Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Magdalena Derbis"'
Autor:
Magdalena Derbis, Emre Kul, Daria Niewiadomska, Michał Sekrecki, Agnieszka Piasecka, Katarzyna Taylor, Renate K. Hukema, Oliver Stork, Krzysztof Sobczak
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Fragile X-associated tremor/ataxia syndrome is a neurodegenerative disease caused by toxic RNA containing expanded CGG repeats. Here, the authors show that synthetic oligonucleotides targeting the RNA repeats decrease the pleiotropic effect of this t
Externí odkaz:
https://doaj.org/article/c6498e46fb154abdbc4b08a40653c26d
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder caused by expanded CGG (CGGexp) trinucleotides in the 5′UTR of the FMR1 gene encoding fragile X mental retardation protein (FMRP). The patients, with the
Externí odkaz:
https://doaj.org/article/d542fea809da4226bd9af91640bd144e
Autor:
Agnieszka Piasecka, Magdalena Derbis, Oliver Stork, Katarzyna Taylor, Renate K. Hukema, Michał Sekrecki, Emre Kul, Daria Niewiadomska, Krzysztof Sobczak
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Nature Communications, 12(1):1265. Nature Publishing Group
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Nature Communications, 12(1):1265. Nature Publishing Group
Fragile X-associated tremor/ataxia syndrome (FXTAS) is an incurable neurodegenerative disorder caused by expansion of CGG repeats in the FMR1 5’UTR. The RNA containing expanded CGG repeats (rCGGexp) causes cell damage by interaction with complement
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)
Frontiers in Genetics, Vol 9 (2018)
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder caused by expanded CGG (CGGexp) trinucleotides in the 5′UTR of the FMR1 gene encoding fragile X mental retardation protein (FMRP). The patients, with the
Autor:
Marta Szajnik, Andrzej Nowakowski, Paulina Patalas, Theresa L. Whiteside, Hanna Drzewiecka, Marcin Michalak, WÅodzimierz Baranowski, Magdalena Derbis, Michał Stefan Lach, Marek Spaczyński, Dariusz Szpurek
Background: In patients with Ovarian Cancer (OvCa) exosomes released by tumor cells are present in the plasma and could be involved in tumor progression. This study examines the association between the exosome presence/protein content in plasma of Ov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f924f61a5b955665074457b3f228a5
https://europepmc.org/articles/PMC3899646/
https://europepmc.org/articles/PMC3899646/
Autor:
Michał Stefan Lach, Marcin Michalak, Paulina Patalas, Magdalena Derbis, Hanna Drzewiecka, Theresa L. Whiteside, Ewa Nowak-Markwitz, Marek Spaczyński, Marta E. Szajnik-Szczepanski, Marta Glura
Publikováno v:
Clinical Cancer Research. 19:A79-A79
Background: Ectonucleotidases CD39/CD73 have been reported to play an important role in functional supression of various immune cells via adenosine that is generated locally in the tumor microenvironment. In patients with ovarian cancer (OvCa) exosom
Publikováno v:
WIREs RNA. 13(4)
Short tandem repeats are repetitive nucleotide sequences robustly distributed in the human genome. Their expansion underlies the pathogenesis of multiple neurological disorders, including Huntington's disease, amyotrophic lateral sclerosis, and front