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

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F15%3A10295613" target="_blank" >RIV/00216208:11110/15:10295613 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064165:_____/15:10295613

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jtemb.2014.05.007" target="_blank" >http://dx.doi.org/10.1016/j.jtemb.2014.05.007</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jtemb.2014.05.007" target="_blank" >10.1016/j.jtemb.2014.05.007</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

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

  • Original language description

    Impaired cellular homeostasis of metals, particularly of Cu, Fe and Mn may trigger neurodegeneration through various mechanisms, notably induction of oxidative stress, promotion of a-synuclein aggregation and fibril formation, activation of microglial cells leading to inflammation and impaired production of metalloproteins. In this article we review available studies concerning Fe, Cu and Mn in Parkinson's disease and Wilson's disease. In Parkinson's disease local dysregulation of iron metabolism in thesubstantia nigra (SN) seems to be related to neurodegeneration with an increase in SN iron concentration, accompanied by decreased SN Cu and ceruloplasmin concentrations and increased free Cu concentrations and decreased ferroxidase activity in the cerebrospinal fluid. Available data in Wilson's disease suggest that substantial increases in CNS Cu concentrations persist for a long time during chelating treatment and that local accumulation of Fe in certain brain nuclei may occur during

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FH - Neurology, neuro-surgery, nuero-sciences

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/7F14308" target="_blank" >7F14308: Comparative study of Huntington's disease using biochemical, immunocytochemical and molecular genetic methods on the mouse, minipig and human tissues and cells</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Trace Elements in Medicine and Biology

  • ISSN

    0946-672X

  • e-ISSN

  • Volume of the periodical

    31

  • Issue of the periodical within the volume

    July

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    11

  • Pages from-to

    193-203

  • UT code for WoS article

    000356192400031

  • EID of the result in the Scopus database

    2-s2.0-84929654685