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