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A Cell Junctional Protein Network Associated with Connexin-26.
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni-Netto RC, Haddad LA. Batissoco AC, et al. Among authors: mingroni netto rc. Int J Mol Sci. 2018 Aug 27;19(9):2535. doi: 10.3390/ijms19092535. Int J Mol Sci. 2018. PMID: 30150563 Free PMC article.
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
Salazar-Silva R, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Mingroni-Netto RC. Salazar-Silva R, et al. Among authors: mingroni netto rc. Hum Mol Genet. 2021 Jan 21;29(22):3691-3705. doi: 10.1093/hmg/ddaa240. Hum Mol Genet. 2021. PMID: 33326993 Free PMC article.
Stem-cell therapy for hearing loss: are we there yet?
Dufner-Almeida LG, Cruz DBD, Mingroni Netto RC, Batissoco AC, Oiticica J, Salazar-Silva R. Dufner-Almeida LG, et al. Among authors: mingroni netto rc. Braz J Otorhinolaryngol. 2019 Jul-Aug;85(4):520-529. doi: 10.1016/j.bjorl.2019.04.006. Epub 2019 May 18. Braz J Otorhinolaryngol. 2019. PMID: 31186186 Free PMC article. Review.
Novel OTOF mutations in Brazilian patients with auditory neuropathy.
Romanos J, Kimura L, Fávero ML, Izarra FA, de Mello Auricchio MT, Batissoco AC, Lezirovitz K, Abreu-Silva RS, Mingroni-Netto RC. Romanos J, et al. Among authors: mingroni netto rc. J Hum Genet. 2009 Jul;54(7):382-5. doi: 10.1038/jhg.2009.45. Epub 2009 May 22. J Hum Genet. 2009. PMID: 19461658
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.
Lezirovitz K, Vieira-Silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Pedroso-Campos V, Nascimento LR, Sonoda CY, Borges VM, Vasconcelos LG, Beck RMO, Grasel SS, Jagger DJ, Grillet N, Bento RF, Mingroni-Netto RC, Oiticica J. Lezirovitz K, et al. Among authors: mingroni netto rc. Hum Mol Genet. 2020 Jun 3;29(9):1520-1536. doi: 10.1093/hmg/ddaa075. Hum Mol Genet. 2020. PMID: 32337552 Free PMC article.
73 results