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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
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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: 14 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. 14 ] 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. 14 ] Available from: https://doi.org/10.1177/0963689718809090
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
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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: 14 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. 14 ] 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. 14 ] Available from: https://doi.org/10.1371/journal.pone.0196360
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
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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: 14 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. 14 ] 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. 14 ] Available from: https://doi.org/10.1002/ajhb.22930
Artigo de periodico
Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes (2016)
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 MÉDICA, QUILOMBOS, GENÓTIPOS, ANTROPOLOGIA, EVOLUÇÃO MOLECULAR
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ABNT
KIMURA, Lilian et al. Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes. American Journal of Human Biology, p. 1-11, 2016Tradução . . Disponível em: https://doi.org/10.1002/ajhb.22930. Acesso em: 14 nov. 2024.
APA
Kimura, L., Nunes, K., Macedo-Souza, L. I., Rocha, J., Meyer, D., & Mingroni Netto, R. C. (2016). Inferring paternal history of rural African-derived Brazilian populations from Y chromosomes. American Journal of Human Biology, 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. 2016 ; 1-11.[citado 2024 nov. 14 ] 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. 2016 ; 1-11.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajhb.22930
Artigo de periodico
Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, São Paulo – Brazil (2016)
Nunes, Kelly; Piovezan, Bruno; Torres, Margareth A.; Pontes, Gerlândia N.; Kimura, Lilian; Carnavalli, Juliana E.P.; Mingroni Netto, Regina Celia ; Moraes, Maria Elisa; Meyer, Diogo
Source: Human Immunology. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, QUILOMBOS, IMUNOGENÉTICA, GENÉTICA
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ABNT
NUNES, Kelly et al. Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, São Paulo – Brazil. Human Immunology, p. online, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.humimm.2016.04.007. Acesso em: 14 nov. 2024.
APA
Nunes, K., Piovezan, B., Torres, M. A., Pontes, G. N., Kimura, L., Carnavalli, J. E. P., et al. (2016). Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, São Paulo – Brazil. Human Immunology, online. doi:10.1016/j.humimm.2016.04.007
NLM
Nunes K, Piovezan B, Torres MA, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Moraes ME, Meyer D. Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, São Paulo – Brazil [Internet]. Human Immunology. 2016 ; online.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.humimm.2016.04.007
Vancouver
Nunes K, Piovezan B, Torres MA, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Moraes ME, Meyer D. Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, São Paulo – Brazil [Internet]. Human Immunology. 2016 ; online.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.humimm.2016.04.007
Artigo de periodico
HLA imputation in an admixed population: an assessment of the 1000 Genomes data as a training set (2015)
Nunes, Kelly; Zheng, Xiuwen; Torres, Margareth; Moraes, Maria Elisa; Piovezan, Bruno Z; Pontes, Gerlândia N; Kimura, Lilian; Carnavalli, Juliana E.P; Mingroni Netto, Regina Celia ; Meyer, Diogo
Source: Human Immunology. Unidade: IB
Subjects: GENOMAS, QUILOMBOS, GENÓTIPOS, ANTROPOLOGIA, GENÉTICA DE POPULAÇÕES
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ABNT
NUNES, Kelly et al. HLA imputation in an admixed population: an assessment of the 1000 Genomes data as a training set. Human Immunology, v. No 2015, n. 3, p. 307-312, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.humimm.2015.11.004. Acesso em: 14 nov. 2024.
APA
Nunes, K., Zheng, X., Torres, M., Moraes, M. E., Piovezan, B. Z., Pontes, G. N., et al. (2015). HLA imputation in an admixed population: an assessment of the 1000 Genomes data as a training set. Human Immunology, No 2015( 3), 307-312. doi:10.1016/j.humimm.2015.11.004
NLM
Nunes K, Zheng X, Torres M, Moraes ME, Piovezan BZ, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Meyer D. HLA imputation in an admixed population: an assessment of the 1000 Genomes data as a training set [Internet]. Human Immunology. 2015 ; No 2015( 3): 307-312.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.humimm.2015.11.004
Vancouver
Nunes K, Zheng X, Torres M, Moraes ME, Piovezan BZ, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Meyer D. HLA imputation in an admixed population: an assessment of the 1000 Genomes data as a training set [Internet]. Human Immunology. 2015 ; No 2015( 3): 307-312.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.humimm.2015.11.004
Trabalho de evento-resumo periodico
A new HLA-C⁄02 nulL allele described in QUILOMBO remnants samples from Southrrn Brazil (2015)
Nunes, Kelly; Torres, Margareth A; Piovezan, Bruno Z; Pontes, Gerlandia N; Kimura, Lilian; Carnavalli, Juliana E. P; Mingroni Netto, Regina Celia ; Meyer, Diogo ; Moraes, Maria E
Source: Human Immunology. Conference titles: Annual Meeting of the American Society for Histocompatibility and Immunogenetics. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, EVOLUÇÃO MOLECULAR, QUILOMBOS, IMUNOGENÉTICA, GENÉTICA (VARIABILIDADE)
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ABNT
NUNES, Kelly et al. A new HLA-C⁄02 nulL allele described in QUILOMBO remnants samples from Southrrn Brazil. Human Immunology. Philadelphia: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2015
APA
Nunes, K., Torres, M. A., Piovezan, B. Z., Pontes, G. N., Kimura, L., Carnavalli, J. E. P., et al. (2015). A new HLA-C⁄02 nulL allele described in QUILOMBO remnants samples from Southrrn Brazil. Human Immunology. Philadelphia: Instituto de Biociências, Universidade de São Paulo.
NLM
Nunes K, Torres MA, Piovezan BZ, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Meyer D, Moraes ME. A new HLA-C⁄02 nulL allele described in QUILOMBO remnants samples from Southrrn Brazil. Human Immunology. 2015 ; 76 140.[citado 2024 nov. 14 ]
Vancouver
Nunes K, Torres MA, Piovezan BZ, Pontes GN, Kimura L, Carnavalli JEP, Mingroni Netto RC, Meyer D, Moraes ME. A new HLA-C⁄02 nulL allele described in QUILOMBO remnants samples from Southrrn Brazil. Human Immunology. 2015 ; 76 140.[citado 2024 nov. 14 ]
Texto na web
Estimation of inbreeding and substructure levels in African-derived Brazilian Quilombo populations (2015)
Lemes, Renan Barbosa; Nunes, Kelly; Meyer, Diogo ; Mingroni Netto, Regina Celia ; Otto, Paulo A
Unidade: IB
Subjects: QUILOMBOS, POPULAÇÃO, GENEALOGIA (ANÁLISE), MARCADOR MOLECULAR (ANÁLISE), GENÉTICA DE POPULAÇÕES, EVOLUÇÃO MOLECULAR, AFRODESCENDENTES
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ABNT
LEMES, Renan Barbosa et al. Estimation of inbreeding and substructure levels in African-derived Brazilian Quilombo populations. . Detroit: Instituto de Biociências, Universidade de São Paulo. Disponível em: http://digitalcommons.wayne.edu/humbiol_preprints/62/. Acesso em: 14 nov. 2024. , 2015
APA
Lemes, R. B., Nunes, K., Meyer, D., Mingroni Netto, R. C., & Otto, P. A. (2015). Estimation of inbreeding and substructure levels in African-derived Brazilian Quilombo populations. Detroit: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://digitalcommons.wayne.edu/humbiol_preprints/62/
NLM
Lemes RB, Nunes K, Meyer D, Mingroni Netto RC, Otto PA. Estimation of inbreeding and substructure levels in African-derived Brazilian Quilombo populations [Internet]. 2015 ;[citado 2024 nov. 14 ] Available from: http://digitalcommons.wayne.edu/humbiol_preprints/62/
Vancouver
Lemes RB, Nunes K, Meyer D, Mingroni Netto RC, Otto PA. Estimation of inbreeding and substructure levels in African-derived Brazilian Quilombo populations [Internet]. 2015 ;[citado 2024 nov. 14 ] Available from: http://digitalcommons.wayne.edu/humbiol_preprints/62/
Artigo de periodico
Genomic copy number alterations in non-syndromic hearing loss (2015)
Rosenberg, Carla ; Freitas, E L; Uehara, D. T; Auricchio, M T B M; Costa, S. S; Oiticica, J; Silva, A G; Krepischi, Ana Cristina Victorino ; Mingroni Netto, Regina Celia
Source: Clinical Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, GENES, GENÉTICA MÉDICA
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ABNT
ROSENBERG, Carla et al. Genomic copy number alterations in non-syndromic hearing loss. Clinical Genetics, v. 89, n. 4, p. 473-477, 2015Tradução . . Disponível em: https://doi.org/10.1111/cge.12683. Acesso em: 14 nov. 2024.
APA
Rosenberg, C., Freitas, E. L., Uehara, D. T., Auricchio, M. T. B. M., Costa, S. S., Oiticica, J., et al. (2015). Genomic copy number alterations in non-syndromic hearing loss. Clinical Genetics, 89( 4), 473-477. doi:10.1111/cge.12683
NLM
Rosenberg C, Freitas EL, Uehara DT, Auricchio MTBM, Costa SS, Oiticica J, Silva AG, Krepischi ACV, Mingroni Netto RC. Genomic copy number alterations in non-syndromic hearing loss [Internet]. Clinical Genetics. 2015 ; 89( 4): 473-477.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/cge.12683
Vancouver
Rosenberg C, Freitas EL, Uehara DT, Auricchio MTBM, Costa SS, Oiticica J, Silva AG, Krepischi ACV, Mingroni Netto RC. Genomic copy number alterations in non-syndromic hearing loss [Internet]. Clinical Genetics. 2015 ; 89( 4): 473-477.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/cge.12683
Artigo de periodico
Strategies for genetic study of hearing loss in the Brazilian northeastern region (2014)
Melo, Uirá Souto ; Santos, Silvana; Cavalcanti, Hannalice Gottschalck ; Andrade, Wagner T; Dantas, Vitor G; Rosa, Marine Raquel Diniz da ; Mingroni Netto, Regina Celia
Source: International Journal of Molecular Epidemiology and Genetics. Unidade: IB
Subjects: GENÉTICA (ESTUDO), EPIDEMIOLOGIA, PERDA AUDITIVA, MUTAÇÃO GENÉTICA
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ABNT
MELO, Uirá Souto et al. Strategies for genetic study of hearing loss in the Brazilian northeastern region. International Journal of Molecular Epidemiology and Genetics, v. 5, n. 1, p. 11-21, 2014Tradução . . Disponível em: http://www.ijmeg.org/files/ijmeg1311003.pdf. Acesso em: 14 nov. 2024.
APA
Melo, U. S., Santos, S., Cavalcanti, H. G., Andrade, W. T., Dantas, V. G., Rosa, M. R. D. da, & Mingroni Netto, R. C. (2014). Strategies for genetic study of hearing loss in the Brazilian northeastern region. International Journal of Molecular Epidemiology and Genetics, 5( 1), 11-21. Recuperado de http://www.ijmeg.org/files/ijmeg1311003.pdf
NLM
Melo US, Santos S, Cavalcanti HG, Andrade WT, Dantas VG, Rosa MRD da, Mingroni Netto RC. Strategies for genetic study of hearing loss in the Brazilian northeastern region [Internet]. International Journal of Molecular Epidemiology and Genetics. 2014 ; 5( 1): 11-21.[citado 2024 nov. 14 ] Available from: http://www.ijmeg.org/files/ijmeg1311003.pdf
Vancouver
Melo US, Santos S, Cavalcanti HG, Andrade WT, Dantas VG, Rosa MRD da, Mingroni Netto RC. Strategies for genetic study of hearing loss in the Brazilian northeastern region [Internet]. International Journal of Molecular Epidemiology and Genetics. 2014 ; 5( 1): 11-21.[citado 2024 nov. 14 ] Available from: http://www.ijmeg.org/files/ijmeg1311003.pdf
Trabalho de evento
Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family (2014)
Mingroni Netto, Regina Celia ; Dantas, V. G. L.; Freitas, E.L.; Moraes, A. M. S. M.; Braga, M. C. C.; Ramos, S. B.; Rosenberg, Carla ; Della-Rosa, V.A.
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, MAPEAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
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ABNT
MINGRONI NETTO, Regina Celia et al. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. 2014, Anais.. Boston: Instituto de Biociências, Universidade de São Paulo, 2014. Disponível em: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm. Acesso em: 14 nov. 2024.
APA
Mingroni Netto, R. C., Dantas, V. G. L., Freitas, E. L., Moraes, A. M. S. M., Braga, M. C. C., Ramos, S. B., et al. (2014). Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family. In Abstracts. Boston: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
NLM
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Vancouver
Mingroni Netto RC, Dantas VGL, Freitas EL, Moraes AMSM, Braga MCC, Ramos SB, Rosenberg C, Della-Rosa VA. Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family [Internet]. Abstracts. 2014 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2013meeting/abstracts/fulltext/f130123586.htm
Artigo de periodico
Genomic ancestry of rural african-derived populations from southeastern Brazil (2013)
Kimura, Lilian; Ribeiro-Rodrigues, Elzemar Martins; Auricchio, Maria Teresa Ballester de Melo; Vicente, João Pedro; Santos, Sidney Emanuel Batista; Mingroni Netto, Regina Celia
Source: American Journal of Human Biology. Unidade: IB
Assunto: GENOMAS
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ABNT
KIMURA, Lilian et al. Genomic ancestry of rural african-derived populations from southeastern Brazil. American Journal of Human Biology, v. 25, n. Ja/Dec. 2013, p. 35-41, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajhb.22335. Acesso em: 14 nov. 2024.
APA
Kimura, L., Ribeiro-Rodrigues, E. M., Auricchio, M. T. B. de M., Vicente, J. P., Santos, S. E. B., & Mingroni Netto, R. C. (2013). Genomic ancestry of rural african-derived populations from southeastern Brazil. American Journal of Human Biology, 25( Ja/Dec. 2013), 35-41. doi:10.1002/ajhb.22335
NLM
Kimura L, Ribeiro-Rodrigues EM, Auricchio MTB de M, Vicente JP, Santos SEB, Mingroni Netto RC. Genomic ancestry of rural african-derived populations from southeastern Brazil [Internet]. American Journal of Human Biology. 2013 ; 25( Ja/Dec. 2013): 35-41.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajhb.22335
Vancouver
Kimura L, Ribeiro-Rodrigues EM, Auricchio MTB de M, Vicente JP, Santos SEB, Mingroni Netto RC. Genomic ancestry of rural african-derived populations from southeastern Brazil [Internet]. American Journal of Human Biology. 2013 ; 25( Ja/Dec. 2013): 35-41.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajhb.22335
Artigo de periodico
Genomic ancestry of rural african-derived populations from Southeastern Brazil (2012)
Kimura, Lilian; Rodrigues, Elzemar Martins Ribeiro; Auricchio, Maria Teresa Balester De Mello; Vicente, João Pedro; Santos, Sidney Emanuel Batista; Mingroni Netto, Regina Celia
Source: American Journal of Human Biology. Unidade: IB
Subjects: GENÉTICA DE POPULAÇÕES, AFRODESCENDENTES, POPULAÇÃO RURAL
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ABNT
KIMURA, Lilian et al. Genomic ancestry of rural african-derived populations from Southeastern Brazil. American Journal of Human Biology, v. 25, n. Ja/Feb. 2012, p. 35-41, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajhb.22335. Acesso em: 14 nov. 2024.
APA
Kimura, L., Rodrigues, E. M. R., Auricchio, M. T. B. D. M., Vicente, J. P., Santos, S. E. B., & Mingroni Netto, R. C. (2012). Genomic ancestry of rural african-derived populations from Southeastern Brazil. American Journal of Human Biology, 25( Ja/Feb. 2012), 35-41. doi:10.1002/ajhb.22335
NLM
Kimura L, Rodrigues EMR, Auricchio MTBDM, Vicente JP, Santos SEB, Mingroni Netto RC. Genomic ancestry of rural african-derived populations from Southeastern Brazil [Internet]. American Journal of Human Biology. 2012 ; 25( Ja/Feb. 2012): 35-41.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajhb.22335
Vancouver
Kimura L, Rodrigues EMR, Auricchio MTBDM, Vicente JP, Santos SEB, Mingroni Netto RC. Genomic ancestry of rural african-derived populations from Southeastern Brazil [Internet]. American Journal of Human Biology. 2012 ; 25( Ja/Feb. 2012): 35-41.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/ajhb.22335
Trabalho de evento-resumo
Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci (2012)
Freitas, E.L.; Uehara, D.T.; Dantas, V.G.L.; Silva, A.G.; Krepischi, Ana Cristina Victorino ; Mingroni Netto, Regina Celia ; Rosenberg, Carla
Source: Posters: Cytogenetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, GENÉTICA MÉDICA, CITOGENÉTICA
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ABNT
FREITAS, E.L. et al. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 14 nov. 2024.
APA
Freitas, E. L., Uehara, D. T., Dantas, V. G. L., Silva, A. G., Krepischi, A. C. V., Mingroni Netto, R. C., & Rosenberg, C. (2012). Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
NLM
Freitas EL, Uehara DT, Dantas VGL, Silva AG, Krepischi ACV, Mingroni Netto RC, Rosenberg C. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Vancouver
Freitas EL, Uehara DT, Dantas VGL, Silva AG, Krepischi ACV, Mingroni Netto RC, Rosenberg C. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Artigo de periodico
Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population (2012)
Kimura, L; Angeli, C. B; Auricchio, M T B M; Fernandes, G. R; Pereira, A C; Vicente, J. P; Pereira, T. V; Mingroni Netto, Regina Celia
Source: International Journal of Hypertension. Unidade: IB
Subjects: POLIMORFISMO, FENÓTIPOS, HIPERTENSÃO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIMURA, L et al. Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population. International Journal of Hypertension, p. on-line, 2012Tradução . . Disponível em: https://doi.org/10.1155/2012/859219. Acesso em: 14 nov. 2024.
APA
Kimura, L., Angeli, C. B., Auricchio, M. T. B. M., Fernandes, G. R., Pereira, A. C., Vicente, J. P., et al. (2012). Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population. International Journal of Hypertension, on-line. doi:10.1155/2012/859219
NLM
Kimura L, Angeli CB, Auricchio MTBM, Fernandes GR, Pereira AC, Vicente JP, Pereira TV, Mingroni Netto RC. Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population [Internet]. International Journal of Hypertension. 2012 ; on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2012/859219
Vancouver
Kimura L, Angeli CB, Auricchio MTBM, Fernandes GR, Pereira AC, Vicente JP, Pereira TV, Mingroni Netto RC. Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population [Internet]. International Journal of Hypertension. 2012 ; on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2012/859219
Trabalho de evento-resumo periodico
Viable, proliferating progenitor cells (2011)
Oiticica, Jeanne; Batissoco, Ana Carla; Lezirovitz, Karina; Barboza Junior, Luiz C. M; Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Bento, Ricardo F
Source: Otolaryngology - Head and Neck Surgery. Conference titles: Annual Meeting of the American Academy of Otolaryngology-Head and Neck Surgery Foundantion. Unidades: IB, FM
Subjects: IMUNOFLUORESCÊNCIA, FIBROBLASTOS, OUVIDO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OITICICA, Jeanne et al. Viable, proliferating progenitor cells. Otolaryngology - Head and Neck Surgery. Alexandria: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1177/0194599811415823a320. Acesso em: 14 nov. 2024. , 2011
APA
Oiticica, J., Batissoco, A. C., Lezirovitz, K., Barboza Junior, L. C. M., Haddad, L. A., Mingroni Netto, R. C., & Bento, R. F. (2011). Viable, proliferating progenitor cells. Otolaryngology - Head and Neck Surgery. Alexandria: Instituto de Biociências, Universidade de São Paulo. doi:10.1177/0194599811415823a320
NLM
Oiticica J, Batissoco AC, Lezirovitz K, Barboza Junior LCM, Haddad LA, Mingroni Netto RC, Bento RF. Viable, proliferating progenitor cells [Internet]. Otolaryngology - Head and Neck Surgery. 2011 ; 145( 2): P232-P233.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1177/0194599811415823a320
Vancouver
Oiticica J, Batissoco AC, Lezirovitz K, Barboza Junior LCM, Haddad LA, Mingroni Netto RC, Bento RF. Viable, proliferating progenitor cells [Internet]. Otolaryngology - Head and Neck Surgery. 2011 ; 145( 2): P232-P233.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1177/0194599811415823a320
Artigo de periodico
ADRB2 and LEPR gene polymorphisms: synergistic effects on the risk of obesity in japanese (2011)
Pereira, Tiago V; Mingroni Netto, Regina Celia ; Yamada, Yoshiji
Source: Obesity. Unidade: IB
Subjects: POLIMORFISMO, FENÓTIPOS, OBESIDADE, JAPONESES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Tiago V e MINGRONI NETTO, Regina Celia e YAMADA, Yoshiji. ADRB2 and LEPR gene polymorphisms: synergistic effects on the risk of obesity in japanese. Obesity, v. 19, n. 7, p. 1523-1527, 2011Tradução . . Disponível em: https://doi.org/10.1038/oby.2010.322. Acesso em: 14 nov. 2024.
APA
Pereira, T. V., Mingroni Netto, R. C., & Yamada, Y. (2011). ADRB2 and LEPR gene polymorphisms: synergistic effects on the risk of obesity in japanese. Obesity, 19( 7), 1523-1527. doi:10.1038/oby.2010.322
NLM
Pereira TV, Mingroni Netto RC, Yamada Y. ADRB2 and LEPR gene polymorphisms: synergistic effects on the risk of obesity in japanese [Internet]. Obesity. 2011 ; 19( 7): 1523-1527.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/oby.2010.322
Vancouver
Pereira TV, Mingroni Netto RC, Yamada Y. ADRB2 and LEPR gene polymorphisms: synergistic effects on the risk of obesity in japanese [Internet]. Obesity. 2011 ; 19( 7): 1523-1527.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/oby.2010.322
Artigo de periodico
Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations (2011)
Angeli, Claudia Blanes; Kimura, Lilian; Auricchio, Maria Teresa Ballester de Melo; Vicente, Joao P; Mattevi, Vanessa S; Zembrzuski, Verônica M; Hutz, Mara H; Pereira, Alexandre C; Pereira, Tiago V; Mingroni Netto, Regina Celia
Source: Obesity. Unidade: IB
Subjects: FENÓTIPOS, OBESIDADE, QUILOMBOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANGELI, Claudia Blanes et al. Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations. Obesity, v. 19, n. Ja 2011, p. 1244-1251, 2011Tradução . . Disponível em: https://doi.org/10.1038/oby.2010.325. Acesso em: 14 nov. 2024.
APA
Angeli, C. B., Kimura, L., Auricchio, M. T. B. de M., Vicente, J. P., Mattevi, V. S., Zembrzuski, V. M., et al. (2011). Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations. Obesity, 19( Ja 2011), 1244-1251. doi:10.1038/oby.2010.325
NLM
Angeli CB, Kimura L, Auricchio MTB de M, Vicente JP, Mattevi VS, Zembrzuski VM, Hutz MH, Pereira AC, Pereira TV, Mingroni Netto RC. Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations [Internet]. Obesity. 2011 ; 19( Ja 2011): 1244-1251.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/oby.2010.325
Vancouver
Angeli CB, Kimura L, Auricchio MTB de M, Vicente JP, Mattevi VS, Zembrzuski VM, Hutz MH, Pereira AC, Pereira TV, Mingroni Netto RC. Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations [Internet]. Obesity. 2011 ; 19( Ja 2011): 1244-1251.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1038/oby.2010.325
Artigo de periodico
Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss (2010)
Uehara, Daniela Tiaki; Rincon, Daniel; Abreu-Silva, Ronaldo Serafim; Auricchio, Maria Teresa Ballester de Melo; Tabith Junior, Alfredo; Kok, Fernando; Mingroni Netto, Regina Celia
Source: Genetic Testing and Molecular Biomarkers. Unidade: IB
Subjects: GENÉTICA MÉDICA, PERDA AUDITIVA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
UEHARA, Daniela Tiaki et al. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss. Genetic Testing and Molecular Biomarkers, v. 14, n. 5, p. 611-616, 2010Tradução . . Disponível em: https://doi.org/10.1089/gtmb.2010.0011. Acesso em: 14 nov. 2024.
APA
Uehara, D. T., Rincon, D., Abreu-Silva, R. S., Auricchio, M. T. B. de M., Tabith Junior, A., Kok, F., & Mingroni Netto, R. C. (2010). Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss. Genetic Testing and Molecular Biomarkers, 14( 5), 611-616. doi:10.1089/gtmb.2010.0011
NLM
Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MTB de M, Tabith Junior A, Kok F, Mingroni Netto RC. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 5): 611-616.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1089/gtmb.2010.0011
Vancouver
Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MTB de M, Tabith Junior A, Kok F, Mingroni Netto RC. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss [Internet]. Genetic Testing and Molecular Biomarkers. 2010 ; 14( 5): 611-616.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1089/gtmb.2010.0011
Artigo de periodico
Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling (2009)
Batissoco, Ana Carla; Abreu-Silva, Ronaldo Serafim; Braga, Maria Cristina Célia; Lezirovitz, Karina; Della Rosa, Valter Augusto; Tabith Jr, Alfredo; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Ear and Hearing. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISSOCO, Ana Carla et al. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, v. 30, n. 1, p. 1-7, 2009Tradução . . Acesso em: 14 nov. 2024.
APA
Batissoco, A. C., Abreu-Silva, R. S., Braga, M. C. C., Lezirovitz, K., Della Rosa, V. A., Tabith Jr, A., et al. (2009). Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, 30( 1), 1-7.
NLM
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 nov. 14 ]
Vancouver
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 nov. 14 ]

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