Zobrazeno 1 - 10
of 132
pro vyhledávání: '"Wojciech Mlynarski"'
Autor:
Damian Krzyzanowski, Aleksandra Oszer, Joanna Madzio, Maciej Zdunek, Julia Kolodrubiec, Bartosz Urbanski, Wojciech Mlynarski, Szymon Janczar
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Congenital defects of neutrophil number or function are associated with a severe infectious phenotype that may require intensive medical attention and interventions to be controlled. While the infectious complications in inherited neutrophil disorder
Externí odkaz:
https://doaj.org/article/f4dca9757e184936ac5e26c274330279
Autor:
Agata Pastorczak, Bartosz Szmyd, Marcin Braun, Joanna Madzio, Kamila Wypyszczak, Pawel Sztromwasser, Wojciech Fendler, Marzena Wojtaszewska, Jedrzej Chrzanowski, Wieslawa Grajkowska, Hanna Gregorek, Anna Wakulinska, Bernarda Kazanowska, Zdenka Krenova, Dilys D. Weijers, Roland P. Kuiper, Wojciech Mlynarski
Publikováno v:
Haematologica, Vol 108, Iss 10 (2023)
Externí odkaz:
https://doaj.org/article/98fb008f6de641828a6b3d6bc7fcbdca
Autor:
Camilla Grud Nielsen, Birthe Lykke Thomsen, Bodil Als-Nielsen, Rachel Conyers, Sima Jeha, Marion K. Mateos, Wojciech Mlynarski, Rob Pieters, Mathias Rathe, Kjeld Schmiegelow, Liv Andrés-Jensen
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Overall survival after cancer is increasing for the majority of cancer types, but survivors can be burdened lifelong by treatment-related severe toxicities. Integration of long-term toxicities in treatment evaluation is not least important for childr
Externí odkaz:
https://doaj.org/article/b89bb3cfc140497ab276ae9fe44af2ec
Autor:
Justyna Walenciak, Zuzanna Urbanska, Agata Pastorczak, Katarzyna Babol-Pokora, Kamila Wypyszczak, Ewa Bien, Aleksandra Gawlowska-Marciniak, Jozef Kobos, Wieslawa Grajkowska, Joanna Smyczynska, Wojciech Mlynarski, Szymon Janczar
Publikováno v:
Children, Vol 10, Iss 11, p 1793 (2023)
Adrenocortical carcinoma (ACC) is a rare cancer in childhood. ACC is frequently associated with germline TP53 variants, with founder effects especially due to the p.Arg337His mutation. ACC leads to the secretion of adrenocortical hormones, resulting
Externí odkaz:
https://doaj.org/article/cd00cc3431084a569657ea7f32b9cbc8
Autor:
Agnieszka Zmyslowska, Miljan Kuljanin, Beata Malachowska, Marcin Stanczak, Dominika Michalek, Aneta Wlodarczyk, Dagmara Grot, Joanna Taha, Bartłomiej Pawlik, Magdalena Lebiedzińska-Arciszewska, Hanna Nieznanska, Mariusz R. Wieckowski, Piotr Rieske, Joseph D. Mancias, Maciej Borowiec, Wojciech Mlynarski, Wojciech Fendler
Publikováno v:
Cell Communication and Signaling, Vol 19, Iss 1, Pp 1-14 (2021)
Abstract Background Wolfram syndrome (WFS) is a rare autosomal recessive syndrome in which diabetes mellitus and neurodegenerative disorders occur as a result of Wolframin deficiency and increased ER stress. In addition, WFS1 deficiency leads to calc
Externí odkaz:
https://doaj.org/article/e9ae24e4ded347729d7a31887a6ccfdf
Autor:
Katarzyna Bobeff, Agata Pastorczak, Zuzanna Urbanska, Walentyna Balwierz, Edyta Juraszewska, Jacek Wachowiak, Katarzyna Derwich, Magdalena Samborska, Krzysztof Kalwak, Iwona Dachowska-Kalwak, Paweł Laguna, Iwona Malinowska, Katarzyna Smalisz, Jolanta Gozdzik, Aleksandra Oszer, Bartosz Urbanski, Maciej Zdunek, Tomasz Szczepanski, Wojciech Mlynarski, Szymon Janczar
Publikováno v:
Children, Vol 10, Iss 4, p 745 (2023)
Venetoclax, the best established BH3-mimetic, is a practice-changing proapoptotic drug in blood cancers in adults. In paediatrics the data are fewer but exciting results were recently presented in relapsed or refractory leukaemias demonstrating signi
Externí odkaz:
https://doaj.org/article/98a8dfe4a61d4af7bc0b568d64fad2c4
Autor:
Anna Repczynska, Agata Pastorczak, Katarzyna Babol-Pokora, Jolanta Skalska-Sadowska, Malgorzata Drozniewska, Wojciech Mlynarski, Olga Haus
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Fanconi anemia is a rare genetic disorder caused by mutations in genes which protein products are involved in replication, cell cycle control and DNA repair. It is characterized by congenital malformations, bone marrow failure, an
Externí odkaz:
https://doaj.org/article/fc8a5a92aaad474e93003b6203963989
Autor:
Aleksandra Pyziak-Skupien, Katarzyna Bobeff, Krystyna Wyka, Katarzyna Banach, Beata Malachowska, Wojciech Fendler, Agnieszka Szadkowska, Wojciech Mlynarski, Agnieszka Zmyslowska
Publikováno v:
Iranian Journal of Immunology, Vol 17, Iss 2, Pp 144-153 (2020)
Background: Clinical partial remission (CPR) in most patients with type 1 diabetes (T1D) is observed shortly after clinical diagnosis. Increasing body weight and impaired insulin sensitivity may play a role in the pathogenesis of CPR. Several cytokin
Externí odkaz:
https://doaj.org/article/8a5d7eeb37ed4ef980c61ab35b9760bc
Autor:
Klaudyna Fidyt, Agata Pastorczak, Agnieszka Goral, Kacper Szczygiel, Wojciech Fendler, Angelika Muchowicz, Marcin Adam Bartlomiejczyk, Joanna Madzio, Julia Cyran, Agnieszka Graczyk‐Jarzynka, Eugene Jansen, Elzbieta Patkowska, Ewa Lech‐Maranda, Deepali Pal, Helen Blair, Anna Burdzinska, Piotr Pedzisz, Eliza Glodkowska‐Mrowka, Urszula Demkow, Karolina Gawle‐Krawczyk, Michal Matysiak, Magdalena Winiarska, Przemyslaw Juszczynski, Wojciech Mlynarski, Olaf Heidenreich, Jakub Golab, Malgorzata Firczuk
Publikováno v:
Molecular Oncology, Vol 13, Iss 5, Pp 1180-1195 (2019)
B‐cell precursor acute lymphoblastic leukemia (BCP‐ALL) is a genetically heterogeneous blood cancer characterized by abnormal expansion of immature B cells. Although intensive chemotherapy provides high cure rates in a majority of patients, subty
Externí odkaz:
https://doaj.org/article/45a979d9ef364d65aa674b4bb09f8254
Publikováno v:
Iranian Journal of Immunology, Vol 16, Iss 1, Pp 92-95 (2019)
Externí odkaz:
https://doaj.org/article/2ed76ae000594aa1b194dac20a3ba233