M. Koudova

Details der Publikationsliste

Zeitraum

2000 - 2000

Anzahl

2

Co-Autoren

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe (2000)

Dork, T, Macek, M, Mekus, F, Tummler, B, Tzountzouris, J, Casals, T, ...

We report a large genomic deletion of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, viz., a deletion that is frequently observed in Central and Eastern Europe. The mutation,...

Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases

Verlaan, M, Drenth, J, Truninger, K, Koudova, M, Schulz, H, Bargetzi, M, ...

Background: Xenobiotic mediated cellular injury is thought to play a major role in the pathogenesis of pancreatic diseases. Genetic variations that reduce the expression or activity of detoxifying...