Human plasma protein N-glycosylation

F Clerc, KR Reiding, BC Jansen, GSM Kammeijer… - Glycoconjugate …, 2016 - Springer
Glycosylation is the most abundant and complex protein modification, and can have a
profound structural and functional effect on the conjugate. The oligosaccharide fraction is …

The neurotoxicity of iron, copper and manganese in Parkinson's and Wilson's diseases

P Dusek, PM Roos, T Litwin, SA Schneider… - Journal of trace …, 2015 - Elsevier
Impaired cellular homeostasis of metals, particularly of Cu, Fe and Mn may trigger
neurodegeneration through various mechanisms, notably induction of oxidative stress …

Changes in oxidative stress, inflammation, and muscle damage markers following diet and beetroot juice supplementation in elite fencers

L Kozłowska, O Mizera, J Gromadzińska, B Janasik… - Antioxidants, 2020 - mdpi.com
The aim of this study was to assess the impact of diet and active substances in beetroot juice
on the parameters of oxidative stress, inflammation, and muscle damage as well as on the …

Meta-analysis of serum non-ceruloplasmin copper in Alzheimer's disease

R Squitti, I Simonelli, M Ventriglia… - Journal of …, 2014 - content.iospress.com
The fraction of copper not bound to ceruloplasmin seems altered in Alzheimer's disease
(AD). We have addressed this notion evaluating all the studies carried out from 1996 until …

A fluorometric assay to determine labile copper (II) ions in serum

M Maares, A Haupt, C Schüßler, M Kulike-Koczula… - Scientific Reports, 2023 - nature.com
Labile copper (II) ions (Cu2+) in serum are considered to be readily available for cellular
uptake and to constitute the biologically active Cu2+ species in the blood. It might also be …

Relative exchangeable copper: a new highly sensitive and highly specific biomarker for Wilson's disease diagnosis

S El Balkhi, JM Trocello, J Poupon, P Chappuis… - Clinica chimica acta, 2011 - Elsevier
Wilson disease (WD) is an autosomal recessive inherited disorder of copper metabolism.
Failure to diagnose WD can be dramatic leading to irreversible damages. The molecular …

Copper assisted sequence-specific chemical protein conjugation at a single backbone amide

M Guo, K Zhao, L Guo, R Zhou, Q He, K Lu, T Li… - Nature …, 2023 - nature.com
Direct, site-specific methods of protein functionalization are highly desirable for
biotechnology. However, such methods are challenging due to the difficulty of chemically …

Diagnosis of Wilson's disease: a comprehensive review

CM Mak, CW Lam - Critical reviews in clinical laboratory sciences, 2008 - Taylor & Francis
Wilson's disease is an autosomal recessive disorder of copper metabolism. The culprit gene
is ATP7B. The worldwide prevalence is about 1 in 30,000, which may vary by population …

A fit-for-purpose copper speciation method for the determination of exchangeable copper relevant to Wilson's disease

ME del Castillo Busto, S Cuello-Nunez… - Analytical and …, 2022 - Springer
Exchangeable copper (CuEXC), mainly comprised copper (Cu) bound to albumin, has been
proposed as a specific marker of Cu overload in Wilson's disease (WD). To the author's …

Review about powerful combinations of advanced and hyphenated sample introduction techniques with inductively coupled plasma-mass spectrometry (ICP-MS) for …

B Michalke - International Journal of Molecular Sciences, 2022 - mdpi.com
Element analysis in clinical or biological samples is important due to the essential role in
clinical diagnostics, drug development, and drug-effect monitoring. Particularly, the specific …