Výsledky vyhledávání - "Dita Zezulkova"

Presence of heterozygous ATM deletion may not be critical in the primary response of chronic lymphocytic leukemia cells to fludarabine

Autor: Jana Šmardová, Martin Klabusay, David Potesil, Michael Doubek, Jitka Chumchalová, Marek Borsky, Dita Zezulkova, Šárka Pospíšilová, Jiri Mayer, Vera Novakova, Ludmila Rocnova, Sona Cejkova, Yvona Brychtová, Martin Trbušek

Publikováno v: European Journal of Haematology. 82:133-142

Objectives: Abnormalities of the TP53 or ATM, cooperating tumor-suppressor genes, significantly worsen the treatment options for chronic lymphocytic leukemia (CLL) patients. Although the aberrations seem to be mutually exclusive in this leukemia, ina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62c80a18ba1277cef423369bc524d54c
https://doi.org/10.1111/j.1600-0609.2008.01177.x

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Identification of 2.3-Mb Gene Locus for Congenital Aural Atresia in 18q22.3 Deletion

Autor: Petr Kuglík, Dita Zezulkova, Renata Gaillyová, Zuzana Dostalova, Ivo Slapak, Mojmir Lejska, Ales Dostal, Jitka Nemeckova, Vladimíra Vranová

Publikováno v: Otology & Neurotology. 27:427-432

18q deletion syndrome is a multiple-anomaly mental retardation syndrome associated with congenital aural atresia. The purpose of this study was to determine the frequency of the congenital aural atresia phenotype in 18q deletion syndrome patients and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73435e543baa8e51a8dece6602584989
https://doi.org/10.1097/00129492-200604000-00022

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Low-level copy number changes of MYC genes have a prognostic impact in medulloblastoma

Autor: Hana Filková, Martina Pešáková, Iva Slámová, Renata Veselská, Dagmar Kantorová, Eva Nečesalová, Jaroslav Sterba, Lenka Tomášiková, Zdenek Pavelka, Iva Staniczková Zambo, Dita Zezulkova, Karel Zitterbart, Petr Kuglík, Vladimíra Vranová

Publikováno v: Journal of neuro-oncology. 102(1)

High-level amplifications of MYC genes are associated with poor outcomes in childhood medulloblastoma (MB). However, the occurrence of MYCN and MYCC copy number increases below the intense amplification pattern is rarely reported, and its clinical im

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bf35c8b399663af73667c805a6736a3
https://pubmed.ncbi.nlm.nih.gov/20607354

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