Výpis publikací

BOULET, Inge, Markéta BÉBAROVÁ, Roel SPÄTJENS, Jan GEELEN, Roselie JONGBLOED, Yvonne ARENS, Joep GERAEDTS, Harry CRIJNS a Paul VOLDERS. LQT1 mutation K557E: Clinical and biophysical characteristics including cAMP-mediated regulation. 2009. ISSN 1547-5271.

RAUDENSKÁ, Martina, Tomáš NOVOTNÝ, Alexandra BITTNEROVÁ a Anna VAŠKŮ. Mutational Screening of SCN5A in Patients Suspected of LQTS. In European Journal of Heart Failure Supplements 2009; Vol. 8(2). 2009.

CHRISTÉ, Georges, Mohamed CHAHINE, Philippe CHEVALIER a Michal PÁSEK. Changes in action potentials and intracellular ionic homeostasis in a ventricular cell model related to a persistent sodium current in SCN5A mutations underlying LQT3. Progress in Biophysics and Molecular Biology. Great Britain: Elsevier Ltd., 2008, roč. 96, 1-3, s. 281-293, 12 s. ISSN 0079-6107.

RAUDENSKÁ, Martina, Alexandra BITTNEROVÁ, Tomáš NOVOTNÝ, Alena FLORIÁNOVÁ, Karel CHROUST, Renata GAILLYOVÁ, Bořivoj SEMRÁD, Jitka KADLECOVÁ, Martina ŠIŠÁKOVÁ, Ondřej TOMAN a Jindřich ŠPINAR. Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome. Physiological Research. Praha: Akademie věd České republiky, 2008, roč. 57/2008, č. 6, s. 857-862. ISSN 1802-9973.

BÉBAROVÁ, Markéta, Jan GEELEN, Roel SPÄTJENS, Roselie JONGBLOED, Yvonne ARENS a Paul VOLDERS. K557E mutation in C-terminus of KCNQ1 gene as a cause of long QT syndrome. In Physiological Research. 2007. ISSN 0862-8408.

RAUDENSKÁ, Martina, Ivo PAPOUŠEK a Karel CHROUST. Mutational Screening of Human Genes which Are Associated with Long QT Syndrome Occurrence. In XI. setkání biochemiků a molekulárních biologů. Česká republika, Brno: Masarykova univerzita, 2007, s. 35-35. ISBN 978-80-210-4234-6.

BÉBAROVÁ, Markéta, Jan GEELEN, Roselie JONGBLOED, Yvonne ARENS a Paul VOLDERS. Electrophysiological properties of C-terminal KCNQ1 mutation K557E detected in family with long QT syndrome. In Program and abstracts: 7th meeting New Frontiers in Basic Cardiovascular Research. 2006.