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Photochemistry and Photobiology|January 9, 2008
Photodynamic therapy of nonmelanoma skin cancer with topical hypericum perforatum extract--a pilot studyDenisa Kacerovská, Karel Pizinger, Filip Majer, et al.Biomedical Chromatography : BMC|March 16, 2007
Estrogen-induced cholestasis results in a dramatic increase of b-series gangliosides in the rat liverFilip Majer, Ladislav Trnka, Libor Vítek, et al.Biological Chemistry|January 27, 2009
Two aspartic proteinases secreted by the pathogenic yeast Candida parapsilosis differ in expression pattern and catalytic propertiesOlga Hrusková-Heidingsfeldová, Jirí Dostál, Filip Majer, et al.Biological Chemistry|September 16, 2006
Structure-based specificity mapping of secreted aspartic proteases of Candida parapsilosis, Candida albicans, and Candida tropicalis using peptidomimetic inhibitors and homology modelingFilip Majer, Libuse Pavlícková, Pavel Majer, et al.Molecular and Cellular Biochemistry|March 30, 2010
Bioinformatic and biochemical studies point to AAGR-1 as the ortholog of human acid alpha-glucosidase in Caenorhabditis elegansJakub Sikora, Jana Urinovská, Filip Majer, et al.Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 1, 2006
Identification of bilirubin reduction products formed by Clostridium perfringens isolated from human neonatal fecal floraLibor Vítek, Filip Majer, Lucie Muchová, et al.Journal of Inherited Metabolic Disease|January 28, 2022
Loading of cell cultures with cholesterol-dextran particles as a new functional test for Niemann-Pick type C diseaseFilip Majer, Befekadu Asfaw, Ladislav Kuchař, et al.Glycoconjugate Journal|March 3, 2007
Changes in GM1 ganglioside content and localization in cholestatic rat liverMarie Jirkovská, Filip Majer, Jaroslava Smídová, et al.Journal of Inherited Metabolic Disease|May 30, 2013
Mosaic tissue distribution of the tandem duplication of LAMP2 exons 4 and 5 demonstrates the limits of Danon disease cellular and molecular diagnosticsFilip Majer, Ondrej Pelak, Tomas Kalina, et al.Molecular Genetics & Genomic Medicine|April 28, 2020
Spinal muscular atrophy caused by a novel Alu-mediated deletion of exons 2a-5 in SMN1 undetectable with routine genetic testingIvana Jedličková, Anna Přistoupilová, Lenka Nosková, et al.Pageof 2