Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aleksandra Oksiejuk"'
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-18 (2023)
Abstract Mortality of Duchenne Muscular Dystrophy (DMD) is a consequence of progressive wasting of skeletal and cardiac muscle, where dystrophinopathy affects not only muscle fibres but also myogenic cells. Elevated activity of P2X7 receptors and inc
Externí odkaz:
https://doaj.org/article/e1cce0c2c23a422ab87448d43fb7c223
Autor:
Marta Narczyk, Łukasz Mioduszewski, Aleksandra Oksiejuk, Maria Winiewska-Szajewska, Beata Wielgus-Kutrowska, Adrian Gojdź, Joanna Cieśla, Agnieszka Bzowska
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract E. coli purine nucleoside phosphorylase is a homohexamer, which structure, in the apo form, can be described as a trimer of dimers. Earlier studies suggested that ligand binding and kinetic properties are well described by two binding consta
Externí odkaz:
https://doaj.org/article/496f274ca99b4a1f857d7a1fc80b317d
Mortality of Duchenne Muscular Dystrophy (DMD) is a direct consequence of progressive wasting of muscle fibres leading to skeletal muscle deterioration and cardiomyopathy. However pathophysiological effects of mutations in the dystrophin encoding gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a62877f11c5f84ffd0e772577c39a67
https://doi.org/10.1101/2022.02.16.478175
https://doi.org/10.1101/2022.02.16.478175
Autor:
Maxime R. F. Gosselin, Natalia Nowak, Wojciech Brutkowski, Dorota Dymkowska, Dariusz C. Górecki, Justyna Róg, Krzysztof Zabłocki, Aleksandra Oksiejuk, Samuel Robson
Publikováno v:
Róg, J, Oksiejuk, A, Gosselin, M R F, Brutkowski, W, Dymkowska, D, Nowak, N, Robson, S, Górecki, D C & Zabłocki, K 2019, ' Dystrophic mdx mouse myoblasts exhibit elevated ATP/UTP-evoked metabotropic purinergic responses and alterations in calcium signalling ', Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease . https://doi.org/10.1016/j.bbadis.2019.01.002
Pathophysiology of Duchenne Muscular Dystrophy (DMD) is still elusive. Although progressive wasting of muscle fibres is a cause of muscle deterioration, there is a growing body of evidence that the triggering effects of DMD mutation are present at th
Autor:
Aleksandra Oksiejuk, Marta Narczyk, Agnieszka Bzowska, Beata Wielgus-Kutrowska, Joanna Cieśla, Maria Winiewska-Szajewska, Adrian Gojdź, Łukasz Mioduszewski
Publikováno v:
Scientific reports 11(1), 11144 (2021). doi:10.1038/s41598-021-90472-4
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Scientific reports 11(1), 11144 (2021). doi:10.1038/s41598-021-90472-4
E. coli purine nucleoside phosphorylase is a homohexamer, which structure, in the apo form, can be described as a trimer of dimers. Earlier studies suggested that ligand bind
E. coli purine nucleoside phosphorylase is a homohexamer, which structure, in the apo form, can be described as a trimer of dimers. Earlier studies suggested that ligand bind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e40bfcef7708005a79afcf6dd674cf12
https://bib-pubdb1.desy.de/record/459569
https://bib-pubdb1.desy.de/record/459569
Autor:
J. Dunlop, Darek Gorecki, Aleksandra Oksiejuk, Maxime R. F. Gosselin, Kacper Łukasiewicz, Natalia Chira, Paweł Matryba, Robin M. H. Rumney, Alexander P. Kao, Christopher N. J. Young, Samuel Robson, Krzysztof Zabłocki, Lukasz Bozycki
Publikováno v:
Young, C, Gosselin, M R F, Rumney, R M H, Oksiejuk, A, Chira, N, Bozycki, L, Matryba, P, Łukasiewicz, K, Kao, A, Dunlop, J N, Robson, S, Zabłocki, K & Gorecki, D 2020, ' Total absence of dystrophin expression exacerbates ectopic myofiber calcification and fibrosis and alters macrophage infiltration patterns ', American Journal of Pathology, vol. 190, no. 1, pp. 190-205 . https://doi.org/10.1016/j.ajpath.2019.09.021
The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link. Duchenne muscular dystrophy (DMD) causes severe disability and death of young men due to progressive m