Results 11 to 20 of about 24,157 (174)

Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia

open access: yesEMBO Molecular Medicine, 2017
Aceruloplasminemia is a monogenic disease caused by mutations in the ceruloplasmin gene that result in loss of protein ferroxidase activity. Ceruloplasmin plays a role in iron homeostasis, and its activity impairment leads to iron accumulation in liver ...
Alan Zanardi   +9 more
doaj   +2 more sources

Therapeutic Reversal of Severe Neuropsychiatric Symptoms in Wilson's Disease: A Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Wilsons disease is an autosomal recessive genetic disorder of copper metabolism that results in copper accumulation in liver and other organs. Hepatic manifestation tends to occur earlier than the neurological manifestation. We present a case with psychiatric presentation.
Penjor T, Dorji S, Wangchuk S.
europepmc   +2 more sources

Copper-Induced Oligomerization of Ceruloplasmin

open access: yes, 2021
Oligomerization of copper-containing ferroxidase of ceruloplasmin in the presence of protein-unbound copper in a solution has been investigated by small-angle X-ray scattering (SAXS). Ceruloplasmin is a monomer with a molecular weight of ~132 kDa. Copper
Petoukhov, M. V.   +7 more
core   +1 more source

Expression of ceruloplasmin in cavernosal tissue of paradoxical sleep deprived rats

open access: yesSleep Science, 2012
Objective: Ceruloplasmin (Cp) is a copper-binding protein expressed in several tissues that plays distinct functions depending on the physiological context.
Monica Levy Andersen   +4 more
doaj   +1 more source

Plasma zinc, copper and serum ceruloplasmin levels of autism spectrum disorder children in Bangladesh

open access: yesHeliyon, 2023
Neural and cognitive processes require zinc and copper homeostasis and a normal zinc/copper ratio. Ceruloplasmin, an intrinsic antioxidant protein, maintains copper homeostasis, which might also influence autism spectrum disorder (ASD).
Umme Raihan Siddiqi   +6 more
doaj   +1 more source

Ceruloplasmin (2-D PAGE) Pattern and Copper Content in Serum and Brain of Alzheimer Disease Patients

open access: yesBiomarker Insights, 2006
A dysfunction in copper homeostasis seems to occur in Alzheimer's disease (AD). We previously evidenced that an excess of non-ceruloplasmin-copper (NCC) correlated with the main functional, anatomical as well as cerebrospinal markers of the disease.
Rosanna Squitti   +7 more
doaj   +2 more sources

Mechanism of Copper Uptake from Blood Plasma Ceruloplasmin by Mammalian Cells. [PDF]

open access: yesPLoS ONE, 2016
Ceruloplasmin, the main copper binding protein in blood plasma, has been of particular interest for its role in efflux of iron from cells, but has additional functions.
Danny Ramos   +6 more
doaj   +1 more source

Sertoli Cells Synthesize and Secrete a Ceruloplasmin-Like Protein [PDF]

open access: yes, 1983
Sertoli cells synthesize and secrete a ceruloplasmin-like protein (testicularceruloplasmin) that is immunologically similar to serum ceruloplasmin.
Michael K. Skinner   +3 more
core   +1 more source

Ceruloplasmin and the Extent of Heart Failure in Ischemic and Nonischemic Cardiomyopathy Patients

open access: yesMediators of Inflammation, 2013
Objective. Ceruloplasmin was elevated in patients with coronary heart disease, but the relationship between ceruloplasmin and heart failure was still unknown.
Yifei Xu   +4 more
doaj   +1 more source

High ceruloplasmin levels are associated with obsessive compulsive disorder: a case control study

open access: yesBehavioral and Brain Functions, 2008
Background Alterations in ceruloplasmin are currently assumed as one of the mechanisms underlying the development of a number of neurodegenerative disorders.
Celik Hakim   +6 more
doaj   +1 more source

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