Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Agnieszka Piasecka"'
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Myocyte enhancer factor 2C (MEF2C) is a transcription factor that regulates heart and skeletal muscle differentiation and growth. Several protein-encoding genes were identified as targets of this factor; however, little is known about its co
Externí odkaz:
https://doaj.org/article/fb929136498a4e399644d825635f831a
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
Autor:
Karol Czubak, Katarzyna Taylor, Agnieszka Piasecka, Krzysztof Sobczak, Katarzyna Kozlowska, Anna Philips, Saam Sedehizadeh, J. David Brook, Marzena Wojciechowska, Piotr Kozlowski
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Splicing aberrations induced as a consequence of the sequestration of muscleblind-like splicing factors on the dystrophia myotonica protein kinase transcript, which contains expanded CUG repeats, present a major pathomechanism of myotonic dystrophy t
Externí odkaz:
https://doaj.org/article/f9a23745cc8a47ba826633b93a12d216
Autor:
Agnieszka Piasecka-Robak
Publikováno v:
Tiltai. 88:22-31
The article presents the situation of patients in Poland, based on existing data (non reactive research), and individual interviews with Patients’ Agents in the given clinic or hospital and Patient’s Ombudsmen. It presents doctor-patient relation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8078b1a5063d26857111c0f0f322df1f
https://doi.org/10.15181/tbb.v88i1.2408
https://doi.org/10.15181/tbb.v88i1.2408
Autor:
Chikara Dohno, Daria Niewiadomska, Anna Baud, Katarzyna Taylor, Krzysztof Sobczak, Patryk Konieczny, Agnieszka Walczak, Ewa Stepniak-Konieczna, Sanjukta Mukherjee, Agnieszka Piasecka, Kazuhiko Nakatani
Publikováno v:
Nucleic Acids Research
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder caused by a limited expansion of CGG repeats in the FMR1 gene. Degeneration of neurons in FXTAS cell models can be triggered by accumulation of polyglycine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c19261f4c341322535888439d1dcec98
https://doi.org/10.1093/nar/gkab669
https://doi.org/10.1093/nar/gkab669
Autor:
Agnieszka Piasecka-Robak
Publikováno v:
Tiltai. :1-27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::421c398fc8977d41000370f20055fd72
https://doi.org/10.15181/tbb.v86i1.2258
https://doi.org/10.15181/tbb.v86i1.2258
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports
Scientific Reports
Myocyte enhancer factor 2C (MEF2C) is a transcription factor that regulates heart and skeletal muscle differentiation and growth. Several protein-encoding genes were identified as targets of this factor; however, little is known about its contributio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902079f6491ff4dd174cfc0a494ba0f8
https://doaj.org/article/fb929136498a4e399644d825635f831a
https://doaj.org/article/fb929136498a4e399644d825635f831a
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced9d097e6e2ffdac59a5c7fa24f0300
https://doi.org/10.1038/s41467-021-21021-w
https://doi.org/10.1038/s41467-021-21021-w
Autor:
Agnieszka Piasecka
Publikováno v:
PROBLEMY JAKOŚCI. 1:34-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::177563fe9fc00de4b0b8e576e11da740
https://doi.org/10.15199/48.2018.11.4
https://doi.org/10.15199/48.2018.11.4
Publikováno v:
PROBLEMY JAKOŚCI. 1:11-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::998c6775ad7718b1aca259576ae9cb17
https://doi.org/10.15199/48.2018.1.2
https://doi.org/10.15199/48.2018.1.2