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Artigo de periodico
Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort (2021)
Barbieri, Manuela Ramos; Fontes, Aparecida Maria ; Barbieri, Marco Antonio ; Saraiva, Maria da Conceição Pereira ; Simões, Vanda Maria Ferreira; Silva, A. A. M. da; Abraham, Kuruvilla Joseph ; Bettiol, Heloisa
Source: Brazilian Journal of Medical and Biological Research. Unidades: FMRP, FORP, ICMC
Subjects: ÍNDICE DE MASSA CORPORAL, ESTUDOS DE CASOS E CONTROLES, FETO, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, GENÓTIPOS, POLIMORFISMO
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ABNT
BARBIERI, Manuela Ramos et al. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort. Brazilian Journal of Medical and Biological Research, v. 54, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1590/1414-431X202010465. Acesso em: 19 nov. 2024.
APA
Barbieri, M. R., Fontes, A. M., Barbieri, M. A., Saraiva, M. da C. P., Simões, V. M. F., Silva, A. A. M. da, et al. (2021). Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort. Brazilian Journal of Medical and Biological Research, 54( 1). doi:10.1590/1414-431X202010465
NLM
Barbieri MR, Fontes AM, Barbieri MA, Saraiva M da CP, Simões VMF, Silva AAM da, Abraham KJ, Bettiol H. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/1414-431X202010465
Vancouver
Barbieri MR, Fontes AM, Barbieri MA, Saraiva M da CP, Simões VMF, Silva AAM da, Abraham KJ, Bettiol H. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/1414-431X202010465
Artigo de periodico
Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5 (2013)
Magalhães, H. R.; Leite, S. B. P.; Paz, C. C. P. de; Duarte, Geraldo; Ramos, Ester Silveira
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ALQUILAÇÃO, PLACENTA, IMPRINTING (GENÉTICA), REGULAÇÃO GÊNICA
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ABNT
MAGALHÃES, H. R. et al. Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5. Brazilian Journal of Medical and Biological Research, v. 46, n. 11, p. 919-919, 2013Tradução . . Disponível em: https://doi.org/10.1590/1414-431X20133035. Acesso em: 19 nov. 2024.
APA
Magalhães, H. R., Leite, S. B. P., Paz, C. C. P. de, Duarte, G., & Ramos, E. S. (2013). Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5. Brazilian Journal of Medical and Biological Research, 46( 11), 919-919. doi:10.1590/1414-431X20133035
NLM
Magalhães HR, Leite SBP, Paz CCP de, Duarte G, Ramos ES. Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5 [Internet]. Brazilian Journal of Medical and Biological Research. 2013 ; 46( 11): 919-919.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/1414-431X20133035
Vancouver
Magalhães HR, Leite SBP, Paz CCP de, Duarte G, Ramos ES. Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5 [Internet]. Brazilian Journal of Medical and Biological Research. 2013 ; 46( 11): 919-919.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/1414-431X20133035
Artigo de periodico
Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer (2011)
López, R. V. M; Zago, Marco Antonio; Eluf Neto, José; Curado, M. P.; Daudt, A W.; Silva Júnior, Wilson Araújo da; Zanette, D. L.; Levi, J. E.; Carvalho, M. B. de; Kowalski, L. P.; Abrahão, M.; Góis-Filho, J. F. de; Boffetta, P.; Wunsch Filho, Victor
Source: Brazilian Journal of Medical and Biological Research. Unidades: FMRP, FM, FSP
Subjects: NEOPLASIAS DE CABEÇA E PESCOÇO (RELAÇÃO), EDUCAÇÃO, ALCOOLISMO, TABAGISMO, POLIMORFISMO
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ABNT
LÓPEZ, R. V. M et al. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer. Brazilian Journal of Medical and Biological Research, v. 44, n. 10, p. 1006-1012, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500097. Acesso em: 19 nov. 2024.
APA
López, R. V. M., Zago, M. A., Eluf Neto, J., Curado, M. P., Daudt, A. W., Silva Júnior, W. A. da, et al. (2011). Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer. Brazilian Journal of Medical and Biological Research, 44( 10), 1006-1012. doi:10.1590/S0100-879X2011007500097
NLM
López RVM, Zago MA, Eluf Neto J, Curado MP, Daudt AW, Silva Júnior WA da, Zanette DL, Levi JE, Carvalho MB de, Kowalski LP, Abrahão M, Góis-Filho JF de, Boffetta P, Wunsch Filho V. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 10): 1006-1012.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/S0100-879X2011007500097
Vancouver
López RVM, Zago MA, Eluf Neto J, Curado MP, Daudt AW, Silva Júnior WA da, Zanette DL, Levi JE, Carvalho MB de, Kowalski LP, Abrahão M, Góis-Filho JF de, Boffetta P, Wunsch Filho V. Education, tobacco smoking, alcohol consumption, and IL-2 and IL-6 gene polymorphisms in the survival of head and neck cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 10): 1006-1012.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/S0100-879X2011007500097
Artigo de periodico
Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas (2010)
Castelli, Luciana Caricati Veiga; Silva, Júlio César Rosa e; Meola, Juliana; Ferriani, Rui Alberto; Yoshimoto, M.; Santos, Silvio Avelino dos; Squire, J. A.; Martelli, Lúcia Regina
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ENDOMETRIOSE, HIBRIDIZAÇÃO
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ABNT
CASTELLI, Luciana Caricati Veiga et al. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas. Brazilian Journal of Medical and Biological Research, v. 43, n. 8, p. 799-805, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2010007500072. Acesso em: 19 nov. 2024.
APA
Castelli, L. C. V., Silva, J. C. R. e, Meola, J., Ferriani, R. A., Yoshimoto, M., Santos, S. A. dos, et al. (2010). Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas. Brazilian Journal of Medical and Biological Research, 43( 8), 799-805. doi:10.1590/s0100-879x2010007500072
NLM
Castelli LCV, Silva JCR e, Meola J, Ferriani RA, Yoshimoto M, Santos SA dos, Squire JA, Martelli LR. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 8): 799-805.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2010007500072
Vancouver
Castelli LCV, Silva JCR e, Meola J, Ferriani RA, Yoshimoto M, Santos SA dos, Squire JA, Martelli LR. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 8): 799-805.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2010007500072
Artigo de periodico
Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer (2008)
Lima, E. M.; Leal, M. F.; Burbano, R. R.; Khayat, A. S.; Assumpção, P. P.; Bello, M. J.; Rey, J. A.; Smith, M. A. C.; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, DNA
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ABNT
LIMA, E. M. et al. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, v. 41, n. 6, p. 539-543, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000600017. Acesso em: 19 nov. 2024.
APA
Lima, E. M., Leal, M. F., Burbano, R. R., Khayat, A. S., Assumpção, P. P., Bello, M. J., et al. (2008). Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, 41( 6), 539-543. doi:10.1590/s0100-879x2008000600017
NLM
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Vancouver
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Artigo de periodico
Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype (2008)
Rodríguez, Viviana Rita; Mazzucatto, Luiz Fernando; Pina Neto, João Monteiro de
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: CITOGENÉTICA, FENÓTIPOS
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ABNT
RODRÍGUEZ, Viviana Rita e MAZZUCATTO, Luiz Fernando e PINA NETO, João Monteiro de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype. Brazilian Journal of Medical and Biological Research, v. 41, n. 8, p. 681-683, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000800007. Acesso em: 19 nov. 2024.
APA
Rodríguez, V. R., Mazzucatto, L. F., & Pina Neto, J. M. de. (2008). Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype. Brazilian Journal of Medical and Biological Research, 41( 8), 681-683. doi:10.1590/s0100-879x2008000800007
NLM
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 8): 681-683.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000800007
Vancouver
Rodríguez VR, Mazzucatto LF, Pina Neto JM de. Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 8): 681-683.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000800007
Artigo de periodico
Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome (2008)
Araújo, A.; Ramos, Ester Silveira
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Assunto: MAPEAMENTO CROMOSSÔMICO
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ABNT
ARAÚJO, A. e RAMOS, Ester Silveira. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Brazilian Journal of Medical and Biological Research, v. 41, n. 5, p. 368-372, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000500004. Acesso em: 19 nov. 2024.
APA
Araújo, A., & Ramos, E. S. (2008). Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Brazilian Journal of Medical and Biological Research, 41( 5), 368-372. doi:10.1590/s0100-879x2008000500004
NLM
Araújo A, Ramos ES. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 5): 368-372.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000500004
Vancouver
Araújo A, Ramos ES. Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 5): 368-372.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2008000500004
Artigo de periodico
miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia (2007)
Zanette, D. L.; Rivadavia, F.; Molfetta, Greice Andreotti de; Barbuzano, F. G.; Proto-Siqueira, R.; Falcão, Roberto Passetto; Zago, Marco Antônio; Silva Júnior, Wilson Araújo da
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: LEUCEMIA, LINFÓCITOS, RNA
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ABNT
ZANETTE, D. L. et al. miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia. Brazilian Journal of Medical and Biological Research, v. 40, n. 11, p. 1435-1440, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2007001100003. Acesso em: 19 nov. 2024.
APA
Zanette, D. L., Rivadavia, F., Molfetta, G. A. de, Barbuzano, F. G., Proto-Siqueira, R., Falcão, R. P., et al. (2007). miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia. Brazilian Journal of Medical and Biological Research, 40( 11), 1435-1440. doi:10.1590/s0100-879x2007001100003
NLM
Zanette DL, Rivadavia F, Molfetta GA de, Barbuzano FG, Proto-Siqueira R, Falcão RP, Zago MA, Silva Júnior WA da. miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40( 11): 1435-1440.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2007001100003
Vancouver
Zanette DL, Rivadavia F, Molfetta GA de, Barbuzano FG, Proto-Siqueira R, Falcão RP, Zago MA, Silva Júnior WA da. miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40( 11): 1435-1440.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2007001100003
Artigo de periodico
No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure (2007)
Dentillo, D. B.; Souza, F. R. P.; Meola, J.; Vieira, G. S.; Yazlle, Marta Edna Holanda Diógenes; Goulart, L. R.; Martelli, Lúcia Regina
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: POLIMORFISMO, REPRODUÇÃO
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ABNT
DENTILLO, D. B. et al. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure. Brazilian Journal of Medical and Biological Research, v. 40, p. 793-797, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2007000600007. Acesso em: 19 nov. 2024.
APA
Dentillo, D. B., Souza, F. R. P., Meola, J., Vieira, G. S., Yazlle, M. E. H. D., Goulart, L. R., & Martelli, L. R. (2007). No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure. Brazilian Journal of Medical and Biological Research, 40, 793-797. doi:10.1590/s0100-879x2007000600007
NLM
Dentillo DB, Souza FRP, Meola J, Vieira GS, Yazlle MEHD, Goulart LR, Martelli LR. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40 793-797.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2007000600007
Vancouver
Dentillo DB, Souza FRP, Meola J, Vieira GS, Yazlle MEHD, Goulart LR, Martelli LR. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40 793-797.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2007000600007
Artigo de periodico
Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men (2006)
Pina Neto, João Monteiro de; Carrara, R. C. V.; Bisinella, R.; Mazzucatto, Luiz Fernando; Martins, M. D.; Sartoratto, E.; Yamasaki, R.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: INFERTILIDADE MASCULINA, CROMOSSOMOS (ANOMALIAS), CARIOTIPAGEM
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ABNT
PINA NETO, João Monteiro de et al. Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men. Brazilian Journal of Medical and Biological Research, v. 39, n. 4, p. 1-7, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2006000400017. Acesso em: 19 nov. 2024.
APA
Pina Neto, J. M. de, Carrara, R. C. V., Bisinella, R., Mazzucatto, L. F., Martins, M. D., Sartoratto, E., & Yamasaki, R. (2006). Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men. Brazilian Journal of Medical and Biological Research, 39( 4), 1-7. doi:10.1590/s0100-879x2006000400017
NLM
Pina Neto JM de, Carrara RCV, Bisinella R, Mazzucatto LF, Martins MD, Sartoratto E, Yamasaki R. Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 1-7.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2006000400017
Vancouver
Pina Neto JM de, Carrara RCV, Bisinella R, Mazzucatto LF, Martins MD, Sartoratto E, Yamasaki R. Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 1-7.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2006000400017
Artigo de periodico
The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma (2006)
Huber, J.; Ramos, Ester Silveira
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA
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ABNT
HUBER, J. e RAMOS, Ester Silveira. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research, v. 39, p. 237-241, 2006Tradução . . Acesso em: 19 nov. 2024.
APA
Huber, J., & Ramos, E. S. (2006). The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research, 39, 237-241.
NLM
Huber J, Ramos ES. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research. 2006 ; 39 237-241.[citado 2024 nov. 19 ]
Vancouver
Huber J, Ramos ES. The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma. Brazilian Journal of Medical and Biological Research. 2006 ; 39 237-241.[citado 2024 nov. 19 ]
Artigo de periodico
Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil (2006)
Wünsch-Filho, V.; Eluf Neto, José; Lotufo, P. A.; Silva Junior, W. A.; Zago, M. A.
Source: Brazilian Journal of Medical and Biological Research. Unidades: FSP, FM, HU, FMRP
Subjects: NEOPLASIAS (ESTUDO), EPIDEMIOLOGIA (CLASSIFICAÇÃO;GENÉTICA), GENOMAS (EPIDEMIOLOGIA), SAÚDE PÚBLICA
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ABNT
WÜNSCH-FILHO, V. et al. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil. Brazilian Journal of Medical and Biological Research, v. 39, n. 4, p. 545-553, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2006000400016. Acesso em: 19 nov. 2024.
APA
Wünsch-Filho, V., Eluf Neto, J., Lotufo, P. A., Silva Junior, W. A., & Zago, M. A. (2006). Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil. Brazilian Journal of Medical and Biological Research, 39( 4), 545-553. doi:10.1590/s0100-879x2006000400016
NLM
Wünsch-Filho V, Eluf Neto J, Lotufo PA, Silva Junior WA, Zago MA. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 545-553.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2006000400016
Vancouver
Wünsch-Filho V, Eluf Neto J, Lotufo PA, Silva Junior WA, Zago MA. Epidemiological studies in the information and genomics era: experience of the Clinical Genome of Cancer Project in São Paulo, Brazil [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 4): 545-553.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2006000400016
Artigo de periodico
Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients (2004)
Bassi, C. L.; Martelli, Lúcia Regina; Cipolotti, R.; Scrideli, C. A.; Defavery, R.; Tone, Luiz Gonzaga
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA
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ABNT
BASSI, C. L. et al. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, v. 37, n. 11, p. 1683-1687, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001100014. Acesso em: 19 nov. 2024.
APA
Bassi, C. L., Martelli, L. R., Cipolotti, R., Scrideli, C. A., Defavery, R., & Tone, L. G. (2004). Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, 37( 11), 1683-1687. doi:10.1590/s0100-879x2004001100014
NLM
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Vancouver
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Artigo de periodico
Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor (2004)
Lima, E. M.; Rissino, J. D.; Harada, M. L.; Assumpção, P. P.; Demachki, S.; Guimarães, A. C.; Casartelli, Cacilda; Smith, M. A. C.; Burbano, R. R.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEOPLASIAS
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ABNT
LIMA, E. M. et al. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, v. 37, n. 12, p. 1831-1838, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001200008. Acesso em: 19 nov. 2024.
APA
Lima, E. M., Rissino, J. D., Harada, M. L., Assumpção, P. P., Demachki, S., Guimarães, A. C., et al. (2004). Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, 37( 12), 1831-1838. doi:10.1590/s0100-879x2004001200008
NLM
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Vancouver
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Artigo de periodico
DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells (2004)
Ribeiro, C. N. M.; Peres, Luiz César; Pina Neto, João Monteiro de
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: REAÇÃO EM CADEIA POR POLIMERASE, DNA, AUTÓPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, C. N. M. e PERES, Luiz César e PINA NETO, João Monteiro de. DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells. Brazilian Journal of Medical and Biological Research, v. 37, n. 5, p. 635-642, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004000500002. Acesso em: 19 nov. 2024.
APA
Ribeiro, C. N. M., Peres, L. C., & Pina Neto, J. M. de. (2004). DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells. Brazilian Journal of Medical and Biological Research, 37( 5), 635-642. doi:10.1590/s0100-879x2004000500002
NLM
Ribeiro CNM, Peres LC, Pina Neto JM de. DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 5): 635-642.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004000500002
Vancouver
Ribeiro CNM, Peres LC, Pina Neto JM de. DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 5): 635-642.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2004000500002
Artigo de periodico
Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer (2000)
Burbano, R. R.; Medeiros, A. C.; Mello, A. A.; Lemos, José Alexandre; Bahia, Marcelo de Oliveira; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURBANO, R. R. et al. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, v. 33, n. 11, p. 1325-1328, 2000Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2000001100010. Acesso em: 19 nov. 2024.
APA
Burbano, R. R., Medeiros, A. C., Mello, A. A., Lemos, J. A., Bahia, M. de O., & Casartelli, C. (2000). Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, 33( 11), 1325-1328. doi:10.1590/s0100-879x2000001100010
NLM
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010
Vancouver
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010

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