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Artigo de periodico
Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
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ABNT
NASLAVSKY, Michel et al. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1831, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29575-z. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1831). doi:10.1038/s41467-022-29575-z
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
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ABNT
NASLAVSKY, Michel et al. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1004, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-28648-3. Acesso em: 15 nov. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1004). doi:10.1038/s41467-022-28648-3
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1004):[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico
Seascape genetics in a polychaete worm: Disentangling the roles of a biogeographic barrier and environmental factors (2022)
Mendes, Cecili B. ; Cortez, Thainá ; Santos, Cinthya S. G. ; Sobral-Souza, Thadeu ; Santos, Arian Dielactaquiz ; Sasaki, Dalton Kei ; Silva, Danilo Augusto ; Dottori, Marcelo ; Andrade, Sónia C. S
Source: Journal biogeography (print). Unidades: IO, IB
Subjects: DIVERSIDADE GENÉTICA, CORRENTES OCEÂNICAS
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ABNT
MENDES, Cecili B. et al. Seascape genetics in a polychaete worm: Disentangling the roles of a biogeographic barrier and environmental factors. Journal biogeography (print), v. 49, n. 12, p. 2296-2308, 2022Tradução . . Disponível em: https://doi.org/10.1111/jbi.14504. Acesso em: 15 nov. 2024.
APA
Mendes, C. B., Cortez, T., Santos, C. S. G., Sobral-Souza, T., Santos, A. D., Sasaki, D. K., et al. (2022). Seascape genetics in a polychaete worm: Disentangling the roles of a biogeographic barrier and environmental factors. Journal biogeography (print), 49( 12), 2296-2308. doi:10.1111/jbi.14504
NLM
Mendes CB, Cortez T, Santos CSG, Sobral-Souza T, Santos AD, Sasaki DK, Silva DA, Dottori M, Andrade SCS. Seascape genetics in a polychaete worm: Disentangling the roles of a biogeographic barrier and environmental factors [Internet]. Journal biogeography (print). 2022 ; 49( 12): 2296-2308.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/jbi.14504
Vancouver
Mendes CB, Cortez T, Santos CSG, Sobral-Souza T, Santos AD, Sasaki DK, Silva DA, Dottori M, Andrade SCS. Seascape genetics in a polychaete worm: Disentangling the roles of a biogeographic barrier and environmental factors [Internet]. Journal biogeography (print). 2022 ; 49( 12): 2296-2308.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/jbi.14504
Artigo de periodico
Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism (2016)
Machado, Camila Oliveira Freitas; Griesi-Oliveira, Karina; Rosenberg, Carla ; Kok, Fernando; Martins, Stephanie; Passos-Bueno, Maria Rita ; Sertie, Andrea Laurato
Source: European Journal of Human Genetics. Unidades: FM, IB
Subjects: SÍNDROME X METABÓLICA, FIBROBLASTOS, TÉCNICAS CITOLÓGICAS
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ABNT
MACHADO, Camila Oliveira Freitas et al. Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism. European Journal of Human Genetics, v. 24, n. 1, p. 59-65, 2016Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2015.69. Acesso em: 15 nov. 2024.
APA
Machado, C. O. F., Griesi-Oliveira, K., Rosenberg, C., Kok, F., Martins, S., Passos-Bueno, M. R., & Sertie, A. L. (2016). Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism. European Journal of Human Genetics, 24( 1), 59-65. doi:10.1038/ejhg.2015.69
NLM
Machado COF, Griesi-Oliveira K, Rosenberg C, Kok F, Martins S, Passos-Bueno MR, Sertie AL. Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism [Internet]. European Journal of Human Genetics. 2016 ; 24( 1): 59-65.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2015.69
Vancouver
Machado COF, Griesi-Oliveira K, Rosenberg C, Kok F, Martins S, Passos-Bueno MR, Sertie AL. Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism [Internet]. European Journal of Human Genetics. 2016 ; 24( 1): 59-65.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2015.69
Artigo de periodico
Early Holocene ritual complexity in South America: the archaeological record of Lapa do Santo (east-central Brazil) (2016)
Strauss, Andre ; Oliveira, Rodrigo Elias ; Bernardo, Danilo ; Salazar-García, Domingo C. ; Bissaro Júnior, Marcos César ; Pugliese, Francisco ; Hermenegildo, Tiago ; Santos, Rafael; Barioni, Alberto ; Oliveira, Emiliano Castro de ; Sousa, João Carlos Moreno de ; Jaouen, Klervia ; Ernani, Max; Hübbe, Mark ; Inglez, Mariana ; Gratão, Marina; Rockwell, H.; Machado, Márcia; Souza, Gustavo de; Chemale Junior, Farid ; Kawashita, Koji; O'Connell, Tamsin ; Israde, Isabel ; Feathers, James K. ; Castro, Claudio Campi ; Richards, Michael ; Wahl, Joachim; Kipnis, Renato ; Araujo, Astolfo Gomes de Mello ; Neves, Walter ; Villagrán, Ximena Suárez
Source: Antiquity. Unidades: IGC, IB, MAE, FM, FFCLRP, FFLCH
Subjects: PALEOÍNDIOS, RITOS FUNERÁRIOS
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ABNT
STRAUSS, Andre et al. Early Holocene ritual complexity in South America: the archaeological record of Lapa do Santo (east-central Brazil). Antiquity, v. 90, p. 1454-1473, 2016Tradução . . Disponível em: https://doi.org/10.15184/aqy.2016.220. Acesso em: 15 nov. 2024.
APA
Strauss, A., Oliveira, R. E., Bernardo, D., Salazar-García, D. C., Bissaro Júnior, M. C., Pugliese, F., et al. (2016). Early Holocene ritual complexity in South America: the archaeological record of Lapa do Santo (east-central Brazil). Antiquity, 90, 1454-1473. doi:10.15184/aqy.2016.220
NLM
Strauss A, Oliveira RE, Bernardo D, Salazar-García DC, Bissaro Júnior MC, Pugliese F, Hermenegildo T, Santos R, Barioni A, Oliveira EC de, Sousa JCM de, Jaouen K, Ernani M, Hübbe M, Inglez M, Gratão M, Rockwell H, Machado M, Souza G de, Chemale Junior F, Kawashita K, O'Connell T, Israde I, Feathers JK, Castro CC, Richards M, Wahl J, Kipnis R, Araujo AG de M, Neves W, Villagrán XS. Early Holocene ritual complexity in South America: the archaeological record of Lapa do Santo (east-central Brazil) [Internet]. Antiquity. 2016 ; 90 1454-1473.[citado 2024 nov. 15 ] Available from: https://doi.org/10.15184/aqy.2016.220
Vancouver
Strauss A, Oliveira RE, Bernardo D, Salazar-García DC, Bissaro Júnior MC, Pugliese F, Hermenegildo T, Santos R, Barioni A, Oliveira EC de, Sousa JCM de, Jaouen K, Ernani M, Hübbe M, Inglez M, Gratão M, Rockwell H, Machado M, Souza G de, Chemale Junior F, Kawashita K, O'Connell T, Israde I, Feathers JK, Castro CC, Richards M, Wahl J, Kipnis R, Araujo AG de M, Neves W, Villagrán XS. Early Holocene ritual complexity in South America: the archaeological record of Lapa do Santo (east-central Brazil) [Internet]. Antiquity. 2016 ; 90 1454-1473.[citado 2024 nov. 15 ] Available from: https://doi.org/10.15184/aqy.2016.220
Trabalho de evento-resumo
Bioarchaeology for children (2015)
Eggers, Sabine; Pezo, L; Petronilho, C
Source: Abstracts. Conference titles: Annual Conference of the British Association for Biological Anthropology and Osteoarchaeology. Unidade: IB
Subjects: ARQUEOLOGIA (ESTUDO;ENSINO), ANTROPOLOGIA BIOLÓGICA
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ABNT
EGGERS, Sabine e PEZO, L e PETRONILHO, C. Bioarchaeology for children. 2015, Anais.. Sheffield: British Association for Biological Anthropology and Osteoarchaeology (BABAO), 2015. . Acesso em: 15 nov. 2024.
APA
Eggers, S., Pezo, L., & Petronilho, C. (2015). Bioarchaeology for children. In Abstracts. Sheffield: British Association for Biological Anthropology and Osteoarchaeology (BABAO).
NLM
Eggers S, Pezo L, Petronilho C. Bioarchaeology for children. Abstracts. 2015 ;[citado 2024 nov. 15 ]
Vancouver
Eggers S, Pezo L, Petronilho C. Bioarchaeology for children. Abstracts. 2015 ;[citado 2024 nov. 15 ]
Artigo de periodico
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome (2015)
Yamamoto, Guilherme Lopes; Aguena, Meire; Gos, Monika; Hung, Christina; Pilch, Jacek; Fahiminiya, Somayyeh; Abramowicz, Anna; Cristian, Ingrid; Buscarilli, Michelle; Naslavsky, Michel ; Malaquias, Alexsandra C.; Zatz, Mayana ; Bodamer, Olaf; Majewski, Jacek; Jorge, Alexander A. L.; Pereira, Alexandre C.; Kim, Chong Ae; Passos-Bueno, Maria Rita ; Bertola, Débora Romeo
Source: Journal of Medical Genetics. Unidades: FM, IB
Subjects: ESTUDOS DE COORTES, ESTATÍSTICA (MÉTODOS), ANORMALIDADES CARDIOVASCULARES, ANORMALIDADES CRANIOFACIAIS
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ABNT
YAMAMOTO, Guilherme Lopes et al. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. Journal of Medical Genetics, v. 52, n. 6, p. 413-421, 2015Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2015-103018. Acesso em: 15 nov. 2024.
APA
Yamamoto, G. L., Aguena, M., Gos, M., Hung, C., Pilch, J., Fahiminiya, S., et al. (2015). Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. Journal of Medical Genetics, 52( 6), 413-421. doi:10.1136/jmedgenet-2015-103018
NLM
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky M, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AAL, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome [Internet]. Journal of Medical Genetics. 2015 ; 52( 6): 413-421.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2015-103018
Vancouver
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky M, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AAL, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome [Internet]. Journal of Medical Genetics. 2015 ; 52( 6): 413-421.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2015-103018
Artigo de periodico
Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells (2015)
Ishiy, Felipe Augusto Andre; Fanganiello, Roberto Dalto; Karina Griesi-Oliveira; Suzuki, Angela May; Kobayashi, Gerson Shigeru; Morales, Andressa Gois; Capelo, Luciane Portas; Passos-Bueno, Maria Rita
Source: Stem Cells International. Unidade: IB
Subjects: TECIDO ADIPOSO, CÉLULAS-TRONCO, REGENERAÇÃO ÓSSEA
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ABNT
ISHIY, Felipe Augusto Andre et al. Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells. Stem Cells International, p. 9 , 2015Tradução . . Disponível em: https://doi.org/10.1155/2015/249098. Acesso em: 15 nov. 2024.
APA
Ishiy, F. A. A., Fanganiello, R. D., Karina Griesi-Oliveira,, Suzuki, A. M., Kobayashi, G. S., Morales, A. G., et al. (2015). Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells. Stem Cells International, 9 . doi:10.1155/2015/249098
NLM
Ishiy FAA, Fanganiello RD, Karina Griesi-Oliveira, Suzuki AM, Kobayashi GS, Morales AG, Capelo LP, Passos-Bueno MR. Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells [Internet]. Stem Cells International. 2015 ; 9 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1155/2015/249098
Vancouver
Ishiy FAA, Fanganiello RD, Karina Griesi-Oliveira, Suzuki AM, Kobayashi GS, Morales AG, Capelo LP, Passos-Bueno MR. Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells [Internet]. Stem Cells International. 2015 ; 9 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1155/2015/249098
Artigo de periodico
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect (2015)
Tavares, Vanessa Luiza Romanelli ; Gordon, Christopher T; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Voisin, Norine; Tan, Tiong Y; Heggie, Andrew A; Pittoli, Siulan Vendramini Paulovich ; Propst, Evan J; Papsin, Blake C; Torres, Tatiana Teixeira ; Buermans, Henk; Capelo, Luciane Portas; Den Dunnen, Johan T; Guion-Almeida, Maria Leine; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS, GENES
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ABNT
TAVARES, Vanessa Luiza Romanelli et al. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, v. 23, n. 4, p. 481-485, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.132. Acesso em: 15 nov. 2024.
APA
Tavares, V. L. R., Gordon, C. T., Zechi-Ceide, R. M., Nakata, N. M. K., Voisin, N., Tan, T. Y., et al. (2015). Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, 23( 4), 481-485. doi:10.1038/ejhg.2014.132
NLM
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Vancouver
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Artigo de periodico
Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies (2012)
Aguena, Meire; Fanganiello, Roberto Dalto; Tissiani, Luiz Alexandre Lorico; Ishiy, Felipe Augusto André; Atique, Rodrigo; Alonso, Nivaldo; Passos-Bueno, Maria Rita
Source: Stem Cells International. Unidades: FM, IB
Subjects: TECIDO ADIPOSO, CÉLULAS-TRONCO, TRANSPLANTE AUTÓLOGO, CIRURGIA PLÁSTICA, IMUNOFENOTIPAGEM, CITOMETRIA DE FLUXO
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ABNT
AGUENA, Meire et al. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies. Stem Cells International, p. 7 , 2012Tradução . . Disponível em: https://doi.org/10.1155/2012/303610. Acesso em: 15 nov. 2024.
APA
Aguena, M., Fanganiello, R. D., Tissiani, L. A. L., Ishiy, F. A. A., Atique, R., Alonso, N., & Passos-Bueno, M. R. (2012). Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies. Stem Cells International, 7 . doi:10.1155/2012/303610
NLM
Aguena M, Fanganiello RD, Tissiani LAL, Ishiy FAA, Atique R, Alonso N, Passos-Bueno MR. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies [Internet]. Stem Cells International. 2012 ; 7 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1155/2012/303610
Vancouver
Aguena M, Fanganiello RD, Tissiani LAL, Ishiy FAA, Atique R, Alonso N, Passos-Bueno MR. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies [Internet]. Stem Cells International. 2012 ; 7 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1155/2012/303610
Artigo de periodico
A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features (2012)
Molin, A. M; Andrieux, J; Koolen, D. A; Malan, V; Carella, M; Colleaux, L; Cormier-Daire, V; David, A; Leeuw, N de; Delobel, B; Duban-Bedu, B; Fischetto, R; Flinter, F; Kjaergaard, S; Kok, Fernando; Krepischi, Ana Cristina Victorino ; Le Caignec, C; Mackie Ogilvie, C; Maia, S; Mathieu-Dramard, M; Minnich, A; Palumbo, O; Papadia, F; Pfundt, R; Reardon, W; Receveur, A; Rio, M; Ronsbro Darling,L; Rosenberg, Carla ; Sá, J; Vallee, L; Vincent-Delorme, C; Zelante, L; Bondeson, M-L; Annerén, G
Source: Journal of Medical Genetics. Unidade: IB
Subjects: RETARDO MENTAL, GENÓTIPOS, FENÓTIPOS, ANOMALIA FACIAL, GENÉTICA MÉDICA
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ABNT
MOLIN, A. M et al. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features. Journal of Medical Genetics, v. 49, n. 2, p. 104-109, 2012Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2011-100534. Acesso em: 15 nov. 2024.
APA
Molin, A. M., Andrieux, J., Koolen, D. A., Malan, V., Carella, M., Colleaux, L., et al. (2012). A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features. Journal of Medical Genetics, 49( 2), 104-109. doi:10.1136/jmedgenet-2011-100534
NLM
Molin AM, Andrieux J, Koolen DA, Malan V, Carella M, Colleaux L, Cormier-Daire V, David A, Leeuw N de, Delobel B, Duban-Bedu B, Fischetto R, Flinter F, Kjaergaard S, Kok F, Krepischi ACV, Le Caignec C, Mackie Ogilvie C, Maia S, Mathieu-Dramard M, Minnich A, Palumbo O, Papadia F, Pfundt R, Reardon W, Receveur A, Rio M, Ronsbro Darling L, Rosenberg C, Sá J, Vallee L, Vincent-Delorme C, Zelante L, Bondeson M-L, Annerén G. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 104-109.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100534
Vancouver
Molin AM, Andrieux J, Koolen DA, Malan V, Carella M, Colleaux L, Cormier-Daire V, David A, Leeuw N de, Delobel B, Duban-Bedu B, Fischetto R, Flinter F, Kjaergaard S, Kok F, Krepischi ACV, Le Caignec C, Mackie Ogilvie C, Maia S, Mathieu-Dramard M, Minnich A, Palumbo O, Papadia F, Pfundt R, Reardon W, Receveur A, Rio M, Ronsbro Darling L, Rosenberg C, Sá J, Vallee L, Vincent-Delorme C, Zelante L, Bondeson M-L, Annerén G. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 104-109.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100534
Artigo de periodico
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion (2012)
Klopocki, Eva; Lohan, Silke; Doelken Sandra C; Stricker, Sigmar; Ockeloen, Charlotte W; Aguiar, Renata Soares Thiele de; Lezirovitz, Karina; Mingroni Netto, Regina Celia ; Jamsheer, Aleksander; Shah, Hitesh; Kurth, Ingo; Habenicht, Rolf; Warman, Matthew; Devriendt, Koenraad; Kordaß, Ulrike; Hempel, Maja; Rajab, Anna; Mäkitie, Outi; Naveed, Mohammed; Radhakrishna, Uppala; Antonarakis, Stylianos E
Source: Journal of Medical Genetics. Unidade: IB
Subjects: MALFORMAÇÕES, DOENÇAS GENÉTICAS, GENÉTICA MÉDICA
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ABNT
KLOPOCKI, Eva et al. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics, v. 49, n. 2, p. 119-125, 2012Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2011-100409. Acesso em: 15 nov. 2024.
APA
Klopocki, E., Lohan, S., Doelken Sandra C,, Stricker, S., Ockeloen, C. W., Aguiar, R. S. T. de, et al. (2012). Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics, 49( 2), 119-125. doi:10.1136/jmedgenet-2011-100409
NLM
Klopocki E, Lohan S, Doelken Sandra C, Stricker S, Ockeloen CW, Aguiar RST de, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordaß U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 119-125.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100409
Vancouver
Klopocki E, Lohan S, Doelken Sandra C, Stricker S, Ockeloen CW, Aguiar RST de, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordaß U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion [Internet]. Journal of Medical Genetics. 2012 ; 49( 2): 119-125.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1136/jmedgenet-2011-100409
Artigo de periodico
Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy (2012)
Giannetti, Juliana Gurgel; Zanoteli, Edmar; Concentino, Eralda Luiza de Castro; Abath Neto, Osorio; Pesquero, João Bosco; Reed, Umbertina Conti; Vainzof, Mariz
Source: Neuromuscular Disorders. Unidades: FM, IB
Subjects: FENÓTIPOS, FIBRAS MUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS (GENÉTICA), MUTAÇÃO GENÉTICA, FIBRAS NERVOSAS, PROGNÓSTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIANNETTI, Juliana Gurgel et al. Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy. Neuromuscular Disorders, v. 22, n. 6, p. 541\2013545, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2011.12.005. Acesso em: 15 nov. 2024.
APA
Giannetti, J. G., Zanoteli, E., Concentino, E. L. de C., Abath Neto, O., Pesquero, J. B., Reed, U. C., & Vainzof, M. (2012). Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy. Neuromuscular Disorders, 22( 6), 541\2013545. doi:10.1016/j.nmd.2011.12.005
NLM
Giannetti JG, Zanoteli E, Concentino EL de C, Abath Neto O, Pesquero JB, Reed UC, Vainzof M. Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy [Internet]. Neuromuscular Disorders. 2012 ; 22( 6): 541\2013545.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.nmd.2011.12.005
Vancouver
Giannetti JG, Zanoteli E, Concentino EL de C, Abath Neto O, Pesquero JB, Reed UC, Vainzof M. Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy [Internet]. Neuromuscular Disorders. 2012 ; 22( 6): 541\2013545.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.nmd.2011.12.005
Artigo de periodico
A palaeobiogeographic model for biotic diversification within Amazonia over the past three million years (2012)
Ribas, Camila Cherem ; Aleixo, Alexandre ; Nogueira, Afonso César Rodrigues ; Miyaki, Cristina Yumi ; Cracraft, Joel
Source: Proceedings of the Royal Society B: Biological Sciences. Unidade: IB
Subjects: PALEOBIOGEOGRAFIA, FILOGENIA, AVES
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ABNT
RIBAS, Camila Cherem et al. A palaeobiogeographic model for biotic diversification within Amazonia over the past three million years. Proceedings of the Royal Society B: Biological Sciences, v. 279, n. 1729, p. 681-689, 2012Tradução . . Disponível em: https://doi.org/10.1098/rspb.2011.1120. Acesso em: 15 nov. 2024.
APA
Ribas, C. C., Aleixo, A., Nogueira, A. C. R., Miyaki, C. Y., & Cracraft, J. (2012). A palaeobiogeographic model for biotic diversification within Amazonia over the past three million years. Proceedings of the Royal Society B: Biological Sciences, 279( 1729), 681-689. doi:10.1098/rspb.2011.1120
NLM
Ribas C C, Aleixo A, Nogueira ACR, Miyaki CY, Cracraft J. A palaeobiogeographic model for biotic diversification within Amazonia over the past three million years [Internet]. Proceedings of the Royal Society B: Biological Sciences. 2012 ; 279( 1729): 681-689.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rspb.2011.1120
Vancouver
Ribas C C, Aleixo A, Nogueira ACR, Miyaki CY, Cracraft J. A palaeobiogeographic model for biotic diversification within Amazonia over the past three million years [Internet]. Proceedings of the Royal Society B: Biological Sciences. 2012 ; 279( 1729): 681-689.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1098/rspb.2011.1120
Artigo de periodico
Disulfide biochemistry in 2-Cys peroxiredoxin: requirement of Glu50 and Arg146 for the reduction of yeast Tsa1 by thioredoxin (2012)
Tairum, Carlos A; Oliveira, Marcos A. de; Horta, Bruno B; Zara, Fernando J; Netto, Luis Eduardo Soares
Source: Journal of Molecular Biology. Unidade: IB
Subjects: PROTEÍNAS, SACCHAROMYCES, ANTIOXIDANTES
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ABNT
TAIRUM, Carlos A et al. Disulfide biochemistry in 2-Cys peroxiredoxin: requirement of Glu50 and Arg146 for the reduction of yeast Tsa1 by thioredoxin. Journal of Molecular Biology, v. No 2012, n. 1-2, p. 28-41, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.jmb.2012.09.008. Acesso em: 15 nov. 2024.
APA
Tairum, C. A., Oliveira, M. A. de, Horta, B. B., Zara, F. J., & Netto, L. E. S. (2012). Disulfide biochemistry in 2-Cys peroxiredoxin: requirement of Glu50 and Arg146 for the reduction of yeast Tsa1 by thioredoxin. Journal of Molecular Biology, No 2012( 1-2), 28-41. doi:10.1016/j.jmb.2012.09.008
NLM
Tairum CA, Oliveira MA de, Horta BB, Zara FJ, Netto LES. Disulfide biochemistry in 2-Cys peroxiredoxin: requirement of Glu50 and Arg146 for the reduction of yeast Tsa1 by thioredoxin [Internet]. Journal of Molecular Biology. 2012 ; No 2012( 1-2): 28-41.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jmb.2012.09.008
Vancouver
Tairum CA, Oliveira MA de, Horta BB, Zara FJ, Netto LES. Disulfide biochemistry in 2-Cys peroxiredoxin: requirement of Glu50 and Arg146 for the reduction of yeast Tsa1 by thioredoxin [Internet]. Journal of Molecular Biology. 2012 ; No 2012( 1-2): 28-41.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jmb.2012.09.008
Artigo de periodico
Recombinant expression, localization and in vitro inhibition of midgut cysteine peptidase (Sl-CathL) from sugarcane weevil, Sphenophorus levis (2012)
Fonseca, Fernando P. P; Soares-Costa, Andrea; Ribeiro, Alberto de Freitas ; Rosa, José César; Terra, Walter Ribeiro ; Henrique-Silva, Flávio
Source: Insect Biochemistry and Molecular Biology. Unidades: FMRP, IQ, IB
Subjects: CANA-DE-AÇÚCAR, DIGESTÃO ANIMAL
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ABNT
FONSECA, Fernando P. P et al. Recombinant expression, localization and in vitro inhibition of midgut cysteine peptidase (Sl-CathL) from sugarcane weevil, Sphenophorus levis. Insect Biochemistry and Molecular Biology, v. 42, n. 1, p. 58-69, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ibmb.2011.10.008. Acesso em: 15 nov. 2024.
APA
Fonseca, F. P. P., Soares-Costa, A., Ribeiro, A. de F., Rosa, J. C., Terra, W. R., & Henrique-Silva, F. (2012). Recombinant expression, localization and in vitro inhibition of midgut cysteine peptidase (Sl-CathL) from sugarcane weevil, Sphenophorus levis. Insect Biochemistry and Molecular Biology, 42( 1), 58-69. doi:10.1016/j.ibmb.2011.10.008
NLM
Fonseca FPP, Soares-Costa A, Ribeiro A de F, Rosa JC, Terra WR, Henrique-Silva F. Recombinant expression, localization and in vitro inhibition of midgut cysteine peptidase (Sl-CathL) from sugarcane weevil, Sphenophorus levis [Internet]. Insect Biochemistry and Molecular Biology. 2012 ; 42( 1): 58-69.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ibmb.2011.10.008
Vancouver
Fonseca FPP, Soares-Costa A, Ribeiro A de F, Rosa JC, Terra WR, Henrique-Silva F. Recombinant expression, localization and in vitro inhibition of midgut cysteine peptidase (Sl-CathL) from sugarcane weevil, Sphenophorus levis [Internet]. Insect Biochemistry and Molecular Biology. 2012 ; 42( 1): 58-69.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ibmb.2011.10.008
Artigo de periodico
The search of a genetic basis for noise-induced hearing loss (NIHL) (2011)
Abreu-Silva, Ronaldo Serafim; Rincon, Daniel; Horimoto, Andréa Roseli Vançan Russo; Sguillar, Ary Papa; Ricardo, Luiz Artur Costa; Kimura, Lilian; Batissoco, Ana Carla; Auricchio, Maria Teresa Ballester de Melo; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Annals of Human Biology. Unidade: IB
Subjects: SURDEZ, MUTAÇÃO GENÉTICA
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ABNT
ABREU-SILVA, Ronaldo Serafim et al. The search of a genetic basis for noise-induced hearing loss (NIHL). Annals of Human Biology, v. 38, n. 2, p. 210-218, 2011Tradução . . Disponível em: https://doi.org/10.3109/03014460.2010.513774. Acesso em: 15 nov. 2024.
APA
Abreu-Silva, R. S., Rincon, D., Horimoto, A. R. V. R., Sguillar, A. P., Ricardo, L. A. C., Kimura, L., et al. (2011). The search of a genetic basis for noise-induced hearing loss (NIHL). Annals of Human Biology, 38( 2), 210-218. doi:10.3109/03014460.2010.513774
NLM
Abreu-Silva RS, Rincon D, Horimoto ARVR, Sguillar AP, Ricardo LAC, Kimura L, Batissoco AC, Auricchio MTB de M, Otto PA, Mingroni Netto RC. The search of a genetic basis for noise-induced hearing loss (NIHL) [Internet]. Annals of Human Biology. 2011 ; 38( 2): 210-218.[citado 2024 nov. 15 ] Available from: https://doi.org/10.3109/03014460.2010.513774
Vancouver
Abreu-Silva RS, Rincon D, Horimoto ARVR, Sguillar AP, Ricardo LAC, Kimura L, Batissoco AC, Auricchio MTB de M, Otto PA, Mingroni Netto RC. The search of a genetic basis for noise-induced hearing loss (NIHL) [Internet]. Annals of Human Biology. 2011 ; 38( 2): 210-218.[citado 2024 nov. 15 ] Available from: https://doi.org/10.3109/03014460.2010.513774
Trabalho de evento-resumo periodico
A candidate gene for X-linked genomic imprinting in human full-term placenta (2011)
Mello, Joana Carvalho Moreira de; Sábio, Fernando G; Pereira, Lygia da Veiga
Conference titles: IFPA Meeting. Unidade: IB
Subjects: PLACENTA, IMPRINTING (GENÉTICA), EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELLO, Joana Carvalho Moreira de e SÁBIO, Fernando G e PEREIRA, Lygia da Veiga. A candidate gene for X-linked genomic imprinting in human full-term placenta. . London: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 15 nov. 2024. , 2011
APA
Mello, J. C. M. de, Sábio, F. G., & Pereira, L. da V. (2011). A candidate gene for X-linked genomic imprinting in human full-term placenta. London: Instituto de Biociências, Universidade de São Paulo.
NLM
Mello JCM de, Sábio FG, Pereira L da V. A candidate gene for X-linked genomic imprinting in human full-term placenta. 2011 ; 32( 9): A137.[citado 2024 nov. 15 ]
Vancouver
Mello JCM de, Sábio FG, Pereira L da V. A candidate gene for X-linked genomic imprinting in human full-term placenta. 2011 ; 32( 9): A137.[citado 2024 nov. 15 ]
Artigo de periodico
Mesenchymal and embryonic characteristics of stem cells obtained from mouse dental pulp (2011)
Guimarães, Elisalva Teixeira; Cruz, Gabriela Silva; Jesus, Alan Araújo de; Carvalho, Acácia Fernandes Lacerda de; Rogatto, Silvia Regina; Pereira, Lygia da Veiga ; Ribeiro-dos-Santos, Ricardo; Soares, Milena Botelho Pereira
Source: Archives of Oral Biology. Unidade: IB
Subjects: CÉLULAS-TRONCO, POLPA DENTÁRIA, RATOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUIMARÃES, Elisalva Teixeira et al. Mesenchymal and embryonic characteristics of stem cells obtained from mouse dental pulp. Archives of Oral Biology, v. No 2011, n. 11, p. 1247-1255, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.archoralbio.2011.05.008. Acesso em: 15 nov. 2024.
APA
Guimarães, E. T., Cruz, G. S., Jesus, A. A. de, Carvalho, A. F. L. de, Rogatto, S. R., Pereira, L. da V., et al. (2011). Mesenchymal and embryonic characteristics of stem cells obtained from mouse dental pulp. Archives of Oral Biology, No 2011( 11), 1247-1255. doi:10.1016/j.archoralbio.2011.05.008
NLM
Guimarães ET, Cruz GS, Jesus AA de, Carvalho AFL de, Rogatto SR, Pereira L da V, Ribeiro-dos-Santos R, Soares MBP. Mesenchymal and embryonic characteristics of stem cells obtained from mouse dental pulp [Internet]. Archives of Oral Biology. 2011 ; No 2011( 11): 1247-1255.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2011.05.008
Vancouver
Guimarães ET, Cruz GS, Jesus AA de, Carvalho AFL de, Rogatto SR, Pereira L da V, Ribeiro-dos-Santos R, Soares MBP. Mesenchymal and embryonic characteristics of stem cells obtained from mouse dental pulp [Internet]. Archives of Oral Biology. 2011 ; No 2011( 11): 1247-1255.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2011.05.008
Artigo de periodico
A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms (2011)
Pereira, Tiago V; Mingroni Netto, Regina Celia
Source: BMC Research Notes. Unidade: IB
Subjects: POLIMORFISMO, GENÉTICA MÉDICA, METANÁLISE, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Tiago V e MINGRONI NETTO, Regina Celia. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. BMC Research Notes, v. 4, p. on-line art. 172, 2011Tradução . . Disponível em: https://doi.org/10.1186/1756-0500-4-172. Acesso em: 15 nov. 2024.
APA
Pereira, T. V., & Mingroni Netto, R. C. (2011). A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. BMC Research Notes, 4, on-line art. 172. doi:10.1186/1756-0500-4-172
NLM
Pereira TV, Mingroni Netto RC. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms [Internet]. BMC Research Notes. 2011 ; 4 on-line art. 172.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1756-0500-4-172
Vancouver
Pereira TV, Mingroni Netto RC. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms [Internet]. BMC Research Notes. 2011 ; 4 on-line art. 172.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1756-0500-4-172

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