Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Genomic copy number alterations in non-syndromic hearing lossRosenberg, C. ; Freitas, É. L. ; Uehara, D. T. ; Auricchio, M. T. B. M. ; Costa, S. S. ; Oiticica, J. ; Silva, A. G. ; Krepischi, A. C. ; Mingroni-Netto, R. C.Clinical genetics, 2016-04, Vol.89 (4), p.473-477 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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2 |
Material Type: Artigo
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NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing lossSalazar-Silva, R ; Dantas, Vitor Lima Goes ; Alves, Leandro Ucela ; Batissoco, Ana Carla ; Oiticica, Jeanne ; Lawrence, Elizabeth A ; Kawafi, Abdelwahab ; Yang, Yushi ; Nicastro, Fernanda Stávale ; Novaes, Beatriz Caiuby ; Hammond, Chrissy ; Kague, Erika ; Mingroni-Netto, R CHuman molecular genetics, 2021-01, Vol.29 (22), p.3691-3705 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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3 |
Material Type: Artigo
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A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21Lezirovitz, K ; Braga, MCC ; Thiele-Aguiar, RS ; Auricchio, MTBM ; Pearson, PL ; Otto, PA ; Mingroni-Netto, RCClinical genetics, 2009-05, Vol.75 (5), p.490-493 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian PopulationKimura, L. ; Angeli, C. B. ; Auricchio, M. T. B. M. ; Fernandes, G. R. ; Pereira, A. C. ; Vicente, J. P. ; Pereira, T. V. ; Mingroni-Netto, R. C. Domenech, MonicaInternational Journal of Hypertension, 2012-01, Vol.2012, p.859219-8 [Periódico revisado por pares]United States: Hindawi LimitedsTexto completo disponível |
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5 |
Material Type: Artigo
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Chromosome imbalances in syndromic hearing lossCatelani, ALPM ; Krepischi, ACV ; Kim, CA ; Kok, F ; Otto, PA ; Auricchio, MTBM ; Mazzeu, JF ; Uehara, DT ; Costa, SS ; Knijnenburg, J ; Tabith Jr, A ; Vianna-Morgante, AM ; Mingroni-Netto, RC ; Rosenberg, CClinical genetics, 2009-11, Vol.76 (5), p.458-464 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Cochlea cell-specific marker expression upon in vitro Hes1 knockdownBatissoco, A C ; Lezirovitz, K ; Zanatta, D B ; Hemza, C R M L ; Vasques, L R ; Strauss, B E ; Mingroni-Netto, R C ; Haddad, L A ; Bento, R F ; Oiticica, JBrazilian journal of medical and biological research, 2021-01, Vol.54 (7), p.e10579-e10579 [Periódico revisado por pares]Brazil: Associacao Brasileira de Divulgacao Cientifica (ABDC)Texto completo disponível |
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7 |
Material Type: Artigo
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Correspondence regarding Ballana et al., “Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment”Abreu-Silva, R.S. ; Batissoco, A.C. ; Lezirovitz, K. ; Romanos, J. ; Rincon, D. ; Auricchio, M.T.B.M. ; Otto, P.A. ; Mingroni-Netto, R.C.Biochemical and biophysical research communications, 2006-05, Vol.343 (3), p.675-676 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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8 |
Material Type: Artigo
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Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary resultsBarboza, Jr, L C M ; Lezirovitz, K ; Zanatta, D B ; Strauss, B E ; Mingroni-Netto, R C ; Oiticica, J ; Haddad, L A ; Bento, R FBrazilian journal of medical and biological research, 2016-01, Vol.49 (4), p.e5064-e5064 [Periódico revisado por pares]Brazil: Associacao Brasileira de Divulgacao Cientifica (ABDC)Texto completo disponível |
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9 |
Material Type: Artigo
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Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsKrepischi-Santos, A.C.V. ; Vianna-Morgante, A.M. ; Jehee, F.S. ; Passos-Bueno, M.R. ; Knijnenburg, J. ; Szuhai, K. ; Sloos, W. ; Mazzeu, J.F. ; Kok, F. ; Cheroki, C. ; Otto, P.A. ; Mingroni-Netto, R.C. ; Varela, M. ; Koiffmann, C. ; Kim, C.A. ; Bertola, D.R. ; Pearson, P.L. ; Rosenberg, C.Cytogenetic and genome research, 2006-01, Vol.115 (3-4), p.254-261 [Periódico revisado por pares]Basel, Switzerland: S. Karger AGTexto completo disponível |
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10 |
Material Type: Artigo
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A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian familyBatissoco, A C ; Auricchio, M T B M ; Kimura, L ; Tabith-Junior, A ; Mingroni-Netto, R CBrazilian journal of medical and biological research, 2009-02, Vol.42 (2), p.168-171 [Periódico revisado por pares]Brazil: Associação Brasileira de Divulgação CientíficaTexto completo disponível |