Search Results - "Staffova, Katerina"

Dual Effect of Taxifolin on ZEB2 Cancer Signaling in HepG2 Cells by Dostal, Zdenek, Sebera, Martin, Srovnal, Josef, Staffova, Katerina, Modriansky, Martin

“…Polyphenols, secondary metabolites of plants, exhibit different anti-cancer and cytoprotective properties such as anti-radical, anti-angiogenic,…”
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Epithelial to mesenchymal transition and microRNA expression are associated with spindle and apocrine cell morphology in triple-negative breast cancer by Koleckova, Marketa, Ehrmann, Jiri, Bouchal, Jan, Janikova, Maria, Brisudova, Aneta, Srovnal, Josef, Staffova, Katerina, Svoboda, Marek, Slaby, Ondrej, Radova, Lenka, Vomackova, Katherine, Melichar, Bohuslav, Veverkova, Lucia, Kolar, Zdenek

“…Triple negative breast cancers (TNBC) are a morphologically and genetically heterogeneous group of breast cancers with uncertain prediction of biological…”
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Differences in the importance of microcephaly, dysmorphism, and epilepsy in the detection of pathogenic CNVs in ID and ASD patients by Capkova, Zuzana, Capkova, Pavlina, Srovnal, Josef, Staffova, Katerina, Becvarova, Vera, Trkova, Marie, Adamova, Katerina, Santava, Alena, Curtisova, Vaclava, Hajduch, Marian, Prochazka, Martin

“…Autism spectrum disorders (ASD) and intellectual disabilities (ID) are heterogeneous and complex developmental diseases with significant genetic backgrounds…”
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MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism by Capkova, Pavlina, Srovnal, Josef, Capkova, Zuzana, Staffova, Katerina, Becvarova, Vera, Trkova, Marie, Adamova, Katerina, Santava, Alena, Curtisova, Vaclava, Hajduch, Marian, Prochazka, Martin

“…Autism spectrum disorder (ASD) is a complex heterogeneous developmental disease with a significant genetic background that is frequently caused by rare copy…”
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Haploinsufficiency of BMP4 and OTX2 in the Foetus with an abnormal facial profile detected in the first trimester of pregnancy by Capkova, Pavlina, Santava, Alena, Markova, Ivana, Stefekova, Andrea, Srovnal, Josef, Staffova, Katerina, Durdová, Veronika

“…Interstitial microdeletion 14q22q23 is a rare chromosomal syndrome associated with variable defects: microphthalmia/anophthalmia, pituitary anomalies,…”
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Abstract 5396: Identification of meningioma patients in high risk of tumor recurrence using microRNA profiling by Srovnal, Josef, Balik, Vladimir, Slavik, Hanus, Megova, Magdalena Houdova, Vaverka, Miroslav, Hrabalek, Lumir, Ehrmann, Jiri, Staffova, Katerina, Hajduch, Marian

“…Abstract Introduction: Meningioma represents one of the most common intracranial tumors. They are generally thought to progress from low to high-grade lesions…”
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Abstract 3170: Analysis of copy number variations in meningioma samples using microarrays revealed 22q deletions more frequent in higher grade tumors by Srovnal, Josef, Balik, Vladimir, Ehrmann, Jiri, Vaverka, Miroslav, Hrabalek, Lumir, Staffova, Katerina, Hajduch, Marian

“…Abstract Background: Meningiomas represent one of the most common intracranial tumors. They are generally thought to progress from low to high-grade lesions…”
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Abstract 4006: MiRNA profiling in esophageal precancerous for malignancy progression risk assessment by Srovnal, Josef, Slaby, Ondrej, Ehrmann, Jiri, Gregar, Jan, Radova, Lenka, Staffova, Katerina, Hajduch, Marian

“…Abstract Background: Barrett's esophagus (BE) is a metaplastic disease with risk to develop esophageal adenocarcinoma (EAC). Current screening method for BE…”
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Abstract 2717: Identification of three distinct molecular subtypes in meningioma samples using microarrays for copy-number variants by Srovnal, Josef, Balik, Vladimir, Megova, Magdalena Houdova, Ehrmann, Jiri, Vaverka, Miroslav, Hrabalek, Lumir, Trojanec, Radek, Staffova, Katerina, Vrbkova, Jana, Hajduch, Marian

“…Abstract Background: Meningioma represents one of the most common intracranial tumors. They are generally thought to progress from low to high-grade lesions…”
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Haploinsufficiency of BMP4 and OTX2 in the Foetus with an abnormal facial profile detected in the first trimester of pregnancy by Capkova, Pavlina, Santava, Alena, Markova, Ivana, Stefekova, Andrea, Srovnal, Josef, Staffova, Katerina, Durdová, Veronika

“…BACKGROUNDInterstitial microdeletion 14q22q23 is a rare chromosomal syndrome associated with variable defects: microphthalmia/anophthalmia, pituitary…”
Get full text