ReP USP - Resultado da busca

Artigo de periodico
TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil (2021)
Bride, Lais; Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Scliar, Marilia ; Pimassoni, Lucia H. S; Aguiar, Paola Sossai; Paula, Flavia de; Wang, Jaqueline; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana ; Errera, Flávia Imbroisi Valle
Source: PeerJ. Unidades: IB, EE, FM, BIOINFORMÁTICA
Subjects: GENÉTICA, DIABETES MELLITUS, OBESIDADE, IDOSOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRIDE, Lais et al. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil. PeerJ, v. 9, 2021Tradução . . Disponível em: https://doi.org/10.7717/peerj.11349. Acesso em: 18 nov. 2024.
APA
Bride, L., Naslavsky, M., Yamamoto, G. L., Scliar, M., Pimassoni, L. H. S., Aguiar, P. S., et al. (2021). TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil. PeerJ, 9. doi:10.7717/peerj.11349
NLM
Bride L, Naslavsky M, Yamamoto GL, Scliar M, Pimassoni LHS, Aguiar PS, Paula F de, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M, Errera FIV. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil [Internet]. PeerJ. 2021 ; 9[citado 2024 nov. 18 ] Available from: https://doi.org/10.7717/peerj.11349
Vancouver
Bride L, Naslavsky M, Yamamoto GL, Scliar M, Pimassoni LHS, Aguiar PS, Paula F de, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M, Errera FIV. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil [Internet]. PeerJ. 2021 ; 9[citado 2024 nov. 18 ] Available from: https://doi.org/10.7717/peerj.11349
Trabalho de evento-resumo
Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation (2019)
Naslavsky, Michel ; Yamamoto, Guilherme Lopes ; Scliar, M. O; Wang, J; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Abstracts. Conference titles: ASHG Annual Meeting. Unidades: EE, IB, BIOINFORMÁTICA, FM
Subjects: GENÉTICA, IDOSOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. 2019, Anais.. Houston: Escola de Enfermagem, Universidade de São Paulo, 2019. Disponível em: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf. Acesso em: 18 nov. 2024.
APA
Naslavsky, M., Yamamoto, G. L., Scliar, M. O., Wang, J., Duarte, Y. A. de O., Passos-Bueno, M. R., & Zatz, M. (2019). Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation. In Abstracts. Houston: Escola de Enfermagem, Universidade de São Paulo. Recuperado de https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
NLM
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 18 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Vancouver
Naslavsky M, Yamamoto GL, Scliar MO, Wang J, Duarte YA de O, Passos-Bueno MR, Zatz M. Pathogenic loss of function in genes associated to monogenic pediatric disorders in healthy elderly Brazilians improves molecular diagnosis interpretation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 18 ] Available from: https://www.ashg.org/wp-content/uploads/2019/10/ASHG-2019-poster-abstracts.pdf
Artigo de periodico
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations (2014)
Longuini, Viviane Cristina; Lourenço Júnior, Delmar M; Sekiya, Tomoko; Meirelles, Osorio; Goncalves, Tatiana D.; Coutinho, Flavia L.; Francisco, Guilherme; Osaki, Luciana H.; Chammas, Roger; Alves, Venâncio Avancini Ferreira; Siqueira, Sheila A. C.; Schlesinger, David; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lucia; Gama, Patrícia ; Lee, Misu; Molatore, Sara; Pereira, Maria Adelaide A.; Jallad, Raquel S.; Bronstein, Marcello D.; Cunha-Neto, Malebranche B.; Liberman, Bernardo; Fragoso, Maria Candida B. V.; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo A.
Source: European Journal of Endocrinology. Unidades: FM, IB, EE, FSP, ICB
Subjects: MUTAÇÃO GENÉTICA, GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LONGUINI, Viviane Cristina et al. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, n. Ju 2014, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0130. Acesso em: 18 nov. 2024.
APA
Longuini, V. C., Lourenço Júnior, D. M., Sekiya, T., Meirelles, O., Goncalves, T. D., Coutinho, F. L., et al. (2014). Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, ( Ju 2014). doi:10.1530/EJE-14-0130
NLM
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 nov. 18 ] Available from: https://doi.org/10.1530/EJE-14-0130
Vancouver
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 nov. 18 ] Available from: https://doi.org/10.1530/EJE-14-0130
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
Source: Endocrine-Related Cancer. Unidades: ICB, FM, EE, IB, FSP
Subjects: BIOLOGIA CELULAR, GENÉTICA, MUTAÇÃO GENÉTICA, RATOS, POLIMORFISMO, GENÓTIPOS, NEOPLASIAS DA TIREOIDE, ADENOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 18 nov. 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 nov. 18 ] 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 nov. 18 ] Available from: https://doi.org/10.1530/ERC-13-0486

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Subjects

Indexado em

Non normalized affiliation