Characterization, mapping, and expression of the human ceruloplasmin gene
about
Shared and distinct mechanisms of iron acquisition by bacterial and fungal pathogens of humansHuman alpha 2-HS-glycoprotein: the A and B chains with a connecting sequence are encoded by a single mRNA transcriptCaeruloplasmin biosynthesis by the human uterusAceruloplasminemia: molecular characterization of this disorder of iron metabolismIdentification of Ceruloplasmin as a Gene that Affects Susceptibility to Glomerulonephritis Through Macrophage Function.Delayed translational silencing of ceruloplasmin transcript in gamma interferon-activated U937 monocytic cells: role of the 3' untranslated regionMechanisms of biological S-nitrosation and its measurement.Is copper an antioxidant nutrient?Single gene disorders affecting the gastrointestinal tract.Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumorsCeruloplasmin has two nearly identical sites that bind myeloperoxidase.Aceruloplasminemia.Iron in neurodegenerative disorders.Protective role of macrophage-derived ceruloplasmin in inflammatory bowel disease.The regulation of cellular iron metabolism.Metal ions in macrophage antimicrobial pathways: emerging roles for zinc and copperA general map of iron metabolism and tissue-specific subnetworks.Role of endogenous ceruloplasmin in low density lipoprotein oxidation by human U937 monocytic cells.Iron Together with Lipid Downregulates Protein Levels of Ceruloplasmin in Macrophages Associated with Rapid Foam Cell Formation.Chromosome maps of man and mouse. IV.Hepatic caeruloplasmin-gene expression during development in the guinea-pig. Correlation with changes in hepatic copper metabolism.Genes of the copper pathway.New insights into the pathogenesis of copper toxicosis in Wilson's disease: evidence for copper incorporation and defective canalicular transport of caeruloplasmin.Molecular and biochemical analysis of ceruloplasmin expression in rabbit and rat ciliary body.The man behind the syndrome: S.A. Kinnier Wilson.Absence of linkage between the retinoblastoma gene and hts gene in the LEC rat: a model of human Wilson's disease.
P2860
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P2860
Characterization, mapping, and expression of the human ceruloplasmin gene
description
1986 nî lūn-bûn
@nan
1986 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Characterization, mapping, and expression of the human ceruloplasmin gene
@ast
Characterization, mapping, and expression of the human ceruloplasmin gene
@en
Characterization, mapping, and expression of the human ceruloplasmin gene
@nl
type
label
Characterization, mapping, and expression of the human ceruloplasmin gene
@ast
Characterization, mapping, and expression of the human ceruloplasmin gene
@en
Characterization, mapping, and expression of the human ceruloplasmin gene
@nl
prefLabel
Characterization, mapping, and expression of the human ceruloplasmin gene
@ast
Characterization, mapping, and expression of the human ceruloplasmin gene
@en
Characterization, mapping, and expression of the human ceruloplasmin gene
@nl
P2093
P2860
P3181
P356
P1476
Characterization, mapping, and expression of the human ceruloplasmin gene
@en
P2093
D R Barnett
G S Adrian
J L McCombs
J R McGill
K H Naberhaus
S L Naylor
P2860
P304
P3181
P356
10.1073/PNAS.83.10.3257
P407
P577
1986-05-01T00:00:00Z