Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ewa Duszenko"'
Autor:
Monika Siemieniuk-Rys, Ewa Duszenko, Ewa Wawrzyniak, Marzena Watek, Aleksandra Kotkowska, Katarzyna Skonieczka, Wanda Knopinska-Posluszny, Sebastian Grosicki, Aleksandra Gołos, Jadwiga Hołojda, Justyna Rybka, Jerzy Holowiecki, Agnieszka Pluta, Barbara Pienkowska-Grela, Malgorzata Wach, Lidia Gil, Agnieszka Wierzbowska, Tadeusz Robak, Mariola Iliszko, Anna Jaskowiec, Renata Woroniecka, Anna Jachalska, Malgorzata Jarmuz-Szymczak, Olga Haus, Maria Czyżewska, Anna Ejduk, Barbara Mucha, Marta Szarawarska, Anna Przybylowicz-Chalecka, Agnieszka Kopacz, Agnieszka Klonowska
Publikováno v:
Leukemia & Lymphoma. 58:889-897
Monosomal karyotype (MK) and complex karyotype (CK) are poor prognostic factors in acute myeloid leukemia (AML). A comprehensive analysis of cytogenetic and clinical factors influencing an outcome of AML-CK+ was performed. The impact of cladribine co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adbf3e11f74b3bc095cf830c3dd8cf36
https://doi.org/10.1080/10428194.2016.1219901
https://doi.org/10.1080/10428194.2016.1219901
Autor:
Wanda Knopinska-Posluszny, Anna Jaskowiec, Aleksandra Kotkowska, Barbara Pienkowska-Grela, Mariola Iliszko, Sebastian Grosicki, Jerzy Holowiecki, Malgorzata Jakobczyk, Agnieszka Pluta, Olga Haus, Malgorzata Wach, Anna Ejduk, Renata Woroniecka, Monika Siemieniuk-Rys, Ewa Wawrzyniak, Ewa Duszenko, Agnieszka Wierzbowska, Joanna Kosny, Agnieszka Klonowska, Barbara Mucha, Tadeusz Robak
Publikováno v:
Leukemia Research. 37:293-299
A monosomal karyotype (MK) was identified by banding techniques (BT) in acute myeloid leukemia (AML). However, BT may be insufficient to determine the actual loss of a complete chromosome, especially in complex karyotypes. We have investigated the ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8006d7a1195b3aa7e815d10aba5c808
https://doi.org/10.1016/j.leukres.2012.10.022
https://doi.org/10.1016/j.leukres.2012.10.022
Publikováno v:
Polish Archives of Internal Medicine. 119:366-372
Introduction Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal diseases of pluripotent hematopoietic stem or progenitor cells. MDS are characterized by ineffective hematopoiesis, increased apoptosis, peripheral blood cytopenias, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0763b3bbba06e8f80557cf5d09212f8c
https://doi.org/10.20452/pamw.711
https://doi.org/10.20452/pamw.711
Autor:
Mariusz Wysocki, Ewa Duszenko, Andrzej Kołtan, Katarzyna Skonieczka, Robert Dębski, Barbara Mucha, Krystyna Soszyńska, Olga Haus
Publikováno v:
Annals of Hematology. 87:991-1002
We investigated bone marrow cells of 70 acute lymphoblastic leukemia children by conventional cytogenetics (CC), fluorescence in situ hybridization (FISH), and reverse transcription polymerase chain reaction (RT-PCR) methods. CC and RT-PCR for fusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdd2d8bcd12629e360b80bdb6faefdae
https://doi.org/10.1007/s00277-008-0540-6
https://doi.org/10.1007/s00277-008-0540-6
Autor:
Magdalena Pasińska, Małgorzata Piotrowicz, Olga Haus, Malgorzata Drozniewska, Ewa Duszenko, Grzegorz Ludwikowski
Publikováno v:
Pediatria Polska. 82:292-299
Wstep Czestośc wad u zywo urodzonych noworodkow wynosi od 0,94 do 4%, u martwo urodzonych jest kilkakrotnie wieksza i wynosi od ok. 9 do 20%. Spośrod wad o znanej etiologii ok. 35% jest spowodowanych przez czynniki wylącznie genetyczne. Cel pracy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5a15c7a364fe4cdf169209902973970
https://doi.org/10.1016/s0031-3939(07)70402-x
https://doi.org/10.1016/s0031-3939(07)70402-x
Autor:
Aleksander B. Skotnicki, Karolina Karabin, Malgorzata Calbecka, Krzysztof Warzocha, Dariusz Kata, Sylwia Czekalska, Wiesław Wiktor Jęrzejczak, Marta Pawelczyk, Olga Haus, Ewa Duszenko, Grażyna Gadomska, Jolanta Libura, Katarzyna Borg, Justyna Gajkowska-Kulig, Z. Salamanczuk, I. Florek, Beata Piątkowska-Jakubas, Anna Ejduk, Magdalena Zawada, Malgorzata Jakobczyk, Bożena Jaźwiec, Barbara Mucha, Marek Kielbinski, Krystyna Soszyńska, Karolina Matiakowska, Sebastian Grosicki, Slawomira Kyrcz-Krzemien, Kazimierz Kuliczkowski, Marta Libura, Iwona Solarska
Copy number variations (CNV) in CEBPA locus represent heterogeneous group of mutations accompanying acute myeloid leukemia (AML). The aim of this study was to characterize different CEBPA mutation categories in regard to biological data like age, cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd3f991ea6f8b295d69f2e1a82248fef
https://ruj.uj.edu.pl/xmlui/handle/item/136787
https://ruj.uj.edu.pl/xmlui/handle/item/136787
Autor:
Ewa Duszenko, Artur Gurgul, Izabela Zawlik, Tomasz Szmatoła, Radosław Chaber, Olga Haus, Blanka Rybka, Anna Tomoń, Grażyna Wróbel, Natalia Potocka, Krzysztof Ciebiera, Christopher J. Arthur, Sylwia Stąpor, Igor Jasielczuk, Jerzy Kowalczyk, Sylwia Paszek, Renata Ryczan-Krawczyk
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 11, p e0187422 (2017)
Arthur, C 2017, ' Whole-genome DNA methylation characteristics in pediatric precursor B cell acute lymphoblastic leukemia (BCP ALL) ', PLoS ONE, vol. 12, no. 11 . https://doi.org/10.1371/journal.pone.0187422
PLoS ONE, Vol 12, Iss 11, p e0187422 (2017)
Arthur, C 2017, ' Whole-genome DNA methylation characteristics in pediatric precursor B cell acute lymphoblastic leukemia (BCP ALL) ', PLoS ONE, vol. 12, no. 11 . https://doi.org/10.1371/journal.pone.0187422
In addition to genetic alterations, epigenetic abnormalities have been shown to underlie the pathogenesis of acute lymphoblastic leukemia (ALL)—the most common pediatric cancer. The purpose of this study was to characterize the whole genome DNA met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1178665ae9c6599f2001aa28643d5776
https://doi.org/10.1371/journal.pone.0187422
https://doi.org/10.1371/journal.pone.0187422
Publikováno v:
Pediatria Polska. 82:239-241
Unbalanced chromosomal aberrations are one of the most common causes of mental retardation and congenital defects. We analized genotype-phenotype correlations in a girl with dysmorphism, heart defect and hypoglycaemic attacks. The proband was born at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::001102edb5522e6b92373dc323758d67
https://doi.org/10.1016/s0031-3939(07)70425-0
https://doi.org/10.1016/s0031-3939(07)70425-0
Autor:
Beata Stella-Holowiecka, Kazimierz Kuliczkowski, Renata Mika-Witkowska, Hanna Makuch-Lasica, Miroslaw Majewski, Olga Haus, Jacek Nowak, Andzelika Krawcewicz, Krzysztof Warzocha, Ewa Duszenko, Dariusz Wołowiec, Grazyna Nowak
Publikováno v:
Annals of hematology. 87(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47208e30c03cf7a5bb0c0fdaa7a92647
https://pubmed.ncbi.nlm.nih.gov/18180922
https://pubmed.ncbi.nlm.nih.gov/18180922
Autor:
Aleksandra Kotkowska, Renata Woroniecka, Barbara Mucha, Agnieszka Kopacz, Anna Jachalska, Malgorzata Jarmuz-Szymczak, Olga Haus, Malgorzata Wach, Agnieszka Wierzbowska, Marzena Watek, Maria Czyżewska, Lidia Gil, Anna Ejduk, Anna Jaskowiec, Katarzyna Skonieczka, Jerzy Holowiecki, Justyna Rybka, Ewa Duszenko, Marta Szarawarska, Wanda Knopinska-Posluszny, Sebastian Grosicki, Jadwiga Hołojda, Barbara Pienkowska-Grela, Agnieszka Klonowska, Mariola Iliszko, Anna Przybylowicz-Chalecka, Monika Siemieniuk-Rys, Ewa Wawrzyniak, Tadeusz Robak, Agnieszka Pluta
Publikováno v:
Blood. 124:2347-2347
Objectives:Cytogenetics is one of the most important prognostic factors in acute myeloid leukemia (AML). Two major, partially overlapping cytogenetic subsets of AML associated with an adverse prognosis, are AML with complex karyotype (CK) and AML wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dfe88edda9f6dea4d5d550da0f6d218
https://doi.org/10.1182/blood.v124.21.2347.2347
https://doi.org/10.1182/blood.v124.21.2347.2347