Academic article
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Christensen, Anne Elisabeth; Cristea, Ileana; Stevenson, Thomas Michael James
et al. (2025). On subcellular distribution of the zinc finger 469 protein (ZNF469) and observed discrepancy in the localization of endogenous and overexpressed ZNF469. (external link)
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Gladkauskas, Titas; Rundgren, Ida Marie; Cristea, Ileana
et al. (2025). Treatment Options for Alkali Burn-Induced Corneal Neovascularization: A Comparative Analysis of Two Tyrosine Kinase Inhibitors. (external link)
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Gladkauskas, Titas; Cristea, Ileana; Mehrasa, Roya
et al. (2025). Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overview. (external link)
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Gladkauskas, Titas; Cristea, Ileana; Mehrasa, Roya
et al. (2025). Temperature as a Key Modulator: Investigating Phosphorylation Patterns of p.Asn666 PDGFRB Variants and Their Role in Downstream Signaling. (external link)
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Cristea, Ileana; Abarca, Hugo; Christensen, Anne Elisabeth
et al. (2023). A Pellino-2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium–digital keloid dysplasia. (external link)
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Mehrasa, Roya; Cristea, Ileana; Bredrup, Cecilie
et al. (2023). Functional characterization of all-trans retinoic acid-induced differentiation factor (ATRAID). (external link)
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Bredrup, Cecilie; Cristea, Ileana; Safieh, Leen Abu
et al. (2021). Temperature-dependent autoactivation associated with clinical variability of PDGFRB Asn666 substitutions. (external link)
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Cristea, Ileana; Bruland, Ove; Aukrust, Ingvild
et al. (2021). Pellino-2 in nonimmune cells: novel interaction partners and intracellular localization. (external link)
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Cristea, Ileana; Bruland, Ove; Rødahl, Eyvind
et al. (2021). K+ regulates relocation of Pellino-2 to the site of NLRP3 inflammasome activation in macrophages. (external link)
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Bredrup, Cecilie; Stokowy, Tomasz; McGaughran, Julie
et al. (2018). A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome.. (external link)
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Xu, Linda Zi Yan; Jensen, Hanne; Johnston, Jennifer
et al. (2018). Recurrent, activating variants in the receptor tyrosine kinase DDR2 cause Warburg-Cinotti syndrome. (external link)
See a complete overview of publications in Cristin.
