Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Tomas, Olejar"'
Autor:
Nikol Jankovska, Robert Rusina, Jiri Keller, Jaromir Kukal, Magdalena Bruzova, Eva Parobkova, Tomas Olejar, Radoslav Matej
Publikováno v:
Biomedicines, Vol 10, Iss 3, p 680 (2022)
Creutzfeldt–Jakob disease (CJD), the most common human prion disorder, may occur as “pure” neurodegeneration with isolated prion deposits in the brain tissue; however, comorbid cases with different concomitant neurodegenerative diseases have be
Externí odkaz:
https://doaj.org/article/12872e8d15424f4893994aa58940fd61
Autor:
Nikol Jankovska, Robert Rusina, Magdalena Bruzova, Eva Parobkova, Tomas Olejar, Radoslav Matej
Publikováno v:
Diagnostics, Vol 11, Iss 10, p 1821 (2021)
Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and fatal neurodegenerative diseases caused by aggregation of misfolded prion protein in neuronal tissue. Due to the potential transmission, human TSEs a
Externí odkaz:
https://doaj.org/article/760cf9e50f9e4926824bcfb6b79e2ff8
Publikováno v:
Physiol Res
Europe PubMed Central
Europe PubMed Central
It has been 30 years since the first member of the protease-activated receptor (PAR) family was discovered. This was followed by the discovery of three other receptors, including PAR2. PAR2 is a G protein-coupled receptor activated by trypsin site-sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92b146f965f05809fa58e9a5323bf8b8
https://europepmc.org/articles/PMC9841802/
https://europepmc.org/articles/PMC9841802/
Autor:
Ondřej Sobek, Adam Pavličko, Eva Malá, Radoslav Matěj, Robert Rusina, Tomas Olejar, Kateřina Matějová
Publikováno v:
Neurologia i Neurochirurgia Polska. 55:499-501
Publikováno v:
Current Alzheimer Research. 17:948-958
Background: Bulbous neuritic changes in neuritic plaques have already been described, and their possible effect on the clinical course of the disease has been discussed. Objective: In our study, we focused on the location and density of these structu
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13303, p 13303 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 22; Issue 24; Pages: 13303
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 22; Issue 24; Pages: 13303
Gerstmann–Sträussler–Scheinker syndrome (GSS) is a hereditary neurodegenerative disease characterized by extracellular aggregations of pathological prion protein (PrP) forming characteristic plaques. Our study aimed to evaluate the micromorpholo
Autor:
Michal Zabrodsky, Pavla Pouckova, Martina Kabesova, Jiri Benes, Tomas Olejar, Jan Bouček, David Vetvicka
Publikováno v:
Anticancer Research. 40:349-356
BACKGROUND/AIM Follicle-stimulating hormone receptor (FSHr), expressed on endothelial cells of vessels in different malignant tumors, has been recently investigated as a potential pan-receptor of cancer treatment. However, the expression of this rece
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 2099, p 2099 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 2099, p 2099 (2021)
Alzheimer’s disease (AD) and sporadic Creutzfeldt–Jakob disease (sCJD) are both characterized by extracellular pathologically conformed aggregates of amyloid proteins—amyloid β-protein (Aβ) and prion protein (PrPSc), respectively. To investig
Autor:
Tomas Olejar, Magdalena Bruzova, Nikol Jankovska, Eva Parobkova, Radoslav Matej, Robert Rusina
Publikováno v:
Diagnostics
Diagnostics, Vol 11, Iss 1821, p 1821 (2021)
Diagnostics, Vol 11, Iss 1821, p 1821 (2021)
Human prion disorders (transmissible spongiform encephalopathies, TSEs) are unique, progressive, and fatal neurodegenerative diseases caused by aggregation of misfolded prion protein in neuronal tissue. Due to the potential transmission, human TSEs a
Autor:
David Habart, Tomas Olejar, Frantisek Saudek, A. Lodererova, Zuzana Papackova, Zuzana Berková, Monika Cahova, Marie Heczkova, Helena Daňková
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
ResearcherID
Scopus-Elsevier
ResearcherID
Lipasin is a recently identified lipokine expressed predominantly in liver and in adipose tissue. It was linked to insulin resistance in mice and to type 1 and type 2 diabetes (T1D, T2D) in humans. No metabolic studies concerning lipasin were perform