Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Jan, Gursky"'
Autor:
Katarina Chroma, Zdenek Skrott, Jan Gursky, Jaroslav Bacovsky, Pavel Moudry, Tereza Buchtova, Martin Mistrik, Jiri Bartek
Publikováno v:
Cell Death and Disease, Vol 13, Iss 3, Pp 1-11 (2022)
Abstract Despite several approved therapeutic modalities, multiple myeloma (MM) remains an incurable blood malignancy and only a small fraction of patients achieves prolonged disease control. The common anti-MM treatment targets proteasome with speci
Externí odkaz:
https://doaj.org/article/3a153f215b3941189abf8b25abc8d0bc
Autor:
Katerina Smesny, Trtkova, Petra, Luzna, Denisa Weiser, Drozdkova, Katerina, Cizkova, Lucie, Janovska, Jan, Gursky, Dana, Prukova, Ivo, Frydrych, Marian, Hajduch, Jiri, Minarik
Publikováno v:
Molecular Medicine Reports. 26
Gene inactivation of the cyclin‑dependent kinase inhibitors p16
Autor:
Veronika Kropackova, Jan Gursky, Jana Balounova, Vladimir Korinek, Vladimir Divoky, Lucie Lanikova
Publikováno v:
Blood. 140:3858-3859
Autor:
Pavla Koralkova, Nikola Niederlova, Iveta Hradilova, Jan Gursky, Barbora Cudova, Helena Urbankova, Eva Reznickova, Tomas Gucky, Denisa Myslivcova, Monika Belickova, Vladimir Krystof, Vladimir Divoky
Publikováno v:
Blood. 140:8823-8824
Autor:
Zdenek Kolar, Denisa Hrckova Drozdkova, Jiri Minarik, Katerina Smesny Trtkova, Ivo Uberall, Jan Gursky
Publikováno v:
Anticancer Research. 40:4979-4987
Background/aim Multiple myeloma is a highly heterogeneous disease of clonal plasma cells. Histone deacetylase (HDAC) inhibitors are promising anticancer drugs but their precise mechanisms of actions are not well understood. Materials and methods Cell
Autor:
Jiri Bartek, Martin Mistrik, Tereza Buchtova, Jan Gursky, Marian Hajduch, Zdenek Skrott, Dusana Majera
Publikováno v:
Oncogene. 38:6711-6722
Aldehyde dehydrogenase (ALDH) is a proposed biomarker and possible target to eradicate cancer stem cells. ALDH inhibition as a treatment approach is supported by anti-cancer effects of the alcohol-abuse drug disulfiram (DSF, Antabuse). Given that met
Autor:
Sona Hubackova, Patrik Flodr, Jiri Bartek, Vladimir Divoky, Jan Gursky, Pavla Koralkova, Zdenek Hodny, Pavla Vyhlidalova, Jan Stetka, A Hlusi, Lucie Lanikova
Publikováno v:
Oncogene
Inflammatory and oncogenic signaling converge in disease evolution of BCR–ABL-negative myeloproliferative neoplasms, clonal hematopoietic stem cell disorders characterized by gain-of-function mutation in JAK2 kinase (JAK2V617F), with highest preval
Autor:
Monika Horvathova, Lucie Lanikova, Jan Gursky, Vladimir Divoky, Pavla Koralkova, Katarina Kapralova, Dagmar Pospisilova, Ondrej Jahoda
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 24
International Journal of Molecular Sciences, Vol 21, Iss 9652, p 9652 (2020)
Volume 21
Issue 24
International Journal of Molecular Sciences, Vol 21, Iss 9652, p 9652 (2020)
Molecular pathophysiology of Diamond-Blackfan anemia (DBA) involves disrupted erythroid-lineage proliferation, differentiation and apoptosis
with the activation of p53 considered as a key component. Recently, oxidative stress was proposed to pla
with the activation of p53 considered as a key component. Recently, oxidative stress was proposed to pla
Autor:
Julie Liñan Velasquez, Pavla Vyhlidalova, Jiri Bartek, Jan Gursky, Renata Mojzikova, Jan Stetka, Vladimir Divoky, Lucia Vráblová
Publikováno v:
Cancers, Vol 12, Iss 903, p 903 (2020)
Cancers
Cancers
Inflammatory and oncogenic signaling, both known to challenge genome stability, are key drivers of BCR-ABL-positive chronic myeloid leukemia (CML) and JAK2 V617F-positive chronic myeloproliferative neoplasms (MPNs). Despite similarities in chronic in
Autor:
Zdenek Hodny, Jirina Bartkova, Mariam Gachechiladze, Dana Simkova, Martin Mistrik, Dusana Majera, Jan Bouchal, Jana Steigerova, Karel Cwiertka, Jan Gursky, Gabriela Korinkova, Zdenek Skrott, Daniela Kurfürstová, Jiri Bartek
Publikováno v:
The Prostate. 79:352-362
Background Castration-resistant prostate cancer (PCa) represents a serious health challenge. Based on mechanistically-supported rationale we explored new therapeutic options based on clinically available drugs with anticancer effects, including inhib