Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Maja, Štalekar"'
Autor:
Mojca Janc, Kaja Zevnik, Ana Dolinar, Tjaša Jakomin, Maja Štalekar, Katarina Bačnik, Denis Kutnjak, Magda Tušek Žnidarič, Lorena Zentilin, Dmitrii Fedorov, David Dobnik
Publikováno v:
Viruses, Vol 16, Iss 8, p 1235 (2024)
Recombinant adeno-associated viruses (rAAVs) play a pivotal role in the treatment of genetic diseases. However, current production and purification processes yield AAV-based preparations that often contain unwanted empty, partially filled or damaged
Externí odkaz:
https://doaj.org/article/4f69d64191ff470891c30bb36291e679
Autor:
Ivana Sedej, Maja Štalekar, Magda Tušek Žnidarič, Katja Goričar, Nika Kojc, Polona Kogovšek, Vita Dolžan, Miha Arnol, Metka Lenassi
Publikováno v:
Journal of Extracellular Vesicles, Vol 11, Iss 9, Pp n/a-n/a (2022)
Abstract Extracellular vesicle‐bound DNA (evDNA) is an understudied extracellular vesicle (EV) cargo, particularly in cancer‐unrelated research. Although evDNA has been detected in urine, little is known about its characteristics, localization, a
Externí odkaz:
https://doaj.org/article/d13f6bf55eef4706a8a3853750664106
Autor:
Barbara Jerič Kokelj, Maja Štalekar, Sebastian Vencken, David Dobnik, Polona Kogovšek, Matjaž Stanonik, Miha Arnol, Maja Ravnikar
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Increasing research demonstrates the potential of donor-derived cell-free DNA (dd-cfDNA) as a biomarker for monitoring the health of various solid organ transplants. Several methods have been proposed for cfDNA analysis, including real-time PCR, digi
Externí odkaz:
https://doaj.org/article/271cc744d59341db92a1eb2f1f004fd6
Autor:
Youn-Bok Lee, Han-Jou Chen, João N. Peres, Jorge Gomez-Deza, Jan Attig, Maja Štalekar, Claire Troakes, Agnes L. Nishimura, Emma L. Scotter, Caroline Vance, Yoshitsugu Adachi, Valentina Sardone, Jack W. Miller, Bradley N. Smith, Jean-Marc Gallo, Jernej Ule, Frank Hirth, Boris Rogelj, Corinne Houart, Christopher E. Shaw
Publikováno v:
Cell Reports, Vol 5, Iss 5, Pp 1178-1186 (2013)
The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Intranuclear neuronal RNA foci have been observed in ALS and FTD tissues, suggesting
Externí odkaz:
https://doaj.org/article/9cf3164a2c9e4faabd2f8beeacdd1d31
Autor:
David Dobnik, Maja Ravnikar, Polona Kogovšek, Barbara Jerič Kokelj, Miha Arnol, Sebastian Vencken, Matjaž Stanonik, Maja Štalekar
Publikováno v:
Frontiers in Medicine
Frontiers in Medicine, Vol 8 (2021)
Frontiers in Medicine, Vol 8 (2021)
Increasing research demonstrates the potential of donor-derived cell-free DNA (dd-cfDNA) as a biomarker for monitoring the health of various solid organ transplants. Several methods have been proposed for cfDNA analysis, including real-time PCR, digi
Autor:
Ivana Sedej, Maja Štalekar, Magda Tušek Žnidarič, Katja Goričar, Nika Kojc, Polona Kogovšek, Vita Dolžan, Metka Lenassi, Miha Arnol
Publikováno v:
Transplantation. 106:S55-S55
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:
Vera Župunski, Matja Zalar, Maja Štalekar, Janez Plavec, Anja Kovanda, Jure Pohleven, Boris Rogelj, Primož Šket
Publikováno v:
Neurobiology of Aging. 36:1091-1096
The G4C2 hexanucleotide repeat expansion, located in the first intron of the C9ORF72 gene, represents a major genetic hallmark of amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Several hypotheses have been proposed on how the tr
Autor:
Claire Troakes, Yoshitsugu Adachi, Caroline Vance, Bradley N. Smith, Youn-Bok Lee, Jan Attig, Jernej Ule, Maja Štalekar, Frank Hirth, Jack W. Miller, Corinne Houart, João N. Peres, Jorge Gomez-Deza, Jean-Marc Gallo, Han-Jou Chen, Emma L. Scotter, Christopher Shaw, Valentina Sardone, Agnes L. Nishimura, Boris Rogelj
Publikováno v:
Cell Reports, Vol 5, Iss 5, Pp 1178-1186 (2013)
Cell Reports
Cell Reports
Summary The GGGGCC (G4C2) intronic repeat expansion within C9ORF72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Intranuclear neuronal RNA foci have been observed in ALS and FTD tissues, su