| 1 | CP, HEPH
|
| Multi-copper ferroxidase deficiency leads to iron accumulation and oxidative damage in astrocytes and oligodendrocytes.
|
| Chen Z, Jiang R, Chen M, Zheng J, Chen M, Braidy N, Liu S, Liu G, Maimaitiming Z, Shen T, Dunaief JL, Vulpe CD, Anderson GJ, Chen H.
|
| Sci Rep. Jul 1;9(1):9437. doi: 10.1038/s41598-019-46019-9. 2019
|
| 2 | CP, HEPH
|
| Multi-Copper Ferroxidase-Deficient Mice Have Increased Brain Iron Concentrations and Learning and Memory Deficits.
|
| Zheng J, Jiang R, Chen M, Maimaitiming Z, Wang J, Anderson GJ, Vulpe CD, Dunaief JL, Chen H.
|
| J Nutr. Apr 1;148(4):643-649. doi: 10.1093/jn/nxy012. 2018
|
| 3 | CP, HEPH
|
| Deletion of hephaestin and ceruloplasmin induces a serious systemic iron deficiency and disrupts iron homeostasis.
|
| Xu E, Chen M, Zheng J, Maimaitiming Z, Zhong T, Chen H.
|
| Biochem Biophys Res Commun. Sep 10;503(3):1905-1910. doi: 10.1016/j.bbrc.2018.07.134. Epub 2018 Jul 27 2018
|
| 4 | CP, 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
|
| 5 | CP, HEPH
|
| Age-dependent expression of hephaestin in the brain of ceruloplasmin-deficient mice.
|
| Cui R, Duan XL, Anderson GJ, Qiao YT, Yu P, Qian ZM, Yoshida K, Takeda S, Guo P, Yang ZL, Chang YZ.
|
| Biol. J Trace Elem Med 23(4):290-9. doi: 10.1016/j.jtemb.2009.05.004. Epub 2009 Jun 21. 2009
|
| 6 | CP, 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
|
| 7 | CP, 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
|
| 8 | CP, 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
|
| 9 | CP, 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
|
| 10 | CP, CPD
|
| Hereditary ceruloplasmin deficiency with hemosiderosis.
|
| Okamoto N, et al.
|
| Hum Genet 97 : 755-758. 1996
|
| 11 | CP, 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
|
| 12 | CP
|
| Dinucleotide repeat polymorphism in the human ceruloplasmin gene.
|
| Daimon M, et al.
|
| Hum Genet 96 : 736. 1995
|
| 13 | CP, 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
|
| 14 | CP, CPD
|
| A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.
|
| Yoshida K, et al.
|
| Nat Genet 9 : 267-272. 1995
|
| 15 | CP, 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
|
| 16 | CP
|
| Fine structure of the human ceruloplasmin gene.
|
| Daimon M, et al.
|
| Biochem Biophys Res Commun 208 : 1028-1035. 1995
|
| 17 | CP, CPD
|
| Hereditary ceruloplasmin deficiency with hemosiderosis : a clinicopathological study of a Japanese family.
|
| Morita H, et al.
|
| Ann Neurol 37 : 646-656. 1995
|
| 18 | CP
|
| Restriction polymorphisms of the ceruloplasmin gene on chromosome 3.
|
| Bost M, et al.
|
| Hum Genet 96 : 239-240. 1995
|
| 19 | CP
|
| Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
|
| Logan JI, et al.
|
| Q J Med 87 : 663-670. 1994
|
| 20 | CP, 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
|
| 21 | CP, 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
|
| 22 | F2, 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
|
| 23 | CP
|
| Characterization, mapping, and expression of the human ceruloplasmin gene.
|
| Yang F, et al.
|
| Proc Natl Acad Sci U S A 83 : 3257-3261. 1986
|
| 24 | CP
|
| Mapping ceruloplasmin cDNA to human chromosome 3.
|
| Naylor SL, et al.
|
| (HGM8) Cytogenet Cell Genet 40 : 711. 1985
|
| 25 | CP
|
| Evidence for linkage between the loci for transferrin and ceruloplasmin in man.
|
| Weitkamp LR.
|
| Ann Hum Genet 47 : 293-297. 1983
|
| 26 | CP
|
| Hereditary hypoceruloplasminemia.
|
| Edwards CQ, et al.
|
| Clin Genet 15 : 311-316. 1979
|