Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Michał Świerniak"'
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:
Ella R. Thompson, Michelle Wong-Brown, Simone M. Rowley, Susan Dooley, Na Lil, Michael Hipwell, Simone McInerny, Cliff Meldrum, Lisa Devereux, David Mossman, Alison H. Trainer, Briar-Rose Millar, Gillian Mitchell, Cate Smith, Paul A. James, Ian G. Campbell, Rodney J. Scott, Katarzyna Klonowska, Anna Jakubowska, Jelena Maksimenko, Arvids Irmejs, Miki Nakazawa-Miklasevica, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, Edvins Miklasevics, Karolina Tęcza, Jolanta Pamuła-Piłat, Joanna Łanuszewska, Ewa Grzybowska, M. Szwiec, J. Tomiczek-Szwiec, M. Gełej, C. Cybulski, T. Huzarski, E. Kilar, Małgorzata Oczko-Wojciechowska, Michał Świerniak, Jolanta Krajewska, Małgorzata Kowalska, Tomasz Tyszkiewicz, Agnieszka Pawlaczek, Michał Jarząb, Monika Kowal, Dagmara Rusinek, Jadwiga Zebracka-Gala, Agnieszka Czarniecka, Barbara Jarzab, Andrzej Plawski, Paweł Borun, Joanna Szczepinska, Monika Siolek, Beata Kozak-Klonowska, Katarzyna Kaczmarek, Magdalena Muszyńska, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Jan Lubiński, Michał Post
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss S1, Pp 1-5 (2017)
Externí odkaz:
https://doaj.org/article/959ca802658e4fe59a0522035180cc7e
Autor:
Agnieszka Furmańczyk-Zawiska, Anna Kubiak-Dydo, Ewelina Użarowska-Gąska, Marta Kotlarek-Łysakowska, Katarzyna Salata, Monika Kolanowska, Michał Świerniak, Paweł Gaj, Beata Leszczyńska, Maria Daniel, Krystian Jażdżewski, Magdalena Durlik, Anna Wójcicka
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 4, 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
Externí odkaz:
https://doaj.org/article/12475646fa0642a3b7b6b5785d600ecb
Autor:
Marta Kotlarek, Anna Kubiak, Małgorzata Czetwertyńska, Michał Świerniak, Wojciech Gierlikowski, Monika Kolanowska, Elwira Bakuła-Zalewska, Sissy M. Jhiang, Krystian Jażdżewski, Anna Wójcicka
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 655 (2018)
Aberrant expression of the sodium-iodide symporter (NIS) and the resistance to post-operative radioactive iodide treatment is a crucial cause of higher mortality of some thyroid cancer patients. In this study, we analyzed the impact of miR-146a on th
Externí odkaz:
https://doaj.org/article/60d3d34237664124acbcc3e1d2e7819d
Autor:
Krystian Jażdżewski, Wiesław Wiechno, Magdalena Bogdańska, Łukasz Koperski, Barbara Górnicka, Adam Kot, Wojciech Gierlikowski, Elżbieta Stachlewska, Joanna Długosińska, Małgorzata Czetwertyńska, Anna Wójcicka, Michał Świerniak
Purpose: Five germline genetic variants (rs116909374, rs965513, rs944289, rs966423, and rs2439302) have been associated in genome-wide association studies (GWAS) with increased risk of differentiated thyroid cancer (DTC), but their role in mortality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d5cbf41d557633f8bffde0b9b0d8111
https://doi.org/10.1158/1078-0432.c.6523637
https://doi.org/10.1158/1078-0432.c.6523637
Autor:
Krystian Jażdżewski, Wiesław Wiechno, Magdalena Bogdańska, Łukasz Koperski, Barbara Górnicka, Adam Kot, Wojciech Gierlikowski, Elżbieta Stachlewska, Joanna Długosińska, Małgorzata Czetwertyńska, Anna Wójcicka, Michał Świerniak
Supplementary Table 1 Overall Mortality_legend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dfa233530adaa6d49260972b274243f
https://doi.org/10.1158/1078-0432.22457645
https://doi.org/10.1158/1078-0432.22457645
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:
Adrienne M. Dorrance, Andrew J. Carroll, Deedra Nicolet, Ann-Kathrin Eisfeld, Allison E. Walker, Michał Świerniak, Christopher J. Walker, Felice Pepe, Krzysztof Mrózek, Marius Bill, Stefano Volinia, Richard Stone, Jonathan E. Kolitz, Jessica Kohlschmidt, Ramiro Garzon, Bayard L. Powell, Sakari Kauppinen, Andreas Petri, Dimitrios Papaioannou, Eunice S. Wang, Clara D. Bloomfield, Geoffrey L. Uy, John C. Byrd
Publikováno v:
Papaioannou, D, Volinia, S, Nicolet, D, Świerniak, M, Petri, A, Mrózek, K, Bill, M, Pepe, F, Walker, C J, Walker, A E, Carroll, A J, Kohlschmidt, J, Eisfeld, A-K, Powell, B L, Uy, G L, Kolitz, J E, Wang, E S, Kauppinen, S, Dorrance, A, Stone, R M, Byrd, J C, Bloomfield, C D & Garzon, R 2020, ' Clinical and functional significance of circular RNAs in cytogenetically normal AML ', Blood advances, vol. 4, no. 2, pp. 239-251 . https://doi.org/10.1182/bloodadvances.2019000568
Circular RNAs (circRNAs) are noncoding RNA molecules that display a perturbed arrangement of exons, called backsplicing. To examine the prognostic and biologic significance of circRNA expression in cytogenetically normal acute myeloid leukemia (CN-AM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c2eb89548dfe66eacf2fabbea796ed
https://vbn.aau.dk/ws/files/336993210/advancesadv2019000568.pdf
https://vbn.aau.dk/ws/files/336993210/advancesadv2019000568.pdf
Autor:
Łukasz Koperski, Barbara Górnicka, Krystian Jazdzewski, Anna Wojcicka, Marta Kotlarek, Anna Kubiak, Michał Świerniak, Monika Kolanowska
Publikováno v:
Oncotarget
// Łukasz Koperski 1 , Marta Kotlarek 2 , Michal Świerniak 2, 3 , Monika Kolanowska 2, 3 , Anna Kubiak 2, 3 , Barbara Gornicka 1 , Krystian Jazdzewski 2, 3 and Anna Wojcicka 2, 3 1 Department of Pathology, Medical University of Warsaw, Warsaw, Pola