Mgr. Martina Raudenská, Ph.D.
Researcher, Department of Physiology
Office: bldg. A20/215
Kamenice 753/5
625 00 Brno
Phone: | +420 549 49 8526 |
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E‑mail: |
social and academic networks: |
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Total number of publications: 140
2011
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Interleukin-1 gene variations in post-orthodontic external root resorption
Year: 2011, type: Conference abstract
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Mutation Analysis Ion Channel Genes Ventricular Fibrillation Survivors with Coronary Artery Disease
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, year: 2011, volume: 34, edition: 6, DOI
2010
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Four promoter polymorphisms (-1823T/C, -1744 G/C, -834 C/T a -775 A/T) in SCN5A gene in ischemic patients with impantable cardiovertor defibrillator
Year: 2010, type: Conference abstract
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Mutation analysis of ion channel genes in ventricular fibrillation survivors with coronary artery disease
Year: 2010, type: Conference abstract
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Risk genotypes in SCN5A and ANK2 genes for hyperthrophy in patients with severe arrhythmias
Year: 2010, type: Conference abstract
2009
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Mutational Screening of SCN5A in Patients Suspected of LQTS
Year: 2009, type: Conference abstract
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Variants of SCN5A gene and severe arrhythmias
Year: 2009, type: Conference abstract
2008
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Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome.
Physiological Research, year: 2008, volume: 57/2008, edition: 6
2007
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Mutational Screening of Human Genes which Are Associated with Long QT Syndrome Occurrence
XI. setkání biochemiků a molekulárních biologů, year: 2007
2006
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Použití metod SSCP a TGGE pro screening kandidátních genů LQTS
X. Pracovní setkání biochemiků a molekulárních biologů, year: 2006