Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Zbyněk Houdek"'
Publikováno v:
Advances in experimental medicine and biology. 1376
Embryonic stem cells and induced pluripotent stem cells provided us with fascinating new knowledge in recent years. Mechanistic insight into intricate regulatory circuitry governing pluripotency stemness and disclosing parallels between pluripotency
Autor:
Michaela, Kripnerová, Hamendra Singh, Parmar, Jiří, Šána, Alena, Kopková, Lenka, Radová, Sieghart, Sopper, Krzysztof, Biernacki, Jan, Jedlička, Michaela, Kohoutová, Jitka, Kuncová, Jan, Peychl, Emil, Rudolf, Miroslav, Červinka, Zbyněk, Houdek, Pavel, Dvořák, Kateřina, Houfková, Martin, Pešta, Zdeněk, Tůma, Martina, Dolejšová, Filip, Tichánek, Václav, Babuška, Martin, Leba, Ondřej, Slabý, Jiří, Hatina
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 11
Journal of Clinical Medicine, Vol 10, Iss 2297, p 2297 (2021)
Volume 10
Issue 11
Journal of Clinical Medicine, Vol 10, Iss 2297, p 2297 (2021)
Sarcomas are a heterogeneous group of mesenchymal tumours, with a great variability in their clinical behaviour. While our knowledge of sarcoma initiation has advanced rapidly in recent years, relatively little is known about mechanisms of sarcoma pr
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783031023774
Embryonic stem cells and induced pluripotent stem cells provided us with fascinating new knowledge in recent years. Mechanistic insight into intricate regulatory circuitry governing pluripotency stemness and disclosing parallels between pluripotency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd7dbdb86561b333d3ac74109c90a5e9
https://doi.org/10.1007/5584_2021_663
https://doi.org/10.1007/5584_2021_663
Autor:
Nicolas H. Zech, Milena Králíčková, Lenka Černá, Cedíková M, František Vožeh, Jan Cendelin, Kristýna Krakorová, Vlastimil Kulda, Zbyněk Houdek, Vaclav Babuska
Publikováno v:
Journal of Applied Biomedicine. 12:17-23
The possibility of regeneration in a damaged central nervous system (CNS) is limited and therapy of CNS diseases accompanied with neuronal loss is problematic. Lurcher (Lc) mutant mice represent a model for olivocerebellar degeneration. Heterozygotes
Autor:
Hamendra Singh Parmar, Michaela Kripnerova, Ondrej Slaby, Jiri Sana, Martin Pesta, Pavel Dvorak, Zbyněk Houdek, Kateřina Houfková, Jiří Hatina, Jitka Kuncova
Publikováno v:
ESMO Open. 3:A84-A85
Introduction Soft tissue sarcomas are known for their great variability in clinical behaviour, ranging from almost indolent lesions to rapidly metastasing tumours. Genes responsible for sarcoma progression have been poorly characterised by now. Towar
Publikováno v:
Neuroscience Letters. 515:23-27
Lurcher mutant mice represent a natural model of olivocerebellar degeneration. They serve as a tool to study pathogenesis, the functional impact of the degeneration as well as therapeutic approaches. Wild type littermates are used as healthy controls
Autor:
Milena Králíčková, Hana Kotasová, Jiřina Procházková, Jiří Pacherník, Jan Kučera, Zbyněk Houdek, Iva Vesela
Publikováno v:
Journal of Cellular Biochemistry. 113:563-570
Retinoic acid (RA) is able to induce the differentiation of embryonic stem cells into neuronal lineages. The mechanism of this effect is unknown but it has been evidenced to be dependent on the formation of floating spheroids called embryoid bodies.
Publikováno v:
Journal of Reproductive Immunology. 81:155-156
Autor:
Milena Králíčková, Jan Cendelin, Vaclav Babuska, Vlastimil Kulda, Zbyněk Houdek, Jiří Pacherník, George B. Stefano, Cedíková M, František Vožeh
Publikováno v:
ResearcherID
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
Scopus-Elsevier
Europe PubMed Central
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
Scopus-Elsevier
Europe PubMed Central
Summary Background Neurotransplantation has great potential for future treatments of various neurodegenerative disorders. Preclinically, the Lurcher mutant mouse represents an appropriate model of genetically-determined olivocerebellar degeneration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b920878a17d961dea80135c0c565c6
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000304535900003&KeyUID=WOS:000304535900003
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000304535900003&KeyUID=WOS:000304535900003
Autor:
Čedíková, Miroslava1,2, Houdek, Zbyněk3,4, Babuška, Václav5, Kulda, Vlastimil5, Vožeh, František2,3, Zech, Nicolas6, Černá, Lenka7, Krakorová, Kristýna7, Králíčková, Milena1,2 milena.kralickova@lfp.cuni.cz, Cendelín, Jan2,3
Publikováno v:
Journal of Applied Biomedicine. Jan2014, Vol. 12 Issue 1, p17-23. 7p.