Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Šalingová A"'
Autor:
Adriana Adamičková, Jan Kyselovic, Matúš Adamička, Nikola Chomaničová, Simona Valášková, Barbara Šalingová, Miroslava Molitorisová, Zdenko Červenák, Ľuboš Danišovič, Andrea Gažová
Publikováno v:
Medicina, Vol 60, Iss 5, p 787 (2024)
Background and Objectives: Stem cell-based regeneration strategies have shown therapeutic efficacy in various fields of regenerative medicine. These include bone healing after bone augmentation, often complicated by pain, which is managed by using no
Externí odkaz:
https://doaj.org/article/84e11285d51443f3b3ae21b6c2759100
Autor:
Zdenko Červenák, Filip Červenák, Adriana Adamičková, Barbara Šalingová, Andrea Gažová, Ján Kyselovič
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background Quantitative RT-PCR is a valuable tool for assessing the gene expression in different human tissues, particularly due to its exceptional sensitivity, accuracy and reliability. However, the choice of adequate control for normalizat
Externí odkaz:
https://doaj.org/article/0833aa58abaf47d790a744b4d60f2e80
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
Akademický článek
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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
Publikováno v:
In Analytical Biochemistry 15 May 2018 549:113-118
Autor:
Stanik, Juraj, Skopkova, Martina, Brennerova, Katarina, Danis, Daniel, Rosolankova, Monika, Salingova, Anna, Bzduch, Vladimir, Klimes, Iwar, Gasperikova, Daniela
Publikováno v:
In Diabetes Research and Clinical Practice April 2017 126:144-150
Publikováno v:
Chemical Papers. 77:2193-2199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b17a61cccf9dcf2806abca2454856e
https://doi.org/10.1007/s11696-022-02622-1
https://doi.org/10.1007/s11696-022-02622-1
Publikováno v:
Zdravotnicke listy; 2023, Vol. 11 Issue 4, p71-77, 7p