Fakulta prírodných vied

Mgr. Dominika-Vešelényiová

doktorand

  • Téma práce: Identifikácia a štúdium kalpaínov u eukaryotických mikroorganizmov, najmä euglenoidných bičíkovcov. Evolúcia a fylogenetika zástupcov Euglenozoa, bioinformatická analýza genómov, transkriptómov a proteómov.
  • Zameranie: Magisterský titul získala na Prírodovedeckej fakulte Univerzity Komenského - genetika (2017). V rámci externých projektov výskum v oblasti klinickej genetiky, výskum a diagnostika vzácnych genetických ochorení
  • Projekty:
  • Publikácie:
  1. S. PAOLACCI, A. BORRELLI, L. STUPPIA, F.C. CAMPANILE, T. DALLAVILLA, J. KRAJČOVIČ, D. Vešelényiová, T. BECCARI, V. UNFER, M. BERTELLI; GENEOB PROJECT. Mendelian obesity, molecular pathways and pharmacological therapies: a review. European review for medical and pharmacological sciences, 2019, 23: 1357-1378.
  2. Vanda Adamcová, Ascensionato Carna, Martin Valica, D. Vešelényiová, Jozef Krajčovič, Miroslav Horník. Removal of Cd and Zn by living euglena gracilis from aqueous solutions. Journal of Biotechnology, 2019, 305: S42.
  3. Vešelényiová D., KRAJCOVIC J., Kalpainy - cysteínové proteázy a ich biomedicínsky význam. Zpravodaj Československej Biologickej spoločnosti, 2019, (1)
  4. Vešelényiová D., Krajčovič J., 2019. Calpain proteases in the flagellate Euglena gracilis and Euglena longa. In: European journal of phycology 54(1), 182-182.
  5. Raabová L., Císarová M., Vešelényiová D., Krajčoviechová I., 2019. Impact of antibiotics on microscopic phototrophs in water environment. In: European journal of phycology 54(1), 162-162
  6. Michelini S, Amato B, Kenanoglu S, Vešelényiová D., Dautaj A, Kurti D, Baglivo M, Dundar M, Krajcovic J, Miggiano GA, Aquilanti B, Matera G, Velluti V, Gagliardi L, Basha SH, Bertelli M. Rare PECAM1 variants in three families with lymphedema. Lymphology. 2020;53(3):141-151. PMID: 33350288.
  7. Michelini S, Ricci M, Serrani R, Barati S, Kenanoglu S, Vešelényiová D., Kurti D, Baglivo M, Basha SH, Priya S, Dautaj A, Dundar M, Krajcovic J, Bertelli M. NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants. Mol Genet Genomic Med. 2020 Nov 28:e1529. doi: 10.1002/mgg3.1529. Epub ahead of print. PMID: 33247628.
  8. Michelini S, Amato B, Ricci M, Kenanoglu S, Vešelényiová D., Kurti D, Baglivo M, Manara E, Dundar M, Krajcovic J, Basha SH, Priya S, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Velluti V, Gagliardi L, Dautaj A, Bertelli M. Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema. Genes (Basel). 2020 Nov 17;11(11):1361. doi: 10.3390/genes11111361. PMID: 33212964; PMCID: PMC7698471.
  9. Ricci M, Daolio C, Amato B, Kenanoglu S, Vešelényiová D., Kurti D, Dautaj A, Baglivo M, Basha SH, Priya S, Serrani R, Dundar M, Krajcovic J, Bertelli M. Review of the function of SEMA3A in lymphatic vessel maturation and its potential as a candidate gene for lymphedema: Analysis of three families with rare causative variants. Lymphology. 2020;53(2):63-75. PMID: 33190429.
  10. Michelini S, Ricci M, Serrani R, Stuppia L, Beccari T, Vešelényiová D., Kenanoglu S, Barati S, Kurti D, Baglivo M, Basha SH, Krajcovic J, Dundar M, Bertelli M. Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants. Lymphat Res Biol. 2020 Sep 22. doi: 10.1089/lrb.2020.0030. Epub ahead of print. PMID: 32960152.
  11. Michelini S, Ricci M, Vešelényiová D., Kenanoglu S, Kurti D, Baglivo M, Fiorentino A, Basha SH, Priya S, Serrani R, Krajcovic J, Dundar M, Dautaj A, Bertelli M. TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema. Int J Mol Sci. 2020 Sep 16;21(18):6780. doi: 10.3390/ijms21186780. PMID: 32947856; PMCID: PMC7555018.
  12. Ricci M, Compagna R, Amato B, Kenanoglu S, Vešelényiová D., Kurti D, Baglivo M, Basha SH, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Marceddu G, Velluti V, Gagliardi L, Dundar M, Krajcovic J, Bertelli M. Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes. Int J Genomics. 2020 Aug 25;2020:3781791. doi: 10.1155/2020/3781791. PMID: 32908855; PMCID: PMC7468673.
  13. Ricci M, Amato B, Barati S, Compagna R, Vešelényiová D., Kenanoglu S, Stuppia L, Beccari T, Baglivo M, Kurti D, Krajcovic J, Serrani R, Dundar M, Basha SH, Chiurazzi P, Bertelli M. Two rare PROX1 variants in patients with lymphedema. Mol Genet Genomic Med. 2020 Oct;8(10):e1424. doi: 10.1002/mgg3.1424 PMID: 32757260; PMCID: PMC7549596.
  14. Ricci M, Serrani R, Amato B, Compagna R, Vešelényiová D., Kenanoglu S, Kurti D, Baglivo M, Krajcovic J, Miggiano GAD, Aquilanti B, Matera G, Velluti V, Gagliardi L, Dundar M, Basha SH, Bertelli M. CYP26B1 and its implications in lymphangiogenesis: Literature review and study of rare variants in two families. Lymphology. 2020;53(1):20-28. PMID: 32521127.
  15. Gatticchi, L., Vešelényiová, D.,, Miertus, J., Maltese, PE., Manara, E., Costantini, A:, Benedetti S., Durovcikova, D., Krajcovic, J., Bertelli, M. Recessive multiple epiphyseal dysplasia and Stargardt disease in two sisters. Molecular Genetics & Genomic Medicine (2021), DOI: 10.1002/mgg3.1630
  16. Krajčovič J., Vešelényiová D., 2021. Calpains - calcium dependent cysteine proteases - their evolution and biomedical importance In: Biotechnology & Biotechnological Equipment 35(1), 25.
  17. Vešelényiová D., Patlevičová A., Schneiderová M., Krajčovič J., 2021. In silico analysis of calpains among pro- and eukaryotic microorganisms. In: Biotechnology & Biotechnological Equipment 35(1), 108.
  18. Kenanoglu S., Vešelényiová D., Michelini S., Maltese E.P., Paolacci S., Krajčovič J., Dundar M., Beccari T., Bertelli M., 2021. Identification of possibly pathogenic variants in candidate genes in lymphedema patients by NGS analysis. In: Biotechnology & Biotechnological Equipment 35(1), 32.

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