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miR-9-5p suppresses pro-fibrogenic transformation of fibroblasts and prevents organ fibrosis by targeting NOX4 and TGFBR2.
Fierro-Fernández M, Busnadiego Ó, Sandoval P, Espinosa-Díez C, Blanco-Ruiz E, Rodríguez M, Pian H, Ramos R, López-Cabrera M, García-Bermejo ML, Lamas S. Fierro-Fernández M, et al. Among authors: rodriguez m. EMBO Rep. 2015 Oct;16(10):1358-77. doi: 10.15252/embr.201540750. Epub 2015 Aug 27. EMBO Rep. 2015. PMID: 26315535 Free PMC article.
MicroRNAs in the kidney: novel biomarkers of acute kidney injury.
Aguado-Fraile E, Ramos E, Conde E, Rodríguez M, Liaño F, García-Bermejo ML. Aguado-Fraile E, et al. Among authors: rodriguez m. Nefrologia. 2013 Nov 13;33(6):826-34. doi: 10.3265/Nefrologia.pre2013.Aug.12198. Epub 2013 Oct 25. Nefrologia. 2013. PMID: 24158125 Free article. Review.
A genetic risk score predicts recurrent events after myocardial infarction in young adults.
Rincón LM, Sanmartín M, Alonso GL, Rodríguez JA, Muriel A, Casas E, Navarro M, Carbonell A, Lázaro C, Fernández S, González P, Rodríguez M, Jiménez-Mena M, Fernández-Golfín C, Esteban A, García-Bermejo ML, Zamorano JL. Rincón LM, et al. Among authors: rodriguez ja, rodriguez m. Rev Esp Cardiol (Engl Ed). 2020 Aug;73(8):623-631. doi: 10.1016/j.rec.2019.08.006. Epub 2019 Oct 17. Rev Esp Cardiol (Engl Ed). 2020. PMID: 31629691 English, Spanish.
Investigating the impact of screen-sharing visual aids during genomic results disclosure via telehealth in diverse families in the TeleKidSeq pilot study.
Odgis JA, Kelly NR, Sebastin M, Scarimbolo L, Insel BJ, Suckiel SA, Bonini KE, Marathe PN, Di Biase M, Brown K, Gallagher KM, Ramos MA, Rodriguez JE, Yelton N, López Aguiñiga K, Rodriguez MA, María E, Lopez J, Zinberg RE, Diaz GA, Greally JM, Abul-Husn NS, Bauman LJ, Gelb BD, Horowitz CR, Kenny EE, Wasserstein MP. Odgis JA, et al. Among authors: rodriguez ma. Public Health Genomics. 2025 Jan 17:1-24. doi: 10.1159/000542444. Online ahead of print. Public Health Genomics. 2025. PMID: 39827879 Free article.
Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders.
Copeland H, Low KJ, Wynn SL, Ahmed A, Arthur V, Balasubramanian M, Bennett K, Berg J, Bertoli M, Bryson L, Bucknall C, Campbell J, Chandler K, Chauhan J, Clarkson A, Coles R, Conti H, Costello P, Coupar T, Craig A, Dean J, Dillon A, Dixit A, Drew K, Eason J, Forzano F, Foulds N, Gardham A, Ghali N, Green A, Hanna W, Harrison R, Hegarty M, Higgs J, Holder M, Irving R, Jain V, Johnson K, Jolley R, Jones WD, Jones G, Joss S, Kalinauskiene R, Kanani F, Kavanagh K, Khan M, Khan N, Kivuva E, Lahiri N, Lakhani N, Lampe A, Lynch SA, Mansour S, Marsden A, Massey H, McKee S, Mohammed S, Naik S, Nesarajah M, Newbury-Ecob R, Osborne F, Parker MJ, Patterson J, Pottinger C, Prapa M, Prescott K, Quinn S, Radley JA, Robart S, Ross A, Rosti G, Sansbury FH, Sarkar A, Searle C, Shannon N, Shears D, Smithson S, Stewart H, Suri M, Tadros S, Theobald R, Thomas R, Tsoulaki O, Vasudevan P, Rodriguez MV, Vittery E, Whyte S, Woods E, Wright T, Zocche D, Firth HV, Wright CF; DDD Study28. Copeland H, et al. Among authors: rodriguez mv. Genet Med Open. 2024 Oct 14;2:101864. doi: 10.1016/j.gimo.2024.101864. eCollection 2024. Genet Med Open. 2024. PMID: 39822267 Free PMC article.
8,746 results