Avidity of antibodies against tau protein in patients with multiple sclerosis
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F09%3A00001018" target="_blank" >RIV/00023752:_____/09:00001018 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11110/09:5085
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Avidity of antibodies against tau protein in patients with multiple sclerosis
Popis výsledku v původním jazyce
Background: The low-molecular-weight tau protein belongs to the microtubule-associated proteins abundantly present in the central nervous system and expressed predominantly in axons (1). The function of these phosphoproteins is associated with the neuronal cytoskeleton. Tau stabilizes microtubules and promotes their polymerization (1). Some neurological diseases of the CNS include axonal injury. Multiple sclerosis (MS) is one of the disorders in whose pathogenesis the axonal damage is involved (2). Several cytoskeletal structures have been explored to reflect this event. Tubulin, neurofilaments, actin or tau proteins were examined as markers of the axonal damage (3, 4). During this process cytoskeletal structures are released into the extracellular environment, where the synthesis of specific antibodies may be induced (5, 6). It was observed that immunization of mice by the recombinant tau protein induced the synthesis of anti-tau antibodies. Moreover, these specific anti-tau antibodie
Název v anglickém jazyce
Avidity of antibodies against tau protein in patients with multiple sclerosis
Popis výsledku anglicky
Background: The low-molecular-weight tau protein belongs to the microtubule-associated proteins abundantly present in the central nervous system and expressed predominantly in axons (1). The function of these phosphoproteins is associated with the neuronal cytoskeleton. Tau stabilizes microtubules and promotes their polymerization (1). Some neurological diseases of the CNS include axonal injury. Multiple sclerosis (MS) is one of the disorders in whose pathogenesis the axonal damage is involved (2). Several cytoskeletal structures have been explored to reflect this event. Tubulin, neurofilaments, actin or tau proteins were examined as markers of the axonal damage (3, 4). During this process cytoskeletal structures are released into the extracellular environment, where the synthesis of specific antibodies may be induced (5, 6). It was observed that immunization of mice by the recombinant tau protein induced the synthesis of anti-tau antibodies. Moreover, these specific anti-tau antibodie
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
FH - Neurologie, neurochirurgie, neurovědy
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/NS10369" target="_blank" >NS10369: Využití neurocytoskeletálních proteinů a protilátek proti nim v diagnostice Alzheimerovy nemoci</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2009
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
From Pathogenesis to Therapy of Autoimmune Diseases. Autoantigens, Autoantibodies, Autoimmunity
ISBN
978-3-89967-579-5
ISSN
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e-ISSN
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Počet stran výsledku
3
Strana od-do
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Název nakladatele
Pabst Science Publishers
Místo vydání
Dresden
Místo konání akce
Dresden
Datum konání akce
2. 9. 2009
Typ akce podle státní příslušnosti
EUR - Evropská akce
Kód UT WoS článku
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