Citations for
1CP, 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
2CP, 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
3CPD
Characterization of a novel, cytokine-inducible carboxypeptidase D isoform in haematopoietic tumour cells.
O'Malley PG, Sangster SM, Abdelmagid SA, Bearne SL, Too CK.
Biochem J 390(Pt 3):665-73. 2005
4CPD, TGOLN2
Identification and nuclear localization of a novel prolactin and cytokine-responsive carboxypeptidase D.
Too CK, Vickaryous N, Boudreau RT, Sangster SM.
Endocrinology 142(3):1357-67. 2001
5CPN1, CPD
Chromosomal localization of the genes for human carboxypeptidase D (CPD) and the active 50-kilodalton subunit of human carboxypeptidase N (CPN1).
Riley DA, et al.
Genomics 50 : 105-108. 1998
6CPD
Cloning, functional expression, and chromosomal localization of the human and mouse gp180-carboxypeptidase D-like enzyme.
Ishikawa T, Murakami K, Kido Y, Ohnishi S, Yazaki Y, Harada F, Kuroki K.
Gene 215(2):361-70. 1998
7CPD
Sequence of human carboxypeptidase D reveals it to be a member of the regulatory carboxypeptidase family with three tandem active site domains.
Tan F, et al.
Biochem J 327 : 81-87. 1997
8CPD
Identification of a membrane-bound carboxypeptidase as the mammalian homolog of duck gp180, a hepatitis B virus-binding protein.
McGwire GB, et al.
Life Sci 60 : 715-724. 1997
9CP, 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
10CP, CPD
Hereditary ceruloplasmin deficiency with hemosiderosis.
Okamoto N, et al.
Hum Genet 97 : 755-758. 1996
11CP, 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
12CP, 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
13CP, CPD
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.
Yoshida K, et al.
Nat Genet 9 : 267-272. 1995
14CP, 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
15CP, CPD
Hereditary ceruloplasmin deficiency with hemosiderosis : a clinicopathological study of a Japanese family.
Morita H, et al.
Ann Neurol 37 : 646-656. 1995