Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings von Hyblova, Michaela, Harsanyova, Maria, Nikulenkov-Grochova, Diana, Kadlecova, Jitka, Kucharik, Marcel, Budis, Jaroslav, Minarik, Gabriel

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Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing von Andrsova, Irena, MD, Novotny, Tomas, MD, PhD, Kadlecova, Jitka, DrS, PhD, Bittnerova, Alexandra, MA, Vit, Pavel, MD, PhD, Florianova, Alena, MD, Sisakova, Martina, MD, Gaillyova, Renata, MD, PhD, Manouskova, Lenka, RN, Spinar, Jindrich, MD, PhD

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A new homozygous mutation of the KCNQ1 gene associated with both Romano-Ward and incomplete Jervell Lange-Nielsen syndromes in two sisters von Kanovsky, Jan, MD, Novotny, Tomas, MD, PhD, Kadlecova, Jitka, DrS, PhD, Gaillyova, Renata, MD, PhD

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Mutation analysis of ion channel genes promoters in ventricular fibrillation survivors with coronary artery disease von Novotny, Tomas, Raudenska, Martina, Kadlecova, Jitka, Andrsova, Irena, Florianova, Alena, Vasku, Anna, Kozak, Milan, Sepsi, Milan, Krivan, Lubomir, Gaillyova, Renata, Spinar, Jindrich

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Mutation analysis of RyR2 gene in patients after arrhythmic storm von Andršová, I., Novotný, T., Valášková, I., Kadlecová, J., Kuderová, D., Sepši, M., Kozák, M., Křivan, M., Gaillyová, R., Špinar, J.

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Clinical characteristics of three Czech families with catecholaminergic polymorphic ventricular tachycardia and pilot results of RyR2 gene mutation analysis von Novotný, Tomáš, Kubuš, Peter, Vít, Pavel, Floriánová, Alena, Dohnalová, Irena, Valášková, Iveta, Kadlecová, Jitka, Gaillyová, Renata, Švandová, Eva, Špinar, Jindřich

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p73 expression in medulloblastoma: TAp73/ΔNp73 transcript detection and possible association of p73α/ΔNp73 immunoreactivity with survival von Zitterbart, Karel, Zavrelova, Iva, Kadlecova, Jitka, Spesna, Renata, Kratochvilova, Adela, Pavelka, Zdenek, Sterba, Jaroslav

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Clinical Characteristics and Mutational Analysis of the RyR2 Gene in Seven Czech Families with Catecholaminergic Polymorphic Ventricular Tachycardia von ANDRSOVA, IRENA, VALASKOVA, IVETA, KUBUS, PETER, VIT, PAVEL, GAILLYOVA, RENATA, KADLECOVA, JITKA, MANOUSKOVA, LENKA, NOVOTNY, TOMAS

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Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease von NOVOTNY, TOMAS, KADLECOVA, JITKA, RAUDENSKA, MARTINA, BITTNEROVA, ALEXANDRA, ANDRSOVA, IRENA, FLORIANOVA, ALENA, VASKU, ANNA, NEUGEBAUER, PETR, KOZAK, MILAN, SEPSI, MILAN, KRIVAN, LUBOMIR, GAILLYOVA, RENATA, SPINAR, JINDRICH

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Expression of MAGE-A1 and MAGE-A3 in Bone Marrow from Monoclonal Gammapathy to Myeloma Patients von Necasova, Jana, Kadlecova, Jitka, Spesna, Renata, Penka, Miroslav, Hajek, Roman

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p73 expression in medulloblastoma: TAp73/[Delta]Np73 transcript detection and possible association of p73[alpha]/[Delta]Np73 immunoreactivity with survival von Zitterbart, Karel, Zavrelova, Iva, Kadlecova, Jitka, Spesna, Renata, Kratochvilova, Adela, Pavelka, Zdenek, Sterba, Jaroslav

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p73 expression in medulloblastoma: TAp73/ΔNp73 transcript detection and possible association of p73α/ΔNp73 immunoreactivity with survival von Zitterbart, Karel, Zavrelova, Iva, Kadlecova, Jitka, Spesna, Renata, Kratochvilova, Adela, Pavelka, Zdenek, Sterba, Jaroslav

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Monozygotic twins with discordant karyotypes following preimplantation genetic screening and single embryo transfer: case report von Tauwinklova, Gabriela, Gaillyova, Renata, Travnik, Pavel, Oracova, Eva, Vesela, Katerina, Hromadova, Lenka, Vesely, Jan, Musilova, Petra, Rubes, Jiri, Kadlecova, Jitka, Slamova, Iva, Makaturova, Eva, Vranova, Vladimira

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p73 expression in medulloblastoma: TAp73/DeltaNp73 transcript detection and possible association of p73alpha/DeltaNp73 immunoreactivity with survival von Zitterbart, Karel, Zavrelova, Iva, Kadlecova, Jitka, Spesna, Renata, Kratochvilova, Adela, Pavelka, Zdenek, Sterba, Jaroslav

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p73 expression in medulloblastoma: TAp73/[Delta]Np73 transcript detection and possible association of p73[alpha]/[Delta]Np73 immunoreactivity with survival von Zitterbart, Karel, Zavrelova, Iva, Kadlecova, Jitka, Spesna, Renata, Kratochvilova, Adela, Pavelka, Zdenek, Sterba, Jaroslav

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The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano–Ward Syndrome von NOVOTNY, TOMAS, KADLECOVA, JITKA, JANOUSEK, JAN, GAILLYOVA, RENATA, BITTNEROVA, ALEXANDRA, FLORIANOVA, ALENA, SISAKOVA, MARTINA, TOMAN, ONDREJ, CHROUST, KAREL, PAPOUSEK, IVO, SPINAR, JINDRICH

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Occurrence of notched T wave in healthy family members with the long QT interval syndrome von Novotny, Tomas, Sisakova, Martina, Kadlecova, Jitka, Florianova, Alena, Semrad, Borivoj, Gaillyova, Renata, Vlasinova, Jitka, Chroust, Karel, Toman, Ondrej

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CASE REPORTS: The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano-Ward Syndrome von Novotny, Tomas, Kadlecova, Jitka, Janousek, Jan, Gaillyova, Renata, Bittnerova, Alexandra, Florianova, Alena, Sisakova, Martina, Toman, Ondrej, Chroust, Karel, Papousek, Ivo, Spinar, Jindrich

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The Homozygous KCNQ1 Gene Mutation Associated with Recessive Romano-Ward Syndrome von NOVOTNY, TOMAS, KADLECOVA, JITKA, JANOUSEK, JAN, GAILLYOVA, RENATA, BITTNEROVA, ALEXANDRA, FLORIANOVA, ALENA, SISAKOVA, MARTINA, TOMAN, ONDREJ, CHROUST, KAREL, PAPOUSEK, IVO, SPINAR, JINDRICH

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New cytokinin derivatives possess UVA and UVB photoprotective effect on human skin cells and prevent oxidative stress von Hönig, Martin, Plíhalová, Lucie, Spíchal, Lukáš, Grúz, Jiří, Kadlecová, Alena, Voller, Jiří, Svobodová, Alena Rajnochová, Vostálová, Jitka, Ulrichová, Jitka, Doležal, Karel, Strnad, Miroslav

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