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Dr LAURA SIDNEY's Outputs (3)

Cultivation and characterisation of the surface markers and carbohydrate profile of human corneal endothelial cells (2016)
Journal Article
Nagymihály, R., Veréb, Z., Albert, R., Sidney, L., Dua, H., Hopkinson, A., & Petrovski, G. (2017). Cultivation and characterisation of the surface markers and carbohydrate profile of human corneal endothelial cells. Clinical and Experimental Ophthalmology, 45(5), 509-519. https://doi.org/10.1111/ceo.12903

Background
The study aims to characterise human corneal endothelial cell (HCEnC) cultures generated by the peel?and?digest method based on their surface protein/carbohydrate expression pattern.

Methods
Quantitative polymerase chain reaction was... Read More about Cultivation and characterisation of the surface markers and carbohydrate profile of human corneal endothelial cells.

Terminal sterilization: conventional methods versus emerging cold atmospheric pressure plasma technology for non-viable biological tissues (2016)
Journal Article
Marsit, N. M., Sidney, L. E., Branch, M. J., Wilson, S. L., & Hopkinson, A. (in press). Terminal sterilization: conventional methods versus emerging cold atmospheric pressure plasma technology for non-viable biological tissues. Plasma Processes and Polymers, https://doi.org/10.1002/ppap.201600134

Tissue products are susceptible to microbial contamination from different sources, which may cause disease transmission upon transplantation. Terminal sterilization using gamma radiation, electron-beam, and ethylene oxide protocols are well-establish... Read More about Terminal sterilization: conventional methods versus emerging cold atmospheric pressure plasma technology for non-viable biological tissues.

Corneal keratocyte transition to mesenchymal stem cell phenotype and reversal using serum-free medium supplemented with FGF-2, TGF-ß3 and retinoic acid (2016)
Journal Article
Sidney, L. E., & Hopkinson, A. (in press). Corneal keratocyte transition to mesenchymal stem cell phenotype and reversal using serum-free medium supplemented with FGF-2, TGF-ß3 and retinoic acid. Journal of Tissue Engineering and Regenerative Medicine, https://doi.org/10.1002/term.2316

Keratocytes of the corneal limbal stroma can derive populations of mesenchymal stem cells (MSC) when expanded in vitro. However, once a corneal MSC (cMSC) phenotype is achieved, regaining the keratocyte phenotype can be challenging, and there is no s... Read More about Corneal keratocyte transition to mesenchymal stem cell phenotype and reversal using serum-free medium supplemented with FGF-2, TGF-ß3 and retinoic acid.