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Adoptive transfer of allergen-expressing B cells prevents IgE-mediated allergy.
Prickler L, Baranyi U, Mengrelis K, Weijler AM, Kainz V, Kratzer B, Steiner R, Mucha J, Rudoph E, Pilat N, Bohle B, Strobl H, Pickl WF, Valenta R, Linhart B, Wekerle T. Prickler L, et al. Among authors: mengrelis k. Front Immunol. 2023 Nov 23;14:1286638. doi: 10.3389/fimmu.2023.1286638. eCollection 2023. Front Immunol. 2023. PMID: 38077381 Free PMC article.
T cell phenotype in paediatric heart transplant recipients.
Mengrelis K, Kucera F, Shahid N, Watt E, Ross S, Lau CI, Adams S, Gilmour K, Pils D, Crompton T, Burch M, Davies EG. Mengrelis K, et al. Pediatr Transplant. 2021 Aug;25(5):e13930. doi: 10.1111/petr.13930. Epub 2020 Dec 16. Pediatr Transplant. 2021. PMID: 33326675
Hedgehog Signalling in the Embryonic Mouse Thymus.
Barbarulo A, Lau CI, Mengrelis K, Ross S, Solanki A, Saldaña JI, Crompton T. Barbarulo A, et al. Among authors: mengrelis k. J Dev Biol. 2016 Jul 16;4(3):22. doi: 10.3390/jdb4030022. J Dev Biol. 2016. PMID: 27504268 Free PMC article.
Optimum timing of antithymocyte globulin in relation to adoptive regulatory T cell therapy.
Muckenhuber M, Mucha J, Mengrelis K, How C, Reindl-Schwaighofer R, Heinzel A, Kainz V, Worel N, Berlakovich G, Edinger M, Oberbauer R, Wekerle T. Muckenhuber M, et al. Among authors: mengrelis k. Am J Transplant. 2023 Jan;23(1):84-92. doi: 10.1016/j.ajt.2022.09.002. Epub 2023 Jan 11. Am J Transplant. 2023. PMID: 36695625 Free article.
Thymus transplantation for complete DiGeorge syndrome: European experience.
Davies EG, Cheung M, Gilmour K, Maimaris J, Curry J, Furmanski A, Sebire N, Halliday N, Mengrelis K, Adams S, Bernatoniene J, Bremner R, Browning M, Devlin B, Erichsen HC, Gaspar HB, Hutchison L, Ip W, Ifversen M, Leahy TR, McCarthy E, Moshous D, Neuling K, Pac M, Papadopol A, Parsley KL, Poliani L, Ricciardelli I, Sansom DM, Voor T, Worth A, Crompton T, Markert ML, Thrasher AJ. Davies EG, et al. Among authors: mengrelis k. J Allergy Clin Immunol. 2017 Dec;140(6):1660-1670.e16. doi: 10.1016/j.jaci.2017.03.020. Epub 2017 Apr 8. J Allergy Clin Immunol. 2017. PMID: 28400115 Free PMC article.
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.
Thomas AC, Williams H, Setó-Salvia N, Bacchelli C, Jenkins D, O'Sullivan M, Mengrelis K, Ishida M, Ocaka L, Chanudet E, James C, Lescai F, Anderson G, Morrogh D, Ryten M, Duncan AJ, Pai YJ, Saraiva JM, Ramos F, Farren B, Saunders D, Vernay B, Gissen P, Straatmaan-Iwanowska A, Baas F, Wood NW, Hersheson J, Houlden H, Hurst J, Scott R, Bitner-Glindzicz M, Moore GE, Sousa SB, Stanier P. Thomas AC, et al. Among authors: mengrelis k. Am J Hum Genet. 2014 Nov 6;95(5):611-21. doi: 10.1016/j.ajhg.2014.10.007. Epub 2014 Nov 6. Am J Hum Genet. 2014. PMID: 25439728 Free PMC article.