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pro vyhledávání: '"Ana, Bajc Česnik"'
Autor:
Ana Bajc Česnik, Urban Švajger
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Mesenchymal stromal stem cells (MSCs) possess a remarkable potential for numerous clinical applications due to their unique properties including self-renewal, immunomodulation, paracrine actions and multilineage differentiation. However, the translat
Externí odkaz:
https://doaj.org/article/ba8c33af16f14dbbb1f359752d4db87b
Publikováno v:
Cells, Vol 9, Iss 8, p 1791 (2020)
Amyotrophic lateral sclerosis is a progressive neurodegenerative disorder, characterized by cytoplasmic inclusions of RNA-binding protein TDP-43. Despite decades of research and identification of more than 50 genes associated with amyotrophic lateral
Externí odkaz:
https://doaj.org/article/b40f0944d16a415f8faf9c9845ee15df
Publikováno v:
Biomaterials science. 8(19)
Cold atmospheric plasma is an ionized gas that shows promise in regenerative medical treatments, yet the mechanisms underlying its effects are still poorly understood. Plasma treatment promotes cell growth or cell death depending on the cell type and
Autor:
Helena Motaln, Youn-Bok Lee, Maja Štalekar, Christopher Shaw, Markus Grosch, Ana Bajc Česnik, Sonja Prpar Mihevc, Jure Pohleven, Micha Drukker, Julija Mazej, Mirjana Malnar, Boris Rogelj, Marko Fonović, Miha Modic, Simona Darovic, Boris Turk
Publikováno v:
J. Cell Sci. 132:jcs224303 (2019)
The GGGGCC (G(4)C(2)) repeat expansion mutation in the C9ORF72 gene is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Transcription of the repeat and formation of nuclear RNA foci, which seques
Autor:
Ana, Bajc Česnik, Simona, Darovic, Sonja, Prpar Mihevc, Maja, Štalekar, Mirjana, Malnar, Helena, Motaln, Youn-Bok, Lee, Julija, Mazej, Jure, Pohleven, Markus, Grosch, Miha, Modic, Marko, Fonovič, Boris, Turk, Micha, Drukker, Christopher E, Shaw, Boris, Rogelj
Publikováno v:
Journal of cell science. 132(5)
The GGGGCC (G
Autor:
Ana Bajc Česnik, Sonja Prpar Mihevc, Simona Darovic, Anja Kovanda, Vera Župunski, Boris Rogelj
Publikováno v:
Brain : a journal of neurology. 140(1)
Amyotrophic lateral sclerosis and frontotemporal lobar degeneration are two ends of a phenotypic spectrum of disabling, relentlessly progressive and ultimately fatal diseases. A key characteristic of both conditions is the presence of TDP-43 (encoded