Characterization, mapping, and expression of the human ceruloplasmin gene - Wikidata - wikimedia - TriplyDB

Characterization, mapping, and expression of the human ceruloplasmin gene

Characterization, mapping, and expression of the human ceruloplasmin gene

http://www.wikidata.org/entity/Q24630091

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Shared and distinct mechanisms of iron acquisition by bacterial and fungal pathogens of humans Human alpha 2-HS-glycoprotein: the A and B chains with a connecting sequence are encoded by a single mRNA transcript Caeruloplasmin biosynthesis by the human uterus Aceruloplasminemia: molecular characterization of this disorder of iron metabolism Identification 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 region Mechanisms 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' tumors Ceruloplasmin 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 copper A 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.

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Characterization, mapping, and expression of the human ceruloplasmin gene

http://www.wikidata.org/entity/Q24630091

description

1986 nî lūn-bûn

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1986 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1986 թվականի մայիսին հրատարակված գիտական հոդված

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1986年の論文

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1986年論文

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1986年論文

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1986年論文

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1986年論文

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1986年論文

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1986年论文

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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Characterization, mapping, and expression of the human ceruloplasmin gene

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PNAS.83.10.3257

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Proceedings of the National Academy of Sciences of the United States of America

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Characterization, mapping, and expression of the human ceruloplasmin gene

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C M Moore

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D R Barnett

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F Yang

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G S Adrian

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J B Lum

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S Cutshaw

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S L Naylor

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P2860

DNA sequencing with chain-terminating inhibitors

Human transferrin: cDNA characterization and chromosomal localization

Single-chain structure of human ceruloplasmin: the complete amino acid sequence of the whole molecule

Sequencing end-labeled DNA with base-specific chemical cleavages

Structure of human factor VIII

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

Ceruloplasmin: the copper transport protein with essential oxidase activity.

Nucleotide sequence of cloned rat serum albumin messenger RNA.

Two new ceruloplasmin variants in Negroes--data on three populations.

Structural model of human ceruloplasmin based on internal triplication, hydrophilic/hydrophobic character, and secondary structure of domains.

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