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Trabalho de evento-resumo
Genetic polymorphisms in promoter region of DEFB1 associated persistent apical periodontitis (2020)
Sousa Neto, Manoel Damião de ; Antunes, Leonardo; Carvalho, Léo de; Petean, Igor Bassi Ferreira ; Antunes, Livia Azeredo Alves; Freitas, Jéssica Vavassori de; Salles, Alessandro Guimarães; Olej, Beni; Oliveira, Daniela Barroso de; Küchler, Erika Calvano
Source: Abstracts. Conference titles: IADR/AADR/CADR General Session. Unidade: FORP
Subjects: ODONTOLOGIA, PERIODONTITE PERIAPICAL, SISTEMA IMUNE, POLIMORFISMO, CANAL RADICULAR
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ABNT
SOUSA NETO, Manoel Damião de et al. Genetic polymorphisms in promoter region of DEFB1 associated persistent apical periodontitis. 2020, Anais.. Alexandria: IADR, 2020. Disponível em: https://iadr.abstractarchives.com/abstract/20iags-3321475/genetic-polymorphisms-in-promoter-region-of-defb1-associated-persistent-apical-periodontitis. Acesso em: 16 nov. 2024.
APA
Sousa Neto, M. D. de, Antunes, L., Carvalho, L. de, Petean, I. B. F., Antunes, L. A. A., Freitas, J. V. de, et al. (2020). Genetic polymorphisms in promoter region of DEFB1 associated persistent apical periodontitis. In Abstracts. Alexandria: IADR. Recuperado de https://iadr.abstractarchives.com/abstract/20iags-3321475/genetic-polymorphisms-in-promoter-region-of-defb1-associated-persistent-apical-periodontitis
NLM
Sousa Neto MD de, Antunes L, Carvalho L de, Petean IBF, Antunes LAA, Freitas JV de, Salles AG, Olej B, Oliveira DB de, Küchler EC. Genetic polymorphisms in promoter region of DEFB1 associated persistent apical periodontitis [Internet]. Abstracts. 2020 ;[citado 2024 nov. 16 ] Available from: https://iadr.abstractarchives.com/abstract/20iags-3321475/genetic-polymorphisms-in-promoter-region-of-defb1-associated-persistent-apical-periodontitis
Vancouver
Sousa Neto MD de, Antunes L, Carvalho L de, Petean IBF, Antunes LAA, Freitas JV de, Salles AG, Olej B, Oliveira DB de, Küchler EC. Genetic polymorphisms in promoter region of DEFB1 associated persistent apical periodontitis [Internet]. Abstracts. 2020 ;[citado 2024 nov. 16 ] Available from: https://iadr.abstractarchives.com/abstract/20iags-3321475/genetic-polymorphisms-in-promoter-region-of-defb1-associated-persistent-apical-periodontitis
Trabalho de evento-resumo
Validation of TREML4 mRNA expression and polymorphisms in blood leukocytes as potential biomarker of atherosclerosis (2019)
Duarte, V. H. R; Manfredi, A. B; Araújo, J. N; Borges, J. B; Bastos, G. M; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Luchessi, André Ducati; Silbiger, Vivian Nogueira
Source: Abstracts. Conference titles: American Association for Clinical Chemistry/AACC. Unidade: FCF
Subjects: POLIMORFISMO, BIOMARCADORES, ARTERIOSCLEROSE
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ABNT
DUARTE, V. H. R et al. Validation of TREML4 mRNA expression and polymorphisms in blood leukocytes as potential biomarker of atherosclerosis. 2019, Anais.. Washington: AACC, 2019. . Acesso em: 16 nov. 2024.
APA
Duarte, V. H. R., Manfredi, A. B., Araújo, J. N., Borges, J. B., Bastos, G. M., Hirata, M. H., et al. (2019). Validation of TREML4 mRNA expression and polymorphisms in blood leukocytes as potential biomarker of atherosclerosis. In Abstracts. Washington: AACC.
NLM
Duarte VHR, Manfredi AB, Araújo JN, Borges JB, Bastos GM, Hirata MH, Hirata RDC, Luchessi AD, Silbiger VN. Validation of TREML4 mRNA expression and polymorphisms in blood leukocytes as potential biomarker of atherosclerosis. Abstracts. 2019 ;[citado 2024 nov. 16 ]
Vancouver
Duarte VHR, Manfredi AB, Araújo JN, Borges JB, Bastos GM, Hirata MH, Hirata RDC, Luchessi AD, Silbiger VN. Validation of TREML4 mRNA expression and polymorphisms in blood leukocytes as potential biomarker of atherosclerosis. Abstracts. 2019 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Influence of polymorphisms LEP c.-2548A>G and LEPR c.668A>G on metabolic alterations in a pediatric population of Southern Chile (2019)
Hirata, Rosario Dominguez Crespo ; Brito, R; Manriquez, Victor; Aguilar-Farias, N; Chandía-Poblete, D; Navarro, J; Fajardo, Cristina Moreno ; Hirata, Mario Hiroyuki ; Cerda, Alvaro
Source: Abstracts. Conference titles: American Association for Clinical Chemistry/AACC. Unidade: FCF
Subjects: POLIMORFISMO, OBESIDADE
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ABNT
HIRATA, Rosario Dominguez Crespo et al. Influence of polymorphisms LEP c.-2548A>G and LEPR c.668A>G on metabolic alterations in a pediatric population of Southern Chile. 2019, Anais.. Washington: AACC, 2019. . Acesso em: 16 nov. 2024.
APA
Hirata, R. D. C., Brito, R., Manriquez, V., Aguilar-Farias, N., Chandía-Poblete, D., Navarro, J., et al. (2019). Influence of polymorphisms LEP c.-2548A>G and LEPR c.668A>G on metabolic alterations in a pediatric population of Southern Chile. In Abstracts. Washington: AACC.
NLM
Hirata RDC, Brito R, Manriquez V, Aguilar-Farias N, Chandía-Poblete D, Navarro J, Fajardo CM, Hirata MH, Cerda A. Influence of polymorphisms LEP c.-2548A>G and LEPR c.668A>G on metabolic alterations in a pediatric population of Southern Chile. Abstracts. 2019 ;[citado 2024 nov. 16 ]
Vancouver
Hirata RDC, Brito R, Manriquez V, Aguilar-Farias N, Chandía-Poblete D, Navarro J, Fajardo CM, Hirata MH, Cerda A. Influence of polymorphisms LEP c.-2548A>G and LEPR c.668A>G on metabolic alterations in a pediatric population of Southern Chile. Abstracts. 2019 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Could SNPs predict Cisplatin toxicity? (2018)
Cursino, Maria Aparecida; Quintanilha, Julia Coelho de França; Visacri, Marilia Berlofa ; Vaz, Camila de Oliveira; Guarnieri, João Paulo de Oliveira; Bastos, Larissa Brito; Torso, Nadine de G; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Lima, C. S. P; Moriel, Patricia
Source: Abstracts. Conference titles: AAPS PharmSci. Unidade: FCF
Subjects: BIOMARCADORES, POLIMORFISMO
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ABNT
CURSINO, Maria Aparecida et al. Could SNPs predict Cisplatin toxicity? 2018, Anais.. Arlington: American Association of Pharmaceutical Scientists, 2018. . Acesso em: 16 nov. 2024.
APA
Cursino, M. A., Quintanilha, J. C. de F., Visacri, M. B., Vaz, C. de O., Guarnieri, J. P. de O., Bastos, L. B., et al. (2018). Could SNPs predict Cisplatin toxicity? In Abstracts. Arlington: American Association of Pharmaceutical Scientists.
NLM
Cursino MA, Quintanilha JC de F, Visacri MB, Vaz C de O, Guarnieri JP de O, Bastos LB, Torso N de G, Hirata MH, Hirata RDC, Lima CSP, Moriel P. Could SNPs predict Cisplatin toxicity? Abstracts. 2018 ;[citado 2024 nov. 16 ]
Vancouver
Cursino MA, Quintanilha JC de F, Visacri MB, Vaz C de O, Guarnieri JP de O, Bastos LB, Torso N de G, Hirata MH, Hirata RDC, Lima CSP, Moriel P. Could SNPs predict Cisplatin toxicity? Abstracts. 2018 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
HLA-G haplotype diversity in a brazilian population sample stratified using ancestry informative markers (2017)
Oliveira, M. L. G; Veiga-Castelli, L. C; Marcorin, L; Pereira, A. L. E; Debortoli, G; Fracasso, N. C. A; Valle-Silva, G; Massaro, J. D; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, E. C; Mendes Júnior, Celso Teixeira
Source: Abstracts. Conference titles: Brazilian International Congress of Genetics - Genética 2017. Unidades: FMRP, FFCLRP
Subjects: ANTÍGENOS DE HISTOCOMPATIBILIDADE, POLIMORFISMO, HAPLOTIPOS
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ABNT
OLIVEIRA, M. L. G et al. HLA-G haplotype diversity in a brazilian population sample stratified using ancestry informative markers. 2017, Anais.. Águas de Lindóia: SBG, 2017. . Acesso em: 16 nov. 2024.
APA
Oliveira, M. L. G., Veiga-Castelli, L. C., Marcorin, L., Pereira, A. L. E., Debortoli, G., Fracasso, N. C. A., et al. (2017). HLA-G haplotype diversity in a brazilian population sample stratified using ancestry informative markers. In Abstracts. Águas de Lindóia: SBG.
NLM
Oliveira MLG, Veiga-Castelli LC, Marcorin L, Pereira ALE, Debortoli G, Fracasso NCA, Valle-Silva G, Massaro JD, Simões AL, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G haplotype diversity in a brazilian population sample stratified using ancestry informative markers. Abstracts. 2017 ;[citado 2024 nov. 16 ]
Vancouver
Oliveira MLG, Veiga-Castelli LC, Marcorin L, Pereira ALE, Debortoli G, Fracasso NCA, Valle-Silva G, Massaro JD, Simões AL, Donadi EA, Castelli EC, Mendes Júnior CT. HLA-G haplotype diversity in a brazilian population sample stratified using ancestry informative markers. Abstracts. 2017 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Association of SNPs with index body mass in a mixed urban population: a case-control study (2017)
Ribeiro, D. O; Diniz, I. G; Silva Júnior, Wilson Araújo da; Guerreiro, J. F
Source: Abstracts. Conference titles: Brazilian International Congress of Genetics - Genética 2017. Unidade: FMRP
Subjects: OBESIDADE, GENÓTIPOS, POLIMORFISMO
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ABNT
RIBEIRO, D. O et al. Association of SNPs with index body mass in a mixed urban population: a case-control study. 2017, Anais.. Águas de Lindóia: SBG, 2017. . Acesso em: 16 nov. 2024.
APA
Ribeiro, D. O., Diniz, I. G., Silva Júnior, W. A. da, & Guerreiro, J. F. (2017). Association of SNPs with index body mass in a mixed urban population: a case-control study. In Abstracts. Águas de Lindóia: SBG.
NLM
Ribeiro DO, Diniz IG, Silva Júnior WA da, Guerreiro JF. Association of SNPs with index body mass in a mixed urban population: a case-control study. Abstracts. 2017 ;[citado 2024 nov. 16 ]
Vancouver
Ribeiro DO, Diniz IG, Silva Júnior WA da, Guerreiro JF. Association of SNPs with index body mass in a mixed urban population: a case-control study. Abstracts. 2017 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Formal description of genetic insertion: deletion markers (2016)
Rodrigues, M. L. B.; Ng, A. M.; Wiezel, Cláudia Emília Vieira; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: Brazilian-International Congress of Genetics. Unidade: FMRP
Subjects: POLIMORFISMO, MARCADOR MOLECULAR
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ABNT
RODRIGUES, M. L. B. et al. Formal description of genetic insertion: deletion markers. 2016, Anais.. Caxambu: SBG, 2016. . Acesso em: 16 nov. 2024.
APA
Rodrigues, M. L. B., Ng, A. M., Wiezel, C. E. V., & Simões, A. L. (2016). Formal description of genetic insertion: deletion markers. In Abstracts. Caxambu: SBG.
NLM
Rodrigues MLB, Ng AM, Wiezel CEV, Simões AL. Formal description of genetic insertion: deletion markers. Abstracts. 2016 ;[citado 2024 nov. 16 ]
Vancouver
Rodrigues MLB, Ng AM, Wiezel CEV, Simões AL. Formal description of genetic insertion: deletion markers. Abstracts. 2016 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Identification of new SNPs associated with susceptibility to systemic lupus erythematosus (2016)
Maso, V. E.; Barbosa, F. B.; Wiezel, Cláudia Emília Vieira; Simioni, M.; Torres, F. R.; Molck, M. C.; Araújo, T. K.; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, Vera Lúcia; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: Brazilian-International Congress of Genetics. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO, POLIMORFISMO
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ABNT
MASO, V. E. et al. Identification of new SNPs associated with susceptibility to systemic lupus erythematosus. 2016, Anais.. Caxambu: SBG, 2016. . Acesso em: 16 nov. 2024.
APA
Maso, V. E., Barbosa, F. B., Wiezel, C. E. V., Simioni, M., Torres, F. R., Molck, M. C., et al. (2016). Identification of new SNPs associated with susceptibility to systemic lupus erythematosus. In Abstracts. Caxambu: SBG.
NLM
Maso VE, Barbosa FB, Wiezel CEV, Simioni M, Torres FR, Molck MC, Araújo TK, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Identification of new SNPs associated with susceptibility to systemic lupus erythematosus. Abstracts. 2016 ;[citado 2024 nov. 16 ]
Vancouver
Maso VE, Barbosa FB, Wiezel CEV, Simioni M, Torres FR, Molck MC, Araújo TK, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Identification of new SNPs associated with susceptibility to systemic lupus erythematosus. Abstracts. 2016 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
HLA-G 3' untranslated region polymorphisms are associated with neuromyelitis optica (2015)
Souza, A. S.; Souza, R. B.; Assis, P. M. S.; Porto, I. O. P.; Castelli, E. C.; Guerreiro, C. T.; Rocha, F. C. G.; Barreira, Amilton Antunes; Donadi, Eduardo Antônio; Brum, Doralina Guimarães
Source: Abstracts. Conference titles: Congress of the European Committee for Treatment and Research in Multiple Sclerosis. Unidade: FMRP
Subjects: ESCLEROSE MÚLTIPLA, NEUROMIELITE ÓPTICA, POLIMORFISMO, AUTOIMUNIDADE
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ABNT
SOUZA, A. S. et al. HLA-G 3' untranslated region polymorphisms are associated with neuromyelitis optica. 2015, Anais.. Barcelona: ECTRIMS, 2015. . Acesso em: 16 nov. 2024.
APA
Souza, A. S., Souza, R. B., Assis, P. M. S., Porto, I. O. P., Castelli, E. C., Guerreiro, C. T., et al. (2015). HLA-G 3' untranslated region polymorphisms are associated with neuromyelitis optica. In Abstracts. Barcelona: ECTRIMS.
NLM
Souza AS, Souza RB, Assis PMS, Porto IOP, Castelli EC, Guerreiro CT, Rocha FCG, Barreira AA, Donadi EA, Brum DG. HLA-G 3' untranslated region polymorphisms are associated with neuromyelitis optica. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Vancouver
Souza AS, Souza RB, Assis PMS, Porto IOP, Castelli EC, Guerreiro CT, Rocha FCG, Barreira AA, Donadi EA, Brum DG. HLA-G 3' untranslated region polymorphisms are associated with neuromyelitis optica. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Validation of an ancestry informative marker panel for population stratification in Brazilian case-control studies performed by genome-wide human cytoscan HD array (2015)
Barbosa, F. B.; Simioni, M.; Cagnin, N. F.; Torres, F. R.; Molck, M. C.; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, V. L.; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO (GENÉTICA), ESTUDOS DE CASOS E CONTROLES, POLIMORFISMO
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ABNT
BARBOSA, F. B. et al. Validation of an ancestry informative marker panel for population stratification in Brazilian case-control studies performed by genome-wide human cytoscan HD array. 2015, Anais.. Águas de Lindóia: SBG, 2015. . Acesso em: 16 nov. 2024.
APA
Barbosa, F. B., Simioni, M., Cagnin, N. F., Torres, F. R., Molck, M. C., Donadi, E. A., et al. (2015). Validation of an ancestry informative marker panel for population stratification in Brazilian case-control studies performed by genome-wide human cytoscan HD array. In Abstracts. Águas de Lindóia: SBG.
NLM
Barbosa FB, Simioni M, Cagnin NF, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Validation of an ancestry informative marker panel for population stratification in Brazilian case-control studies performed by genome-wide human cytoscan HD array. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Vancouver
Barbosa FB, Simioni M, Cagnin NF, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Validation of an ancestry informative marker panel for population stratification in Brazilian case-control studies performed by genome-wide human cytoscan HD array. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome (2015)
Martins, Clarissa Silva; Elias, Daniel; Colli, Leandro Machado; Couri, Carlos Eduardo; Souza, Manoel Carlos L. A; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara; Foss, Milton César; Castro, Margaret de
Source: Abstracts. Conference titles: Annual Meeting and Expo of the Endocrine Society (ENDO). Unidade: FMRP
Subjects: GLÂNDULA PITUITÁRIA, POLIMORFISMO
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ABNT
MARTINS, Clarissa Silva et al. HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome. 2015, Anais.. San Diego: Endocrine Society, 2015. Disponível em: http://press.endocrine.org/doi/abs/10.1210/endo-meetings.2015.AHPAA.5.THR-400. Acesso em: 16 nov. 2024.
APA
Martins, C. S., Elias, D., Colli, L. M., Couri, C. E., Souza, M. C. L. A., Moreira, A. C., et al. (2015). HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome. In Abstracts. San Diego: Endocrine Society. Recuperado de http://press.endocrine.org/doi/abs/10.1210/endo-meetings.2015.AHPAA.5.THR-400
NLM
Martins CS, Elias D, Colli LM, Couri CE, Souza MCLA, Moreira AC, Elias LLK, Foss MC, Castro M de. HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome [Internet]. Abstracts. 2015 ;[citado 2024 nov. 16 ] Available from: http://press.endocrine.org/doi/abs/10.1210/endo-meetings.2015.AHPAA.5.THR-400
Vancouver
Martins CS, Elias D, Colli LM, Couri CE, Souza MCLA, Moreira AC, Elias LLK, Foss MC, Castro M de. HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome [Internet]. Abstracts. 2015 ;[citado 2024 nov. 16 ] Available from: http://press.endocrine.org/doi/abs/10.1210/endo-meetings.2015.AHPAA.5.THR-400
Trabalho de evento-resumo
A set of single nucleotide polymorphisms in susceptibility to systemic Lupus erythematosus (2015)
Maso, V. E.; Barbosa, F. B.; Simioni, M.; Torres, F. R.; Molck, M. C.; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, V. L.; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO (GENÉTICA), POLIMORFISMO
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ABNT
MASO, V. E. et al. A set of single nucleotide polymorphisms in susceptibility to systemic Lupus erythematosus. 2015, Anais.. Águas de Lindóia: SBG, 2015. . Acesso em: 16 nov. 2024.
APA
Maso, V. E., Barbosa, F. B., Simioni, M., Torres, F. R., Molck, M. C., Donadi, E. A., et al. (2015). A set of single nucleotide polymorphisms in susceptibility to systemic Lupus erythematosus. In Abstracts. Águas de Lindóia: SBG.
NLM
Maso VE, Barbosa FB, Simioni M, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. A set of single nucleotide polymorphisms in susceptibility to systemic Lupus erythematosus. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Vancouver
Maso VE, Barbosa FB, Simioni M, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. A set of single nucleotide polymorphisms in susceptibility to systemic Lupus erythematosus. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
FunciSNP tool to identify risk regions associated with ovarian cancer (2015)
Saraiva da Silva, M. F.; Coetzee, S. G.; Malta, T. M.; Gayther, S.; Noushmehr, Houtan
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidade: FMRP
Subjects: NEOPLASIAS OVARIANAS, POLIMORFISMO
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ABNT
SARAIVA DA SILVA, M. F. et al. FunciSNP tool to identify risk regions associated with ovarian cancer. 2015, Anais.. Águas de Lindóia: SBG, 2015. . Acesso em: 16 nov. 2024.
APA
Saraiva da Silva, M. F., Coetzee, S. G., Malta, T. M., Gayther, S., & Noushmehr, H. (2015). FunciSNP tool to identify risk regions associated with ovarian cancer. In Abstracts. Águas de Lindóia: SBG.
NLM
Saraiva da Silva MF, Coetzee SG, Malta TM, Gayther S, Noushmehr H. FunciSNP tool to identify risk regions associated with ovarian cancer. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Vancouver
Saraiva da Silva MF, Coetzee SG, Malta TM, Gayther S, Noushmehr H. FunciSNP tool to identify risk regions associated with ovarian cancer. Abstracts. 2015 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Impact of chromosomal polymorphisms of heterochromatin on male meiosis in humans (2014)
Pereira, C. S.; Santana, V. P.; Santos, S. A.; Dantas, Marilda Hatsumi Yamada; Prata, M.; Squire, Jeremy Andrew; Martelli, Lucia Regina
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidade: FMRP
Subjects: POLIMORFISMO, INFERTILIDADE MASCULINA, SÊMEN, PEIXES (EXPERIMENTOS)
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ABNT
PEREIRA, C. S. et al. Impact of chromosomal polymorphisms of heterochromatin on male meiosis in humans. 2014, Anais.. Guarujá: SBG, 2014. . Acesso em: 16 nov. 2024.
APA
Pereira, C. S., Santana, V. P., Santos, S. A., Dantas, M. H. Y., Prata, M., Squire, J. A., & Martelli, L. R. (2014). Impact of chromosomal polymorphisms of heterochromatin on male meiosis in humans. In Abstracts. Guarujá: SBG.
NLM
Pereira CS, Santana VP, Santos SA, Dantas MHY, Prata M, Squire JA, Martelli LR. Impact of chromosomal polymorphisms of heterochromatin on male meiosis in humans. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Vancouver
Pereira CS, Santana VP, Santos SA, Dantas MHY, Prata M, Squire JA, Martelli LR. Impact of chromosomal polymorphisms of heterochromatin on male meiosis in humans. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Analysis of global DNA methylation in irradiated fig selections (2014)
Rodrigues, Maria Gabriela Fontanetti; Soares, Murilo Racy; Moraes Filho, Romulo Maciel; Mondin, Mateus; Ramos, Ester Silveira; Giuliatti, Silvana
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidades: FMRP, ESALQ
Subjects: GENÉTICA, DNA, POLIMORFISMO
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ABNT
RODRIGUES, Maria Gabriela Fontanetti et al. Analysis of global DNA methylation in irradiated fig selections. 2014, Anais.. Guarujá: SBG, 2014. . Acesso em: 16 nov. 2024.
APA
Rodrigues, M. G. F., Soares, M. R., Moraes Filho, R. M., Mondin, M., Ramos, E. S., & Giuliatti, S. (2014). Analysis of global DNA methylation in irradiated fig selections. In Abstracts. Guarujá: SBG.
NLM
Rodrigues MGF, Soares MR, Moraes Filho RM, Mondin M, Ramos ES, Giuliatti S. Analysis of global DNA methylation in irradiated fig selections. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Vancouver
Rodrigues MGF, Soares MR, Moraes Filho RM, Mondin M, Ramos ES, Giuliatti S. Analysis of global DNA methylation in irradiated fig selections. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Plasma arginase activity may affect the responses to sildenafil in patients with erectile dysfunction (2014)
Lacchini, Riccardo ; Pinheiro, Lucas C.; Muniz, Jaqueline; Nobre, Yuri; Cologna, Adauto Jose; Martins, Antônio; Tanus-Santos, José Eduardo
Source: Abstracts. Conference titles: Nitrite Oxide-Nitrite/Nitrate Conference. Unidades: FMRP, EERP
Subjects: DISFUNÇÃO ERÉTIL, POLIMORFISMO, FÁRMACOS (SISTEMA CARDIOVASCULAR)
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ABNT
LACCHINI, Riccardo et al. Plasma arginase activity may affect the responses to sildenafil in patients with erectile dysfunction. 2014, Anais.. Cleveland: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2014. . Acesso em: 16 nov. 2024.
APA
Lacchini, R., Pinheiro, L. C., Muniz, J., Nobre, Y., Cologna, A. J., Martins, A., & Tanus-Santos, J. E. (2014). Plasma arginase activity may affect the responses to sildenafil in patients with erectile dysfunction. In Abstracts. Cleveland: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Lacchini R, Pinheiro LC, Muniz J, Nobre Y, Cologna AJ, Martins A, Tanus-Santos JE. Plasma arginase activity may affect the responses to sildenafil in patients with erectile dysfunction. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Vancouver
Lacchini R, Pinheiro LC, Muniz J, Nobre Y, Cologna AJ, Martins A, Tanus-Santos JE. Plasma arginase activity may affect the responses to sildenafil in patients with erectile dysfunction. Abstracts. 2014 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Integrative analysis identifies functional prostate cancer risk SNPs in genomic regulatory regions defined as enhancers (2013)
Noushmehr, Houtan; Coetzee, Simon G.; Rhie, Suhn K.; Yan, Chunli; Haiman, Christopher A.; Berman, Benjamin P.; Frenkel, Baruch; Coetzee, Gerhard A.
Source: Abstracts. Conference titles: Advances in Genome Biology and Technology Conference (AGBT). Unidade: FMRP
Subjects: NEOPLASIAS PROSTÁTICAS, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOUSHMEHR, Houtan et al. Integrative analysis identifies functional prostate cancer risk SNPs in genomic regulatory regions defined as enhancers. 2013, Anais.. Marco Island: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 16 nov. 2024.
APA
Noushmehr, H., Coetzee, S. G., Rhie, S. K., Yan, C., Haiman, C. A., Berman, B. P., et al. (2013). Integrative analysis identifies functional prostate cancer risk SNPs in genomic regulatory regions defined as enhancers. In Abstracts. Marco Island: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Noushmehr H, Coetzee SG, Rhie SK, Yan C, Haiman CA, Berman BP, Frenkel B, Coetzee GA. Integrative analysis identifies functional prostate cancer risk SNPs in genomic regulatory regions defined as enhancers. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Vancouver
Noushmehr H, Coetzee SG, Rhie SK, Yan C, Haiman CA, Berman BP, Frenkel B, Coetzee GA. Integrative analysis identifies functional prostate cancer risk SNPs in genomic regulatory regions defined as enhancers. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Discovery of new SNPs and INDELs variants in a native South America individual (2013)
Ribeiro-dos-Santos, A. M.; Souza, J. E.; Almeida, R.; Alencar, D. O.; Barbosa, M. S. R.; Gusmão, L.; Silva Júnior, Wilson Araújo da; Souza, S. J.; Silva, A.; Ribeiro-dos-Santos, A.; Darnet, S.; Santos, S.
Source: Abstracts. Conference titles: Congresso Brasileiro de Genética. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO-DOS-SANTOS, A. M. et al. Discovery of new SNPs and INDELs variants in a native South America individual. 2013, Anais.. Águas de Lindóia: SBG, 2013. . Acesso em: 16 nov. 2024.
APA
Ribeiro-dos-Santos, A. M., Souza, J. E., Almeida, R., Alencar, D. O., Barbosa, M. S. R., Gusmão, L., et al. (2013). Discovery of new SNPs and INDELs variants in a native South America individual. In Abstracts. Águas de Lindóia: SBG.
NLM
Ribeiro-dos-Santos AM, Souza JE, Almeida R, Alencar DO, Barbosa MSR, Gusmão L, Silva Júnior WA da, Souza SJ, Silva A, Ribeiro-dos-Santos A, Darnet S, Santos S. Discovery of new SNPs and INDELs variants in a native South America individual. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Vancouver
Ribeiro-dos-Santos AM, Souza JE, Almeida R, Alencar DO, Barbosa MSR, Gusmão L, Silva Júnior WA da, Souza SJ, Silva A, Ribeiro-dos-Santos A, Darnet S, Santos S. Discovery of new SNPs and INDELs variants in a native South America individual. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population (2013)
Marano, L. A.; Simões, Aguinado Luiz; Donadi, Eduardo Antônio; Mendes Júnior, Celso Teixeira
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FMRP, FFCLRP
Subjects: POLIMORFISMO, MELANINAS, GENÉTICA DE POPULAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARANO, L. A. et al. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. 2013, Anais.. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 16 nov. 2024.
APA
Marano, L. A., Simões, A. L., Donadi, E. A., & Mendes Júnior, C. T. (2013). Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. In Abstracts. Boston: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Vancouver
Marano LA, Simões AL, Donadi EA, Mendes Júnior CT. Melanocortin 1-receptor haplotypes associated to pigmentation phenotypes in the Brazilian population. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Trabalho de evento-resumo
Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients (2013)
Kiminami, Daniel Ossamu Goldschmidt; Coeli-Lacchini, Fernanda Borchers; Roa, Silvia Ruiz; Castro, Margaret de; Antonini, Sonir Roberto Rauber; Moreira, Ayrton Custódio
Source: Abstracts. Conference titles: Annual Meeting and Expo of the Endocrine Society. Unidade: FMRP
Subjects: POLIMORFISMO, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIMINAMI, Daniel Ossamu Goldschmidt et al. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. 2013, Anais.. San Francisco: Endocrine Society, 2013. . Acesso em: 16 nov. 2024.
APA
Kiminami, D. O. G., Coeli-Lacchini, F. B., Roa, S. R., Castro, M. de, Antonini, S. R. R., & Moreira, A. C. (2013). Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. In Abstracts. San Francisco: Endocrine Society.
NLM
Kiminami DOG, Coeli-Lacchini FB, Roa SR, Castro M de, Antonini SRR, Moreira AC. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. Abstracts. 2013 ;[citado 2024 nov. 16 ]
Vancouver
Kiminami DOG, Coeli-Lacchini FB, Roa SR, Castro M de, Antonini SRR, Moreira AC. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. Abstracts. 2013 ;[citado 2024 nov. 16 ]

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