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Trabalho de evento-resumo
HLA-G gene associated with vitiligo in a Brazilian population sample (2019)
Oliveira, Maria Luiza Guimarães de ; Castelli, Luciana Caricati Veiga ; Pereira, Alison Luis Eburneo; Debortoli, Guilherme ; Marcorin, Letícia ; Fracasso, Nádia Carolina de Aguiar; Silva, Guilherme do Valle ; Souza, A. S.; Massaro, Juliana Doblas ; Simões, Aguinaldo Luiz ; Sabbagh, A.; Cardili, Renata Nahas; Donadi, Eduardo Antônio ; Castelli, E. C.; Mendes Júnior, Celso Teixeira
Fonte: Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Assuntos: GENES, VITILIGO, DOENÇAS AUTOIMUNES, POPULAÇÃO
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ABNT
OLIVEIRA, Maria Luiza Guimarães de et al. HLA-G gene associated with vitiligo in a Brazilian population sample. 2019, Anais.. Houston: ASHG, 2019. Disponível em: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf. Acesso em: 19 nov. 2024.
APA
Oliveira, M. L. G. de, Castelli, L. C. V., Pereira, A. L. E., Debortoli, G., Marcorin, L., Fracasso, N. C. de A., et al. (2019). HLA-G gene associated with vitiligo in a Brazilian population sample. In Abstracts. Houston: ASHG. Recuperado de https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
NLM
Oliveira MLG de, Castelli LCV, Pereira ALE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G gene associated with vitiligo in a Brazilian population sample [Internet]. Abstracts. 2019 ;[citado 2024 nov. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Vancouver
Oliveira MLG de, Castelli LCV, Pereira ALE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza AS, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G gene associated with vitiligo in a Brazilian population sample [Internet]. Abstracts. 2019 ;[citado 2024 nov. 19 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Trabalho de evento-resumo
MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil (2017)
Mendes Júnior, Celso Teixeira; Pereira, A. L. E.; Marcorin, L.; Oliveira, M. L. G.; Fracasso, N. C. A.; Debortoli, G.; Silva, G. V.; Massaro, J. D.; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz
Fonte: Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Assuntos: DIVERSIDADE GENÉTICA, MELANINAS, POPULAÇÃO
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. 2017, Anais.. Orlando: ASHG, 2017. . Acesso em: 19 nov. 2024.
APA
Mendes Júnior, C. T., Pereira, A. L. E., Marcorin, L., Oliveira, M. L. G., Fracasso, N. C. A., Debortoli, G., et al. (2017). MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. In Abstracts. Orlando: ASHG.
NLM
Mendes Júnior CT, Pereira ALE, Marcorin L, Oliveira MLG, Fracasso NCA, Debortoli G, Silva GV, Massaro JD, Simões AL, Donadi EA, Castelli E da C. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. Abstracts. 2017 ;[citado 2024 nov. 19 ]
Vancouver
Mendes Júnior CT, Pereira ALE, Marcorin L, Oliveira MLG, Fracasso NCA, Debortoli G, Silva GV, Massaro JD, Simões AL, Donadi EA, Castelli E da C. MC1R regulatory and coding polymorphisms and pigmentation in an admixed population from Brazil. Abstracts. 2017 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population (2016)
Debortoli, G.; Marcorin, L.; Oliveira, M. L. G.; Pereira, A. L. E.; Fracasso, N. C. A.; Massaro, Juliana Doblas; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz; Mendes Júnior, Celso Teixeira
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
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ABNT
DEBORTOLI, G. et al. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 19 nov. 2024.
APA
Debortoli, G., Marcorin, L., Oliveira, M. L. G., Pereira, A. L. E., Fracasso, N. C. A., Massaro, J. D., et al. (2016). Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. In Poster Abstracts. Vancouver: ASHG.
NLM
Debortoli G, Marcorin L, Oliveira MLG, Pereira ALE, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Mendes Júnior CT. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Vancouver
Debortoli G, Marcorin L, Oliveira MLG, Pereira ALE, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Mendes Júnior CT. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population (2016)
Mendes Júnior, Celso Teixeira; Pereira, A. L. E.; Debortoli, G.; Oliveira, M. L. G.; Fracasso, N. C. A.; Massaro, Juliana Doblas; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz; Marcorin, L.
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDES JÚNIOR, Celso Teixeira et al. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 19 nov. 2024.
APA
Mendes Júnior, C. T., Pereira, A. L. E., Debortoli, G., Oliveira, M. L. G., Fracasso, N. C. A., Massaro, J. D., et al. (2016). MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. In Poster Abstracts. Vancouver: ASHG.
NLM
Mendes Júnior CT, Pereira ALE, Debortoli G, Oliveira MLG, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Marcorin L. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Vancouver
Mendes Júnior CT, Pereira ALE, Debortoli G, Oliveira MLG, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Marcorin L. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development (2016)
Cagnin, N. F.; Barbosa, F. B.; Marano, L.; Mendes Júnior, Celso Teixeira; Donadi, Eduardo Antônio; Simões, Aguinaldo Luiz
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FFCLRP, FMRP
Assuntos: GENÉTICA MÉDICA, LÚPUS ERITEMATOSO SISTÊMICO
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ABNT
CAGNIN, N. F. et al. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 19 nov. 2024.
APA
Cagnin, N. F., Barbosa, F. B., Marano, L., Mendes Júnior, C. T., Donadi, E. A., & Simões, A. L. (2016). Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. In Poster Abstracts. Vancouver: ASHG.
NLM
Cagnin NF, Barbosa FB, Marano L, Mendes Júnior CT, Donadi EA, Simões AL. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Vancouver
Cagnin NF, Barbosa FB, Marano L, Mendes Júnior CT, Donadi EA, Simões AL. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. Poster Abstracts. 2016 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil (2012)
Andrade, E. S.; Fracasso, N. C. A.; Strazza Júnior, P. S.; Simões, Aguinaldo Luiz; Mendes Júnior, Celso Teixeira
Fonte: Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, E. S. et al. Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil. 2012, Anais.. San Francisco: ASHG, 2012. . Acesso em: 19 nov. 2024.
APA
Andrade, E. S., Fracasso, N. C. A., Strazza Júnior, P. S., Simões, A. L., & Mendes Júnior, C. T. (2012). Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil. In Abstracts. San Francisco: ASHG.
NLM
Andrade ES, Fracasso NCA, Strazza Júnior PS, Simões AL, Mendes Júnior CT. Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil. Abstracts. 2012 ;[citado 2024 nov. 19 ]
Vancouver
Andrade ES, Fracasso NCA, Strazza Júnior PS, Simões AL, Mendes Júnior CT. Allelic and genotypic associations of SNPs of the OCA2 and HERC2 genes with eye, hair and skin pigmentation and the presence of freckles in Brazil. Abstracts. 2012 ;[citado 2024 nov. 19 ]
Trabalho de evento-resumo
Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence (2012)
Marano, L. A.; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Mendes Júnior, Celso Teixeira
Fonte: Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, MARCADOR MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARANO, L. A. et al. Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence. 2012, Anais.. San Francisco: ASHG, 2012. . Acesso em: 19 nov. 2024.
APA
Marano, L. A., Simões, A. L., Donadi, E. A., & Mendes Júnior, C. T. (2012). Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence. In Abstracts. San Francisco: ASHG.
NLM
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence. Abstracts. 2012 ;[citado 2024 nov. 19 ]
Vancouver
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Alleles at the rs3212368 SNP at the 3’UTR of the MC1R gene are associated with human pigmentation by possible microRNA influence. Abstracts. 2012 ;[citado 2024 nov. 19 ]

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