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

Year Number of Results
2002 1
2004 1
2006 2
2007 1
2008 2
2009 2
2010 3
2011 2
2012 2
2013 1
2014 2
2015 1
2016 3
2017 1
2018 5
2019 3
2021 2
2022 4
2023 1
2024 2

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33 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 PMC article. Review.
Ca2+ binding to the C2E domain of otoferlin is required for hair cell exocytosis and hearing.
Chen H, Monga M, Fang Q, Slitin L, Neef J, Chepurwar SS, Netto RCM, Lezirovitz K, Tabith A Jr, Benseler F, Brose N, Kusch K, Wichmann C, Strenzke N, Vona B, Preobraschenski J, Moser T. Chen H, et al. Among authors: netto rcm. Protein Cell. 2024 Apr 1;15(4):305-312. doi: 10.1093/procel/pwad058. Protein Cell. 2024. PMID: 38066594 Free PMC article. No abstract available.
Whole-genome sequencing of 1,171 elderly admixed individuals from São Paulo, Brazil.
Naslavsky MS, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, de Carvalho DL, da Silva Simões CE, Bozoklian D, Nonaka R, Dos Santos Brito Silva N, da Silva Souza A, de Souza Andrade H, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni-Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YAO, Passos-Bueno MR, Zatz M. Naslavsky MS, et al. Among authors: mingroni netto rc. Nat Commun. 2022 Mar 4;13(1):1004. doi: 10.1038/s41467-022-28648-3. Nat Commun. 2022. PMID: 35246524 Free PMC article.
Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil.
Naslavsky MS, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, de Carvalho DL, da Silva Simões CE, Bozoklian D, Nonaka R, Dos Santos Brito Silva N, da Silva Souza A, de Souza Andrade H, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni-Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YAO, Passos-Bueno MR, Zatz M. Naslavsky MS, et al. Among authors: mingroni netto rc. Nat Commun. 2022 Mar 30;13(1):1831. doi: 10.1038/s41467-022-29575-z. Nat Commun. 2022. PMID: 35354829 Free PMC article. No abstract available.
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.
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
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.
Novel frameshift variant in gene SALL4 causing Okihiro syndrome.
Alves LU, Perez AB, Alonso LG, Otto PA, Mingroni-Netto RC. Alves LU, et al. Among authors: mingroni netto rc. Eur J Med Genet. 2016 Feb;59(2):80-5. doi: 10.1016/j.ejmg.2015.12.015. Epub 2016 Jan 11. Eur J Med Genet. 2016. PMID: 26791099 Free article.
33 results