Marek Nemcovic
Overview
Explore the profile of Marek Nemcovic including associated specialties, affiliations and a list of published articles.
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13
Citations
111
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Recent Articles
1.
Del Greco C, Kuo M, Smith D, Mendes M, Salamons G, Nemcovic M, et al.
Mol Genet Genomic Med
. 2025 Feb;
13(2):e70078.
PMID: 39963003
Background: Mutations in cysteinyl-tRNA synthetase (CARS1) have been implicated in a multisystem disease including microcephaly, developmental delay, and brittle hair and nail phenotypes. Methods: Here, we present a patient with...
2.
Aguedo J, Vojs M, Vrska M, Nemcovic M, Pakanova Z, Dragounova K, et al.
Nanomaterials (Basel)
. 2024 Aug;
14(15).
PMID: 39120346
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...
3.
Kianickova K, Pazitna L, Kundalia P, Pakanova Z, Nemcovic M, Barath P, et al.
Int J Mol Sci
. 2023 May;
24(10).
PMID: 37240090
Changes in protein glycosylation are associated with most biological processes, and the importance of glycomic analysis in the research of disorders is constantly increasing, including in the neurodevelopmental field. We...
4.
Krchnak M, Kodrikova R, Matulova M, Nemcovic M, Uhliarikova I, Katrlik J, et al.
Front Biosci (Landmark Ed)
. 2023 Mar;
28(2):39.
PMID: 36866557
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...
5.
Kodrikova R, Pakanova Z, Krchnak M, Sediva M, Sestak S, Kveton F, et al.
Biomedicines
. 2023 Feb;
11(2).
PMID: 36831116
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...
6.
Aguedo J, Pakanova Z, Lorencova L, Nemcovic M, Kasak P, Barath M, et al.
Anal Chim Acta
. 2022 Nov;
1234:340512.
PMID: 36328727
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...
7.
Ziburova J, Nemcovic M, Sestak S, Bellova J, Pakanova Z, Sivakova B, et al.
Am J Med Genet A
. 2021 Sep;
185(11):3494-3501.
PMID: 34467644
Congenital disorder of glycosylation type Ig (ALG12-CDG) is a rare inherited metabolic disease caused by a defect in alpha-mannosyltransferase 8, encoded by the ALG12 gene (22q13.33). To date, only 15...
8.
Bonaccorsi di Patti M, Cutone A, Nemcovic M, Pakanova Z, Barath P, Musci G
Int J Mol Sci
. 2021 Aug;
22(15).
PMID: 34360993
The ferroxidase ceruloplasmin (CP) plays a crucial role in iron homeostasis in vertebrates together with the iron exporter ferroportin. Mutations in the CP gene give rise to aceruloplasminemia, a rare...
9.
Pazitna L, Nemcovic M, Pakanova Z, Barath P, Aliev T, Dolgikh D, et al.
J Biotechnol
. 2020 Apr;
314-315:34-40.
PMID: 32298669
Glycosylation of therapeutic glycoproteins significantly affects their physico-chemical properties, bioactivity and immunogenicity. The determination of glycan composition is highly important regarding their development and production. Therefore, there is a demand...
10.
Robajac D, Masnikosa R, Nemcovic M, Krizakova M, Belicka Klukova L, Barath P, et al.
Mech Ageing Dev
. 2019 Oct;
183:111151.
PMID: 31589880
Structural changes of glycans are observed in different (patho)physiological conditions. Human placental membrane (glyco)proteins were isolated from the first and third trimester placentas of mothers at different ages. By using...