ReP USP - Resultado da busca

Trabalho de evento-resumo
Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population (2016)
Debortoli, G.; Marcorin, L.; Oliveira, M. L. G.; Pereira, A. L. E.; Fracasso, N. C. A.; Massaro, Juliana Doblas; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz; Mendes Júnior, Celso Teixeira
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
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ABNT
DEBORTOLI, G. et al. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Debortoli, G., Marcorin, L., Oliveira, M. L. G., Pereira, A. L. E., Fracasso, N. C. A., Massaro, J. D., et al. (2016). Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. In Poster Abstracts. Vancouver: ASHG.
NLM
Debortoli G, Marcorin L, Oliveira MLG, Pereira ALE, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Mendes Júnior CT. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Debortoli G, Marcorin L, Oliveira MLG, Pereira ALE, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Mendes Júnior CT. Characterization of OCA2 gene diversity: genetic variation and association with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population (2016)
Mendes Júnior, Celso Teixeira; Pereira, A. L. E.; Debortoli, G.; Oliveira, M. L. G.; Fracasso, N. C. A.; Massaro, Juliana Doblas; Simões, Aguinaldo Luiz; Donadi, Eduardo Antônio; Castelli, Erick da Cruz; Marcorin, L.
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FMRP, FFCLRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Mendes Júnior, C. T., Pereira, A. L. E., Debortoli, G., Oliveira, M. L. G., Fracasso, N. C. A., Massaro, J. D., et al. (2016). MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. In Poster Abstracts. Vancouver: ASHG.
NLM
Mendes Júnior CT, Pereira ALE, Debortoli G, Oliveira MLG, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Marcorin L. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Mendes Júnior CT, Pereira ALE, Debortoli G, Oliveira MLG, Fracasso NCA, Massaro JD, Simões AL, Donadi EA, Castelli E da C, Marcorin L. MITF and ASIP genetic variation and associations with skin, hair and eye pigmentation in an admixed brazilian population. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development (2016)
Cagnin, N. F.; Barbosa, F. B.; Marano, L.; Mendes Júnior, Celso Teixeira; Donadi, Eduardo Antônio; Simões, Aguinaldo Luiz
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidades: FFCLRP, FMRP
Assuntos: GENÉTICA MÉDICA, LÚPUS ERITEMATOSO SISTÊMICO
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ABNT
CAGNIN, N. F. et al. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Cagnin, N. F., Barbosa, F. B., Marano, L., Mendes Júnior, C. T., Donadi, E. A., & Simões, A. L. (2016). Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. In Poster Abstracts. Vancouver: ASHG.
NLM
Cagnin NF, Barbosa FB, Marano L, Mendes Júnior CT, Donadi EA, Simões AL. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Cagnin NF, Barbosa FB, Marano L, Mendes Júnior CT, Donadi EA, Simões AL. Association between variants of melanocortin 1 receptor (MC1R) gene and the systemic lupus erythematosus development. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center (2016)
Baratela, W. A. R.; Yamamoto, G. L.; Testai, L. C.; Honjo, R.; Oliveira, L. A. N.; Doriqui, M. J. R.; Rosa, R; Meira, J. G. C.; Pina Neto, João Monteiro de; Cavalcanti, D. P.; Kim, C. A.; Passos-Bueno, Maria Rita ; Bertola, D. R.
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
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ABNT
BARATELA, W. A. R. et al. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Baratela, W. A. R., Yamamoto, G. L., Testai, L. C., Honjo, R., Oliveira, L. A. N., Doriqui, M. J. R., et al. (2016). Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. In Poster Abstracts. Vancouver: ASHG.
NLM
Baratela WAR, Yamamoto GL, Testai LC, Honjo R, Oliveira LAN, Doriqui MJR, Rosa R, Meira JGC, Pina Neto JM de, Cavalcanti DP, Kim CA, Passos-Bueno MR, Bertola DR. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Baratela WAR, Yamamoto GL, Testai LC, Honjo R, Oliveira LAN, Doriqui MJR, Rosa R, Meira JGC, Pina Neto JM de, Cavalcanti DP, Kim CA, Passos-Bueno MR, Bertola DR. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Copy number variation of ADAM3A gene in systemic lupus erithematosus (2016)
Barbosa, F. B.; Simioni, M.; Wiezel, C. E. V.; Torres, F. R.; Molck, M. C.; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, Vera Lúcia; Simões, Aguinaldo Luiz
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
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ABNT
BARBOSA, F. B. et al. Copy number variation of ADAM3A gene in systemic lupus erithematosus. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Barbosa, F. B., Simioni, M., Wiezel, C. E. V., Torres, F. R., Molck, M. C., Donadi, E. A., et al. (2016). Copy number variation of ADAM3A gene in systemic lupus erithematosus. In Poster Abstracts. Vancouver: ASHG.
NLM
Barbosa FB, Simioni M, Wiezel CEV, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Copy number variation of ADAM3A gene in systemic lupus erithematosus. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Barbosa FB, Simioni M, Wiezel CEV, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Copy number variation of ADAM3A gene in systemic lupus erithematosus. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Association of STAT4 rs7574865 polymorphism with susceptibility to systemic lupus erythematosus (2016)
Maso, V. E.; Barbosa, F. B.; Wiezel, C. E. V.; Simioni, M.; Torres, F. R.; Molck, M. C.; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, Vera Lúcia; Simões, Aguinaldo Luiz
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA DE POPULAÇÕES
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ABNT
MASO, V. E. et al. Association of STAT4 rs7574865 polymorphism with susceptibility to systemic lupus erythematosus. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Maso, V. E., Barbosa, F. B., Wiezel, C. E. V., Simioni, M., Torres, F. R., Molck, M. C., et al. (2016). Association of STAT4 rs7574865 polymorphism with susceptibility to systemic lupus erythematosus. In Poster Abstracts. Vancouver: ASHG.
NLM
Maso VE, Barbosa FB, Wiezel CEV, Simioni M, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Association of STAT4 rs7574865 polymorphism with susceptibility to systemic lupus erythematosus. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Maso VE, Barbosa FB, Wiezel CEV, Simioni M, Torres FR, Molck MC, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Association of STAT4 rs7574865 polymorphism with susceptibility to systemic lupus erythematosus. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Controlled polarization of two-dimensional quantum turbulence in atomic Bose-Einstein condensates (2016)
Cidrim, A.; Santos, F. E. A.; Galantuci, L.; Bagnato, Vanderlei Salvador ; Barenghi, C. F.
Fonte: Poster Abstracts. Nome do evento: Multicomponent Atomic Condensates and Rotational Dynamics Conference (MACRO). Unidade: IFSC
Assuntos: CONDENSADO DE BOSE-EINSTEIN, TURBULÊNCIA, POLARIZAÇÃO
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ABNT
CIDRIM, A. et al. Controlled polarization of two-dimensional quantum turbulence in atomic Bose-Einstein condensates. 2016, Anais.. Durham: Joint Quantum Centre - JQC, 2016. Disponível em: https://conferences.ncl.ac.uk/media/sites/conferencewebsites/jqcmacro/book_of_poster_abstracts.pdf. Acesso em: 16 out. 2025.
APA
Cidrim, A., Santos, F. E. A., Galantuci, L., Bagnato, V. S., & Barenghi, C. F. (2016). Controlled polarization of two-dimensional quantum turbulence in atomic Bose-Einstein condensates. In Poster Abstracts. Durham: Joint Quantum Centre - JQC. Recuperado de https://conferences.ncl.ac.uk/media/sites/conferencewebsites/jqcmacro/book_of_poster_abstracts.pdf
NLM
Cidrim A, Santos FEA, Galantuci L, Bagnato VS, Barenghi CF. Controlled polarization of two-dimensional quantum turbulence in atomic Bose-Einstein condensates [Internet]. Poster Abstracts. 2016 ;[citado 2025 out. 16 ] Available from: https://conferences.ncl.ac.uk/media/sites/conferencewebsites/jqcmacro/book_of_poster_abstracts.pdf
Vancouver
Cidrim A, Santos FEA, Galantuci L, Bagnato VS, Barenghi CF. Controlled polarization of two-dimensional quantum turbulence in atomic Bose-Einstein condensates [Internet]. Poster Abstracts. 2016 ;[citado 2025 out. 16 ] Available from: https://conferences.ncl.ac.uk/media/sites/conferencewebsites/jqcmacro/book_of_poster_abstracts.pdf
Trabalho de evento-resumo
Repair DNA pattern expression and ribosomal genes are associated with adult medulloblastoma subtype (2016)
Fontes, Aparecida Maria; Barbosa, F. B.; Simões, Aguinaldo Luiz; Wiezel, Cláudia Emília Vieira; Ramalho, Fernando Silva; Machado, Hélio Rubens; Gerson, S. L.; Abraham, Kuruvilla Joseph
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics (ASHG). Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, MEDULOBLASTOMA
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ABNT
FONTES, Aparecida Maria et al. Repair DNA pattern expression and ribosomal genes are associated with adult medulloblastoma subtype. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 16 out. 2025.
APA
Fontes, A. M., Barbosa, F. B., Simões, A. L., Wiezel, C. E. V., Ramalho, F. S., Machado, H. R., et al. (2016). Repair DNA pattern expression and ribosomal genes are associated with adult medulloblastoma subtype. In Poster Abstracts. Vancouver: ASHG.
NLM
Fontes AM, Barbosa FB, Simões AL, Wiezel CEV, Ramalho FS, Machado HR, Gerson SL, Abraham KJ. Repair DNA pattern expression and ribosomal genes are associated with adult medulloblastoma subtype. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Vancouver
Fontes AM, Barbosa FB, Simões AL, Wiezel CEV, Ramalho FS, Machado HR, Gerson SL, Abraham KJ. Repair DNA pattern expression and ribosomal genes are associated with adult medulloblastoma subtype. Poster Abstracts. 2016 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions (2015)
Markello, T.; Marchegiani, S.; Davis, T.; Tessadori, F.; van Haaften, G.; Brancati, F.; Pusey, B.; Wolfe, L.; Tifft, C.; Ferraz, Victor Evangelista de Faria; Roche, N.; Ramos, F.; Malicdan, M.; Boerkoel, C.; Gahl, W. A.; Vries, B. de; van Haelst, M.; Zenker, M.
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assuntos: MACROSTOMIA, DOENÇAS GENÉTICAS
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ABNT
MARKELLO, T. et al. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Markello, T., Marchegiani, S., Davis, T., Tessadori, F., van Haaften, G., Brancati, F., et al. (2015). TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. In Poster Abstracts. Baltimore: ASHG.
NLM
Markello T, Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Pusey B, Wolfe L, Tifft C, Ferraz VE de F, Roche N, Ramos F, Malicdan M, Boerkoel C, Gahl WA, Vries B de, van Haelst M, Zenker M. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Markello T, Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Pusey B, Wolfe L, Tifft C, Ferraz VE de F, Roche N, Ramos F, Malicdan M, Boerkoel C, Gahl WA, Vries B de, van Haelst M, Zenker M. TWIST2 is the cause of ablepharon macrostomia and barber say syndromes: reascertainment of two cases lost to follow-up as keys to solving these conditions. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Admixture and ancestry patterns of three Brazilian quilombo remnants communities (2015)
Mendes Júnior, Celso Teixeira; Salvanha, D. M.; Vêncio, Ricardo Zorzetto Nicoliello; Garrido, Leandro Maza; Krieger, Henrique; Castelli, E. C.; Simões, Aguinaldo Luiz; Andrade, E. S
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: FFCLRP, ICB, FMRP
Assuntos: QUILOMBOS, ASCENDENTE, GRUPOS ÉTNICOS
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ABNT
MENDES JÚNIOR, Celso Teixeira et al. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Mendes Júnior, C. T., Salvanha, D. M., Vêncio, R. Z. N., Garrido, L. M., Krieger, H., Castelli, E. C., et al. (2015). Admixture and ancestry patterns of three Brazilian quilombo remnants communities. In Poster Abstracts. Baltimore: ASHG.
NLM
Mendes Júnior CT, Salvanha DM, Vêncio RZN, Garrido LM, Krieger H, Castelli EC, Simões AL, Andrade ES. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Mendes Júnior CT, Salvanha DM, Vêncio RZN, Garrido LM, Krieger H, Castelli EC, Simões AL, Andrade ES. Admixture and ancestry patterns of three Brazilian quilombo remnants communities. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals (2015)
Carvalho, S. C. S.; Grangeiro, C. H. P.; Albuquerque, C. G. P.; Anjos, T. O.; Plaça, J. R.; Araújo, L. F.; Muys, B. R.; Souza, E. M.; Molfetta, Greice Andreotti de; Silva Júnior, Wilson Araújo da; Ferraz, Victor Evangelista de Faria
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assuntos: SURDEZ, GENÉTICA MÉDICA, DIAGNÓSTICO
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ABNT
CARVALHO, S. C. S. et al. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Carvalho, S. C. S., Grangeiro, C. H. P., Albuquerque, C. G. P., Anjos, T. O., Plaça, J. R., Araújo, L. F., et al. (2015). Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. In Poster Abstracts. Baltimore: ASHG.
NLM
Carvalho SCS, Grangeiro CHP, Albuquerque CGP, Anjos TO, Plaça JR, Araújo LF, Muys BR, Souza EM, Molfetta GA de, Silva Júnior WA da, Ferraz VE de F. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Carvalho SCS, Grangeiro CHP, Albuquerque CGP, Anjos TO, Plaça JR, Araújo LF, Muys BR, Souza EM, Molfetta GA de, Silva Júnior WA da, Ferraz VE de F. Mutation screening of the SLC26A4 gene in Brazilian non-syndromic sensorineural prelingual deaf individuals. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome (2015)
Souza, E. M. S. M. M.; Peronni, K. C.; Plaça, J. R.; Molfetta, Greice Andreotti de; Carvalho, S. C. S.; Marques, A. A.; Araújo, L. F.; Silva Júnior, Wilson Araújo da; Ferraz, Victor Evangelista de Faria
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assuntos: MACROSTOMIA, DOENÇAS GENÉTICAS
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ABNT
SOUZA, E. M. S. M. M. et al. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Souza, E. M. S. M. M., Peronni, K. C., Plaça, J. R., Molfetta, G. A. de, Carvalho, S. C. S., Marques, A. A., et al. (2015). Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. In Poster Abstracts. Baltimore: ASHG.
NLM
Souza EMSMM, Peronni KC, Plaça JR, Molfetta GA de, Carvalho SCS, Marques AA, Araújo LF, Silva Júnior WA da, Ferraz VE de F. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Souza EMSMM, Peronni KC, Plaça JR, Molfetta GA de, Carvalho SCS, Marques AA, Araújo LF, Silva Júnior WA da, Ferraz VE de F. Mutation in TWIST2 gene and its relation to a new clinical finding-lipodystrophyc habitus: in ablepharon macrostomia syndrome. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services (2015)
Molfetta, Greice Andreotti de; Marques, A.; Furtado, C.; Ramos, Ester Silveira; Silva Júnior, Wilson Araújo da
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assuntos: SÍNDROME X, ACONSELHAMENTO GENÉTICO
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ABNT
MOLFETTA, Greice Andreotti de et al. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Molfetta, G. A. de, Marques, A., Furtado, C., Ramos, E. S., & Silva Júnior, W. A. da. (2015). Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. In Poster Abstracts. Baltimore: ASHG.
NLM
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Genotype-phenotype correlation of an 8p complex rearrangement (2015)
Martelli, Lúcia Regina; Grangeiro, Carlos Henrique Paiva; Gomes, A. G.; Joaquim, T. M; Laureano, L. A. F.; Grzesiuk, J. D.; Gennaro, F. G. O.; Huber, Jair; Squire, Jeremy Andrew
Fonte: Poster Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assuntos: GENÓTIPOS, FENÓTIPOS
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ABNT
MARTELLI, Lúcia Regina et al. Genotype-phenotype correlation of an 8p complex rearrangement. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 16 out. 2025.
APA
Martelli, L. R., Grangeiro, C. H. P., Gomes, A. G., Joaquim, T. M., Laureano, L. A. F., Grzesiuk, J. D., et al. (2015). Genotype-phenotype correlation of an 8p complex rearrangement. In Poster Abstracts. Baltimore: ASHG.
NLM
Martelli LR, Grangeiro CHP, Gomes AG, Joaquim TM, Laureano LAF, Grzesiuk JD, Gennaro FGO, Huber J, Squire JA. Genotype-phenotype correlation of an 8p complex rearrangement. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Vancouver
Martelli LR, Grangeiro CHP, Gomes AG, Joaquim TM, Laureano LAF, Grzesiuk JD, Gennaro FGO, Huber J, Squire JA. Genotype-phenotype correlation of an 8p complex rearrangement. Poster Abstracts. 2015 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
DNA recognition of Copper complexes using metadynamics simulations and hyperfine coupling calculations (2014)
Nascimento, Rafael Rodrigues do
Fonte: Poster Abstracts. Nome do evento: Symposium on Current Topics in Molecular Biophysics. Unidade: IF
Assuntos: BIOFÍSICA (CONGRESSOS), DNA (CONGRESSOS)
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ABNT
NASCIMENTO, Rafael Rodrigues do. DNA recognition of Copper complexes using metadynamics simulations and hyperfine coupling calculations. 2014, Anais.. São Paulo: IFUSP, 2014. Disponível em: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf. Acesso em: 16 out. 2025.
APA
Nascimento, R. R. do. (2014). DNA recognition of Copper complexes using metadynamics simulations and hyperfine coupling calculations. In Poster Abstracts. São Paulo: IFUSP. Recuperado de http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
NLM
Nascimento RR do. DNA recognition of Copper complexes using metadynamics simulations and hyperfine coupling calculations [Internet]. Poster Abstracts. 2014 ;[citado 2025 out. 16 ] Available from: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
Vancouver
Nascimento RR do. DNA recognition of Copper complexes using metadynamics simulations and hyperfine coupling calculations [Internet]. Poster Abstracts. 2014 ;[citado 2025 out. 16 ] Available from: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
Trabalho de evento-resumo
Analysis of differentially expressed genes in a mouse model of KRAS-induced lung cancer with conditional loss of thep65 subunit of the NF-kBtranscription factor (2014)
Corrêa, Thalita Bueno; Salviatto, Armando Padilha; Beckedorff, Felipe Cesar Ferrarezi; Ebbs, Aaron; Verjovski-Almeida, Sergio ; Baldwin, Albert S; Bassères, Daniela Sanchez
Fonte: Poster Abstracts. Nome do evento: Meeting of the Brazilian Society for Cell Biology. Unidade: IQ
Assuntos: EXPRESSÃO GÊNICA, NEOPLASIAS DO TRATO RESPIRATÓRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORRÊA, Thalita Bueno et al. Analysis of differentially expressed genes in a mouse model of KRAS-induced lung cancer with conditional loss of thep65 subunit of the NF-kBtranscription factor. 2014, Anais.. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC, 2014. . Acesso em: 16 out. 2025.
APA
Corrêa, T. B., Salviatto, A. P., Beckedorff, F. C. F., Ebbs, A., Verjovski-Almeida, S., Baldwin, A. S., & Bassères, D. S. (2014). Analysis of differentially expressed genes in a mouse model of KRAS-induced lung cancer with conditional loss of thep65 subunit of the NF-kBtranscription factor. In Poster Abstracts. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC.
NLM
Corrêa TB, Salviatto AP, Beckedorff FCF, Ebbs A, Verjovski-Almeida S, Baldwin AS, Bassères DS. Analysis of differentially expressed genes in a mouse model of KRAS-induced lung cancer with conditional loss of thep65 subunit of the NF-kBtranscription factor. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Vancouver
Corrêa TB, Salviatto AP, Beckedorff FCF, Ebbs A, Verjovski-Almeida S, Baldwin AS, Bassères DS. Analysis of differentially expressed genes in a mouse model of KRAS-induced lung cancer with conditional loss of thep65 subunit of the NF-kBtranscription factor. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Aurora kinase targeting in lung cancer cells reduces KRAS-dependent oncogenicity (2014)
Santos, Edmilson Ozorio dos; Aoki, Mateus Nobrega; Bassères, Daniela Sanchez
Fonte: Poster Abstracts. Nome do evento: Meeting of the Brazilian Society for Cell Biology. Unidade: IQ
Assuntos: ONCOGENES, NEOPLASIAS DO TRATO RESPIRATÓRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Edmilson Ozorio dos e AOKI, Mateus Nobrega e BASSÈRES, Daniela Sanchez. Aurora kinase targeting in lung cancer cells reduces KRAS-dependent oncogenicity. 2014, Anais.. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC, 2014. . Acesso em: 16 out. 2025.
APA
Santos, E. O. dos, Aoki, M. N., & Bassères, D. S. (2014). Aurora kinase targeting in lung cancer cells reduces KRAS-dependent oncogenicity. In Poster Abstracts. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC.
NLM
Santos EO dos, Aoki MN, Bassères DS. Aurora kinase targeting in lung cancer cells reduces KRAS-dependent oncogenicity. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Vancouver
Santos EO dos, Aoki MN, Bassères DS. Aurora kinase targeting in lung cancer cells reduces KRAS-dependent oncogenicity. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Recently, potential applications of Desferrioxamine and other iron chelators have attracted attention for the clinical management of neurodegenerative diseases (2014)
Díaz Suarez, Eduardo
Fonte: Poster Abstracts. Nome do evento: Symposium on Current Topics in Molecular Biophysics. Unidade: IF
Assuntos: BIOFÍSICA (CONGRESSOS), DOENÇAS NEURODEGENERATIVAS (PESQUISA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DÍAZ SUAREZ, Eduardo. Recently, potential applications of Desferrioxamine and other iron chelators have attracted attention for the clinical management of neurodegenerative diseases. 2014, Anais.. São Paulo: IFUSP, 2014. Disponível em: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf. Acesso em: 16 out. 2025.
APA
Díaz Suarez, E. (2014). Recently, potential applications of Desferrioxamine and other iron chelators have attracted attention for the clinical management of neurodegenerative diseases. In Poster Abstracts. São Paulo: IFUSP. Recuperado de http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
NLM
Díaz Suarez E. Recently, potential applications of Desferrioxamine and other iron chelators have attracted attention for the clinical management of neurodegenerative diseases [Internet]. Poster Abstracts. 2014 ;[citado 2025 out. 16 ] Available from: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
Vancouver
Díaz Suarez E. Recently, potential applications of Desferrioxamine and other iron chelators have attracted attention for the clinical management of neurodegenerative diseases [Internet]. Poster Abstracts. 2014 ;[citado 2025 out. 16 ] Available from: http://biophysics-saopaulo.org/wp-content/uploads/2014/05/ProgramAbstracts_CurrentTopics.pdf
Trabalho de evento-resumo
Neurodegeneration in hippocampus: role of treadmill running in modulating neurodegeneration (2014)
Almeida, Michael Fernandes de; Silva, Carolliny Moura da; Ferrari, Merari de Fátima Ramires
Fonte: Poster Abstracts. Nome do evento: Meeting of the Brazilian Society for Cell Biology. Unidade: IB
Assuntos: DOENÇAS NEURODEGENERATIVAS, DOENÇA DE ALZHEIMER, HIPOTÁLAMO, EXPRESSÃO GÊNICA, EXERCÍCIO FÍSICO, RATOS, MODELOS ANIMAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Michael Fernandes de e SILVA, Carolliny Moura da e FERRARI, Merari de Fátima Ramires. Neurodegeneration in hippocampus: role of treadmill running in modulating neurodegeneration. 2014, Anais.. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC, 2014. . Acesso em: 16 out. 2025.
APA
Almeida, M. F. de, Silva, C. M. da, & Ferrari, M. de F. R. (2014). Neurodegeneration in hippocampus: role of treadmill running in modulating neurodegeneration. In Poster Abstracts. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC.
NLM
Almeida MF de, Silva CM da, Ferrari M de FR. Neurodegeneration in hippocampus: role of treadmill running in modulating neurodegeneration. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Vancouver
Almeida MF de, Silva CM da, Ferrari M de FR. Neurodegeneration in hippocampus: role of treadmill running in modulating neurodegeneration. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Trabalho de evento-resumo
Genomic profile of primary and secondary metastasizing pleomorphic adenoma (2014)
Mariano, Fernanda V; Gondak, Rogério O; Martins, Antonio S; Coletta, Ricardo D; Almeida, Oslei P; Kowalski, Luiz P; Krepischi, Ana Cristina Victorino ; Altemani, Albina
Fonte: Poster Abstracts. Nome do evento: World Congress of International Federation of Head an Neck Oncologic Societies - IFHNOS. Unidade: IB
Assuntos: CARCINOGÊNESE BUCAL, HIBRIDIZAÇÃO, GENOMAS, CARCINOSSARCOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARIANO, Fernanda V et al. Genomic profile of primary and secondary metastasizing pleomorphic adenoma. 2014, Anais.. New York: American Head and Neck Society & International Federation of Head and Neck Oncologic Societies, 2014. . Acesso em: 16 out. 2025.
APA
Mariano, F. V., Gondak, R. O., Martins, A. S., Coletta, R. D., Almeida, O. P., Kowalski, L. P., et al. (2014). Genomic profile of primary and secondary metastasizing pleomorphic adenoma. In Poster Abstracts. New York: American Head and Neck Society & International Federation of Head and Neck Oncologic Societies.
NLM
Mariano FV, Gondak RO, Martins AS, Coletta RD, Almeida OP, Kowalski LP, Krepischi ACV, Altemani A. Genomic profile of primary and secondary metastasizing pleomorphic adenoma. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]
Vancouver
Mariano FV, Gondak RO, Martins AS, Coletta RD, Almeida OP, Kowalski LP, Krepischi ACV, Altemani A. Genomic profile of primary and secondary metastasizing pleomorphic adenoma. Poster Abstracts. 2014 ;[citado 2025 out. 16 ]

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