Characterization of bovine ceruloplasmin [PDF]
Patricia L. Jenkins +3 more
openaire +3 more sources
A hem érfal komponensekre kifejtett közvetlen és közvetett patofiziológiai hatásai = Pathologic effects of heme on components of vessel wall via direct and indirect mechanisms [PDF]
Kimutattuk, hogy az atheroma lipid magja prooxidáns környezetet teremt, ahol a vörösvértestek szétesnek, a hemoglobin ferri- és ferrylhemoglobinná oxidálódik, és a felszabaduló hem és vas lipidoxidációt indít el.
Balla, György +5 more
core
Electrophoretic variation in human serum ceruloplasmin: A new genetic polymorphism [PDF]
D C Shreffler +3 more
openalex +1 more source
Aim of the present study has to focused on the possible relationship between serum malondialdehyde level, an index of lipid peroxidation, and ceruloplasmin levels, as protective agent against lipid peroxidation, in hepatitis C virus.
Rasha H. Jasim
doaj
A Novel Mutation Related to Aceruloplasminemia with Mild Clinical Findings: A Case Report
Background and Clinical Significance: Aceruloplasminemia (ACP), a member of the neurodegeneration with brain iron accumulation (NBIA) spectrum of disorders, is a rare disorder caused by mutations in the ceruloplasmin (CP) gene.
Alexandros Giannakis +4 more
doaj +1 more source
Thiol/disulphide homeostasis, ischemia modified albumin, and ferroxidase as oxidative stress markers in women with obesity with insulin resistance [PDF]
Background: The purpose of the study was to determine oxidative stress-related plasma thiol/disulphide, ischemiamodified albumin (IMA) levels and ferroxidase activity among women with obesity in insulin-resistant and noninsulin-resistant groups in ...
Ates Elif +4 more
doaj
Lafora Disease Masquerading as Hepatic Dysfunction [PDF]
Lafora disease is fatal intractable progressive myoclonic epilepsy. It is frequently characterized by epileptic seizures, difficulty walking, muscle spasms, and dementia in late childhood or adolescence.
Abdullah, Hafez Mohammad A. +6 more
core +1 more source
Inhibition of ascorbic-acid-induced depolymerization of hyaluronic acid by ceruloplasmin in synovial fluid. [PDF]
William Niedermeier
openalex +1 more source
Molecular and pathological basis of aceruloplasminemia
Aceruloplasminemia is an autosomal recessive neurodegenerative disease characterized by iron accumulation in the brain as well as visceral organs. It is a loss-of-function disorder caused by mutations in the ceruloplasmin gene.
SATOSHI KONO, HIROAKI MIYAJIMA
doaj
Differential Regulation of Ceruloplasmin Isoforms Expression in Macrophages and Hepatocytes [PDF]
Prémio de melhor poster.Ceruloplasmin (Cp) is an acute-phase protein that has been implicated in iron metabolism due to its ferroxidase activity, assisting ferroportin (Fpn) on cellular iron efflux.
Auriac, A. +6 more
core

