Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Joanna Taha"'
Autor:
Zuzanna Urbańska, Monika Lejman, Joanna Taha, Joanna Madzio, Kinga Ostrowska, Karolina Miarka-Walczyk, Kamila Wypyszczak, Borys Styka, Justyna Jakubowska, Łukasz Sędek, Tomasz Szczepański, Marcin Stańczak, Wojciech Fendler, Wojciech Młynarski, Agata Pastorczak
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 35, Iss , Pp 100840- (2023)
We analyzed the pattern of whole-genome copy number alterations (CNAs) and their association with the kinetics of blast clearance during the induction treatment among 195 pediatric patients with B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
Externí odkaz:
https://doaj.org/article/34f74e221bac4925ae4720cc46ce51ba
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:
Monika Lejman, Monika Włodarczyk, Borys Styka, Agata Pastorczak, Joanna Zawitkowska, Joanna Taha, Łukasz Sędek, Katarzyna Skonieczka, Marcin Braun, Olga Haus, Tomasz Szczepański, Wojciech Młynarski, Jerzy R. Kowalczyk
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
T-cell acute lymphoblastic leukemia (T-ALL) is a highly heterogeneous disease, and numerous genetic aberrations in the leukemic genome are responsible for the biological and clinical differences among particular ALL subtypes. However, there is limite
Externí odkaz:
https://doaj.org/article/835ccc35fdab439c92ae9b676f7716bb
Autor:
Urszula Smyczynska, Marcin Stanczak, Miljan Kuljanin, Aneta Włodarczyk, Ewelina Stoczynska-Fidelus, Joanna Taha, Bartłomiej Pawlik, Maciej Borowiec, Joseph D. Mancias, Wojciech Mlynarski, Piotr Rieske, Wojciech Fendler, Agnieszka Zmysłowska
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2370
Alström syndrome (ALMS) and Bardet–Biedl syndrome (BBS) are rare genetic diseases with a number of common clinical features ranging from early-childhood obesity and retinal degeneration. ALMS and BBS belong to the ciliopathies, which are known to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::766f3c3ffc799869a7c13366aa04ab41
Autor:
Magdalena Lebiedzinska-Arciszewska, Bartlomiej Pawlik, Piotr Rieske, Joanna Taha, Wojciech Fendler, Hanna Nieznanska, Miljan Kuljanin, Aneta Wlodarczyk, Dominika Michałek, Agnieszka Zmysłowska, Beata Małachowska, Joseph D. Mancias, Wojciech Młynarski, Marcin Stanczak, Maciej Borowiec, Mariusz R. Wieckowski, Dagmara Grot
Publikováno v:
Cell Communication and Signaling, Vol 19, Iss 1, Pp 1-14 (2021)
Cell Communication and Signaling : CCS
Cell Communication and Signaling : CCS
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 calcium homeo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d969bef511c2898189cf414590f38a
https://doaj.org/article/e9ae24e4ded347729d7a31887a6ccfdf
https://doaj.org/article/e9ae24e4ded347729d7a31887a6ccfdf
Autor:
Monika Mielcarek-Siedziuk, Ewa Gorczyńska, Karolina Liszka, Paweł Marschollek, Krzysztof Kałwak, Joanna Taha, Blanka Rybka
Publikováno v:
Acta Haematologica Polonica. 52:211-213
When all of the usually applied treatment methods fail, we have to try something innovative. In this vignette, we present the history of the first in Poland CAR-T cell therapy in a child with refractory B-cell acute lymphoblastic leukemia (ALL). In m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4128b28941e9e440626568bd14bc8a1
https://doi.org/10.5603/ahp.a2021.0028
https://doi.org/10.5603/ahp.a2021.0028
Autor:
Walentyna Balwierz, Jacek Treliński, Teresa Iwaniec, Andrzej Kołtan, Iwona Rurańska, Izabela Jatczak-Pawlik, Karolina Janczar, Edyta Odnoczko, Joanna Zdziarska, Szymon Janczar, Anna Klukowska, Danuta Pietrys, Pawel Laguna, Katarzyna Babol-Pokora, Jerzy Windyga, Michał Jamrozik, Wojciech Młynarski, Tomasz Szczepański, Joanna Taha
Publikováno v:
Thrombosis Research. 193:9-14
Introduction Female hemophilia is an intriguing rare disorder and few larger reports on its genetic etiology are available. While historically the diagnosis was satisfactorily reached by factor VIII activity assays, the clinical and potentially thera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08de5c1d08b102937532a42fa3a948f8
https://doi.org/10.1016/j.thromres.2020.05.041
https://doi.org/10.1016/j.thromres.2020.05.041
Autor:
Marcin, Braun, Agata, Pastorczak, Łukasz, Sędek, Joanna, Taha, Joanna, Madzio, Izabela, Jatczak-Pawlik, Kamila, Wypyszczak, Michał, Matysiak, Katarzyna, Derwich, Monika, Lejman, Bernarda, Kazanowska, Tomasz, Szczepański, Jerzy R, Kowalczyk, Wojciech, Mlynarski
Publikováno v:
Hematological oncologyREFERENCES. 40(3)
The strongest predictors of outcome in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) are minimal residual disease (MRD) and specific molecular abnormalities. One unfavorable prognostic factor is the presence of IKZF1 gene aberrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87d237fdd172ac9a746c61ac2cf1e0c5
https://pubmed.ncbi.nlm.nih.gov/35118711
https://pubmed.ncbi.nlm.nih.gov/35118711
Autor:
Marcin Braun, Agata Pastorczak, Joanna Taha, Wojciech Fendler, Jerzy Kowalczyk, Monika Lejman, Wojciech Młynarski, Ewa Wrona
Publikováno v:
Journal of Applied Genetics
Chromosome 21 abnormalities are the most frequent genetic findings in childhood B cell precursor acute lymphoblastic leukemia (BCP-ALL) cases. Majority of patients are effectively diagnosed with fluorescence in situ hybridization (FISH) and karyotypi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94cc27b5b9d76a4fe93adad7ef613715
http://europepmc.org/articles/PMC6803575
http://europepmc.org/articles/PMC6803575
Autor:
Łukasz Sędek, Joanna Zawitkowska, Agata Pastorczak, Marcin Braun, Olga Haus, Wojciech Młynarski, Monika Włodarczyk, Tomasz Szczepański, Borys Styka, Jerzy Kowalczyk, Katarzyna Skonieczka, Joanna Taha, Monika Lejman
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology
Frontiers in Oncology
T-cell acute lymphoblastic leukemia (T-ALL) is a highly heterogeneous disease, and numerous genetic aberrations in the leukemic genome are responsible for the biological and clinical differences among particular ALL subtypes. However, there is limite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077007c3f25eea8de573adb86356f04c
https://pubmed.ncbi.nlm.nih.gov/32766158
https://pubmed.ncbi.nlm.nih.gov/32766158