Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mirjana, Malnar"'
Autor:
Mirjana Malnar Črnigoj, Urša Čerček, Xiaoke Yin, Manh Tin Ho, Barbka Repic Lampret, Manuela Neumann, Andreas Hermann, Guy Rouleau, Beat Suter, Manuel Mayr, Boris Rogelj
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract The expanded hexanucleotide GGGGCC repeat mutation in the C9orf72 gene is the main genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia. Under one disease mechanism, sense and antisense transcripts of the repeat are pre
Externí odkaz:
https://doaj.org/article/b29cd3b5c510491ea05a97aba7af8fed
Autor:
Alexandra-Larisa Condurat, Sepideh Aminzadeh-Gohari, Mirjana Malnar, Nicole Schider, Leonie Opitz, Ria Thomas, Vishal Menon, Barbara Kofler, Jan Pruszak
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-15 (2023)
Abstract Neuroblastoma (NB) is a highly aggressive extracranial solid tumor in children. Due to its heterogeneity, NB remains a therapeutic challenge. Several oncogenic factors, including the Hippo effectors YAP/TAZ, are associated with NB tumorigene
Externí odkaz:
https://doaj.org/article/be4f03f793154d44b69f2a4c79def987
Autor:
Mirjana Malnar, Urša Čerček, Xiaoke Yin, Manh Tin Ho, Barbka Repič Lampret, Manuela Neuman, Andreas Hermann, Guy Rouleau, Beat Suter, Manuel Mayr, Boris Rogelj
The expanded hexanucleotide GGGGCC repeat mutation in the C9orf72 gene is the main genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia. Under one disease mechanism, sense and antisense transcripts of the repeat are predicted to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aee324b41dae1e3ce46386900982c86
https://doi.org/10.21203/rs.3.rs-2166624/v1
https://doi.org/10.21203/rs.3.rs-2166624/v1
Autor:
Alexandra-Larisa Condurat, Sepideh Aminzadeh-Gohari, Mirjana Malnar, Ria Thomas, Vishal Menon, Barbara Kofler, Jan Pruszak
Neuroblastoma (NB) is a highly aggressive extracranial solid tumor in children. Due to its heterogeneity, NB remains a therapeutic challenge. Several oncogenic factors, including the Hippo effectors YAP/TAZ, are associated with NB tumorigenesis. Vert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::867eeb82677bee2a4505895115b48135
https://doi.org/10.21203/rs.3.rs-2151532/v1
https://doi.org/10.21203/rs.3.rs-2151532/v1
Autor:
Mirjana Malnar, Boris Rogelj
Publikováno v:
Journal of Cell Science
article-version (VoR) Version of Record
article-version (VoR) Version of Record
The expanded GGGGCC repeat mutation in the C9orf72 gene is the most common genetic cause of the neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The expansion is transcribed to sense and antisense RNA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e76cd016556393245a942488d35601
http://europepmc.org/articles/PMC7904093
http://europepmc.org/articles/PMC7904093
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57d9ee9b063796c8ea7706200b168b2e
https://doi.org/10.1242/jcs.224303
https://doi.org/10.1242/jcs.224303
Autor:
Mirjana Malnar, Tadeja Režen
Publikováno v:
Journal of pharmacological and toxicological methods. 96
Introduction FFPE samples represent a rich pool of tissue samples for retrospective analyses of mRNA and miRNA analyses. However, the initial formalin fixation introduces a chemical modification of RNA and causes its degradation, therefore, a longer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eda4bd0219c3af1feba682459da40aa
https://pubmed.ncbi.nlm.nih.gov/30735812
https://pubmed.ncbi.nlm.nih.gov/30735812
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5eab73b36e95efe1c460603c868bce0e
https://pubmed.ncbi.nlm.nih.gov/30745340
https://pubmed.ncbi.nlm.nih.gov/30745340