| Year |
Citation |
Score |
| 2024 |
Vella L, Sternjakob A, Lohse S, Fingerle A, Sperling T, Wickenhauser C, Stöckle M, Vogt T, Roemer K, Ołdak M, Smola S. 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. PMID 38510961 DOI: 10.3389/fcimb.2024.1336492 |
0.649 |
|
| 2020 |
Oziębło D, Pazik J, Stępniak I, Skarżyński H, Ołdak M. Two Novel Pathogenic Variants Confirm Causative Role in Perrault Syndrome with Renal Involvement. Genes. 11. PMID 32911714 DOI: 10.3390/Genes11091060 |
0.32 |
|
| 2020 |
Ścieżyńska A, Soszyńska M, Komorowski M, Podgórska A, Krześniak N, Nogowska A, Smolińska M, Szulborski K, Szaflik JP, Noszczyk B, Ołdak M, Malejczyk J. Molecular Analysis of the Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles. International Journal of Molecular Sciences. 21. PMID 32413971 DOI: 10.3390/Ijms21103430 |
0.355 |
|
| 2019 |
Oziębło D, Sarosiak A, Leja ML, Budde BS, Tacikowska G, Di Donato N, Bolz HJ, Nürnberg P, Skarżyński H, Ołdak M. First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene. Journal of Translational Medicine. 17: 351. PMID 31655630 DOI: 10.1186/S12967-019-2099-5 |
0.301 |
|
| 2018 |
Sarosiak A, Udziela M, Ścieżyńska A, Oziębło D, Wawrzynowska A, Szaflik JP, Ołdak M. 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. PMID 30084067 DOI: 10.1007/S00417-018-4075-9 |
0.306 |
|
| 2018 |
Podgórska M, Ołdak M, Marthaler A, Fingerle A, Walch-Rückheim B, Lohse S, Müller CSL, Vogt T, Ustav M, Wnorowski A, Malejczyk M, Majewski S, Smola S. 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. PMID 29563902 DOI: 10.3389/Fmicb.2018.00392 |
0.712 |
|
| 2018 |
Lechowicz U, Pollak A, Frączak A, Rydzanicz M, Stawiński P, Lorens A, Skarżyński PH, Skarżyński H, Płoski R, Ołdak M. 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. PMID 29257206 DOI: 10.3892/Mmr.2017.8064 |
0.305 |
|
| 2017 |
Ścieżyńska A, Ruszkowska E, Szulborski K, Rydz K, Wierzbowska J, Kosińska J, Rękas M, Płoski R, Szaflik JP, Ołdak M. 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. PMID 28841713 DOI: 10.1371/Journal.Pone.0183866 |
0.354 |
|
| 2017 |
Jacoszek A, Pollak A, Płoski R, Ołdak M. 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. PMID 27771768 DOI: 10.1007/S00405-016-4330-9 |
0.337 |
|
| 2017 |
Ołdak M, Ruszkowska E, Siwiec S, Pollak A, Stawiński P, Szulborski K, Szaflik JP. ORF15 exon of the RPGR gene in retinitis pigmentosa – technically difficult, diagnostically important. Klinika Oczna. 2016: 139-143. DOI: 10.5114/Ko.2016.71690 |
0.315 |
|
| 2016 |
Pollak A, Lechowicz U, Kędra A, Stawiński P, Rydzanicz M, Furmanek M, Brzozowska M, Mrówka M, Skarżyński H, Skarżyński PH, Ołdak M, Płoski R. Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss. Plos One. 11: e0166618. PMID 27941975 DOI: 10.1371/Journal.Pone.0166618 |
0.32 |
|
| 2016 |
Ścieżyńska A, Oziębło D, Ambroziak AM, Korwin M, Szulborski K, Krawczyński M, Stawiński P, Szaflik J, Szaflik JP, Płoski R, Ołdak M. Next-generation sequencing of ABCA4: High frequency of complex alleles and novel mutations in patients with retinal dystrophies from Central Europe. Experimental Eye Research. 145: 93-99. PMID 26593885 DOI: 10.1016/J.Exer.2015.11.011 |
0.331 |
|
| 2016 |
Wertheim-Tysarowska K, Ołdak M, Giza A, Kutkowska-Kaźmierczak AD, Sota J, Przybylska D, Woźniak K, Śniegórska D, Niepokój K, Sobczyńska-Tomaszewska A, Rygiel AM, Płoski R, Bal J, Kowalewski C. Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation. Journal of Applied Genetics. 57: 175-181. PMID 26432462 DOI: 10.1007/S13353-015-0310-9 |
0.352 |
|
| 2016 |
Lechowicz U, Pollak A, Oziębło D, Ołdak M. Pathogenic p.Cys194Metfs*17 variant argues against TMPRSS3/GJB2 digenic inheritance of hearing loss. 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. 273: 1327-8. PMID 26408194 DOI: 10.1007/S00405-015-3782-7 |
0.345 |
|
| 2015 |
Ołdak M, Ruszkowska E, Udziela M, Oziębło D, Bińczyk E, Ścieżyńska A, Płoski R, Szaflik JP. Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level. Biomed Research International. 2015: 640234. PMID 26451375 DOI: 10.1155/2015/640234 |
0.308 |
|
| 2014 |
Ołdak M, Szaflik JP, Ścieżyńska A, Udziela M, Maksym RB, Rymgayłło-Jankowska B, Hofmann-Rummelt C, Menzel-Severing J, Płoski R, Żarnowski T, Kruse FE, Szaflik J. Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene. Cornea. 33: 294-9. PMID 24473223 DOI: 10.1097/Ico.0000000000000062 |
0.306 |
|
| 2014 |
Pahne-Zeppenfeld J, Schröer N, Walch-Rückheim B, Oldak M, Gorter A, Hegde S, Smola S. Cervical cancer cell-derived interleukin-6 impairs CCR7-dependent migration of MMP-9-expressing dendritic cells. International Journal of Cancer. Journal International Du Cancer. 134: 2061-73. PMID 24136650 DOI: 10.1002/ijc.28549 |
0.573 |
|
| 2012 |
Sperling T, Ołdak M, Walch-Rückheim B, Wickenhauser C, Doorbar J, Pfister H, Malejczyk M, Majewski S, Keates AC, Smola S. Human papillomavirus type 8 interferes with a novel C/EBPβ-mediated mechanism of keratinocyte CCL20 chemokine expression and Langerhans cell migration. Plos Pathogens. 8: e1002833. PMID 22911498 DOI: 10.1371/Journal.Ppat.1002833 |
0.681 |
|
| 2011 |
Gatzioufas Z, Oldak M, Schnaidt A, Smola S, Seitz B. Graft-to-host transmission of herpes simplex virus -- myth or reality? Acta Ophthalmologica. 89: e473-4; author reply. PMID 21756291 DOI: 10.1111/j.1755-3768.2011.02192.x |
0.479 |
|
| 2011 |
Oldak M, Tolzmann L, Wnorowski A, Podgórska MJ, Silling S, Lin R, Hiscott J, Müller CS, Vogt T, Smola H, Smola S. Differential regulation of human papillomavirus type 8 by interferon regulatory factors 3 and 7. Journal of Virology. 85: 178-88. PMID 20980500 DOI: 10.1128/Jvi.00998-10 |
0.712 |
|
| 2010 |
Rydzanicz M, Wróbel M, Pollak A, Gawecki W, Brauze D, Kostrzewska-Poczekaj M, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesińska M, Ołdak M, Płoski R, Skarzyński H, Szyfter K. Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss. Biochemical and Biophysical Research Communications. 395: 116-21. PMID 20353758 DOI: 10.1016/J.Bbrc.2010.03.149 |
0.323 |
|
| 2010 |
Oldak M, Maksym RB, Sperling T, Yaniv M, Smola H, Pfister HJ, Malejczyk J, Smola S. Human papillomavirus type 8 E2 protein unravels JunB/Fra-1 as an activator of the beta4-integrin gene in human keratinocytes. Journal of Virology. 84: 1376-86. PMID 19923172 DOI: 10.1128/JVI.01220-09 |
0.619 |
|
| 2010 |
Ołdak M, Kowalewski C, Maksym RB, Woźniak K, Pollak A, Podgórska M, Wnorowski A, Kosińska J, Płoski R. Novel keratin 14 hotspot mutation in Dowling-Meara type of epidermolysis bullosa simplex: strategy to avoid KRT14 pseudogene amplification by a simple approach. Journal of Dermatological Science. 57: 69-70. PMID 19854623 DOI: 10.1016/J.Jdermsci.2009.09.006 |
0.625 |
|
| 2009 |
Dole VS, Smola H, Dooley S, Said HM, Oldak M, Pfister HJ, Smola S. The adenoviral E1A oncoprotein activates the Smad7 promoter: requirement of a functional E-box. International Journal of Oncology. 35: 1493-8. PMID 19885573 |
0.6 |
|
| 2008 |
Pollak A, Mueller-Malesińska M, Skórka A, Kostrzewa G, Ołdak M, Korniszewski L, Skarżyński H, Ploski R. GJB2 and hearing impairment: promoter defects do not explain the excess of monoallelic mutations Journal of Medical Genetics. 45: 607-608. PMID 18762573 DOI: 10.1136/Jmg.2008.059873 |
0.308 |
|
| 2007 |
Pollak A, Skórka A, Mueller-Malesińska M, Kostrzewa G, Kisiel B, Waligóra J, Krajewski P, Ołdak M, Korniszewski L, Skarzyński H, Ploski R. M34T and V37I mutations in GJB2 associated hearing impairment: evidence for pathogenicity and reduced penetrance. American Journal of Medical Genetics. Part A. 143: 2534-43. PMID 17935238 DOI: 10.1002/Ajmg.A.31982 |
0.33 |
|
| 2004 |
Oldak M, Smola H, Aumailley M, Rivero F, Pfister H, Smola-Hess S. The human papillomavirus type 8 E2 protein suppresses beta4-integrin expression in primary human keratinocytes. Journal of Virology. 78: 10738-46. PMID 15367640 DOI: 10.1128/JVI.78.19.10738-10746.2004 |
0.361 |
|
| 2003 |
Hadaschik D, Hinterkeuser K, Oldak M, Pfister HJ, Smola-Hess S. The Papillomavirus E2 protein binds to and synergizes with C/EBP factors involved in keratinocyte differentiation. Journal of Virology. 77: 5253-65. PMID 12692227 DOI: 10.1128/jvi.77.9.5253-5265.2003 |
0.337 |
|
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