| 1 | CP, MPO
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| Ceruloplasmin is an endogenous inhibitor of myeloperoxidase.
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| Chapman AL, Mocatta TJ, Shiva S, Seidel A, Chen B, Khalilova I, Paumann-Page ME, Jameson GN, Winterbourn CC, Kettle AJ.
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| J Biol Chem 288(9):6465-77. doi: 10.1074/jbc.M112.418970. Epub 2013 Jan 10.
2013
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| 2 | CP, MPO
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| Ceruloplasmin and myeloperoxidase in complex affect the enzymatic properties of each other.
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| Sokolov AV, Ageeva KV, Pulina MO, Cherkalina OS, Samygina VR, Vlasova II, Panasenko OM, Zakharova ET, Vasilyev VB.
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| Free Radic Res 42(11-12):989-98.PMID: 19031316 2008
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| 3 | CP, CPD
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| Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus.
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| Shang HF, Jiang XF, Burgunder JM, Chen Q, Zhou D.
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| Mov Disord 21(12):2217-20. 2006
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| 4 | CP, CPD
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| Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia.
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| Kono S, Suzuki H, Takahashi K, Takahashi Y, Shirakawa K, Murakawa Y, Yamaguchi S, Miyajima H.
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| Gastroenterology 131(1):240-5. 2006
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| 5 | CP, CPD
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| Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease.
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| Takahashi Y, et al.
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| Hum Mol Genet 5 : 81-84. 1996
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| 6 | CP, CPD
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| Hereditary ceruloplasmin deficiency with hemosiderosis.
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| Okamoto N, et al.
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| Hum Genet 97 : 755-758. 1996
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| 7 | CP, CPD
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| Expression of the ceruloplasmin gene in the human retina and brain : implications for a pathogenic model in aceruloplasminemia.
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| Klomp LWJ, et al.
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| Hum Mol Genet 5 : 1989-1996. 1996
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| 8 | CP
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| Dinucleotide repeat polymorphism in the human ceruloplasmin gene.
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| Daimon M, et al.
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| Hum Genet 96 : 736. 1995
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| 9 | CP, CPD
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| A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus.
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| Daimon M, et al.
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| Biochem Biophys Res Commun 217 : 89-95. 1995
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| 10 | CP, CPD
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| A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.
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| Yoshida K, et al.
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| Nat Genet 9 : 267-272. 1995
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| 11 | CP, CPD
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| Aceruloplasminemia : molecular characterization of this disorder of iron metabolism.
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| Harris ZL, et al.
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| Proc Natl Acad Sci U S A 92 : 2539-2543. 1995
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| 12 | CP
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| Fine structure of the human ceruloplasmin gene.
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| Daimon M, et al.
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| Biochem Biophys Res Commun 208 : 1028-1035. 1995
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| 13 | CP, CPD
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| Hereditary ceruloplasmin deficiency with hemosiderosis : a clinicopathological study of a Japanese family.
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| Morita H, et al.
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| Ann Neurol 37 : 646-656. 1995
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| 14 | CP
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| Restriction polymorphisms of the ceruloplasmin gene on chromosome 3.
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| Bost M, et al.
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| Hum Genet 96 : 239-240. 1995
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| 15 | CP
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| Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
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| Logan JI, et al.
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| Q J Med 87 : 663-670. 1994
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| 16 | CP, CPP, F2, F5TPH, F12
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| Regional assignment for the human genes encoding FII, FV, FXII, ceruloplasmin and pseudoceruloplasmin.
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| Riddell DC, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 682. 1987
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| 17 | CP, TF
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| Chromosomal localization of ceruloplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes.
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| Baranov VS, et al.
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| Chromosoma 96 : 60-66. 1987
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| 18 | F2, CP, CPL1
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| Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively.
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| Royle NJ, et al.
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| Somat Cell Mol Genet 13 : 285-292. 1987
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| 19 | CP
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| Characterization, mapping, and expression of the human ceruloplasmin gene.
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| Yang F, et al.
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| Proc Natl Acad Sci U S A 83 : 3257-3261. 1986
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| 20 | CP
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| Mapping ceruloplasmin cDNA to human chromosome 3.
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| Naylor SL, et al.
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| (HGM8) Cytogenet Cell Genet 40 : 711. 1985
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| 21 | CP
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| Evidence for linkage between the loci for transferrin and ceruloplasmin in man.
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| Weitkamp LR.
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| Ann Hum Genet 47 : 293-297. 1983
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| 22 | CP
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| Hereditary hypoceruloplasminemia.
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| Edwards CQ, et al.
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| Clin Genet 15 : 311-316. 1979
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