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Artigo de periodico
Association Between Human Leukocyte Antigen Polymorphism and Human Papillomavirus Infection in Brazilian Women (2023)
Araujo-Souza, Patricia Savio de; El-Zein, Mariam; Bolpetti, Aline do N; Maciag, Paulo Cesar; Rabachini, Tatiana; Franco, Eduardo L; Villa, Luisa Lina
Fonte: Sexually transmitted diseases. Unidade: FM
Assuntos: POLIMORFISMO, INFECÇÕES POR PAPILLOMAVIRUS, MULHERES
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ARAUJO-SOUZA, Patricia Savio de et al. Association Between Human Leukocyte Antigen Polymorphism and Human Papillomavirus Infection in Brazilian Women. Sexually transmitted diseases, v. 50, n. 1, p. 50-58, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/51482. Acesso em: 05 ago. 2024.
APA
Araujo-Souza, P. S. de, El-Zein, M., Bolpetti, A. do N., Maciag, P. C., Rabachini, T., Franco, E. L., & Villa, L. L. (2023). Association Between Human Leukocyte Antigen Polymorphism and Human Papillomavirus Infection in Brazilian Women. Sexually transmitted diseases, 50( 1), 50-58. doi:10.1097/OLQ.0000000000001718
NLM
Araujo-Souza PS de, El-Zein M, Bolpetti A do N, Maciag PC, Rabachini T, Franco EL, Villa LL. Association Between Human Leukocyte Antigen Polymorphism and Human Papillomavirus Infection in Brazilian Women [Internet]. Sexually transmitted diseases. 2023 ; 50( 1): 50-58.[citado 2024 ago. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/51482
Vancouver
Araujo-Souza PS de, El-Zein M, Bolpetti A do N, Maciag PC, Rabachini T, Franco EL, Villa LL. Association Between Human Leukocyte Antigen Polymorphism and Human Papillomavirus Infection in Brazilian Women [Internet]. Sexually transmitted diseases. 2023 ; 50( 1): 50-58.[citado 2024 ago. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/51482
Artigo de periodico
The role of single-nucleotide polymorphism (SNPs) in toxicity of induction chemotherapy based on cisplatin and paclitaxel in patients with advanced head and neck cancer (2019)
Marchi, Pedro De; Melendez, Matias E; Laus, Ana C; Kuhlmann, Pamela A; Carvalho, Ana Carolina de; Arantes, Lidia Maria R. B; Evangelista, Adriane F; Andrade, Edilene S; Castro Junior, Gilberto de Castro ; Reis, Rui M
Fonte: Oral oncology. Unidade: FM
Assuntos: NEOPLASIAS DE CABEÇA E PESCOÇO, POLIMORFISMO, CARCINOMA DE CÉLULAS ESCAMOSAS, SEQUENCIAMENTO GENÉTICO, QUIMIOTERAPIA, ANTINEOPLÁSICOS, PROTEÍNAS DE TRANSPORTE, GENÓTIPOS
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MARCHI, Pedro De et al. The role of single-nucleotide polymorphism (SNPs) in toxicity of induction chemotherapy based on cisplatin and paclitaxel in patients with advanced head and neck cancer. Oral oncology, v. 98, p. 48-52, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.oraloncology.2019.09.013. Acesso em: 05 ago. 2024.
APA
Marchi, P. D., Melendez, M. E., Laus, A. C., Kuhlmann, P. A., Carvalho, A. C. de, Arantes, L. M. R. B., et al. (2019). The role of single-nucleotide polymorphism (SNPs) in toxicity of induction chemotherapy based on cisplatin and paclitaxel in patients with advanced head and neck cancer. Oral oncology, 98, 48-52. doi:10.1016/j.oraloncology.2019.09.013
NLM
Marchi PD, Melendez ME, Laus AC, Kuhlmann PA, Carvalho AC de, Arantes LMRB, Evangelista AF, Andrade ES, Castro Junior G de C, Reis RM. The role of single-nucleotide polymorphism (SNPs) in toxicity of induction chemotherapy based on cisplatin and paclitaxel in patients with advanced head and neck cancer [Internet]. Oral oncology. 2019 ; 98 48-52.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.oraloncology.2019.09.013
Vancouver
Marchi PD, Melendez ME, Laus AC, Kuhlmann PA, Carvalho AC de, Arantes LMRB, Evangelista AF, Andrade ES, Castro Junior G de C, Reis RM. The role of single-nucleotide polymorphism (SNPs) in toxicity of induction chemotherapy based on cisplatin and paclitaxel in patients with advanced head and neck cancer [Internet]. Oral oncology. 2019 ; 98 48-52.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.oraloncology.2019.09.013
Artigo de periodico
Variants in immune-related genes and genital HPV 16 persistence in men (2019)
Mainali, Bigyan; Schabath, Matthew B; Sudenga, Staci L; Ye, Yuanfan; Wiener, Howard W; Villa, Luisa Lina; Giuliano, Anna R; Shrestha, Sadeep
Fonte: Papillomavirus research. Unidade: FM
Assuntos: HPV, GENES VIRAIS, VERRUGAS, HOMENS, GENÔMICA, POLIMORFISMO, REGRESSÃO LOGÍSTICA
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MAINALI, Bigyan et al. Variants in immune-related genes and genital HPV 16 persistence in men. Papillomavirus research, v. 7, p. 11-14, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.pvr.2018.08.001. Acesso em: 05 ago. 2024.
APA
Mainali, B., Schabath, M. B., Sudenga, S. L., Ye, Y., Wiener, H. W., Villa, L. L., et al. (2019). Variants in immune-related genes and genital HPV 16 persistence in men. Papillomavirus research, 7, 11-14. doi:10.1016/j.pvr.2018.08.001
NLM
Mainali B, Schabath MB, Sudenga SL, Ye Y, Wiener HW, Villa LL, Giuliano AR, Shrestha S. Variants in immune-related genes and genital HPV 16 persistence in men [Internet]. Papillomavirus research. 2019 ; 7 11-14.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.pvr.2018.08.001
Vancouver
Mainali B, Schabath MB, Sudenga SL, Ye Y, Wiener HW, Villa LL, Giuliano AR, Shrestha S. Variants in immune-related genes and genital HPV 16 persistence in men [Internet]. Papillomavirus research. 2019 ; 7 11-14.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.pvr.2018.08.001
Artigo de periodico
Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer (2018)
Furuya, Tatiane K.; Jacob, Carlos E.; Tomitao, Michele T. P; Camacho, Lizeth C. C; Ramos, Marcus F. K. P; Eluf Neto, José; Alves, Venâncio Avancini Ferreira; Zilberstein, Bruno; Cecconello, Ivan; Ribeiro Júnior, Ulysses; Chammas, Roger
Fonte: Genes. Unidade: FM
Assuntos: NEOPLASIAS GÁSTRICAS, POLIMORFISMO, INFLAMAÇÃO, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, PROGNÓSTICO
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FURUYA, Tatiane K. et al. Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer. Genes, v. 9, n. 12, 2018Tradução . . Disponível em: https://doi.org/10.3390/genes9120631. Acesso em: 05 ago. 2024.
APA
Furuya, T. K., Jacob, C. E., Tomitao, M. T. P., Camacho, L. C. C., Ramos, M. F. K. P., Eluf Neto, J., et al. (2018). Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer. Genes, 9( 12). doi:10.3390/genes9120631
NLM
Furuya TK, Jacob CE, Tomitao MTP, Camacho LCC, Ramos MFKP, Eluf Neto J, Alves VAF, Zilberstein B, Cecconello I, Ribeiro Júnior U, Chammas R. Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer [Internet]. Genes. 2018 ; 9( 12):[citado 2024 ago. 05 ] Available from: https://doi.org/10.3390/genes9120631
Vancouver
Furuya TK, Jacob CE, Tomitao MTP, Camacho LCC, Ramos MFKP, Eluf Neto J, Alves VAF, Zilberstein B, Cecconello I, Ribeiro Júnior U, Chammas R. Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer [Internet]. Genes. 2018 ; 9( 12):[citado 2024 ago. 05 ] Available from: https://doi.org/10.3390/genes9120631
Trabalho de evento-resumo periodico
GAD1 polymorphisms are associated with glutamatergic activity in the anterior cingulare in bipolar I disorder (2017)
Souza, Marcio Soeiro de; Vieira, Rodrigo Machado; Moreno, Ricardo; Chile, Thais; Gouveia, Gisele; Pastorello, Bruno; Leite, Claudia da Costa; Henning, Anke; Otaduy, Maria Concepcion; Vallada Filho, Homero Pinto
Fonte: European neuropsychopharmacology. Nome do evento: Annual World Congress of Psychiatric Genetics (WCPG). Unidade: FM
Assuntos: TRANSTORNO BIPOLAR, ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR, POLIMORFISMO, GENES
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SOUZA, Marcio Soeiro de et al. GAD1 polymorphisms are associated with glutamatergic activity in the anterior cingulare in bipolar I disorder. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 ago. 2024. , 2017
APA
Souza, M. S. de, Vieira, R. M., Moreno, R., Chile, T., Gouveia, G., Pastorello, B., et al. (2017). GAD1 polymorphisms are associated with glutamatergic activity in the anterior cingulare in bipolar I disorder. European neuropsychopharmacology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo.
NLM
Souza MS de, Vieira RM, Moreno R, Chile T, Gouveia G, Pastorello B, Leite C da C, Henning A, Otaduy MC, Vallada Filho HP. GAD1 polymorphisms are associated with glutamatergic activity in the anterior cingulare in bipolar I disorder. European neuropsychopharmacology. 2017 ; 27 S213.[citado 2024 ago. 05 ]
Vancouver
Souza MS de, Vieira RM, Moreno R, Chile T, Gouveia G, Pastorello B, Leite C da C, Henning A, Otaduy MC, Vallada Filho HP. GAD1 polymorphisms are associated with glutamatergic activity in the anterior cingulare in bipolar I disorder. European neuropsychopharmacology. 2017 ; 27 S213.[citado 2024 ago. 05 ]
Artigo de periodico
Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population (2017)
Tomitão, Michele Tatiana Pereira; Nahas, Sergio Carlos; Kubrusly, Marcia Saldanha; Furuya, Tatiane Katsue; Diniz, Marcio Augusto; Marie, Suely Kazue Nagahashi; Safatle-Ribeiro, Adriana Vaz; Eluf-Neto, José; Cecconello, Ivan; Ribeiro Junior, Ulysses
Fonte: Journal of gastrointestinal oncology. Unidade: FM
Assuntos: GENES, RISCO, NEOPLASIAS COLORRETAIS, POLIMORFISMO
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TOMITÃO, Michele Tatiana Pereira et al. Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population. Journal of gastrointestinal oncology, v. 8, n. 4, p. 629-635, 2017Tradução . . Disponível em: https://doi.org/10.1186/s12960-017-0245-9. Acesso em: 05 ago. 2024.
APA
Tomitão, M. T. P., Nahas, S. C., Kubrusly, M. S., Furuya, T. K., Diniz, M. A., Marie, S. K. N., et al. (2017). Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population. Journal of gastrointestinal oncology, 8( 4), 629-635. doi:10.1186/s12960-017-0245-9
NLM
Tomitão MTP, Nahas SC, Kubrusly MS, Furuya TK, Diniz MA, Marie SKN, Safatle-Ribeiro AV, Eluf-Neto J, Cecconello I, Ribeiro Junior U. Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population [Internet]. Journal of gastrointestinal oncology. 2017 ; 8( 4): 629-635.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1186/s12960-017-0245-9
Vancouver
Tomitão MTP, Nahas SC, Kubrusly MS, Furuya TK, Diniz MA, Marie SKN, Safatle-Ribeiro AV, Eluf-Neto J, Cecconello I, Ribeiro Junior U. Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population [Internet]. Journal of gastrointestinal oncology. 2017 ; 8( 4): 629-635.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1186/s12960-017-0245-9
Artigo de periodico
The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder (2017)
Soeiro-de-Souza, M. G.; Lafer, B.; Moreno, R. A.; Nery, F. G.; Chile, T.; Chaim, K.; Leite, C da Costa; Machado-Vieira, R.; Otaduy, M. C. G.; Vallada, H.
Fonte: Translational Psychiatry. Unidade: FM
Assuntos: POLIMORFISMO, CÉREBRO, ALELOS, TRANSTORNO BIPOLAR
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SOEIRO-DE-SOUZA, M. G. et al. The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder. Translational Psychiatry, v. 7, n. 3, p. 6 art. e1086, 2017Tradução . . Disponível em: https://doi.org/10.1038/tp.2017.57. Acesso em: 05 ago. 2024.
APA
Soeiro-de-Souza, M. G., Lafer, B., Moreno, R. A., Nery, F. G., Chile, T., Chaim, K., et al. (2017). The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder. Translational Psychiatry, 7( 3), 6 art. e1086. doi:10.1038/tp.2017.57
NLM
Soeiro-de-Souza MG, Lafer B, Moreno RA, Nery FG, Chile T, Chaim K, Leite C da C, Machado-Vieira R, Otaduy MCG, Vallada H. The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder [Internet]. Translational Psychiatry. 2017 ; 7( 3): 6 art. e1086.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1038/tp.2017.57
Vancouver
Soeiro-de-Souza MG, Lafer B, Moreno RA, Nery FG, Chile T, Chaim K, Leite C da C, Machado-Vieira R, Otaduy MCG, Vallada H. The CACNA1C risk allele rs1006737 is associated with age-related prefrontal cortical thinning in bipolar I disorder [Internet]. Translational Psychiatry. 2017 ; 7( 3): 6 art. e1086.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1038/tp.2017.57
Artigo de periodico
Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria (2015)
Gonzaga, Ana Denise Gomes; Amorim, Lidia Maria da Fonte de; Fonseca, Ana Beatriz Monteiro; Nogueira, Tatiana Lucia Santos; Pereira, Olga Maria Diniz; Nagai, Maria Aparecida; Barretto, Orlando Cesar de Oliveira; Ribeiro, Georgina Severo
Fonte: Annals of Human Genetics. Unidade: FM
Assuntos: SEQUÊNCIA DO DNA, POPULAÇÃO, MUTAÇÃO GENÉTICA, POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE, BRASIL
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GONZAGA, Ana Denise Gomes et al. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, v. 79, n. 3, p. 162-172, 2015Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf. Acesso em: 05 ago. 2024.
APA
Gonzaga, A. D. G., Amorim, L. M. da F. de, Fonseca, A. B. M., Nogueira, T. L. S., Pereira, O. M. D., Nagai, M. A., et al. (2015). Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, 79( 3), 162-172. doi:10.1111/ahg.12102
NLM
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2024 ago. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
Vancouver
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2024 ago. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
Artigo de periodico
Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3′ Untranslated Region 1630 C>T Polymorphism and Copy Number Variation (2014)
Leal, Mariana Ferreira; Cirilo, Priscila Daniele Ramos; Mazzotti, Tatiane Katsue Furuya; Calcagno, Danielle Queiroz; Wisnieski, Fernanda; Demachki, Samia; Martinez, Margarita Cortes; Assumpção, Paulo Pimentel; Chammas, Roger; Burbano, Rommel Rodríguez; Smith, Marília Cardoso
Fonte: PLOS ONE. Unidade: FM
Assuntos: REAÇÃO EM CADEIA POR POLIMERASE, EXPRESSÃO GÊNICA, POLIMORFISMO, NEOPLASIAS GÁSTRICAS (EPIDEMIOLOGIA)
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ABNT
LEAL, Mariana Ferreira et al. Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3′ Untranslated Region 1630 C>T Polymorphism and Copy Number Variation. PLOS ONE, v. 9, n. 5, p. 9 art. e98583, 2014Tradução . . Disponível em: http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0098583&representation=PDF. Acesso em: 05 ago. 2024.
APA
Leal, M. F., Cirilo, P. D. R., Mazzotti, T. K. F., Calcagno, D. Q., Wisnieski, F., Demachki, S., et al. (2014). Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3′ Untranslated Region 1630 C>T Polymorphism and Copy Number Variation. PLOS ONE, 9( 5), 9 art. e98583. doi:10.1371/journal.pone.0098583
NLM
Leal MF, Cirilo PDR, Mazzotti TKF, Calcagno DQ, Wisnieski F, Demachki S, Martinez MC, Assumpção PP, Chammas R, Burbano RR, Smith MC. Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3′ Untranslated Region 1630 C>T Polymorphism and Copy Number Variation [Internet]. PLOS ONE. 2014 ; 9( 5): 9 art. e98583.[citado 2024 ago. 05 ] Available from: http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0098583&representation=PDF
Vancouver
Leal MF, Cirilo PDR, Mazzotti TKF, Calcagno DQ, Wisnieski F, Demachki S, Martinez MC, Assumpção PP, Chammas R, Burbano RR, Smith MC. Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3′ Untranslated Region 1630 C>T Polymorphism and Copy Number Variation [Internet]. PLOS ONE. 2014 ; 9( 5): 9 art. e98583.[citado 2024 ago. 05 ] Available from: http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0098583&representation=PDF
Artigo de periodico
p27 variant and corticotropinoma susceptibility: a genetic and in vitro study (2014)
Sekiya, Tomoko; Bronstein, Marcello Delano ; Benfini, Katiuscia; Longuini, Viviane Cristina; Jallad, Raquel Soares; Machado, Marcio Cardoso; Gonçalves, Tatiana Denk; Osaki, Luciana Harumi; Higashi, Leonardo; Viana Junior, Jose; Kater, Claudio; Lee, Misu; Molatore, Sara; Francisco, Guilherme; Chammas, Roger ; Naslavsky, Michel ; Schlesinger, David; Gama, Patrícia ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lúcia ; Zatz, Mayana ; Meirelles, Osorio; Liberman, Bernardo; Fragoso, Maria Candida Barisson Villares ; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo de Almeida; Zatz, Mayana
Fonte: Endocrine-Related Cancer. Unidades: ICB, FM, EE, IB, FSP
Assuntos: BIOLOGIA CELULAR, GENÉTICA, MUTAÇÃO GENÉTICA, RATOS, POLIMORFISMO, GENÓTIPOS, NEOPLASIAS DA TIREOIDE, ADENOMA
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ABNT
SEKIYA, Tomoko et al. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, v. 21, n. 3, p. 395-404, 2014Tradução . . Disponível em: https://doi.org/10.1530/ERC-13-0486. Acesso em: 05 ago. 2024.
APA
Sekiya, T., Bronstein, M. D., Benfini, K., Longuini, V. C., Jallad, R. S., Machado, M. C., et al. (2014). p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, 21( 3), 395-404. doi:10.1530/ERC-13-0486
NLM
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1530/ERC-13-0486
Vancouver
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1530/ERC-13-0486
Artigo de periodico
ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia (2014)
Alencar, Guilherme Asmar; Lerario, Antonio Marcondes; Nishi, Mirian Yumie; Mariani, Beatriz Marinho de Paula; Almeida, Madson Queiroz; Tremblay, Johanne; Hamet, Pavel; Zerbini, Maria Claudis Nogueira; Gomes, Gilberto Carlos; Bordeau, Isabelle; Pereira, Maria Adelaide Albergaria; Rocha, Manoel de Souza; Chambo, Jose Carlos; Lacroix, Andre; Mendonça, Berenice Bilharinho; Fragoso, Maria Candida B. Villares
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: POLIMORFISMO, MUTAÇÃO GENÉTICA, HIPERPLASIA SUPRARRENAL CONGÊNITA
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ALENCAR, Guilherme Asmar et al. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 8, p. E1501-E1509, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-4237. Acesso em: 05 ago. 2024.
APA
Alencar, G. A., Lerario, A. M., Nishi, M. Y., Mariani, B. M. de P., Almeida, M. Q., Tremblay, J., et al. (2014). ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 99( 8), E1501-E1509. doi:10.1210/jc.2013-4237
NLM
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1210/jc.2013-4237
Vancouver
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1210/jc.2013-4237
Trabalho de evento-resumo periodico
Erlotinib in metastatic pulmonary adenocarcinomas harbouring EGFR activating mutations, in Sao Paulo - Brazil (2013)
Caires-Lima, Rafael; Protasio, Bruno M.; Takahashi, Tiago K.; Mak, Milena P.; Nakazato, Denyei; Mesquita, Cristiane S.; Takagaki, Teresa Y.; Soares, Iberê C.; Mello, Evandro S.; Hoff, Paulo M.; Alves, Venâncio A.; Castro Jr., Gilberto
Fonte: Journal of thoracic oncology. Nome do evento: World Conference on Lung Cancer. Unidade: FM
Assuntos: NEOPLASIAS PULMONARES, POLIMORFISMO, ADENOCARCINOMA, MUTAÇÃO, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAIRES-LIMA, Rafael et al. Erlotinib in metastatic pulmonary adenocarcinomas harbouring EGFR activating mutations, in Sao Paulo - Brazil. Journal of thoracic oncology. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 ago. 2024. , 2013
APA
Caires-Lima, R., Protasio, B. M., Takahashi, T. K., Mak, M. P., Nakazato, D., Mesquita, C. S., et al. (2013). Erlotinib in metastatic pulmonary adenocarcinomas harbouring EGFR activating mutations, in Sao Paulo - Brazil. Journal of thoracic oncology. Faculdade de Medicina, Universidade de São Paulo.
NLM
Caires-Lima R, Protasio BM, Takahashi TK, Mak MP, Nakazato D, Mesquita CS, Takagaki TY, Soares IC, Mello ES, Hoff PM, Alves VA, Castro Jr. G. Erlotinib in metastatic pulmonary adenocarcinomas harbouring EGFR activating mutations, in Sao Paulo - Brazil. Journal of thoracic oncology. 2013 ; 8 S892.[citado 2024 ago. 05 ]
Vancouver
Caires-Lima R, Protasio BM, Takahashi TK, Mak MP, Nakazato D, Mesquita CS, Takagaki TY, Soares IC, Mello ES, Hoff PM, Alves VA, Castro Jr. G. Erlotinib in metastatic pulmonary adenocarcinomas harbouring EGFR activating mutations, in Sao Paulo - Brazil. Journal of thoracic oncology. 2013 ; 8 S892.[citado 2024 ago. 05 ]
Trabalho de evento-resumo periodico
Clinic Evolution of the Cutaneous Melanoma in Patients with Selected Polymorphism in Nucleotide Excison Repair Genes (2013)
Campagnari, M.; Pedreira Duprat, J.; Chammas, R.; Katsue Furuya, T.; Cirilo, P.; Bertolli, E.
Fonte: JDDG: Journal der Deutschen Dermatologischen Gesellschaft. Nome do evento: World Congress of Melanoma. Unidade: FM
Assuntos: MELANOMA, EVOLUÇÃO CLÍNICA, REPARAÇÃO DE DNA, POLIMORFISMO, NUCLEOTÍDEOS, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPAGNARI, M. et al. Clinic Evolution of the Cutaneous Melanoma in Patients with Selected Polymorphism in Nucleotide Excison Repair Genes. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. Berlin: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/ddg.12161/pdf. Acesso em: 05 ago. 2024. , 2013
APA
Campagnari, M., Pedreira Duprat, J., Chammas, R., Katsue Furuya, T., Cirilo, P., & Bertolli, E. (2013). Clinic Evolution of the Cutaneous Melanoma in Patients with Selected Polymorphism in Nucleotide Excison Repair Genes. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. Berlin: Faculdade de Medicina, Universidade de São Paulo. doi:10.1111/ddg.12161
NLM
Campagnari M, Pedreira Duprat J, Chammas R, Katsue Furuya T, Cirilo P, Bertolli E. Clinic Evolution of the Cutaneous Melanoma in Patients with Selected Polymorphism in Nucleotide Excison Repair Genes [Internet]. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2013 ; 11 48.[citado 2024 ago. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ddg.12161/pdf
Vancouver
Campagnari M, Pedreira Duprat J, Chammas R, Katsue Furuya T, Cirilo P, Bertolli E. Clinic Evolution of the Cutaneous Melanoma in Patients with Selected Polymorphism in Nucleotide Excison Repair Genes [Internet]. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2013 ; 11 48.[citado 2024 ago. 05 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ddg.12161/pdf
Trabalho de evento-resumo periodico
Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause (2013)
Souza, M. A.; Fonseca, A. M.; Bagnoli, V. R.; De Barros, N.; Mendonça, E. N.; Hortense, V. H.; Soares Jr., J. M.; Baracat, E. C.
Fonte: Giornale Italiano di Obstetricia e Ginecologia. Nome do evento: World Congress on Human reproduction. Unidade: FM
Assuntos: MENOPAUSA, BRASILEIROS, ESTROGÉNOS, MAMA (FISIOPATOLOGIA), POLIMORFISMO, FATORES DE RISCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, M. A. et al. Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause. Giornale Italiano di Obstetricia e Ginecologia. Torino: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://www.giog.it/common/php/portiere.php?ID=a87b8c19ec6c9f6b9735557c79944910. Acesso em: 05 ago. 2024. , 2013
APA
Souza, M. A., Fonseca, A. M., Bagnoli, V. R., De Barros, N., Mendonça, E. N., Hortense, V. H., et al. (2013). Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause. Giornale Italiano di Obstetricia e Ginecologia. Torino: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://www.giog.it/common/php/portiere.php?ID=a87b8c19ec6c9f6b9735557c79944910
NLM
Souza MA, Fonseca AM, Bagnoli VR, De Barros N, Mendonça EN, Hortense VH, Soares Jr. JM, Baracat EC. Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause [Internet]. Giornale Italiano di Obstetricia e Ginecologia. 2013 ; 35( 1): 343-348.[citado 2024 ago. 05 ] Available from: http://www.giog.it/common/php/portiere.php?ID=a87b8c19ec6c9f6b9735557c79944910
Vancouver
Souza MA, Fonseca AM, Bagnoli VR, De Barros N, Mendonça EN, Hortense VH, Soares Jr. JM, Baracat EC. Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause [Internet]. Giornale Italiano di Obstetricia e Ginecologia. 2013 ; 35( 1): 343-348.[citado 2024 ago. 05 ] Available from: http://www.giog.it/common/php/portiere.php?ID=a87b8c19ec6c9f6b9735557c79944910
Artigo de periodico
Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis (2013)
Walter, Stephen D.; Riddell, Corinne A.; Rabachini, Tatiana; Villa, Luisa L.; Franco, Eduardo L.
Fonte: PLOS ONE. Unidade: FM
Assuntos: FATORES DE RISCO, POLIMORFISMO, PAPILLOMAVIRUS, GENÓTIPOS, NEOPLASIAS DO COLO UTERINO (EPIDEMIOLOGIA;GENÉTICA), SEGUIMENTOS, CARCINOMA DE CÉLULAS ESCAMOSAS (DIAGNÓSTICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WALTER, Stephen D. et al. Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis. PLOS ONE, v. 8, n. 2, p. 7 , 2013Tradução . . Disponível em: http://www.plosone.org/article/info:doi/10.1371/journal.pone.0056430. Acesso em: 05 ago. 2024.
APA
Walter, S. D., Riddell, C. A., Rabachini, T., Villa, L. L., & Franco, E. L. (2013). Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis. PLOS ONE, 8( 2), 7 . doi:10.1371/journal.pone.0056430
NLM
Walter SD, Riddell CA, Rabachini T, Villa LL, Franco EL. Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis [Internet]. PLOS ONE. 2013 ; 8( 2): 7 .[citado 2024 ago. 05 ] Available from: http://www.plosone.org/article/info:doi/10.1371/journal.pone.0056430
Vancouver
Walter SD, Riddell CA, Rabachini T, Villa LL, Franco EL. Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis [Internet]. PLOS ONE. 2013 ; 8( 2): 7 .[citado 2024 ago. 05 ] Available from: http://www.plosone.org/article/info:doi/10.1371/journal.pone.0056430
Trabalho de evento-resumo periodico
Polymorphisms in the exon 20 of EGFR gene in metastatic lung adenocarcinoma: prognostic relevance and sensitivity to erlotinib (2013)
Castro Jr., Gilberto; Soares, Iberê C.; Takahashi, Tiago K.; Maia, Manuel C. D. F.; Caires-Lima, Rafael; Protasio, Bruno M.; Takagaki, Teresa Y.; Shiang, Christina; Mello, Evandro S.; Hoff, Paulo M.; Alves, Venâncio A.
Fonte: Journal of thoracic oncology. Nome do evento: World Conference on Lung Cancer. Unidade: FM
Assuntos: NEOPLASIAS PULMONARES, POLIMORFISMO, ADENOCARCINOMA, TÉCNICAS CITOLÓGICAS (TENDÊNCIAS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO JR., Gilberto et al. Polymorphisms in the exon 20 of EGFR gene in metastatic lung adenocarcinoma: prognostic relevance and sensitivity to erlotinib. Journal of thoracic oncology. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 ago. 2024. , 2013
APA
Castro Jr., G., Soares, I. C., Takahashi, T. K., Maia, M. C. D. F., Caires-Lima, R., Protasio, B. M., et al. (2013). Polymorphisms in the exon 20 of EGFR gene in metastatic lung adenocarcinoma: prognostic relevance and sensitivity to erlotinib. Journal of thoracic oncology. Faculdade de Medicina, Universidade de São Paulo.
NLM
Castro Jr. G, Soares IC, Takahashi TK, Maia MCDF, Caires-Lima R, Protasio BM, Takagaki TY, Shiang C, Mello ES, Hoff PM, Alves VA. Polymorphisms in the exon 20 of EGFR gene in metastatic lung adenocarcinoma: prognostic relevance and sensitivity to erlotinib. Journal of thoracic oncology. 2013 ; 8 S784.[citado 2024 ago. 05 ]
Vancouver
Castro Jr. G, Soares IC, Takahashi TK, Maia MCDF, Caires-Lima R, Protasio BM, Takagaki TY, Shiang C, Mello ES, Hoff PM, Alves VA. Polymorphisms in the exon 20 of EGFR gene in metastatic lung adenocarcinoma: prognostic relevance and sensitivity to erlotinib. Journal of thoracic oncology. 2013 ; 8 S784.[citado 2024 ago. 05 ]
Artigo de periodico
Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity (2012)
Hoff, Paulo M.; Saad, Everardo D.; Costa, Frederico; Coutinho, Anelisa K.; Caponero, Ricardo; Prolla, Gabriel; Gansl, Rene C.
Fonte: Clinical Colorectal Cancer. Unidade: FM
Assuntos: NEOPLASIAS COLORRETAIS (TERAPIA), DROGATERAPIA (TOXIDADE), METÁSTASE NEOPLÁSICA, ANTINEOPLÁSICOS (TOXIDADE), MANIFESTAÇÕES NEUROLÓGICAS, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOFF, Paulo M. et al. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity. Clinical Colorectal Cancer, v. 11, n. 2, p. 93-100, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.clcc.2011.10.004. Acesso em: 05 ago. 2024.
APA
Hoff, P. M., Saad, E. D., Costa, F., Coutinho, A. K., Caponero, R., Prolla, G., & Gansl, R. C. (2012). Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity. Clinical Colorectal Cancer, 11( 2), 93-100. doi:10.1016/j.clcc.2011.10.004
NLM
Hoff PM, Saad ED, Costa F, Coutinho AK, Caponero R, Prolla G, Gansl RC. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity [Internet]. Clinical Colorectal Cancer. 2012 ; 11( 2): 93-100.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.clcc.2011.10.004
Vancouver
Hoff PM, Saad ED, Costa F, Coutinho AK, Caponero R, Prolla G, Gansl RC. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity [Internet]. Clinical Colorectal Cancer. 2012 ; 11( 2): 93-100.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.clcc.2011.10.004
Artigo de periodico
ERCC1 protein, mRNA expression and T19007C polymorphism as prognostic markers in head and neck squamous cell carcinoma patients treated with surgery and adjuvant cisplatin-based chemoradiation (2011)
Castro, Gilberto de; Pasini, Fatima Solange; Siqueira, Sheila Aparecida Coelho; Ferraz, Alberto Rossetti; Villar, Rosangela Correa; Snitcovsky, Igor Moysés Longo; Federico, Miriam Hatsue Honda
Fonte: Oncology reports. Unidade: FM
Assuntos: POLIMORFISMO, MARCADOR MOLECULAR, PROGNÓSTICO, NEOPLASIAS DE CABEÇA E PESCOÇO (QUIMIOTERAPIA), CARCINOMA DE CÉLULAS ESCAMOSAS (CIRURGIA), QUIMIOTERAPIA ADJUVANTE, ANTINEOPLÁSICOS (TOXICIDADE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Gilberto de et al. ERCC1 protein, mRNA expression and T19007C polymorphism as prognostic markers in head and neck squamous cell carcinoma patients treated with surgery and adjuvant cisplatin-based chemoradiation. Oncology reports, v. 25, n. 3, p. 693-699, 2011Tradução . . Disponível em: https://doi.org/10.1200/jco.2010.28.15_suppl.5540. Acesso em: 05 ago. 2024.
APA
Castro, G. de, Pasini, F. S., Siqueira, S. A. C., Ferraz, A. R., Villar, R. C., Snitcovsky, I. M. L., & Federico, M. H. H. (2011). ERCC1 protein, mRNA expression and T19007C polymorphism as prognostic markers in head and neck squamous cell carcinoma patients treated with surgery and adjuvant cisplatin-based chemoradiation. Oncology reports, 25( 3), 693-699. doi:10.1200/jco.2010.28.15_suppl.5540
NLM
Castro G de, Pasini FS, Siqueira SAC, Ferraz AR, Villar RC, Snitcovsky IML, Federico MHH. ERCC1 protein, mRNA expression and T19007C polymorphism as prognostic markers in head and neck squamous cell carcinoma patients treated with surgery and adjuvant cisplatin-based chemoradiation [Internet]. Oncology reports. 2011 ; 25( 3): 693-699.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1200/jco.2010.28.15_suppl.5540
Vancouver
Castro G de, Pasini FS, Siqueira SAC, Ferraz AR, Villar RC, Snitcovsky IML, Federico MHH. ERCC1 protein, mRNA expression and T19007C polymorphism as prognostic markers in head and neck squamous cell carcinoma patients treated with surgery and adjuvant cisplatin-based chemoradiation [Internet]. Oncology reports. 2011 ; 25( 3): 693-699.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1200/jco.2010.28.15_suppl.5540
Artigo de periodico
Arg72Pro TP53 polymorphism and cancer susceptibility: a comprehensive meta-analysis of 302 case-control studies (2011)
Francisco, Guilherme; Menezes, Paulo Rossi; Eluf-Neto, José; Chammas, Roger
Fonte: International journal of cancer. Unidade: FM
Assuntos: NEOPLASIAS, POLIMORFISMO, METANÁLISE, ESTUDO DE CASO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCISCO, Guilherme et al. Arg72Pro TP53 polymorphism and cancer susceptibility: a comprehensive meta-analysis of 302 case-control studies. International journal of cancer, n. 4, p. 920-930, 2011Tradução . . Disponível em: https://doi.org/10.1002/ijc.25710. Acesso em: 05 ago. 2024.
APA
Francisco, G., Menezes, P. R., Eluf-Neto, J., & Chammas, R. (2011). Arg72Pro TP53 polymorphism and cancer susceptibility: a comprehensive meta-analysis of 302 case-control studies. International journal of cancer, ( 4), 920-930. doi:10.1002/ijc.25710
NLM
Francisco G, Menezes PR, Eluf-Neto J, Chammas R. Arg72Pro TP53 polymorphism and cancer susceptibility: a comprehensive meta-analysis of 302 case-control studies [Internet]. International journal of cancer. 2011 ;( 4): 920-930.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1002/ijc.25710
Vancouver
Francisco G, Menezes PR, Eluf-Neto J, Chammas R. Arg72Pro TP53 polymorphism and cancer susceptibility: a comprehensive meta-analysis of 302 case-control studies [Internet]. International journal of cancer. 2011 ;( 4): 920-930.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1002/ijc.25710
Artigo de periodico
European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil (2011)
Gonçalves, Fernanda T.; Eluf Neto, José; Francisco, Guilherme; Souza, Sonia P. de; Luiz, Olinda C.; Festa Neto, Cyro; Sanches, José A.; Chammas, Roger; Gattas, Gilka J. F.
Fonte: Journal of Dermatological Science. Unidade: FM
Assuntos: POLIMORFISMO, RNA, GENES, MELANONA, ESTUDO DE CASO, NEOPLASIAS CUTÂNEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GONÇALVES, Fernanda T. et al. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil. Journal of Dermatological Science, v. 64, n. 1, p. 59-66, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jdermsci.2011.06.003. Acesso em: 05 ago. 2024.
APA
Gonçalves, F. T., Eluf Neto, J., Francisco, G., Souza, S. P. de, Luiz, O. C., Festa Neto, C., et al. (2011). European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil. Journal of Dermatological Science, 64( 1), 59-66. doi:10.1016/j.jdermsci.2011.06.003
NLM
Gonçalves FT, Eluf Neto J, Francisco G, Souza SP de, Luiz OC, Festa Neto C, Sanches JA, Chammas R, Gattas GJF. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil [Internet]. Journal of Dermatological Science. 2011 ; 64( 1): 59-66.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.jdermsci.2011.06.003
Vancouver
Gonçalves FT, Eluf Neto J, Francisco G, Souza SP de, Luiz OC, Festa Neto C, Sanches JA, Chammas R, Gattas GJF. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil [Internet]. Journal of Dermatological Science. 2011 ; 64( 1): 59-66.[citado 2024 ago. 05 ] Available from: https://doi.org/10.1016/j.jdermsci.2011.06.003

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