Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Martina Hruba"'
Autor:
Regina Fillerova, Lenka Kruzova, Tomas Papajik, Michael Doubek, Daniel Lysák, Martina Hruba, Marek Mráz, Vít Procházka, Marie Jarošová, Eva Koritakova, Karel Indrak, Alexandra Oltová, Eva Kriegova, Karla Plevová
Publikováno v:
American Journal of Hematology. 92
Detection of genetic changes has improved the current risk stratification in chronic lymphocytic leukemia (CLL).1,2 Among the known recurrent chromosomal abnormalities,1 6q deletion is less frequent and controversy surrounding its prognostic signific
Autor:
Anna Jonasova, Anna Rykovska, Ivan Subrt, I Sarova, Martina Hruba, Daniel Lysák, Samuel Vokurka, Pavel Dvorak, Kyra Michalova
Publikováno v:
Hematological Oncology. 32:82-86
The translocation t(2;11)(p21;q23) is associated with de novo myelodysplastic syndromes (MDS) and has an overall frequency of approximately 1%. The outcome of MDS patients with this translocation is not clear until now, because most of the clinical d
Autor:
Ivan Subrt, Martina Hruba
Publikováno v:
Leukemia & Lymphoma. 54:413-416
Although 13q14 deletion, as the most frequent chromosomal aberration in chronic lymphocytic leukemia (CLL), has been investigated over a long period of time, the issue is so complex that both its b...
Publikováno v:
Leukemia & Lymphoma. 53:2054-2062
13q14 deletion is the most frequent chromosomal aberration in chronic lymphocytic leukemia (CLL), found by interphase fluorescence in situ hybridization (FISH) in more than 50% of cases of CLL [1]....
Autor:
Monika Pittrova, Jitka Zemanova, Martina Hruba, Romana Vlckova, Libor Hradecky, Barbara Wirleitner, Maximilian Schuff, Pavla Novakova, Astrid Stecher, Maximilian Murtinger, Milena Králíčková
Publikováno v:
Reproductive BioMedicine Online. 36:e23
Autor:
Pavel, Dvorak, Daniel, Lysak, Samuel, Vokurka, Kyra, Michalova, Iveta, Sarova, Anna, Jonasova, Martina, Hruba, Anna, Rykovska, Ivan, Subrt
Publikováno v:
Hematological oncology. 32(2)
The translocation t(2;11)(p21;q23) is associated with de novo myelodysplastic syndromes (MDS) and has an overall frequency of approximately 1%. The outcome of MDS patients with this translocation is not clear until now, because most of the clinical d
Autor:
Alexandra Oltová, Ivan Spicka, Petr Kuglík, Jana Rabasova, Hana Filková, Roman Hájek, Zdenek Adam, Jana Balcarkova, Kyra Michalova, Pavel Nemec, Martina Hruba, Zuzana Zemanova, Vladimir Maisnar, Miroslava Schützová, Evzen Gregora, Jana Tajtlova, Vlastimil Scudla, Milena Holzerova, Petra Kaisarova, Marie Jarošová
Publikováno v:
Leukemialymphoma. 53(5)
The prognostic impact of chromosomal abnormalities was evaluated by fluorescence in situ hybridization with cytoplasmic immunoglobulin light chain staining (cIg-FISH) and by classical metaphase cytogenetics in a cohort of 207 patients with newly diag
Publikováno v:
Leukemia Research. 33:860-861
Autor:
Jiri Sterba, Jan Stary, Petr Sedlacek, Kyra Michalova, Renata Formankova, Marie Jarošová, Martina Hruba, Zuzana Zemanova, Libuse Babicka, Milena Holzerova, Jan Trka, Lenka Pavlistova, Alena Vrzalova, Alexandra Oltová, Katerina Muzikova, Vladimír Mihál, Jan Zuna
Publikováno v:
ResearcherID
Cryptic translocation t(12;21)(p13;q22) which give origin to the ETV6/RUNX1 hybrid gene can be found by I-FISH in approximately 20–25% of children with B precursor ALL as the most frequent specific aberration. This translocation is generally associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34bc2235ed6df12c3bfd93b436a13cf6
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000242440003069&KeyUID=WOS:000242440003069
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000242440003069&KeyUID=WOS:000242440003069