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Year Number of Results
2018 1
2019 2
2020 1
2021 3
2022 1
2023 4
2024 1

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11 results

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Page 1
Deciphering neuronal deficit and protein profile changes in human brain organoids from patients with creatine transporter deficiency.
Broca-Brisson L, Harati R, Disdier C, Mozner O, Gaston-Breton R, Maïza A, Costa N, Guyot AC, Sarkadi B, Apati A, Skelton MR, Madrange L, Yates F, Armengaud J, Hamoudi R, Mabondzo A. Broca-Brisson L, et al. Among authors: mozner o. Elife. 2023 Oct 13;12:RP88459. doi: 10.7554/eLife.88459. Elife. 2023. PMID: 37830910 Free PMC article.
Potential role of the ABCG2-Q141K polymorphism in type 2 diabetes.
Szabó E, Kulin A, Mózner O, Korányi L, Literáti-Nagy B, Vitai M, Cserepes J, Sarkadi B, Várady G. Szabó E, et al. Among authors: mozner o. PLoS One. 2021 Dec 2;16(12):e0260957. doi: 10.1371/journal.pone.0260957. eCollection 2021. PLoS One. 2021. PMID: 34855903 Free PMC article.
Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia.
Pálinkás M, Szabó E, Kulin A, Mózner O, Rásonyi R, Juhász P, Nagy K, Várady G, Vörös D, Zámbó B, Sarkadi B, Poór G. Pálinkás M, et al. Among authors: mozner o. Clin Exp Med. 2023 Aug;23(4):1277-1284. doi: 10.1007/s10238-022-00848-7. Epub 2022 Aug 8. Clin Exp Med. 2023. PMID: 35939175 Free PMC article.
11 results