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Molecular profile of the NF-κB signalling pathway in human colorectal cancer.
Dobre M, Trandafir B, Milanesi E, Salvi A, Bucuroiu IA, Vasilescu C, Niculae AM, Herlea V, Hinescu ME, Constantinescu G. Dobre M, et al. Among authors: vasilescu c. J Cell Mol Med. 2022 Dec;26(24):5966-5975. doi: 10.1111/jcmm.17545. Epub 2022 Nov 25. J Cell Mol Med. 2022. PMID: 36433652 Free PMC article.
Anti-miR-93-5p therapy prolongs sepsis survival by restoring the peripheral immune response.
Dragomir MP, Fuentes-Mattei E, Winkle M, Okubo K, Bayraktar R, Knutsen E, Qdaisat A, Chen M, Li Y, Shimizu M, Pang L, Liu K, Liu X, Anfossi S, Zhang H, Koch I, Tran AM, Mohapatra S, Ton A, Kaplan M, Anderson MW, Rothfuss SJ, Silasi R, Keshari RS, Ferracin M, Ivan C, Rodriguez-Aguayo C, Lopez-Berestein G, Georgescu C, Banerjee PP, Basar R, Li Z, Horst D, Vasilescu C, Bertilaccio MTS, Rezvani K, Lupu F, Yeung SC, Calin GA. Dragomir MP, et al. Among authors: vasilescu c. J Clin Invest. 2023 Jul 17;133(14):e158348. doi: 10.1172/JCI158348. J Clin Invest. 2023. PMID: 37261908 Free PMC article.
Pelvic Exenteration - Past, Present and Future.
Duduş L, Minciună CE, Tudor Ș, Lăcătuş M, Vasilescu C. Duduş L, et al. Among authors: vasilescu c. Chirurgia (Bucur). 2024 Apr;119(2):201-210. doi: 10.21614/chirurgia.2024.v.119.i.2.p.201. Chirurgia (Bucur). 2024. PMID: 38743833
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Aleo SJ, Del Dotto V, Romagnoli M, Fiorini C, Capirossi G, Peron C, Maresca A, Caporali L, Capristo M, Tropeano CV, Zanna C, Ross-Cisneros FN, Sadun AA, Pignataro MG, Giordano C, Fasano C, Cavaliere A, Porcelli AM, Tioli G, Musiani F, Catania A, Lamperti C, Marzoli SB, De Negri A, Cascavilla ML, Battista M, Barboni P, Carbonelli M, Amore G, La Morgia C, Smirnov D, Vasilescu C, Farzeen A, Blickhaeuser B, Prokisch H, Priglinger C, Livonius B, Catarino CB, Klopstock T, Tiranti V, Carelli V, Ghelli AM. Aleo SJ, et al. Among authors: vasilescu c. Cell Rep Med. 2024 Feb 20;5(2):101383. doi: 10.1016/j.xcrm.2023.101383. Epub 2024 Jan 24. Cell Rep Med. 2024. PMID: 38272025 Free PMC article.
Recessive TMOD1 mutation causes childhood cardiomyopathy.
Vasilescu C, Colpan M, Ojala TH, Manninen T, Mutka A, Ylänen K, Rahkonen O, Poutanen T, Martelius L, Kumari R, Hinterding H, Brilhante V, Ojanen S, Lappalainen P, Koskenvuo J, Carroll CJ, Fowler VM, Gregorio CC, Suomalainen A. Vasilescu C, et al. Commun Biol. 2024 Jan 2;7(1):7. doi: 10.1038/s42003-023-05670-9. Commun Biol. 2024. PMID: 38168645 Free PMC article.
240 results