Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marek Nemcovic"'
Autor:
Juvissan Aguedo, Marian Vojs, Martin Vrška, Marek Nemcovic, Zuzana Pakanova, Katerina Aubrechtova Dragounova, Oleksandr Romanyuk, Alexander Kromka, Marian Varga, Michal Hatala, Marian Marton, Jan Tkac
Publikováno v:
Nanomaterials, Vol 14, Iss 15, p 1241 (2024)
We investigated the use of boron-doped diamond (BDD) with different surface morphologies for the enhanced detection of nine different peptides by matrix-assisted laser desorption/ionisation mass spectrometry (MALDI-MS). For the first time, we compare
Externí odkaz:
https://doaj.org/article/df6734d9cc2847a298a76650c4e3f75f
Autor:
Juvissan Aguedo, Zuzana Pakanova, Lenka Lorencova, Marek Nemcovic, Peter Kasak, Marek Barath, Pavol Farkas, Jan Tkac
Publikováno v:
Analytica Chimica Acta
In this study, we applied MXene as column cartridge for N-glycan enrichment from human samples with a focus on the analysis of sialic acid linkages using a derivatisation protocol followed by glycan analysis via Matrix Assisted Laser Desorption Ionis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73bb8eb9f356f8d0e94f402a677913f
https://pubmed.ncbi.nlm.nih.gov/36328727
https://pubmed.ncbi.nlm.nih.gov/36328727
Autor:
Filip Pančík, Zuzana Pakanová, Marek Nemčovič, Filip Květoň, Anna Šalingová, Anna Hlavatá, Stanislav Kozmon, Peter Baráth
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 11 (2023)
Abstract Mucopolysaccharidosis IIIA (MPS IIIA) is a lysosomal storage disorder (LSD) caused by deficiency of lysosomal N-sulphoglucosamine sulphohydrolase, which is one of four enzymes involved in heparan sulfate degradation. Traditional methods used
Externí odkaz:
https://doaj.org/article/3057a8bed4784423b7c36be11fca0b28
Autor:
Maroš Krchňák, Rebeka Kodríková, Mária Matulová, Marek Nemčovič, Iveta Uhliariková, Jaroslav Katrlík, Anna Šalingová, Anna Hlavatá, Katarína Juríčková, Peter Baráth, Ján Mucha, Zuzana Pakanová
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 2, p 39 (2023)
Background: Alpha-mannosidosis is a rare lysosomal storage disorder, caused by decreased activity of α-D-mannosidase. This enzyme is involved in the hydrolysis of mannosidic linkages in N-linked oligosaccharides. Due to the mannosidase defect, undig
Externí odkaz:
https://doaj.org/article/b1d5cf5e688d4082a717eda583be8cca
Autor:
Rebeka Kodríková, Zuzana Pakanová, Maroš Krchňák, Mária Šedivá, Sergej Šesták, Filip Květoň, Gábor Beke, Anna Šalingová, Katarína Skalická, Katarína Brennerová, Emília Jančová, Peter Baráth, Ján Mucha, Marek Nemčovič
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 580 (2023)
Congenital disorders of glycosylation (CDG) are a group of rare inherited metabolic disorders caused by a defect in the process of protein glycosylation. In this work, we present a comprehensive glycoprofile analysis of a male patient with a novel mi
Externí odkaz:
https://doaj.org/article/b8f285849fce43669acafaebbecacf11
Autor:
Simona Lenhartová, Marek Nemčovič, Radka Šebová, Mário Benko, Dirk M. Zajonc, Ivana Nemčovičová
Publikováno v:
Crystals, Vol 11, Iss 7, p 820 (2021)
An increasing number of surface-exposed ligands and receptors acting on immune cells are being considered as a starting point in drug development applications. As they are dedicated to manipulating a wide range of immune responses, accurately predict
Externí odkaz:
https://doaj.org/article/8eddae2a8bf843e890847c720c28c050
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