Search Results - "Gabcova, D"
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Molecular analysis of genes involved in lipoprotein lipase deficiency in Slovak patients with familial chylomicronemia
Published in Atherosclerosis (01-09-2016)Get full text
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Contemporary skull development - palatal angle analysis
Published in Bratislavské lékarské listy (2015)“…The palatal angle is an important angle of the craniofacial complex. It is significant for the diagnosis of craniofacial disorders mainly for nasopharyngeal…”
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The molecular genetic background of familial hypercholesterolemia: data from the Slovak nation-wide survey
Published in Physiological research (01-01-2017)“…Familial hypercholesterolemia (FH) is most frequently caused by LDLR or APOB mutations. Therefore, the aim of our study was to examine the genetic background…”
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Molecular-genetic aspects of familial hypercholesterolemia
Published in Endocrine regulations (Bratislava) (01-07-2015)“…Familial hypercholesterolemia (FH) is the world's most abundant and the most common heritable disorder of lipid metabolism. The prevalence of the disease in…”
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Age of obesity onset in MC4R mutation carriers
Published in Endocrine regulations (Bratislava) (01-07-2015)“…The mutations in gene for the melanocortin-4 receptor (MC4R) are the most common etiology factors of monogenic obesity development. Recently, it has been shown…”
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Further characterization of the role of Pso2 in the repair of DNA interstrand cross-link-associated double-strand breaks in Saccharomyces cerevisiae
Published in Neoplasma (2007)“…DNA interstrand cross-links (ICL) are thought to be one of the most lethal forms of DNA damage. Therefore, they present a colossal challenge for the DNA damage…”
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