Monika Ołdak
Affiliations: | Department of Histology and Embryology | Medical University of Warsaw, Poland |
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| Vella L, Sternjakob A, Lohse S, et al. (2024) The cutaneous beta human papillomavirus type 8 E6 protein induces CCL2 through the CEBPα/miR-203/p63 pathway to support an inflammatory microenvironment in epidermodysplasia verruciformis skin lesions. Frontiers in Cellular and Infection Microbiology. 14: 1336492 |
| Oziębło D, Pazik J, Stępniak I, et al. (2020) Two Novel Pathogenic Variants Confirm Causative Role in Perrault Syndrome with Renal Involvement. Genes. 11 |
| Ścieżyńska A, Soszyńska M, Komorowski M, et al. (2020) Molecular Analysis of the Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles. International Journal of Molecular Sciences. 21 |
| Oziębło D, Sarosiak A, Leja ML, et al. (2019) First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene. Journal of Translational Medicine. 17: 351 |
| Sarosiak A, Udziela M, Ścieżyńska A, et al. (2018) Clinical diversity in patients with Schnyder corneal dystrophy-a novel and known UBIAD1 pathogenic variants. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. 256: 2127-2134 |
| Podgórska M, Ołdak M, Marthaler A, et al. (2018) Chronic Inflammatory Microenvironment in Epidermodysplasia Verruciformis Skin Lesions: Role of the Synergism Between HPV8 E2 and C/EBPβ to Induce Pro-Inflammatory S100A8/A9 Proteins. Frontiers in Microbiology. 9: 392 |
| Lechowicz U, Pollak A, Frączak A, et al. (2018) Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss. Molecular Medicine Reports. 17: 1782-1790 |
| Ścieżyńska A, Ruszkowska E, Szulborski K, et al. (2017) Processing of OPA1 with a novel N-terminal mutation in patients with autosomal dominant optic atrophy: Escape from nonsense-mediated decay. Plos One. 12: e0183866 |
| Jacoszek A, Pollak A, Płoski R, et al. (2017) Advances in genetic hearing loss: CIB2 gene. European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (Eufos) : Affiliated With the German Society For Oto-Rhino-Laryngology - Head and Neck Surgery. 274: 1791-1795 |
| Ołdak M, Ruszkowska E, Siwiec S, et al. (2017) ORF15 exon of the RPGR gene in retinitis pigmentosa – technically difficult, diagnostically important. Klinika Oczna. 2016: 139-143 |