Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Libuse Babicka"'
Autor:
Libuse Babicka, Zuzana Zemanova, Filip Kramar, Petr Kozler, Petr Hrabal, Sarka Ransdorfova, Kyra Michalova
Publikováno v:
Journal of Neuro-Oncology. 84:201-211
Specific gene mutations, loss of heterozygosity, deletions and/or amplifications of entire chromosomal regions and gene silencing have been described in gliomas. 82 samples from 81 patients were investigated to detect the deletion of TP53, RB1, CDKN2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6b44f8aa50ebfb33b5152bbf2cc4ce
https://doi.org/10.1007/s11060-007-9358-7
https://doi.org/10.1007/s11060-007-9358-7
Autor:
Lucie Houskova, Zuzana Zemanova, Libuse Babicka, Lenka Pavlistova, Jana Brezinova, Hana Klamova, Jana Moravcová, Sarka Ransdorfova, Kyra Michalova
Publikováno v:
Cancer Genetics and Cytogenetics. 168:22-29
During progression of chronic myeloid leukemia (CML) from the chronic to the accelerated phase and/or blast crisis, clonal evolution with nonrandom secondary aberrations such as +8, +Ph, i(17q), +19, -Y, +21, +17, and -7 is frequently observed. Compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15e62f6ff42126d1e25c6a38c33b8f8d
https://doi.org/10.1016/j.cancergencyto.2005.11.017
https://doi.org/10.1016/j.cancergencyto.2005.11.017
Analysis of complex chromosomal rearrangements in adult patients with MDS and AML by multicolor FISH
Autor:
Kyra Michalova, Jacqueline Maaloufová, Sarka Ransdorfova, M. Siskova, Zuzana Zemanova, Libuse Babicka, Jaroslav Cermak, Lenka Sindelarova, Jana Brezinova
Publikováno v:
Leukemia research. 31(1)
We analyzed complex chromosomal aberrations in 37 adult patients with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) using classical cytogenetic method, FISH with locus-specific probes, multicolor FISH (mFISH) and multicolor banding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eef2a11dd15f4b7348a8ce284867d1d
https://pubmed.ncbi.nlm.nih.gov/16687173
https://pubmed.ncbi.nlm.nih.gov/16687173
Publikováno v:
Journal of Neuro-Oncology; Sep2007, Vol. 84 Issue 2, p201-211, 11p
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
