Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Alena Musilova"'
Autor:
Michaela Novakova, Marketa Zaliova, Karel Fiser, Barbora Vakrmanova, Lucie Slamova, Alena Musilova, Monika Brüggemann, Matthias Ritgen, Eva Fronkova, Tomas Kalina, Jan Stary, Lucie Winkowska, Peter Svec, Alexandra Kolenova, Jan Stuchly, Jan Zuna, Jan Trka, Ondrej Hrusak, Ester Mejstrikova
Publikováno v:
Haematologica, Vol 106, Iss 8 (2020)
Recently, we described B-cell precursor acute lymphoblastic leukemia (BCP-ALL) subtype with early switch to the monocytic lineage and loss of the B-cell immunophenotype, including CD19 expression. Thus far, the genetic background has remained unknown
Externí odkaz:
https://doaj.org/article/26a5eaf9193b48aaadedfbc17dd78bfa
Autor:
Katerina Rejlova, Alena Musilova, Karolina Skvarova Kramarzova, Marketa Zaliova, Karel Fiser, Meritxell Alberich-Jorda, Jan Trka, Julia Starkova
Publikováno v:
Epigenetics, Vol 13, Iss 1, Pp 73-84 (2018)
Homeobox (HOX) genes are frequently dysregulated in leukemia. Previous studies have shown that aberrant HOX gene expression accompanies leukemogenesis and affects disease progression and leukemia patient survival. Patients with acute myeloid leukemia
Externí odkaz:
https://doaj.org/article/a78aec922106463abf4d02495cb9f808
Autor:
Marketa Zaliova, Eliska Potuckova, Lenka Hovorkova, Alena Musilova, Lucie Winkowska, Karel Fiser, Jan Stuchly, Ester Mejstrikova, Julia Starkova, Jan Zuna, Jan Stary, Jan Trka
Publikováno v:
Haematologica, Vol 104, Iss 7 (2019)
ERG-deletions occur recurrently in acute lymphoblastic leukemia, especially in the DUX4-rearranged subtype. The ERG-deletion was shown to positively impact prognosis of patients with IKZF1-deletion and its presence precludes assignment into IKZF1plus
Externí odkaz:
https://doaj.org/article/b3ac0ac530c4478aaf403b9a1428838a
Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort
Autor:
Marketa Zaliova, Jan Stuchly, Lucie Winkowska, Alena Musilova, Karel Fiser, Martina Slamova, Julia Starkova, Martina Vaskova, Ondrej Hrusak, Lucie Sramkova, Jan Stary, Jan Zuna, Jan Trka
Publikováno v:
Haematologica, Vol 104, Iss 7 (2019)
Novel biological subtypes and clinically important genetic aberrations (druggable lesions, prognostic factors) have been described in B-other acute lymphoblastic leukemia (ALL) during the last decade; however, due to a lack of studies on unselected c
Externí odkaz:
https://doaj.org/article/83a31a02ffa84184a5cd3db59a615b50
Autor:
Barbora Straka, Barbora Hermanovska, Lenka Krskova, Josef Zamecnik, Marketa Vlckova, Miroslava Balascakova, Pavel Tesner, Petr Jezdik, Michal Tichy, Martin Kyncl, Alena Musilova, Petra Lassuthova, Petr Marusic, Pavel Krsek
Publikováno v:
Neurology. Genetics. 8(5)
Background and ObjectivesMalformations of cortical development (MCD), though individually rare, constitute a significant burden of disease. The diagnostic yield of next-generation sequencing (NGS) in these patients varies across studies and methods,
Autor:
Alena Musilova, Jan Stary, Ester Mejstrikova, Jan Zuna, Jan Stuchly, Julia Starkova, Ondrej Hrusak, Michaela Kotrova, Marketa Zaliova, Karel Fiser, Jan Trka
Publikováno v:
Blood. 128:2263-2266
To the editor: Mixed phenotype acute leukemias (MPALs) are a rare subset of acute leukemias that cannot be unambiguously assigned to a single hematopoietic lineage because of the significant expression of antigens from additional lineages. This subse
Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort
Autor:
Marketa, Zaliova, Jan, Stuchly, Lucie, Winkowska, Alena, Musilova, Karel, Fiser, Martina, Slamova, Julia, Starkova, Martina, Vaskova, Ondrej, Hrusak, Lucie, Sramkova, Jan, Stary, Jan, Zuna, Jan, Trka
Publikováno v:
Haematologica
Novel biological subtypes and clinically important genetic aberrations (druggable lesions, prognostic factors) have been described in B-other acute lymphoblastic leukemia (ALL) during the last decade; however, due to a lack of studies on unselected c
Autor:
Alena Musilova, Julia Starkova, Karolina Skvarova Kramarzova, Karel Fiser, Marketa Zaliova, Meritxell Alberich-Jorda, Katerina Rejlova, Jan Trka
Publikováno v:
Epigenetics. 13(1)
Homeobox (HOX) genes are frequently dysregulated in leukemia. Previous studies have shown that aberrant HOX gene expression accompanies leukemogenesis and affects disease progression and leukemia patient survival. Patients with acute myeloid leukemia
Autor:
Barbora Straka, Markéta Vlčková, Zuzana Libá, Barbora Heřmanovská, Martin Kynčl, Jana Dorňáková, Jakub Táborský, Pavel Kršek, Alena Musilová, Jan Janota, Miroslava Balaščaková
Publikováno v:
Epilepsia Open, Vol 8, Iss 1, Pp 211-216 (2023)
Abstract Fetal intracranial hemorrhage represents a rare event with an estimated prevalence of 1:10 000 pregnancies. We report a patient diagnosed prenatally with intracranial hemorrhage and ventriculomegaly carrying a novel, previously unreported, l
Externí odkaz:
https://doaj.org/article/a2e0995e10254ea09c975d92a2e9c41a
Autor:
Petr Mlejnek, Vladimír Křen, Vladimír Landa, Miroslava Šimáková, Alena Musilova, Vaclav Zidek, Jan Šilhavý, Michal Pravenec
Publikováno v:
Publons
The spontaneously hypertensive rat (SHR) is the most widely used animal model of essential hypertension and accompanying metabolic disturbances. Recent advances in sequencing of genomes of BN-Lx and SHR progenitors of the BXH/HXB recombinant inbred (