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Items where Author is "Meimaridou, Eirini"

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Number of items: 12.

Terry, Cassandra, Meimaridou, Eirini, Jorfi, Samireh, Ramchurn, Medah and Encinas, Mabel (2024) “Sweet” detectives: children crack the case for a healthy future. The Biochemist. pp. 1-5. ISSN 1740-1194

Kidd, Elliot, Mooruth, Ravi, Meimaridou, Eirini, Walley, Andrew and Fairbrother, Una (2024) DNA extraction methodologies for ultra long nanopore sequencing to determine chromosome specific rodent telomere lengths. In: ESHG 2024 - European Human Genetics Conference, 1-4 June, Berlin. (In Press)

Kidd, Elliot, Meimaridou, Eirini, Williams, Jack L., Metherell, LA, Walley, Andrew and Fairbrother, Una (2024) Choice of gDNA isolation method has a significant impact on average murine Telomere Length estimates. Preparative Biochemistry & Biotechnology, 54 (6). pp. 788-795. ISSN 1532-2297

Kidd, Elliot, Meimaridou, Eirini, Walley, Andrew and Fairbrother, Una (2023) Adapted qPCR methodology to detect telomere oxidative damage (TOD) associated with telomere attrition (TA) in murine tissue. In: ISHG - Irish society of Human Genetics - 26th Meeting, 2023, 22nd September 2023, Galway, Eire.

Kidd, Elliot, Meimaridou, Eirini, Walley, Andrew and Fairbrother, Una (2023) Telomere oxidation status (TOS) is correlated with relative telomere length (RTL) across different mouse tissues but not with nicotinamide nucleotide transhydrogenase (Nnt) status. In: ESHG 2023 - 56th European Society of Human Genetics Conference, 10-13th June 2023, Glasgow.

Williams, Jack L., Hall, Charlotte L., Meimaridou, Eirini and Metherell, Louise A. (2021) Loss of NNT increases expression of oxidative phosphorylation complexes in C57BL/6J hearts. International Journal of Molecular Sciences, 22 (11). pp. 1-12. ISSN 1422-0067

Williams, Jack L., Paudyal, Anju, Awad, Sherine, Nicholson, James, Grzesik, Dominika, Botta, Joaquin, Meimaridou, Eirini, Maharaj, Avinaash, Stewart, Michelle, Tinker, Andrew, Cox, Roger D. and Metherell, Louise A. (2020) Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not. Life Science Alliance, 3 (4). pp. 1-15. ISSN 2575-1077

Davies, Kate and Meimaridou, Eirini (2020) Biological basis of child health 1: understanding the cell and genetics. Nursing children and young people. ISSN 2046-2344

Maharaj, Avinaash, Buonocore, Federica, Meimaridou, Eirini, Ruiz-Babot, Gerard, Guasti, Leonardo, Peng, Hwei-Ming, Capper, Cameron P., Burgos-Tirado, Neikelyn, Prasad, Rathi, Hughes, Claire R., Maudhoo, Ashwini, Crowne, Elizabeth, Cheetham, Timothy D., Brain, Caroline E., Suntharalingham, Jenifer P., Striglioni, Niccolò, Yuksel, Bilgin, Gurbuz, Fatih, Gupta, Sangay, Lindsay, Robert, Couch, Robert, Spoudeas, Helen A., Guran, Tulay, Johnson, Stephanie, Fowler, Dallas J., Conwell, Louise S., McInerney-Leo, Aideen M., Drui, Delphine, Cariou, Bertrand, Lopez-Siguero, Juan P., Harris, Mark, Duncan, Emma L., Hindmarsh, Peter C., Auchus, Richard J., Donaldson, Malcolm D., Achermann, John C. and Metherell, Louise A. (2018) Predicted benign and synonymous variants in CYP11A1 cause primary adrenal insufficiency through missplicing. Journal of the Endocrine Society, 3 (1). pp. 201-221. ISSN 2472-1972

Chortis, Vasileios, Taylor, Angela E., Doig, Craig L., Walsh, Mark D., Meimaridou, Eirini, Jenkinson, Carl, Rodriguez-Blanco, Giovanny, Ronchi, Cristina L., Jafri, Alisha, Metherell, Louise A., Hebenstreit, Daniel, Dunn, Warwick B., Arlt, Wiebke and Foster, Paul A. (2018) Nicotinamide Nucleotide Transhydrogenase as a novel treatment target in adrenocortical carcinoma. Endocrinology, 159 (8). pp. 2836-2849. ISSN 1945-7170

Meimaridou, Eirini, Goldsworthy, Michelle, Chortis, Vasileios, Fragouli, Elpida, Foster, Paul A., Arlt, Wiebke, Cox, Roger D. and Metherell, Louise A. (2018) NNT is a key regulator of adrenal redox homeostasis and steroidogenesis in male mice. Journal of Endocrinology, 236 (1). pp. 13-28. ISSN 1479-6805

Prasad, Rathi, Hadjidemetriou, Irene, Maharaj, Avinaash, Meimaridou, Eirini, Buonocore, Federica, Saleem, Moin, Hurcombe, Jenny, Bierzynska, Agnieszka, Barbagelata, Eliana, Bergadá, Ignacio, Cassinelli, Hamilton, Das, Urmi, Krone, Ruth, Hacihamdioglu, Bulent, Sari, Erkan, Yesilkaya, Ediz, Storr, Helen L., Clemente, Maria, Fernandez-Cancio, Monica, Camats, Nuria, Ram, Nanik, Achermann, John C., Van Veldhoven, Paul P., Guasti, Leonardo, Braslavsky, Debora, Guran, Tulay and Metherell, Louise A. (2017) Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. Journal of Clinical Investigation, 127 (3). pp. 942-953. ISSN 0021-9738

This list was generated on Thu Nov 21 22:26:31 2024 UTC.