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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1994 1
1996 3
1999 3
2002 1
2004 1
2005 1
2006 5
2007 2
2008 4
2009 5
2010 3
2011 5
2012 4
2013 1
2014 6
2015 5
2016 6
2017 3
2018 8
2019 3
2020 1
2021 5
2022 5
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70 results
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Page 1
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 article. Review.
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: mingroni netto rc. 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.
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.
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.
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: mingroni netto rc. 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.
Waardenburg syndrome: Novel mutations in a large Brazilian sample.
Bocángel MAP, Melo US, Alves LU, Pardono E, Lourenço NCV, Marcolino HVC, Otto PA, Mingroni-Netto RC. Bocángel MAP, et al. Among authors: mingroni netto rc. Eur J Med Genet. 2018 Jun;61(6):348-354. doi: 10.1016/j.ejmg.2018.01.012. Epub 2018 Jan 31. Eur J Med Genet. 2018. PMID: 29407415 Free 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: 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.
Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
Soares de Lima Y, Chiabai M, Shen J, Córdoba MS, Versiani BR, Benício ROA, Pogue R, Mingroni-Netto RC, Lezirovitz K, Pic-Taylor A, Mazzeu JF, Oliveira SF. Soares de Lima Y, et al. Among authors: mingroni netto rc. Hear Res. 2018 Dec;370:181-188. doi: 10.1016/j.heares.2018.10.008. Epub 2018 Oct 16. Hear Res. 2018. PMID: 30390570
Santos syndrome is caused by mutation in the WNT7A gene.
Alves LU, Santos S, Musso CM, Ezquina SA, Opitz JM, Kok F, Otto PA, Mingroni-Netto RC. Alves LU, et al. Among authors: mingroni netto rc. J Hum Genet. 2017 Dec;62(12):1073-1078. doi: 10.1038/jhg.2017.86. Epub 2017 Aug 31. J Hum Genet. 2017. PMID: 28855715
70 results