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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: oiticica j. Int J Mol Sci. 2018 Aug 27;19(9):2535. doi: 10.3390/ijms19092535. Int J Mol Sci. 2018. PMID: 30150563 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: oiticica j. 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.
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: oiticica j. Hum Mol Genet. 2021 Jan 21;29(22):3691-3705. doi: 10.1093/hmg/ddaa240. Hum Mol Genet. 2021. PMID: 33326993 Free PMC article.
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: oiticica j. Hum Mol Genet. 2020 Jun 3;29(9):1520-1536. doi: 10.1093/hmg/ddaa075. Hum Mol Genet. 2020. PMID: 32337552 Free PMC article.
Cochlea cell-specific marker expression upon in vitro Hes1 knockdown.
Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni-Netto RC, Haddad LA, Bento RF, Oiticica J. Batissoco AC, et al. Among authors: oiticica j. Braz J Med Biol Res. 2021 May 17;54(7):e10579. doi: 10.1590/1414-431X2020e10579. eCollection 2021. Braz J Med Biol Res. 2021. PMID: 34008754 Free PMC article.
Corrigendum to: 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: oiticica j. Hum Mol Genet. 2021 Dec 17;31(1):156. doi: 10.1093/hmg/ddab325. Hum Mol Genet. 2021. PMID: 34788418 Free PMC article. No abstract available.
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A).
Kobayashi GS, Vieira-Silva GA, Varella-Branco E, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni-Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Kobayashi GS, et al. Among authors: oiticica j. Stem Cell Res. 2023 Sep;71:103181. doi: 10.1016/j.scr.2023.103181. Epub 2023 Aug 9. Stem Cell Res. 2023. PMID: 37595341 Free article.
Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss.
Batissoco AC, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, da Silva de Oliveira Longati EU, Mariano D, Hoshino ACH, Tsuji RK, Jesus-Santos R, Abath-Neto O, Bento RF, Oiticica J, Lezirovitz K. Batissoco AC, et al. Among authors: oiticica j. Hum Genet. 2022 Apr;141(3-4):519-538. doi: 10.1007/s00439-021-02372-2. Epub 2021 Oct 1. Hum Genet. 2022. PMID: 34599368
39 results