Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Stefan Stamenković"'
Publikováno v:
European Biophysics Journal. 48:475-484
Pathological mechanisms in amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease, are still poorly understood. One subset of familial ALS cases is caused by mutations in the metallo-enzyme copper-zinc superoxide dismutase (SOD1), inc
Publikováno v:
Microscopy and Microanalysis. 27:102-103
Publikováno v:
Journal of Biophotonics. 13
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease, causing death of motor neurons controlling voluntary muscles. The pathological mechanisms of the disease are only partially understood. The hSOD1-G93A ALS rat model is characte
Publikováno v:
Analytical Chemistry. 91:1460-1471
Amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease, is the most common adult onset neurodegenerative disorder affecting motor neurons. Disruptions in metal ion homeostasis have been described in association with ALS, but the patho
Publikováno v:
Neuroscience. 357:37-55
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting motor and cognitive domains of the CNS. Mutations in the Cu,Zn-superoxide dismutase (SOD1) cause 20% of familial ALS and provoke formation of intracellular aggregates and c
Autor:
Aleksandra Pavićević, Ana Popović-Bijelić, Goran Bačić, Vesna Selaković, Miloš Mojović, Stefan Stamenković, Pavle R. Andjus
Publikováno v:
Free Radical Biology and Medicine. 108:258-269
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder affecting the motor pathways of the central nervous system. Although a number of pathophysiological mechanisms have been described in the disease, post mortem and animal model
Autor:
Mojca Pavlin, Joel C. Glover, Dinko Mitrečić, Jasna Lojk, Stefan Stamenković, Stefano Cavalli, Markus Aswendt, Caterina Frati, Francesco Fiori, Federico Quaini, Mathias Hoehn, Jean-Luc Boulland, Pavle R. Andjus
Stem cell-based therapeutics is a rapidly developing field associated with a number of clinical challenges. One such challenge lies in the implementation of methods to track stem cells and stem cell-derived cells in experimental animal models and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c76d68cfd7f03b5160f55d3549cba6a
https://www.bib.irb.hr/1192054
https://www.bib.irb.hr/1192054
Publikováno v:
Neuroscience. 357
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting motor and cognitive domains of the CNS. Mutations in the Cu,Zn-superoxide dismutase (SOD1) cause 20% of familial ALS and provoke formation of intracellular aggregates and c
Autor:
Stefan, Stamenković, Aleksandra, Pavićević, Miloš, Mojović, Ana, Popović-Bijelić, Vesna, Selaković, Pavle, Andjus, Goran, Bačić
Publikováno v:
Free radical biologymedicine. 108
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder affecting the motor pathways of the central nervous system. Although a number of pathophysiological mechanisms have been described in the disease, post mortem and animal model
Autor:
Lidija Radenovic, Leszek Kaczmarek, Pavle R. Andjus, Milos Jovanovic, Tomasz Jaworski, Stefan Stamenković, Igor Jakovcevski, Maciej Gawlak, Grzegorz M. Wilczynski, Melitta Schachner, Vera Stamenković
Publikováno v:
Brain structure & function 222(1), 393-415 (2016). doi:10.1007/s00429-016-1224-y
The importance of the extracellular matrix (ECM) glycoprotein tenascin-C (TnC) and the ECM degrading enzymes, matrix metalloproteinases (MMPs) -2 and -9, in cerebellar histogenesis is well established. This study aimed to examine whether there is a f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::922d7bbbf84af7e5ea0485591aaec4dc
https://pub.dzne.de/record/138984
https://pub.dzne.de/record/138984