ReP USP - Resultado da busca

Artigo de periodico
Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics (2022)
Palmeira, Ondina; Matos, Larissa R. B; Naslavsky, Michel ; Bueno, Heloisa Maria Siqueira ; Soler, Júlia Maria Pavan ; Setubal, João Carlos ; Zatz, Mayana
Source: iScience. Unidades: IB, IQ, IME, BIOINFORMÁTICA
Subjects: BIOTA INTESTINAL, BEBÊS, RNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALMEIRA, Ondina et al. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics. iScience, v. 25, n. 3, p. 1-18 art. 103861, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.isci.2022.103861. Acesso em: 09 nov. 2024.
APA
Palmeira, O., Matos, L. R. B., Naslavsky, M., Bueno, H. M. S., Soler, J. M. P., Setubal, J. C., & Zatz, M. (2022). Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics. iScience, 25( 3), 1-18 art. 103861. doi:10.1016/j.isci.2022.103861
NLM
Palmeira O, Matos LRB, Naslavsky M, Bueno HMS, Soler JMP, Setubal JC, Zatz M. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics [Internet]. iScience. 2022 ; 25( 3): 1-18 art. 103861.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.isci.2022.103861
Vancouver
Palmeira O, Matos LRB, Naslavsky M, Bueno HMS, Soler JMP, Setubal JC, Zatz M. Longitudinal 16S rRNA gut microbiota data of infant triplets show partial susceptibility to host genetics [Internet]. iScience. 2022 ; 25( 3): 1-18 art. 103861.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.isci.2022.103861
Artigo de periodico
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements (2021)
Tavares, Vanessa Luiza Romanelli ; Guimarães-Ramos, Sofia Ligia; Zhou, Yan; Masotti, Cibele; Ezquina, Suzana; Moreira, Danielle de Paula; Buermans, Henk; Freitas, Renato S; Dunnen, Johan T Den; Twigg, Stephen R F; Passos-Bueno, Maria Rita
Source: Journal of Medical Genetics. Unidades: IB, BIOINFORMÁTICA
Subjects: GENÉTICA, DOENÇAS GENÉTICAS, FENÓTIPOS, MALFORMAÇÕES, VARIAÇÃO GENÉTICA, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Vanessa Luiza Romanelli et al. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2021-107825. Acesso em: 09 nov. 2024.
APA
Tavares, V. L. R., Guimarães-Ramos, S. L., Zhou, Y., Masotti, C., Ezquina, S., Moreira, D. de P., et al. (2021). New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements. Journal of Medical Genetics. doi:10.1136/jmedgenet-2021-107825
NLM
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
Vancouver
Tavares VLR, Guimarães-Ramos SL, Zhou Y, Masotti C, Ezquina S, Moreira D de P, Buermans H, Freitas RS, Dunnen JTD, Twigg SRF, Passos-Bueno MR. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1136/jmedgenet-2021-107825
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: 09 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. 09 ] 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. 09 ] Available from: https://doi.org/10.7717/peerj.11349
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) (2020)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly
Source: BioRxiv (The Preprint Server for Biology). Unidades: IB, BIOINFORMÁTICA
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), p. 1-29, 2020Tradução . . Disponível em: https://doi.org/10.1101/2020.09.15.298026. Acesso em: 09 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., & Nunes, K. (2020). Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil). BioRxiv (The Preprint Server for Biology), 1-29. doi:10.1101/2020.09.15.298026
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K. Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil) [Internet]. BioRxiv (The Preprint Server for Biology). 2020 ; 1-29.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1101/2020.09.15.298026
Artigo de periodico
Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate (2019)
Alvizi, Lucas ; Brito, Luciano Abreu; Bischain, Bárbara; Silva, Camila Bassi Fernandes da; Ramos, Sofia Ligia Guimaraes; Kobayashi, Gerson Shigeru; Wang, Jaqueline; Passos-Bueno, Maria Rita
Source: BioRxiv. Unidades: IB, BIOINFORMÁTICA
Subjects: MALFORMAÇÕES, FISSURA LÁBIOPALATINA, EXPRESSÃO GÊNICA, METILAÇÃO DE DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVIZI, Lucas et al. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate. BioRxiv, 2019Tradução . . Disponível em: https://doi.org/10.1101/850016. Acesso em: 09 nov. 2024.
APA
Alvizi, L., Brito, L. A., Bischain, B., Silva, C. B. F. da, Ramos, S. L. G., Kobayashi, G. S., et al. (2019). Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate. BioRxiv. doi:10.1101/850016
NLM
Alvizi L, Brito LA, Bischain B, Silva CBF da, Ramos SLG, Kobayashi GS, Wang J, Passos-Bueno MR. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate [Internet]. BioRxiv. 2019 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1101/850016
Vancouver
Alvizi L, Brito LA, Bischain B, Silva CBF da, Ramos SLG, Kobayashi GS, Wang J, Passos-Bueno MR. Mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate [Internet]. BioRxiv. 2019 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1101/850016

USP Schools

ReP

Filtros

USP Schools

Authors

USP affiliated authors

Subjects

Non normalized affiliation