs, M.S.1
Gierasch, L.M.2
-
5
-
-
0027452091
-
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
-
Bull P.C., Thomas G.R., Rommens J.M., Forbes J.R., Cox D.C. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat. Genet. 5:1993;327-337.
-
(1993)
Nat. Genet.
, vol.5
, pp. 327-337
-
-
Bull, P.C.1
Thomas, G.R.2
Rommens, J.M.3
Forbes, J.R.4
Cox, D.C.5
-
6
-
-
0021858066
-
Absorption, transport and hepatic metabolism of c ovary opper and zinc: Special reference to metallothionein and ceruloplasmin
-
Cousins R.J. Absorption, transport and hepatic metabolism of c ovary opper and zinc: special reference to metallothionein and ceruloplasmin. Physiol. Rev. 2:1985;238-309.
-
(1985)
Physiol. Rev.
, vol.2
, pp. 238-309
-
-
Cousins, R.J.1
-
7
-
-
0000386450
-
Disorders of copper transport
-
C.R. Scriver, A.L. Beaudet, W.M. Sly, & D. Valle. New York: McGraw-Hill
-
Danks D.M. Disorders of copper transport. Scriver C.R., Beaudet A.L., Sly W.M., Valle D. The Metabolic and Molecular Basis of Inherited Disease. 1995;2211-2235 McGraw-Hill, New York.
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 2211-2235
-
-
Danks, D.M.1
-
9
-
-
0025346979
-
Primary structure of rat ceruloplasmin and analysis of tissue-specific gene expression during development
-
Fleming R.E., Gitlin J.D. Primary structure of rat ceruloplasmin and analysis of tissue-specific gene expression during development. J. Biol. Chem. 265:1990;7701-7707.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 7701-7707
-
-
Fleming, R.E.1
Gitlin, J.D.2
-
10
-
-
0015968328
-
Defective biliary excretion of copper in Wilson's disease
-
Frommer D.J. Defective biliary excretion of copper in Wilson's disease. Gut. 15:1974;125-129.
-
(1974)
Gut
, vol.15
, pp. 125-129
-
-
Frommer, D.J.1
-
11
-
-
0018616612
-
A study of caeruloplasmin concentrations found in 75 patients with Wilson's disease, their kinships and various control groups
-
Gibbs K.G., Walshe J.M. A study of caeruloplasmin concentrations found in 75 patients with Wilson's disease, their kinships and various control groups. Q. J. Med. 48:1979;447.
-
(1979)
Q. J. Med.
, vol.48
, pp. 447
-
-
Gibbs, K.G.1
Walshe, J.M.2
-
12
-
-
0019318158
-
Biliary excretion of copper in Wilson's disease
-
Gibbs K., Walshe J.M. Biliary excretion of copper in Wilson's disease. Lancet. 2:1980;538.
-
(1980)
Lancet
, vol.2
, pp. 538
-
-
Gibbs, K.1
Walshe, J.M.2
-
13
-
-
0026521529
-
Mechanisms of ceruloplasmin biosynthesis in normal and copper-deficient rats
-
Gitlin J.D., Schroeder J.J., Lee-Ambrose L.M., Cousins R.J. Mechanisms of ceruloplasmin biosynthesis in normal and copper-deficient rats. Biochem. J. 282:1992;835-839.
-
(1992)
Biochem. J.
, vol.282
, pp. 835-839
-
-
Gitlin, J.D.1
Schroeder, J.J.2
Lee-Ambrose, L.M.3
Cousins, R.J.4
-
14
-
-
0019363278
-
Caeruloplasmin: Physiological and pathological perspectives
-
Gutteridge J.M., Stocks J. Caeruloplasmin: physiological and pathological perspectives. Crit. Rev. Clin. Lab. Sci. 14:1981;257-329.
-
(1981)
Crit. Rev. Clin. Lab. Sci.
, vol.14
, pp. 257-329
-
-
Gutteridge, J.M.1
Stocks, J.2
-
15
-
-
0028903259
-
Aceruloplasminemia: Molecular characterization of this disorder of iron metabolism
-
Harris Z.L., Takahashi Y., Miyajima H., Serizawa M., MacGillivray R.T., Gitlin J.D. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc. Natl. Acad. Sci. USA. 92:1995;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
-
16
-
-
84970567557
-
Experimental copper and Heliotropium Europeaum intoxication in sheep: Clinical syndromes and trace element concentrations
-
Howell J.M., Deol H.S., Dorling P.R. Experimental copper and Heliotropium Europeaum intoxication in sheep: clinical syndromes and trace element concentrations. Aust. J. Agric. Res. 42:1991;979-992.
-
(1991)
Aust. J. Agric. Res.
, vol.42
, pp. 979-992
-
-
Howell, J.M.1
Deol, H.S.2
Dorling, P.R.3
-
18
-
-
0021770224
-
Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs
-
Kozak M. Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs. Nucleic Acids Res. 12:1984;857-872.
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 857-872
-
-
Kozak, M.1
-
20
-
-
0342901001
-
Observations on blood copper in the sheep. 1. Normal copper status and variations induced by different conditions
-
McCosker P.J. Observations on blood copper in the sheep. 1. Normal copper status and variations induced by different conditions. Res. Vet. Sci. 9:1968;91-101.
-
(1968)
Res. Vet. Sci.
, vol.9
, pp. 91-101
-
-
McCosker, P.J.1
-
21
-
-
0022494771
-
Isolation of a human ceruloplasmin cDNA clone that includes the N-terminal leader sequence
-
Mercer J.F., Grimes A. Isolation of a human ceruloplasmin cDNA clone that includes the N-terminal leader sequence. FEBS Lett. 203:1986;185-190.
-
(1986)
FEBS Lett.
, vol.203
, pp. 185-190
-
-
Mercer, J.F.1
Grimes, A.2
-
22
-
-
0025886315
-
Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse
-
Mercer J.F., Grimes A., Danks D.M., Rauch H. Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse. J. Nutr. 121:1991;894-899.
-
(1991)
J. Nutr.
, vol.121
, pp. 894-899
-
-
Mercer, J.F.1
Grimes, A.2
Danks, D.M.3
Rauch, H.4
-
23
-
-
0025372084
-
Analysis of hepatic copper, zinc, metallothionein and metallothionein-1a mRNA in developing sheep
-
Paynter J.A., Camakaris J., Mercer J.F.B. Analysis of hepatic copper, zinc, metallothionein and metallothionein-1a mRNA in developing sheep. Eur. J. Biochem. 190:1990;149-154.
-
(1990)
Eur. J. Biochem.
, vol.190
, pp. 149-154
-
-
Paynter, J.A.1
Camakaris, J.2
Mercer, J.F.B.3
-
25
-
-
0025729544
-
Mechanisms of copper incorporation during the biosynthesis of human ceruloplasmin
-
Sato M., Gitlin J.D. Mechanisms of copper incorporation during the biosynthesis of human ceruloplasmin. J. Biol. Chem. 266:1991;5128-5134.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 5128-5134
-
-
Sato, M.1
Gitlin, J.D.2
-
26
-
-
0000852301
-
Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease)
-
Scheinberg I.H., Gitlin D. Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease). Science. 116:1952;484-485.
-
(1952)
Science
, vol.116
, pp. 484-485
-
-
Scheinberg, I.H.1
Gitlin, D.2
-
27
-
-
0022449964
-
The ontogeny of liver copper metabolism in the guinea-pig: Clues to the etiology of Wilson's disease
-
Srai S.K., Burroughs A.K., Wood B., Epstein O. The ontogeny of liver copper metabolism in the guinea-pig: clues to the etiology of Wilson's disease. Hepatology. 6:1986;427-432.
-
(1986)
Hepatology
, vol.6
, pp. 427-432
-
-
Srai, S.K.1
Burroughs, A.K.2
Wood, B.3
Epstein, O.4
-
28
-
-
0001384460
-
Single-chain structure of human ceruloplasmin: The complete amino acid sequence of the whole molecule
-
Takahashi N., Ortel T.L., Putnam F.W. Single-chain structure of human ceruloplasmin: the complete amino acid sequence of the whole molecule. Proc. Natl. Acad. Sci. USA. 81:1984;390-394.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 390-394
-
-
Takahashi, N.1
Ortel, T.L.2
Putnam, F.W.3
-
29
-
-
0027364961
-
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
-
Tanzi R.E., et al. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat. Genet. 5:1993;344-350.
-
(1993)
Nat. Genet.
, vol.5
, pp. 344-350
-
-
Tanzi, R.E.1
-
30
-
-
0028801746
-
Copper incorporation into ceruloplasmin in rat livers
-
Terada K., Kararada Y., Miura N., Yasui O., Koyama K., Sugiyama T. Copper incorporation into ceruloplasmin in rat livers. Biochim. Biophys. Acta. 2170:1995;58-62.
-
(1995)
Biochim. Biophys. Acta
, vol.2170
, pp. 58-62
-
-
Terada, K.1
Kararada, Y.2
Miura, N.3
Yasui, O.4
Koyama, K.5
Sugiyama, T.6
-
31
-
-
17144458094
-
Restoration of holoceruloplasmin synthesis in LEC rat after infusion of recombinant adenovirus bearing WND cDNA
-
Terada K., Nakako T., Yang X.l., Iida M., Aiba N., Minamiya Y., Nakai M., Sakaki T., Miura N., Sugiyama T. Restoration of holoceruloplasmin synthesis in LEC rat after infusion of recombinant adenovirus bearing WND cDNA. J. Biol. Chem. 373:1998;1815-1820.
-
(1998)
J. Biol. Chem.
, vol.373
, pp. 1815-1820
-
-
Terada, K.1
Nakako, T.2
Yang, X.I.3
Iida, M.4
Aiba, N.5
Minamiya, Y.6
Nakai, M.7
Sakaki, T.8
Miura, N.9
Sugiyama, T.10
-
32
-
-
0029799960
-
The toxic milk mouse is a murine model of Wilson disease
-
Theophilos M.B., Cox D.W., Mercer J.F.B. The toxic milk mouse is a murine model of Wilson disease. Human Mol. Genet. 5:1996;1619-1624.
-
(1996)
Human Mol. Genet.
, vol.5
, pp. 1619-1624
-
-
Theophilos, M.B.1
Cox, D.W.2
Mercer, J.F.B.3
-
33
-
-
0027968068
-
ClustalW: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalities and weight matrix choice
-
Thompson J.D., Higgins D.G., Gibson T.J. ClustalW: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalities and weight matrix choice. Nucleic Acids Res. 22:1994;4673-4680.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
35
-
-
0020770479
-
Patterns of amino acids near signal-sequence cleavage sites
-
von Heijne G. Patterns of amino acids near signal-sequence cleavage sites. Eur. J. Biochem. 133:1983;17-21.
-
(1983)
Eur. J. Biochem.
, vol.133
, pp. 17-21
-
-
Von Heijne, G.1
-
37
-
-
0027431996
-
Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease
-
Yamaguchi Y., Heiny M.E., Gitlin J.D. Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease. Biochem. Biophys. Res. Commun. 197:1993;271-277.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.197
, pp. 271-277
-
-
Yamaguchi, Y.1
Heiny, M.E.2
Gitlin, J.D.3
-
38
-
-
0022512141
-
Characterization, mapping, and expression of the human ceruloplasmin gene
-
Yang F., Naylor S.L., Lum J.B., Cutshaw S., McCombs J.L., Naberhaus K.H., McGill J.R., Adrian G.S., Moore C.M., Barnett D.R., Bowmann B.H. Characterization, mapping, and expression of the human ceruloplasmin gene. Proc. Natl. Acad. Sci. USA. 83:1986;3257-3261.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 3257-3261
-
-
Yang, F.1
Naylor, S.L.2
Lum, J.B.3
Cutshaw, S.4
McCombs, J.L.5
Naberhaus, K.H.6
McGill, J.R.7
Adrian, G.S.8
Moore, C.M.9
Barnett, D.R.10
Bowmann, B.H.11
-
39
-
-
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., Hiyamuta S., Ikeda S., Norikazu S., Yanagisawa N. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nat. Genet. 9:1995;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
Hiyamuta, S.7
Ikeda, S.8
Norikazu, S.9
Yanagisawa, N.10
|