Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ewelina Użarowska"'
Autor:
Marcin Bednarek, Marek Trybus, Monika Kolanowska, Mateusz Koziej, Beata Kiec‐Wilk, Artur Dobosz, Marta Kotlarek‐Łysakowska, Anna Kubiak‐Dydo, Ewelina Użarowska‐Gąska, Julia Staręga‐Rosłan, Paweł Gaj, Izabela Górzyńska, Katarzyna Serwan, Michał Świerniak, Adam Kot, Krystian Jażdżewski, Anna Wójcicka
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Abstract Background Brachydactylies are a group of inherited conditions, characterized mainly by the presence of shortened fingers and toes. Based on the patients’ phenotypes, brachydactylies have been subdivided into 10 subtypes. In this study, we
Externí odkaz:
https://doaj.org/article/affdf9a585db42bda2bb63ae2877b1ff
Autor:
Katarzyna Zabielska-Koczywąs, Anna Wojtalewicz, Ewelina Użarowska, Agata Klejman, Agata Wojtkowska, Izabella Dolka, Marek Wojnicki, Katarzyna Sobczak, Michał Wójcik, Haifa Shen, Mauro Ferrari, Roman Lechowski
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 4, p 1021 (2018)
Feline injection site sarcomas (FISS) are malignant skin tumors with high recurrence rates despite the primary treatment of radical surgical resections. Adjunctive radiotherapy or chemotherapy with doxorubicin is mostly ineffective. Cellular and mole
Externí odkaz:
https://doaj.org/article/96324280bebe4c8abb78bb02d05ae219
Autor:
Monika Kolanowska, Krystian Jazdzewski, Marta Kotlarek-Łysakowska, Magdalena Durlik, Anna Kubiak-Dydo, Katarzyna Salata, Agnieszka Furmańczyk-Zawiska, Pawel Gaj, Michał Świerniak, Anna Wojcicka, Ewelina Użarowska-Gąska, Beata Leszczyńska, Maria Daniel
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 304, p 304 (2021)
Journal of Personalized Medicine, Vol 11, Iss 304, p 304 (2021)
Atypical hemolytic uremic syndrome (aHUS) is a rare disease triggered by dysregulation of the alternative complement pathway, consisting of a characteristic triad of nonimmune hemolytic anemia, thrombocytopenia, and renal failure. The risk of aHUS on
Autor:
Ewelina Użarowska-Gąska, Izabela Górzyńska, Mateusz Koziej, Anna Kubiak-Dydo, Katarzyna Serwan, Pawel Gaj, Marta Kotlarek-Łysakowska, Krystian Jazdzewski, Anna Wojcicka, Julia Staręga-Rosłan, Michał Świerniak, Monika Kolanowska, Adam Kot, Marcin Bednarek, Beata Kieć-Wilk, Artur Dobosz, Marek Trybus
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Brachydactylies are a group of inherited conditions, characterized mainly by the presence of shortened fingers and toes. Based on the patients’ phenotypes, brachydactylies have been subdivided into 10 subtypes. In this study, we have ide
Autor:
Sylwia Olejniczak, Anna Mietelska-Porowska, Urszula Wojda, Jakub Golab, Katarzyna Laskowska-Kaszub, Stanislaw Pikul, Mykola Zdioruk, Andrew Want, Agata Klejman, Paulina Koza, Joanna Wojsiat, Witold Konopka, Ewelina Użarowska
Publikováno v:
Cancers
Volume 12
Issue 8
Cancers, Vol 12, Iss 2161, p 2161 (2020)
Volume 12
Issue 8
Cancers, Vol 12, Iss 2161, p 2161 (2020)
Induction of mitotic catastrophe through the disruption of microtubules is an established target in cancer therapy. However, the molecular mechanisms determining the mitotic catastrophe and the following apoptotic or non-apoptotic cell death remain p
Autor:
Agata Klejman, Ewelina Użarowska, Kamila Barszcz, Eva Sikora, Tytus Bernas, Joanna Czarnecka, Agata Kowalczyk, Halina Was, Paulina Koza, Bozena Kaminska, Katarzyna Piwocka
Publikováno v:
Oncotarget
// Halina Was 1, 2 , Kamila Barszcz 1, 2 , Joanna Czarnecka 1, 2 , Agata Kowalczyk 3 , Tytus Bernas 4 , Ewelina Uzarowska 5 , Paulina Koza 5, 6 , Agata Klejman 5 , Katarzyna Piwocka 3 , Bozena Kaminska 2 , Eva Sikora 1 1 Laboratory of Molecular Basis
Publikováno v:
Europe PubMed Central
Atypical hemolytic-uremic syndrome (aHUS) results from excessive, uncontrolled activation of the alternative pathway of the complement system. It is important to distinguish aHUS from other thrombotic microangiopathies. The aim of this paper is to di
Autor:
Bednarek, Marcin1,2 (AUTHOR), Trybus, Marek1,2 (AUTHOR), Kolanowska, Monika3 (AUTHOR), Koziej, Mateusz4 (AUTHOR), Kiec‐Wilk, Beata1,5 (AUTHOR), Dobosz, Artur6 (AUTHOR), Kotlarek‐Łysakowska, Marta3 (AUTHOR), Kubiak‐Dydo, Anna3 (AUTHOR), Użarowska‐Gąska, Ewelina3 (AUTHOR), Staręga‐Rosłan, Julia3 (AUTHOR), Gaj, Paweł3 (AUTHOR), Górzyńska, Izabela3 (AUTHOR), Serwan, Katarzyna3 (AUTHOR), Świerniak, Michał3 (AUTHOR), Kot, Adam3 (AUTHOR), Jażdżewski, Krystian3,7 (AUTHOR), Wójcicka, Anna3 (AUTHOR) anna.wojcicka@warsawgenomics.pl
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2021, Vol. 9 Issue 3, p1-8. 8p.
Publikováno v:
Wiadomości Lekarskie; 2019, Vol. 72 Issue 10, p2024-2032, 9p