Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alicja, Rabiasz"'
Autor:
Monika Piwecka, Paweł Głodowicz, Katarzyna Rolle, Konrad Kuczyński, Dariusz Wawrzyniak, Małgorzata Lekka, Joanna Zemła, Alicja Rabiasz, Małgorzata Grabowska
Publikováno v:
Journal of Cellular and Molecular Medicine. 26:3913-3930
BackgroundGlioblastoma (GBM) is the most common malignant brain tumour. GBM cells have ability to infiltrate into the surrounding brain tissue, which results in a significant decrease in the patient’s survival rate. Infiltration is a consequence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8075732673e79f6b058f8721e9d5ce7f
https://doi.org/10.1111/jcmm.17428
https://doi.org/10.1111/jcmm.17428
Autor:
Alicja Rabiasz, Ewa Zietkiewicz
Publikováno v:
International Journal of Molecular Sciences. 24:4472
Cilia and flagella are evolutionarily conserved organelles that form protrusions on the surface of many growth-arrested or differentiated eukaryotic cells. Due to the structural and functional differences, cilia can be roughly classified as motile an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d0cce975ae23fed5da917461077b9dc
https://doi.org/10.3390/ijms24054472
https://doi.org/10.3390/ijms24054472
Autor:
Zuzanna, Bukowy-Bieryllo, Alicja, Rabiasz, Maciej, Dabrowski, Andrzej, Pogorzelski, Alina, Wojda, Hanna, Dmenska, Katarzyna, Grzela, Jakub, Sroczynski, Michal, Witt, Ewa, Zietkiewicz
Publikováno v:
Journal of medical genetics. 56(11)
Primary ciliary dyskinesia (PCD) is a motile ciliopathy, whose symptoms include airway infections, male infertility andTo elucidate the role of motile cilia defects in the respiratory phenotype of PCD patients with C-terminal OFD1 mutations.Whole-exo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9cf8d11121c8ee15a07c1f9ae619eba
https://pubmed.ncbi.nlm.nih.gov/31366608
https://pubmed.ncbi.nlm.nih.gov/31366608
Autor:
Alicja Rabiasz, Katarzyna Voelkel, Ewa Ziętkiewicz, Andrzej Pogorzelski, Alina Wojda, Zuzanna Bukowy-Bieryllo, Ewa Rutkiewicz, Margarida Rasteiro, Michał Witt, Patrycja Daca-Roszak
Publikováno v:
National Information Processing Institute
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous hereditary disease from a class of ciliopathies. In spite of the recent progress, the genetic basis of PCD in one-third of pati...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3a7595ec651ea9d5247cebac6ac1457
https://www.atsjournals.org/doi/pdf/10.1165/rcmb.2018-0260OC
https://www.atsjournals.org/doi/pdf/10.1165/rcmb.2018-0260OC
