Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Lucie, Lanikova"'
Autor:
Lucie Janeckova, Michal Kolar, Jiri Svec, Lucie Lanikova, Vendula Pospichalova, Nikol Baloghova, Martina Vojtechova, Eva Sloncova, Hynek Strnad, Vladimir Korinek
Publikováno v:
Translational Oncology, Vol 9, Iss 2, Pp 99-107 (2016)
Neoplastic growth is frequently associated with genomic DNA methylation that causes transcriptional silencing of tumor suppressor genes. We used a collection of colorectal polyps and carcinomas in combination with bioinformatics analysis of large dat
Externí odkaz:
https://doaj.org/article/9f1b1d985a2d49578ef07e9ef602a819
Autor:
Lucie Lanikova, Jiri Svec, Lucie Janeckova, Vendula Pospichalova, Nikol Dibus, Martina Vojtechova, Dusan Hrckulak, Eva Sloncova, Hynek Strnad, Vladimir Korinek
Hypermethylated in Cancer 1 (HIC1) is an established tumor suppressor, which is frequently inactivated in various cancers. In colorectal carcinoma (CRC), silencing of HIC1 has been recognized as one of the important events in malignant tumor progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c48edb23fb7f520702879aa0f7f141a
https://doi.org/10.1101/2022.07.25.501405
https://doi.org/10.1101/2022.07.25.501405
Autor:
Veronika Kropackova, Jan Gursky, Jana Balounova, Vladimir Korinek, Vladimir Divoky, Lucie Lanikova
Publikováno v:
Blood. 140:3858-3859
Autor:
Leona Raskova Kafkova, Vladimir Korinek, Olga Babosova, Vladimir Divoky, Lucie Lanikova, Josef T. Prchal, Katarina Kapralova
Publikováno v:
Journal of Cellular and Molecular Medicine
The patients with mantle cell lymphoma (MCL) have translocation t(11;14) associated with cyclin D1 overexpression. We observed that iron (an essential cofactor of dioxygenases including prolyl hydroxylases [PHDs]) depletion by deferoxamine blocked MC
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 Belickova, Cristina Mambet, Olga Babosova, Daniel Coriu, Stefan N. Constantinescu, Nicoleta Berbec, Vladimir Divoky, Barbora Kralova, Jitka Vesela, Violaine Havelange, Oana Stanca, Carmen C. Diaconu, Emilie Leroy, Pascale Saussoy, Aurelia Tatic, Laura Necula, Christian Pecquet, Jean-Philippe Defour, Lucie Lanikova
Publikováno v:
Blood. 132:2695-2699
TO THE EDITOR: Although the concept of somatic driver mutations in myeloproliferative neoplasms (MPNs) represented by polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis is well established,[1][1][⇓][2]-[3][3] the cont
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
Publikováno v:
Genes
Genes, Vol 10, Iss 10, p 813 (2019)
Genes, Vol 10, Iss 10, p 813 (2019)
Myeloproliferative neoplasms (MPN) are genetically very complex and heterogeneous diseases in which the acquisition of a somatic driver mutation triggers three main myeloid cytokine receptors, and phenotypically expresses as polycythemia vera (PV), e
Autor:
Vladimir Divoky, Robin Miller, Josef T. Prchal, N. Scott Reading, Jihyun Song, Swee Lay Thein, Claire Shooter, Archana M. Agarwal, Lucie Lanikova, Barnaby Clark
Publikováno v:
Human Mutation. 37:1153-1156
We report an infant with sickle cell disease phenotype by biochemical analysis whose β-globin gene (HBB) sequencing showed sickle cell mutation (HBBS ) heterozygosity. The proband has a unique head-to-tail duplication of the β-globin gene cluster h
Autor:
Michal Kolar, Vladimir Korinek, Hynek Strnad, Vendula Pospichalova, Lucie Lanikova, Lucie Janeckova, Martina Vojtechova, Nikol Baloghova, Eva Sloncova, Jiri Svec
Publikováno v:
Translational Oncology, Vol 9, Iss 2, Pp 99-107 (2016)
Neoplastic growth is frequently associated with genomic DNA methylation that causes transcriptional silencing of tumor suppressor genes. We used a collection of colorectal polyps and carcinomas in combination with bioinformatics analysis of large dat