scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.R111.316406 |
P8608 | Fatcat ID | release_amanc6zcfjfabn4pt37ryzd5ce |
P932 | PMC publication ID | 3340201 |
P698 | PubMed publication ID | 22389498 |
P2093 | author name string | Michael J Petris | |
Victoria Hodgkinson | |||
P2860 | cites work | Bacterial killing by dry metallic copper surfaces | Q24633271 |
Contribution of copper ion resistance to survival of Escherichia coli on metallic copper surfaces | Q24641867 | ||
Molecular basis of metal-ion selectivity and zeptomolar sensitivity by CueR | Q27641964 | ||
Hepcidin and iron regulation, 10 years later | Q27690828 | ||
Copper as a biocidal tool | Q28267347 | ||
Structure, regulation and evolution of Nox-family NADPH oxidases that produce reactive oxygen species | Q28282131 | ||
A novel copper-responsive regulon in Mycobacterium tuberculosis | Q28486641 | ||
CsoR is a novel Mycobacterium tuberculosis copper-sensing transcriptional regulator | Q28486657 | ||
CtpV: a putative copper exporter required for full virulence of Mycobacterium tuberculosis | Q28487128 | ||
Identification of a copper-binding metallothionein in pathogenic mycobacteria | Q28487141 | ||
Cu,Zn superoxide dismutase of Mycobacterium tuberculosis contributes to survival in activated macrophages that are generating an oxidative burst | Q28487322 | ||
CsoR regulates the copper efflux operon copZA in Bacillus subtilis | Q29346694 | ||
A role for the ATP7A copper-transporting ATPase in macrophage bactericidal activity | Q33553377 | ||
The multi-copper-ion oxidase CueO of Salmonella enterica serovar Typhimurium is required for systemic virulence | Q33826068 | ||
Copper homeostasis in Salmonella is atypical and copper-CueP is a major periplasmic metal complex | Q34055736 | ||
Controlling Legionella in hospital drinking water: an evidence-based review of disinfection methods | Q34175425 | ||
Potential use of copper surfaces to reduce survival of epidemic meticillin-resistant Staphylococcus aureus in the healthcare environment. | Q34519768 | ||
Copper resistance is essential for virulence of Mycobacterium tuberculosis | Q34534178 | ||
Mechanisms for copper acquisition, distribution and regulation | Q34750485 | ||
Crystal structures of multicopper oxidase CueO bound to copper(I) and silver(I): functional role of a methionine-rich sequence | Q35424254 | ||
Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS) | Q35656072 | ||
Superoxide accelerates DNA damage by elevating free-iron levels | Q35921515 | ||
Bacterial infection as assessed by in vivo gene expression | Q35966527 | ||
Copper metabolism during acute inflammation: studies on liver and serum copper concentrations in normal and inflamed rats | Q36097699 | ||
The role of diet and the reticuloendothelial system in the response of rats to Salmonella typhilmurium infection | Q36168069 | ||
Virulent Salmonella typhimurium has two periplasmic Cu, Zn-superoxide dismutases | Q36398159 | ||
The structure and function of heavy metal transport P1B-ATPases. | Q36706247 | ||
Copper and zinc body levels in inflammation: an overview of the data obtained from animal and human studies | Q36762274 | ||
Function and regulation of human copper-transporting ATPases | Q36872228 | ||
Inflammatory manifestations in chronic granulomatous disease (CGD). | Q37056322 | ||
Copper transport into the secretory pathway is regulated by oxygen in macrophages | Q37166075 | ||
Mycobacterium tuberculosis and the macrophage: maintaining a balance. | Q37186955 | ||
The iron-sulfur clusters of dehydratases are primary intracellular targets of copper toxicity | Q37208556 | ||
Antimicrobial mechanisms of phagocytes and bacterial evasion strategies | Q37445493 | ||
Response of gram-positive bacteria to copper stress. | Q37601995 | ||
The cop operon is required for copper homeostasis and contributes to virulence in Streptococcus pneumoniae | Q84516987 | ||
Human copper transporters: mechanism, role in human diseases and therapeutic potential | Q37747071 | ||
War-Fe-re: iron at the core of fungal virulence and host immunity | Q37852592 | ||
Transcriptional activation of an Escherichia coli copper efflux regulon by the chromosomal MerR homologue, cueR. | Q38310027 | ||
Genes involved in copper resistance influence survival of Pseudomonas aeruginosa on copper surfaces | Q38824427 | ||
Relationships between serum concentrations of C-reactive protein and micronutrients, in patients with tuberculosis. | Q39147140 | ||
Molecular analysis of the copper-transporting efflux system CusCFBA of Escherichia coli | Q39775113 | ||
Linkage between catecholate siderophores and the multicopper oxidase CueO in Escherichia coli | Q40000513 | ||
Structure, oxidant activity, and cardiovascular mechanisms of human ceruloplasmin | Q40518508 | ||
Characteristics of fever and acute-phase response induced in rabbits by IL-1 and TNF. | Q40781130 | ||
Fenton chemistry: an introduction. | Q40980956 | ||
Mutants in the CtpA copper transporting P-type ATPase reduce virulence of Listeria monocytogenes | Q41130491 | ||
Role of Dietary Copper in Enhancing Resistance to Escherichia coli Mastitis | Q42441033 | ||
CueR (YbbI) of Escherichia coli is a MerR family regulator controlling expression of the copper exporter CopA. | Q42640041 | ||
Role of copper in reducing hospital environment contamination | Q43311791 | ||
Trace element alterations in infectious diseases | Q43489850 | ||
Acute phase response in horses: changes in plasma cation concentrations after localised tissue injury | Q43495415 | ||
Mutations in the cueA gene encoding a copper homeostasis P-type ATPase reduce the pathogenicity of Pseudomonas aeruginosa in mice | Q43540663 | ||
CueO is a multi-copper oxidase that confers copper tolerance in Escherichia coli. | Q43722949 | ||
In vivo copper-mediated free radical production: an ESR spin-trapping study | Q43981754 | ||
Copper deficiency increases the virulence of amyocarditic and myocarditic strains of coxsackievirus B3 in mice | Q44034936 | ||
Respiratory burst and candidacidal activity of peritoneal macrophages are impaired in copper-deficient rats | Q44059090 | ||
Effects of inflammation and antiinflammatory treatment on serum trace elements concentrations | Q44497690 | ||
Using wound fluid analyses to identify trace element requirements for efficient healing | Q44578655 | ||
Essential trace elements selenium, zinc, copper, and iron concentrations and their related acute-phase proteins in patients with vivax malaria | Q48014379 | ||
Menkes' disease: case report | Q48209920 | ||
Neuronal and vascular disorders of the brain and spinal cord in Menkes kinky hair disease | Q48249207 | ||
The sctR of Salmonella enterica serova Typhimurium encoding a homologue of MerR protein is involved in the copper-responsive regulation of cuiD. | Q48303329 | ||
Biodistribution of 64Cu in inflamed rats following administration of two anti-inflammatory copper complexes | Q48449768 | ||
Difficulties in the neonatal diagnosis of Menkes' kinky hair syndrome--trichopoliodystrophy | Q48628210 | ||
The global burden of nontyphoidal Salmonella gastroenteritis | Q50050617 | ||
Alternative periplasmic copper-resistance mechanisms in Gram negative bacteria. | Q50054546 | ||
GolS controls the response to gold by the hierarchical induction of Salmonella-specific genes that include a CBA efflux-coding operon | Q50067863 | ||
Bacterial sensing of and resistance to gold salts. | Q50074078 | ||
Clinical and biochemical consequences of copper-histidine therapy in Menkes disease. | Q52222718 | ||
Interaction of nutrition and infection: effect of copper deficiency on resistance to Trypanosoma lewisi. | Q54264859 | ||
Correlation of hypercupremia with other acute phase reactants in malignant lymphoma. | Q54472488 | ||
Trace elements and some extracellular antioxidant proteins levels in serum of patients with systemic lupus erythematosus. | Q54785143 | ||
Copper status and function of neutrophils are reversibly depressed in marginally and severely copper-deficient rats | Q68490471 | ||
Redistribution of minerals and trace elements in chronic inflammation--a study on isolated blood cells from patients with ankylosing spondylitis | Q69229759 | ||
Serum copper concentration as an index of experimental lung injury | Q69274073 | ||
The effect of copper deficiency on the resistance of mice to infection with Pasteurella haemolytica | Q71709747 | ||
Some effects of copper deficiency on leucocyte function in sheep and cattle | Q72919151 | ||
Effects of selenium and copper deficiency on neutrophil function in cattle | Q72936432 | ||
The independent cue and cus systems confer copper tolerance during aerobic and anaerobic growth in Escherichia coli | Q74001289 | ||
The Enterococcus hirae copper chaperone CopZ delivers copper(I) to the CopY repressor | Q74589491 | ||
The Haber-Weiss cycle -- 70 years later: an alternative view | Q78021420 | ||
Impaired zinc and copper status in children with burn injuries: need to reassess nutritional requirements | Q80351143 | ||
Elemental analysis of Mycobacterium avium-, Mycobacterium tuberculosis-, and Mycobacterium smegmatis-containing phagosomes indicates pathogen-induced microenvironments within the host cell's endosomal system | Q81300400 | ||
P433 | issue | 17 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | copper | Q753 |
P304 | page(s) | 13549-13555 | |
P577 | publication date | 2012-03-02 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Copper homeostasis at the host-pathogen interface | |
P478 | volume | 287 |
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