Výsledky vyhledávání - "Renata Taslerová"

Double trouble': Duchenne muscular dystrophy and osteogenesis imperfecta in one patient - a case report

Autor: Renata Taslerová, Hana Ošlejšková, Lenka Fajkusová, Milan Bayer, Lenka Mrázová

Publikováno v: Bone Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::acc8109482212c543a91a6fa52f7e074
https://doi.org/10.1530/boneabs.4.p50

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Cytogenetics and cytology of retinoblastomas

Autor: Jitka Zluvova, Eva Bártová, Michal Kozubek, Pavla Jirsová, Irena Koutná, Hana Gajová, Renata Taslerová, Stanislav Kozubek

Publikováno v: Journal of Cancer Research and Clinical Oncology. 129:89-99

Chromosomal aberrations and the nuclear topography of retinoblastoma tumour cells as well as lymphocytes of patients suffering from the familiar or sporadic form of retinoblastoma were studied. Fluorescence in situ hybridisation (FISH) on fresh, para

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce27dfe6bbcb254c8511581e589b0470
https://doi.org/10.1007/s00432-003-0414-1

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Localization of genetic elements of intact and derivative chromosome 11 and 22 territories in nuclei of Ewing sarcoma cells

Autor: Michal Kozubek, Stanislav Kozubek, Eva Bártová, Pavla Gajdušková, Renata Taslerová, Roman Kodet

Publikováno v: Journal of structural biology. 155(3)

Recurring chromosomal abnormalities are associated with specific tumour types. The EWSR1 and FLI1 genes are involved in balanced translocation t(11;22)(q24;q12), which is present in more than 85% of Ewing sarcomas. In our previous study, we have foun

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09206a2aa13a50b2047a9eb580c57382
https://pubmed.ncbi.nlm.nih.gov/16837212

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Arrangement of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lymphocytes and Ewing sarcoma cells

Autor: Michal Kozubek, Stanislav Kozubek, Eva Bártová, Renata Taslerová, Emilie Lukášová, Pavla Jirsová

Publikováno v: Human genetics. 112(2)

Standard and repeated fluorescence in situ hybridization and high-resolution cytometry were used to study topographical parameters of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lym

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d46f93a3f129e05a39e3bea4f37f53b0
https://pubmed.ncbi.nlm.nih.gov/12522555

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