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Artigo de periodico
Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants (2024)
Torres, William Bertani ; Lezirovitz, Karina ; Coutinho, Danillo Alencar ; Pardono, Eliete; Costa, Silvia Souza da; Antunes, Larissa do Nascimento; Oliveira, Judite de; Otto, Paulo A ; Pingault, Véronique ; Mingroni Netto, Regina Celia
Source: Audiology Research. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, GENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, PIGMENTOS
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ABNT
TORRES, William Bertani et al. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, v. 14, n. 1, p. 9-25, 2024Tradução . . Disponível em: https://doi.org/10.3390/audiolres14010002. Acesso em: 09 nov. 2024.
APA
Torres, W. B., Lezirovitz, K., Coutinho, D. A., Pardono, E., Costa, S. S. da, Antunes, L. do N., et al. (2024). Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants. Audiology Research, 14( 1), 9-25. doi:10.3390/audiolres14010002
NLM
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/audiolres14010002
Vancouver
Torres WB, Lezirovitz K, Coutinho DA, Pardono E, Costa SS da, Antunes L do N, Oliveira J de, Otto PA, Pingault V, Mingroni Netto RC. Waardenburg syndrome: the contribution of next-generation sequencing to the identification of novel causative variants [Internet]. Audiology Research. 2024 ; 14( 1): 9-25.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/audiolres14010002
Artigo de periodico
Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population (2024)
Leite, Jean Michel Rocha Sampaio ; Ribeiro, Adele; Pereira, Jaqueline Lopes ; Souza, Camila Alves de ; Heider, Dominik ; Soler, Júlia Maria Pavan ; Mingroni Netto, Regina Celia ; Fisberg, Regina Mara ; Rogero, Marcelo Macedo ; Sarti, Flávia Mori
Source: Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. Unidades: IME, IB, FSP, EACH
Assunto: POPULAÇÃO
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LEITE, Jean Michel Rocha Sampaio et al. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism, v. 63, p. 311-321, 2024Tradução . . Disponível em: http://dx.doi.org/10.1016/j.clnesp.2024.06.045. Acesso em: 09 nov. 2024.
APA
Leite, J. M. R. S., Ribeiro, A., Pereira, J. L., Souza, C. A. de, Heider, D., Soler, J. M. P., et al. (2024). Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism, 63, 311-321. doi:10.1016/j.clnesp.2024.06.045
NLM
Leite J M R S, Ribeiro A, Pereira JL, Souza CA de, Heider D, Soler JMP, Mingroni Netto RC, Fisberg RM, Rogero MM, Sarti FM. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population [Internet]. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. 2024 ; 63 311-321.[citado 2024 nov. 09 ] Available from: http://dx.doi.org/10.1016/j.clnesp.2024.06.045
Vancouver
Leite J M R S, Ribeiro A, Pereira JL, Souza CA de, Heider D, Soler JMP, Mingroni Netto RC, Fisberg RM, Rogero MM, Sarti FM. Missense genetic variants in major bitter taste receptors are associated with diet quality and food intake in a highly admixed underrepresented population [Internet]. Clinical Nutrition ESPEN: the European e-journal of clinical nutrition and metabolism. 2024 ; 63 311-321.[citado 2024 nov. 09 ] Available from: http://dx.doi.org/10.1016/j.clnesp.2024.06.045
Artigo de periodico
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) (2023)
Kobayashi, Gerson S ; Silva, Gleiciele A. Vieira; Branco, Elisa Varella ; Moreira, Danielle P; Kitajima, João Paulo F. W; Hemza, Claudia R.M.L; Mingroni Netto, Regina Celia ; Lojudice, Fernando H ; Oiticica, Jeanne ; Bento, Ricardo F ; Batissoco, Ana C ; Lezirovitz, Karina
Source: Stem Cell Research. Unidades: IB, FM
Subjects: PERDA AUDITIVA, CÉLULAS-TRONCO
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KOBAYASHI, Gerson S et al. 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). Stem Cell Research, v. 71, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2023.103181. Acesso em: 09 nov. 2024.
APA
Kobayashi, G. S., Silva, G. A. V., Branco, E. V., Moreira, D. P., Kitajima, J. P. F. W., Hemza, C. R. M. L., et al. (2023). 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). Stem Cell Research, 71. doi:10.1016/j.scr.2023.103181
NLM
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. 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) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Vancouver
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. 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) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Artigo de periodico
Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
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ABNT
NASLAVSKY, Michel et al. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1831, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29575-z. Acesso em: 09 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1831). doi:10.1038/s41467-022-29575-z
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, 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 YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, 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 YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Genetic etiology of non-syndromic hearing loss in Latin America (2022)
Lezirovitz, Karina ; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, MUTAÇÃO GENÉTICA
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ABNT
LEZIROVITZ, Karina e MINGRONI NETTO, Regina Celia. Genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, v. 141, p. 539–581, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00439-021-02354-4. Acesso em: 09 nov. 2024.
APA
Lezirovitz, K., & Mingroni Netto, R. C. (2022). Genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, 141, 539–581. doi:10.1007/s00439-021-02354-4
NLM
Lezirovitz K, Mingroni Netto RC. Genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 539–581.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Vancouver
Lezirovitz K, Mingroni Netto RC. Genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 539–581.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Artigo de periodico
Correction to: genetic etiology of non-syndromic hearing loss in Latin America (2022)
Lezirovitz, Karina ; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEZIROVITZ, Karina e MINGRONI NETTO, Regina Celia. Correction to: genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, v. 141, p. 997, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00439-021-02354-4. Acesso em: 09 nov. 2024.
APA
Lezirovitz, K., & Mingroni Netto, R. C. (2022). Correction to: genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, 141, 997. doi:10.1007/s00439-021-02354-4
NLM
Lezirovitz K, Mingroni Netto RC. Correction to: genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 997.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Vancouver
Lezirovitz K, Mingroni Netto RC. Correction to: genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 997.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1004, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-28648-3. Acesso em: 09 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1004). doi:10.1038/s41467-022-28648-3
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, 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 YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, 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 YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico
Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss (2022)
Silva, Rodrigo Salazar da ; Dantas, Vitor Lima Goes ; Alves, Leandro Ucela; Batissoco, Ana Carla ; Oiticica, Jeanne ; Lawrence, Elizabeth A ; Kawafi, Abdelwahab ; Yang, Yishi ; Nicastro, Fernanda Stávale; Novaes, Beatriz Caiuby ; Hammond, Chrissy ; Kague, Érika ; Mingroni Netto, Regina Celia
Source: Human Molecular Genetics. Unidades: IB, FM
Subjects: SURDEZ, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Rodrigo Salazar da et al. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, v. 31, n. Ja 2022, 2022Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddab325. Acesso em: 09 nov. 2024.
APA
Silva, R. S. da, Dantas, V. L. G., Alves, L. U., Batissoco, A. C., Oiticica, J., Lawrence, E. A., et al. (2022). Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, 31( Ja 2022). doi:10.1093/hmg/ddab325
NLM
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2022 ; 31( Ja 2022):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/ddab325
Vancouver
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2022 ; 31( Ja 2022):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/ddab325
Parte de monografia/livro
The human mitocondrial DNA (2021)
Mingroni Netto, Regina Celia
Source: Human genome structure, function and clinical considerations. Unidade: IB
Subjects: DNA MITOCONDRIAL, GENOMAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia. The human mitocondrial DNA. Human genome structure, function and clinical considerations. Tradução . Cham: Instituto de Biociências, Universidade de São Paulo, 2021. p. 301-329. Disponível em: https://doi.org/10.1007/978-3-030-73151-9_10. Acesso em: 09 nov. 2024.
APA
Mingroni Netto, R. C. (2021). The human mitocondrial DNA. In Human genome structure, function and clinical considerations (p. 301-329). Cham: Instituto de Biociências, Universidade de São Paulo. doi:10.1007/978-3-030-73151-9_10
NLM
Mingroni Netto RC. The human mitocondrial DNA [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 301-329.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_10
Vancouver
Mingroni Netto RC. The human mitocondrial DNA [Internet]. In: Human genome structure, function and clinical considerations. Cham: Instituto de Biociências, Universidade de São Paulo; 2021. p. 301-329.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/978-3-030-73151-9_10
Artigo de periodico
Cochlea cell-specific marker expression upon in vitro Hes1 knockdown (2021)
Batissoco, A.C ; Lezirovitz, K ; Zanatta, D. B ; Hemza, C. R. M. L ; Vasques, L. R ; Strauss, B. E ; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Bento, R. F ; Oiticica, J
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, FM, BIOTECNOLOGIA
Subjects: PERDA AUDITIVA, MUTAÇÃO GENÉTICA, EXPRESSÃO GÊNICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISSOCO, A.C et al. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown. Brazilian Journal of Medical and Biological Research, v. 54, n. 7, 2021Tradução . . Disponível em: https://doi.org/10.1590/1414-431X2020e10579. Acesso em: 09 nov. 2024.
APA
Batissoco, A. C., Lezirovitz, K., Zanatta, D. B., Hemza, C. R. M. L., Vasques, L. R., Strauss, B. E., et al. (2021). Cochlea cell-specific marker expression upon in vitro Hes1 knockdown. Brazilian Journal of Medical and Biological Research, 54( 7). doi:10.1590/1414-431X2020e10579
NLM
Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni Netto RC, Haddad LA, Bento RF, Oiticica J. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 7):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/1414-431X2020e10579
Vancouver
Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni Netto RC, Haddad LA, Bento RF, Oiticica J. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 7):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/1414-431X2020e10579
Artigo de periodico
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss (2020)
Silva, Rodrigo Salazar da ; Dantas, Vitor Lima Goes ; Alves, Leandro Ucela; Batissoco, Ana Carla ; Oiticica, Jeanne ; Lawrence, Elizabeth A ; Kawafi, Abdelwahab ; Yang, Yishi ; Nicastro, Fernanda Stávale; Novaes, Beatriz Caiuby ; Hammond, Chrissy ; Kague, Érika ; Mingroni Netto, Regina Celia
Source: Human Molecular Genetics. Unidades: IB, FM
Subjects: AUDIÇÃO, SURDEZ, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Rodrigo Salazar da et al. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, v. 29, n. 2, p. 3691–3705, 2020Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddaa240. Acesso em: 09 nov. 2024.
APA
Silva, R. S. da, Dantas, V. L. G., Alves, L. U., Batissoco, A. C., Oiticica, J., Lawrence, E. A., et al. (2020). NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Human Molecular Genetics, 29( 2), 3691–3705. doi:10.1093/hmg/ddaa240
NLM
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2020 ;29( 2): 3691–3705.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/ddaa240
Vancouver
Silva RS da, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague É, Mingroni Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss [Internet]. Human Molecular Genetics. 2020 ;29( 2): 3691–3705.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/ddaa240
Artigo de periodico
Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration (2019)
Pereira, Larissa Vilela; Bento, Ricardo Ferreira; Cruz, Dayane B; Marchi, Claudia; Salomone, Raquel; Oiticicca, Jeanne; Costa, Marcio Paulino; Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Costa, Heloisa Juliana Zabeu Rossi
Source: Cell transplantation. Unidades: FM, IB
Subjects: CÉLULAS-TRONCO, POLPA DENTÁRIA, NERVO FACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Larissa Vilela et al. Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration. Cell transplantation, v. 28, n. 1, p. 55-64, 2019Tradução . . Disponível em: https://doi.org/10.1177/0963689718809090. Acesso em: 09 nov. 2024.
APA
Pereira, L. V., Bento, R. F., Cruz, D. B., Marchi, C., Salomone, R., Oiticicca, J., et al. (2019). Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration. Cell transplantation, 28( 1), 55-64. doi:10.1177/0963689718809090
NLM
Pereira LV, Bento RF, Cruz DB, Marchi C, Salomone R, Oiticicca J, Costa MP, Haddad LA, Mingroni Netto RC, Costa HJZR. Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration [Internet]. Cell transplantation. 2019 ; 28( 1): 55-64.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1177/0963689718809090
Vancouver
Pereira LV, Bento RF, Cruz DB, Marchi C, Salomone R, Oiticicca J, Costa MP, Haddad LA, Mingroni Netto RC, Costa HJZR. Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration [Internet]. Cell transplantation. 2019 ; 28( 1): 55-64.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1177/0963689718809090
Artigo de periodico
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans (2019)
Dias, Alex Marcel Moreira; Lezirovitz, Karina ; Nicastro, Fernanda Stávale; Mendes, Beatriz C. A; Mingroni Netto, Regina Celia
Source: Journal of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, SEQUENCIAMENTO GENÉTICO, ACONSELHAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Alex Marcel Moreira et al. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, v. 64, p. 257–260, 2019Tradução . . Disponível em: https://doi.org/10.1038/s10038-018-0546-4. Acesso em: 09 nov. 2024.
APA
Dias, A. M. M., Lezirovitz, K., Nicastro, F. S., Mendes, B. C. A., & Mingroni Netto, R. C. (2019). Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, 64, 257–260. doi:10.1038/s10038-018-0546-4
NLM
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s10038-018-0546-4
Vancouver
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s10038-018-0546-4
Artigo de periodico
Waardenburg syndrome: novel mutations in a large Brazilian (2018)
Bocángel, Magnolia Astrid Pretell; Melo, Uirá Souto; Alves, Leandro Ucela; Pardono, Eliete; Lourenço, Naila Cristina Vilaça; Marcolino, Humberto Vicente Cezar; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, GENÉTICA MOLECULAR, GENES
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ABNT
BOCÁNGEL, Magnolia Astrid Pretell et al. Waardenburg syndrome: novel mutations in a large Brazilian. European Journal of Medical Genetics, p. 1-7, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2018.01.012. Acesso em: 09 nov. 2024.
APA
Bocángel, M. A. P., Melo, U. S., Alves, L. U., Pardono, E., Lourenço, N. C. V., Marcolino, H. V. C., et al. (2018). Waardenburg syndrome: novel mutations in a large Brazilian. European Journal of Medical Genetics, 1-7. doi:10.1016/j.ejmg.2018.01.012
NLM
Bocángel MAP, Melo US, Alves LU, Pardono E, Lourenço NCV, Marcolino HVC, Otto PA, Mingroni Netto RC. Waardenburg syndrome: novel mutations in a large Brazilian [Internet]. European Journal of Medical Genetics. 2018 ; 1-7.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ejmg.2018.01.012
Vancouver
Bocángel MAP, Melo US, Alves LU, Pardono E, Lourenço NCV, Marcolino HVC, Otto PA, Mingroni Netto RC. Waardenburg syndrome: novel mutations in a large Brazilian [Internet]. European Journal of Medical Genetics. 2018 ; 1-7.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ejmg.2018.01.012
Artigo de periodico
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss (2018)
Dantas, Vitor G. L; Raval, Dantas1, Manmeet H; Ballesteros, Angela; Cui, Runjia; Gunther, Laura K; Yamamoto, Guilherme L; Alves, Leandro Ucela; Bueno, André Silva; Lezirovitz, Karina; Pirana, Sulene; Mendes, Beatriz C. A; Yengo, Christopher M; Kachar, Bechara; Mingroni Netto, Regina Celia
Source: Scientific Reports. Unidade: IB
Subjects: PERDA AUDITIVA, MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA, GENÉTICA MOLECULAR, GENOMAS
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ABNT
DANTAS, Vitor G. L et al. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific Reports, v. 8, p. 1-15, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-26818-2. Acesso em: 09 nov. 2024.
APA
Dantas, V. G. L., Raval, D. 1, Ballesteros, A., Cui, R., Gunther, L. K., Yamamoto, G. L., et al. (2018). Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific Reports, 8, 1-15. doi:10.1038/s41598-018-26818-2
NLM
Dantas VGL, Raval D1, Ballesteros A, Cui R, Gunther LK, Yamamoto GL, Alves LU, Bueno AS, Lezirovitz K, Pirana S, Mendes BCA, Yengo CM, Kachar B, Mingroni Netto RC. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41598-018-26818-2
Vancouver
Dantas VGL, Raval D1, Ballesteros A, Cui R, Gunther LK, Yamamoto GL, Alves LU, Bueno AS, Lezirovitz K, Pirana S, Mendes BCA, Yengo CM, Kachar B, Mingroni Netto RC. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/s41598-018-26818-2
Artigo de periodico
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects (2018)
Nonose, Renata Watanabe; Lezirovitz, Karina; Auricchio, Maria Teresa Balester De Mello; Batissoco, Ana Carla; Yamamoto, Guilherme Lopes; Mingroni Netto, Regina Celia
Source: BMC Medical Genetics. Unidade: IB
Subjects: SURDEZ, HEREDITARIEDADE, MUTAÇÃO GENÉTICA, PERDA AUDITIVA BILATERAL, PACIENTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NONOSE, Renata Watanabe et al. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects. BMC Medical Genetics, v. 19, p. 1-10, 2018Tradução . . Disponível em: https://doi.org/10.1186/s12881-018-0585-x. Acesso em: 09 nov. 2024.
APA
Nonose, R. W., Lezirovitz, K., Auricchio, M. T. B. D. M., Batissoco, A. C., Yamamoto, G. L., & Mingroni Netto, R. C. (2018). Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects. BMC Medical Genetics, 19, 1-10. doi:10.1186/s12881-018-0585-x
NLM
Nonose RW, Lezirovitz K, Auricchio MTBDM, Batissoco AC, Yamamoto GL, Mingroni Netto RC. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects [Internet]. BMC Medical Genetics. 2018 ; 19 1-10.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1186/s12881-018-0585-x
Vancouver
Nonose RW, Lezirovitz K, Auricchio MTBDM, Batissoco AC, Yamamoto GL, Mingroni Netto RC. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects [Internet]. BMC Medical Genetics. 2018 ; 19 1-10.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1186/s12881-018-0585-x
Artigo de periodico
Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing (2018)
Lima, Yasmin Soares de; Chiabai, Marcela; Shen, Jun; Cordoba, Mara S; Versiani, Beatriz R; Benício, Rosenelle O. A; Pogue, Robert; Mingroni Netto, Regina Celia ; Lezirovitz, Karina; Pic-Taylor, Aline; Mazzeu, Juliana F; Oliveira, Silviene F
Source: Hearing Research. Unidade: IB
Subjects: PERDA AUDITIVA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Yasmin Soares de et al. Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing. Hearing Research, v. 370, p. 181-188, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.heares.2018.10.008. Acesso em: 09 nov. 2024.
APA
Lima, Y. S. de, Chiabai, M., Shen, J., Cordoba, M. S., Versiani, B. R., Benício, R. O. A., et al. (2018). Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing. Hearing Research, 370, 181-188. doi:10.1016/j.heares.2018.10.008
NLM
Lima YS de, Chiabai M, Shen J, Cordoba MS, Versiani BR, Benício ROA, Pogue R, Mingroni Netto RC, Lezirovitz K, Pic-Taylor A, Mazzeu JF, Oliveira SF. Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing [Internet]. Hearing Research. 2018 ; 370 181-188.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.heares.2018.10.008
Vancouver
Lima YS de, Chiabai M, Shen J, Cordoba MS, Versiani BR, Benício ROA, Pogue R, Mingroni Netto RC, Lezirovitz K, Pic-Taylor A, Mazzeu JF, Oliveira SF. Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing [Internet]. Hearing Research. 2018 ; 370 181-188.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.heares.2018.10.008
Artigo de periodico
Inbreeding estimates in human populations: applying new approaches to an admixed Brazilian isolate (2018)
Lemes, Renan B; Nunes, Kelly; Carnavalli, Juliana E. P; Kimura, Lilian; Mingroni Netto, Regina Celia ; Meyer, Diogo ; Otto, Paulo A
Source: PLOS ONE. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, MARCADOR MOLECULAR, GENÉTICA MÉDICA, QUILOMBOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEMES, Renan B et al. Inbreeding estimates in human populations: applying new approaches to an admixed Brazilian isolate. PLOS ONE, v. 13, n. 4, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0196360. Acesso em: 09 nov. 2024.
APA
Lemes, R. B., Nunes, K., Carnavalli, J. E. P., Kimura, L., Mingroni Netto, R. C., Meyer, D., & Otto, P. A. (2018). Inbreeding estimates in human populations: applying new approaches to an admixed Brazilian isolate. PLOS ONE, 13( 4). doi:10.1371/journal.pone.0196360
NLM
Lemes RB, Nunes K, Carnavalli JEP, Kimura L, Mingroni Netto RC, Meyer D, Otto PA. Inbreeding estimates in human populations: applying new approaches to an admixed Brazilian isolate [Internet]. PLOS ONE. 2018 ; 13( 4):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1371/journal.pone.0196360
Vancouver
Lemes RB, Nunes K, Carnavalli JEP, Kimura L, Mingroni Netto RC, Meyer D, Otto PA. Inbreeding estimates in human populations: applying new approaches to an admixed Brazilian isolate [Internet]. PLOS ONE. 2018 ; 13( 4):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1371/journal.pone.0196360
Artigo de periodico
A Cell Junctional Protein Network Associated with Connexin-26 (2018)
Batissoco, Ana C; Salazar-Silva, Rodrigo; Oiticica, Jeanne; Bento, Ricardo F; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral
Source: International Journal of Molecular Sciences. Unidades: FM, IB
Subjects: PERDA AUDITIVA HEREDITÁRIA, CONEXINAS, MUTAÇÃO GENÉTICA, SURDEZ
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISSOCO, Ana C et al. A Cell Junctional Protein Network Associated with Connexin-26. International Journal of Molecular Sciences, v. 19, n. 9, p. 1-20, 2018Tradução . . Disponível em: https://doi.org/10.3390/ijms19092535. Acesso em: 09 nov. 2024.
APA
Batissoco, A. C., Salazar-Silva, R., Oiticica, J., Bento, R. F., Mingroni Netto, R. C., & Haddad, L. A. (2018). A Cell Junctional Protein Network Associated with Connexin-26. International Journal of Molecular Sciences, 19( 9), 1-20. doi:10.3390/ijms19092535
NLM
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni Netto RC, Haddad LA. A Cell Junctional Protein Network Associated with Connexin-26 [Internet]. International Journal of Molecular Sciences. 2018 ; 19( 9): 1-20.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/ijms19092535
Vancouver
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni Netto RC, Haddad LA. A Cell Junctional Protein Network Associated with Connexin-26 [Internet]. International Journal of Molecular Sciences. 2018 ; 19( 9): 1-20.[citado 2024 nov. 09 ] Available from: https://doi.org/10.3390/ijms19092535
Artigo de periodico
Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes (2017)
Kimura, Lilian; Nunes, Kelly; Macedo-Souza, Lúcia Inês; Rocha, Jorge; Meyer, Diogo ; Mingroni Netto, Regina Celia
Source: American Journal of Human Biology. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, GENÉTICA MOLECULAR, CROMOSSOMO Y, ANTROPOLOGIA, QUILOMBOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIMURA, Lilian et al. Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes. American Journal of Human Biology, v. 29, n. 2, p. 1-11, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajhb.22930. Acesso em: 09 nov. 2024.
APA
Kimura, L., Nunes, K., Macedo-Souza, L. I., Rocha, J., Meyer, D., & Mingroni Netto, R. C. (2017). Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes. American Journal of Human Biology, 29( 2), 1-11. doi:10.1002/ajhb.22930
NLM
Kimura L, Nunes K, Macedo-Souza LI, Rocha J, Meyer D, Mingroni Netto RC. Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes [Internet]. American Journal of Human Biology. 2017 ; 29( 2): 1-11.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1002/ajhb.22930
Vancouver
Kimura L, Nunes K, Macedo-Souza LI, Rocha J, Meyer D, Mingroni Netto RC. Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes [Internet]. American Journal of Human Biology. 2017 ; 29( 2): 1-11.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1002/ajhb.22930

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