Search Results - "Schwarzová, Lucie"

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    Tick-borne encephalitis virus expansion to higher altitudes correlated with climate warming by Danielová, Vlasta, Schwarzová, Lucie, Materna, Jan, Daniel, Milan, Metelka, Ladislav, Holubová, Jaroslava, Kříž, Bohumír

    “…Abstract Since 2002, the expansion of Ixodes ricinus ticks and tick-borne infection agents have been studied in the Krkonoše Mts., Czech Republic. Tick-borne…”
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    Extension of Ixodes ricinus ticks and agents of tick-borne diseases to mountain areas in the Czech Republic by Danielová, Vlasta, Rudenko, Natalia, Daniel, Milan, Holubová, Jaroslava, Materna, Jan, Golovchenko, Maryna, Schwarzová, Lucie

    “…Along with the shift of the hard tick Ixodes ricinus to higher altitudes observed in the Czech Republic a corresponding shift of tick-borne infections to…”
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    Synchronous gastric and sebaceous cancers, a rare manifestation of MLH1-related Muir-Torre syndrome by Svec, Jiří, Schwarzová, Lucie, Janošíková, Bohumila, Stekrová, Jitka, Mandys, Václav, Kment, Milan, Vodička, Pavel

    “…Muir-Torre syndrome (MTS), a rare variant of the hereditary non polyposis colorectal cancer syndrome, is an autosomal dominant genodermatosis characterised by…”
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    Aggressive behaviour in subadult and adult black redstarts: status-signalling strategy by SCHWARZOVA, Lucie

    Published in Journal of ethology (2010)
    “…In some birds, yearling males (subadults) are less brightly coloured than the adult ones. To explain this phenomenon known as delayed plumage maturation (DPM),…”
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    Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families by Schwarzová, Lucie, Štekrová, Jitka, Florianová, Martina, Novotný, Aleš, Schneiderová, Michaela, Lněnička, Petr, Kebrdlová, Věra, Kotlas, Jaroslav, Veselá, Kamila, Kohoutová, Milada

    Published in Familial cancer (01-03-2013)
    “…Familial adenomatous polyposis (FAP) is an autosomal dominant syndrome with almost 100 % risk of colorectal cancer. The typical FAP is characterized by…”
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    Molecular genetics of hypercholesterolemia by Schwarzová, Lucie

    Published in Vnitřní lékar̆stvĭ (2016)
    “…The review focuses on the molecular background of an inborn error of lipid metabolism -familial hypercholesterolemia. FH describes a group of genetic defects…”
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    Hyperlipoproteinemia and dyslipidemia as rare diseases. Diagnostics and treatment by Češka, Richard, Štulc, Tomáš, Votavová, Lucie, Schwarzová, Lucie, Vaclová, Martina, Freiberger, Tomáš

    Published in Vnitřní lékar̆stvĭ (2016)
    “…Hyperlipoproteinemia (HLP) and dyslipidemia (DLP) are of course mainly perceived as diseases of common incidence and are typically seen as the greatest risk…”
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    The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case–Control Study by Hubacek, Jaroslav A., Dlouha, Dana, Adamkova, Vera, Schwarzova, Lucie, Lanska, Vera, Ceska, Richard, Satny, Martin, Vrablik, Michal

    Published in Molecular diagnosis & therapy (01-08-2019)
    “…Background Plasma triglyceride (TG) values are significant predictors of cardiovascular and total mortality. The plasma levels of TGs have an important genetic…”
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    Molecular characteristics of mismatch repair genes in sporadic colorectal tumors in Czech patients by Vymetalkova, Veronika Polakova, Slyskova, Jana, Korenkova, Vlasta, Bielik, Ludovit, Langerova, Lucie, Prochazka, Pavel, Rejhova, Alexandra, Schwarzova, Lucie, Pardini, Barbara, Naccarati, Alessio, Vodicka, Pavel

    Published in BMC genetics (31-01-2014)
    “…Mismatch repair (MMR) genes are known to be frequently altered in colorectal cancer (CRC). Both genetics and epigenetics modifications seems to be relevant in…”
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    A novel c. 204 Ile68Met germline variant in exon 2 of the mutL homolog 1 gene in a colorectal cancer patient by VODICKA, PAVEL, CAJA, FABIAN, VYMETALKOVA, VERONIKA, PROCHAZKA, PAVEL, VODICKOVA, LUDMILA, SCHWARZOVA, LUCIE, SLYSKOVA, JANA, KUMAR, RAJIV, SCHNEIDEROVA, MICHAELA

    Published in Oncology letters (01-01-2015)
    “…Mutations in the mutL homolog 1 (MLH1) gene are frequent in patients with hereditary non-polyposis colorectal cancer (CRC). The MLH1 gene was screened for…”
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