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