Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Agnieszka Walczak"'
Autor:
Agnieszka Walczak-Skałecka
Publikováno v:
Journal of Modern Science, Vol 54, Iss 5, Pp 147-162 (2023)
Objectives Personal branding, which is often considered a personal promotion tool, is such a capacious concept that the promotional aspect alone does not seem to capture the complexity of the practices that lead to a strong personal brand. Undoubtedl
Externí odkaz:
https://doaj.org/article/7acdc433e0734eefbfd82eade7a85855
Autor:
Ankur Gadgil, Agnieszka Walczak, Agata Stępień, Jonas Mechtersheimer, Agnes Lumi Nishimura, Christopher E. Shaw, Marc-David Ruepp, Katarzyna Dorota Raczyńska
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Genes encoding replication-dependent histones lack introns, and the mRNAs produced are a unique class of RNA polymerase II transcripts in eukaryotic cells that do not end in a polyadenylated tail. Mature mRNAs are thus formed by a single end
Externí odkaz:
https://doaj.org/article/cc016ad4171f42469bc5c1df58514821
Autor:
Paweł Trzaskoma, Błażej Ruszczycki, Byoungkoo Lee, Katarzyna K. Pels, Katarzyna Krawczyk, Grzegorz Bokota, Andrzej A. Szczepankiewicz, Jesse Aaron, Agnieszka Walczak, Małgorzata A. Śliwińska, Adriana Magalska, Michal Kadlof, Artur Wolny, Zofia Parteka, Sebastian Arabasz, Magdalena Kiss-Arabasz, Dariusz Plewczyński, Yijun Ruan, Grzegorz M. Wilczyński
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
The genome is folded in 3-dimensions, though the lack of robust ultra-resolution imaging makes this difficult to visualise. Here, the authors present 3D-EMISH that combines serial block-face scanning electron microscopy with in situ hybridization.
Externí odkaz:
https://doaj.org/article/314efe399d9e425fbc4fd722009456ec
Autor:
Anna Skupien-Jaroszek, Agnieszka Walczak, Iwona Czaban, Katarzyna Karolina Pels, Andrzej Antoni Szczepankiewicz, Katarzyna Krawczyk, Błażej Ruszczycki, Grzegorz Marek Wilczynski, Joanna Dzwonek, Adriana Magalska
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0239111 (2021)
The Brain-Derived Neurotrophic Factor is one of the most important trophic proteins in the brain. The role of this growth factor in neuronal plasticity, in health and disease, has been extensively studied. However, mechanisms of epigenetic regulation
Externí odkaz:
https://doaj.org/article/d596a654b77a4c9c812038c27972a15b
Autor:
Błażej Ruszczycki, Katarzyna Karolina Pels, Agnieszka Walczak, Katarzyna Zamłyńska, Michał Such, Andrzej Antoni Szczepankiewicz, Małgorzata Hanna Hall, Adriana Magalska, Marta Magnowska, Artur Wolny, Grzegorz Bokota, Subhadip Basu, Ayan Pal, Dariusz Plewczynski, Grzegorz Marek Wilczyński
Publikováno v:
Frontiers in Neuroanatomy, Vol 13 (2019)
The detailed architectural examination of the neuronal nuclei in any brain region, using confocal microscopy, requires quantification of fluorescent signals in three-dimensional stacks of confocal images. An essential prerequisite to any quantificati
Externí odkaz:
https://doaj.org/article/3455ab6482634c019a72a43baa9be4b3
Autor:
Dominika Wolosz, Agnieszka Walczak, Grzegorz Szparecki, Michal Dwojak, Magdalena Winiarska, Ewa Wolinska, Barbara Gornicka
Publikováno v:
European Journal of Histochemistry, Vol 63, Iss 1 (2019)
Deleted in Liver Cancer (DLC) proteins belong to the family of RhoGAPs and are believed to operate as negative regulators of the Rho family of small GTPases. So far, the role of the first identified member from the DLC family, DLC1, was established a
Externí odkaz:
https://doaj.org/article/e3c686369b4847e5a2afd848dcd5fa4b
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 Walczak-Skałecka
Publikováno v:
Scientific Papers of Silesian University of Technology Organization and Management Series. 2023
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::624a322535b06c766783ae0551823685
https://doi.org/10.29119/1641-3466.2022.164.37
https://doi.org/10.29119/1641-3466.2022.164.37
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:
Tomasz Stompór, Piotr M Burak, Agnieszka Walczak, Elżbieta Jurkiewicz, Jan Walczak, Marta Bladowska
Publikováno v:
Polish archives of internal medicine. 131(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e2688e633714b55bc9809ffd023439
https://pubmed.ncbi.nlm.nih.gov/33913674
https://pubmed.ncbi.nlm.nih.gov/33913674