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Artigo de periodico
An evolutionary perspective on complex neuropsychiatric disease (2024)
McClellan, Jon M ; Zoghbi, Anthony W ; Buxbaum, Joseph D ; Cappi, Carolina ; Crowley, James J ; Flint, Jonathan ; Grice, Dorothy E ; Gulsuner, Suleyman ; Iyegbe, Conrad ; Jain, Sanjeev ; Kuo, Po-Hsiu ; Lattig, Maria Claudia ; Passos-Bueno, Maria Rita ; Purushottam, Meera ; Stein, Dan J ; Sunshine, Anna B ; Susser, Ezra S ; Walsh, Christopher A ; Wootton, Olivia ; King, Mary-Claire
Source: Neuron. Unidade: IB
Subjects: NEUROPSIQUIATRIA, MUTAÇÃO GENÉTICA, DERIVA GÊNICA, ALELOS, TRANSTORNO AUTÍSTICO, ESQUIZOFRENIA
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MCCLELLAN, Jon M et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron, v. 112, n. 1, p. 7-24, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.neuron.2023.10.037. Acesso em: 10 maio 2024.
APA
McClellan, J. M., Zoghbi, A. W., Buxbaum, J. D., Cappi, C., Crowley, J. J., Flint, J., et al. (2024). An evolutionary perspective on complex neuropsychiatric disease. Neuron, 112( 1), 7-24. doi:10.1016/j.neuron.2023.10.037
NLM
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Vancouver
McClellan JM, Zoghbi AW, Buxbaum JD, Cappi C, Crowley JJ, Flint J, Grice DE, Gulsuner S, Iyegbe C, Jain S, Kuo P-H, Lattig MC, Passos-Bueno MR, Purushottam M, Stein DJ, Sunshine AB, Susser ES, Walsh CA, Wootton O, King M-C. An evolutionary perspective on complex neuropsychiatric disease [Internet]. Neuron. 2024 ; 112( 1): 7-24.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.neuron.2023.10.037
Artigo de periodico
Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction (2023)
Alvizi, Lucas; Nani, Diogo; Brito, Luciano Abreu; Kobayashi, Gerson Shigeru ; Passos-Bueno, Maria Rita ; Mayor, Roberto
Source: Nature Communications. Unidade: IB
Subjects: LÁBIO FISSURADO, EPIGÊNESE GENÉTICA, ANORMALIDADES CRANIOFACIAIS
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ALVIZI, Lucas et al. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction. Nature Communications, v. 14, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41467-023-38526-1. Acesso em: 10 maio 2024.
APA
Alvizi, L., Nani, D., Brito, L. A., Kobayashi, G. S., Passos-Bueno, M. R., & Mayor, R. (2023). Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction. Nature Communications, 14. doi:10.1038/s41467-023-38526-1
NLM
Alvizi L, Nani D, Brito LA, Kobayashi GS, Passos-Bueno MR, Mayor R. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction [Internet]. Nature Communications. 2023 ; 14[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41467-023-38526-1
Vancouver
Alvizi L, Nani D, Brito LA, Kobayashi GS, Passos-Bueno MR, Mayor R. Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction [Internet]. Nature Communications. 2023 ; 14[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41467-023-38526-1
Artigo de periodico
DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta (2023)
Pramio, Dimitrius Tansini ; Vieceli, Felipe Monteleone ; Branco, Elisa Varella ; Goes, Carolina Purcell ; Kobayashi, Gerson Shigeru ; Pelegrina, Diogo Vieira da Silva; Moraes, Beatriz Caroline de ; Allam, Aicha El ; Kumar, Bony De ; Jara, Gabriel ; Farfel, José Marcelo ; Reis, Eduardo Moraes ; Passos-Bueno, Maria Rita ; Schechtman, Deborah
Source: Biochimica et biophysica acta-gene regulatory mechanisms. Unidades: IQ, IB, FM, ESALQ
Subjects: EPIGÊNESE GENÉTICA, PROTEÍNAS QUINASES, DOENÇA DE ALZHEIMER, METILAÇÃO DE DNA
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PRAMIO, Dimitrius Tansini et al. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta. Biochimica et biophysica acta-gene regulatory mechanisms, v. 1866, n. 1, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54748. Acesso em: 10 maio 2024.
APA
Pramio, D. T., Vieceli, F. M., Branco, E. V., Goes, C. P., Kobayashi, G. S., Pelegrina, D. V. da S., et al. (2023). DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta. Biochimica et biophysica acta-gene regulatory mechanisms, 1866( 1). doi:10.1016/j.bbagrm.2023.194909
NLM
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Reis EM, Passos-Bueno MR, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta [Internet]. Biochimica et biophysica acta-gene regulatory mechanisms. 2023 ; 1866( 1):[citado 2024 maio 10 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54748
Vancouver
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Reis EM, Passos-Bueno MR, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta [Internet]. Biochimica et biophysica acta-gene regulatory mechanisms. 2023 ; 1866( 1):[citado 2024 maio 10 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54748
Artigo de periodico
Three generation families: analysis of de novo variants in autism (2023)
Costa, Claudia I. Samogy; Campos, Gabriele da Silva; Montenegro, Eduarda Morgana da Silva; Wang, Jaqueline Yu Ting; Scliar, Marília; Monfardini, Frederico; Zachi, Elaine Cristina; Lourenço, Naila C. V ; Chan, Ada J. S; Pereira, Sergio L; Engchuan, Worrawat; Thiruvahindrapuram, Bhooma; Zarrei, Mehdi; Scherer, Stephen W; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: IP, IB, BIOINFORMÁTICA
Subjects: TRANSTORNO DO ESPECTRO AUTISTA, GENES
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COSTA, Claudia I. Samogy et al. Three generation families: analysis of de novo variants in autism. European Journal of Human Genetics, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41431-023-01398-6. Acesso em: 10 maio 2024.
APA
Costa, C. I. S., Campos, G. da S., Montenegro, E. M. da S., Wang, J. Y. T., Scliar, M., Monfardini, F., et al. (2023). Three generation families: analysis of de novo variants in autism. European Journal of Human Genetics. doi:10.1038/s41431-023-01398-6
NLM
Costa CIS, Campos G da S, Montenegro EM da S, Wang JYT, Scliar M, Monfardini F, Zachi EC, Lourenço NCV, Chan AJS, Pereira SL, Engchuan W, Thiruvahindrapuram B, Zarrei M, Scherer SW, Passos-Bueno MR. Three generation families: analysis of de novo variants in autism [Internet]. European Journal of Human Genetics. 2023 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41431-023-01398-6
Vancouver
Costa CIS, Campos G da S, Montenegro EM da S, Wang JYT, Scliar M, Monfardini F, Zachi EC, Lourenço NCV, Chan AJS, Pereira SL, Engchuan W, Thiruvahindrapuram B, Zarrei M, Scherer SW, Passos-Bueno MR. Three generation families: analysis of de novo variants in autism [Internet]. European Journal of Human Genetics. 2023 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41431-023-01398-6
Artigo de periodico
DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ (2023)
Pramio, Dimitrius Tansini; Vieceli, Felipe Monteleone ; Branco, Elisa Varella ; Goes, Carolina Purcell ; Kobayashi, Gerson Shigeru ; Pelegrina, Diogo Vieira da Silva; Moraes, Beatriz Caroline de ; Allam, Aicha El ; Kumar, Bony De ; Jara, Gabriel ; Farfel, José Marcelo; Bennett, David Alan; Kundu, Somanath; Viapiano, Mariano S ; Reis, Eduardo Moraes ; Oliveira, Paulo Sérgio Lopes de; Passos-Bueno, Maria Rita ; Rothlin, Carla V; Ghosh, Sourav; Schechtman, Deborah
Source: Biochimica et Biophysica Acta. Unidades: IQ, IB, ICB
Subjects: METILAÇÃO DE DNA, DOENÇA DE ALZHEIMER, EPIGÊNESE GENÉTICA
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ABNT
PRAMIO, Dimitrius Tansini et al. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ. Biochimica et Biophysica Acta, v. 1866, p. 1-13 art. 194909, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.bbagrm.2023.194909. Acesso em: 10 maio 2024.
APA
Pramio, D. T., Vieceli, F. M., Branco, E. V., Goes, C. P., Kobayashi, G. S., Pelegrina, D. V. da S., et al. (2023). DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ. Biochimica et Biophysica Acta, 1866, 1-13 art. 194909. doi:10.1016/j.bbagrm.2023.194909
NLM
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Bennett DA, Kundu S, Viapiano MS, Reis EM, Oliveira PSL de, Passos-Bueno MR, Rothlin CV, Ghosh S, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ [Internet]. Biochimica et Biophysica Acta. 2023 ; 1866 1-13 art. 194909.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.bbagrm.2023.194909
Vancouver
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Bennett DA, Kundu S, Viapiano MS, Reis EM, Oliveira PSL de, Passos-Bueno MR, Rothlin CV, Ghosh S, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ [Internet]. Biochimica et Biophysica Acta. 2023 ; 1866 1-13 art. 194909.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.bbagrm.2023.194909
Artigo de periodico
Updated consensus guidelines on the management of Phelan–McDermid syndrome (2023)
Srivastava, Siddharth ; Sahin, Mustafa ; Buxbaum, Joseph D ; Berry-Kravis, Elizabeth; Soorya, Latha Valluripalli; Thurm, Audrey ; Bernstein, Jonathan A ; Asante-Otoo, Afua; Bennett Jr, William E; Betancur, Catalina ; Brickhouse, Tegwyn H; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: GENÉTICA MÉDICA, NEUROGENÉTICA
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ABNT
SRIVASTAVA, Siddharth et al. Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, v. 191, n. 8, p. 2015-2044, 2023Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63312. Acesso em: 10 maio 2024.
APA
Srivastava, S., Sahin, M., Buxbaum, J. D., Berry-Kravis, E., Soorya, L. V., Thurm, A., et al. (2023). Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, 191( 8), 2015-2044. doi:10.1002/ajmg.a.63312
NLM
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Vancouver
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Artigo de periodico
Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome (2023)
Lazzaro Filho, Ricardo Di; Yamamoto, Guilherme Lopes; Silva, Tiago J; Rocha, Leticia A; Linnenkamp, Bianca D. W; Castro, Matheus Augusto Araújo; Bartholdi, Deborah; Schaller, André; Leeb, Tosso; Kelmann, Samantha; Utagawa, Claudia Y; Steiner, Carlos E; Steinmetz, Leandra; Honjo, Rachel Sayuri; Kim, Chong Ae ; Wang, Lisa; Abourjaili-Bilodeau, Raphaël; Campeau, Philippe M; Warma, Matthew; Passos-Bueno, Maria Rita ; Hoch, Nicolas Carlos ; Bertola, Débora Romeo
Source: Journal of Medical Genetics. Unidades: BIOINFORMÁTICA, FM, IB, IQ
Subjects: GENÉTICA MÉDICA, ANÁLISE DE SEQUÊNCIA DE DNA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
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ABNT
LAZZARO FILHO, Ricardo Di et al. Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome. Journal of Medical Genetics, 2023Tradução . . Disponível em: https://doi.org/10.1136/jmg-2022-109119. Acesso em: 10 maio 2024.
APA
Lazzaro Filho, R. D., Yamamoto, G. L., Silva, T. J., Rocha, L. A., Linnenkamp, B. D. W., Castro, M. A. A., et al. (2023). Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome. Journal of Medical Genetics. doi:10.1136/jmg-2022-109119
NLM
Lazzaro Filho RD, Yamamoto GL, Silva TJ, Rocha LA, Linnenkamp BDW, Castro MAA, Bartholdi D, Schaller A, Leeb T, Kelmann S, Utagawa CY, Steiner CE, Steinmetz L, Honjo RS, Kim CA, Wang L, Abourjaili-Bilodeau R, Campeau PM, Warma M, Passos-Bueno MR, Hoch NC, Bertola DR. Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome [Internet]. Journal of Medical Genetics. 2023 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1136/jmg-2022-109119
Vancouver
Lazzaro Filho RD, Yamamoto GL, Silva TJ, Rocha LA, Linnenkamp BDW, Castro MAA, Bartholdi D, Schaller A, Leeb T, Kelmann S, Utagawa CY, Steiner CE, Steinmetz L, Honjo RS, Kim CA, Wang L, Abourjaili-Bilodeau R, Campeau PM, Warma M, Passos-Bueno MR, Hoch NC, Bertola DR. Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome [Internet]. Journal of Medical Genetics. 2023 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1136/jmg-2022-109119
Artigo de periodico
Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: models for Xia-Gibbs syndrome (2023)
Carvalho, Laura Machado Lara; Branco, Elisa Varella ; Sarafian, Raquel Delgado ; Kobayashi, Gerson Shigeru ; Araújo, Fabiano Tófoli de; Souza, Lucas Santos ; Moreira, Danielle de Paula; Hsia, Gabriella Shih Ping ; Bertollo, Eny Maria Goloni; Buck, Cecília Barbosa; Costa, Silvia Souza da; Fialho, Davi Mendes; Vasconcelos, Felipe Tadeu Galante Rocha de; Brito, Luciano Abreu; Machado, Luciana Elena de Souza Fraga; Ramos, Igor Cabreira; Pereira, Lygia da Veiga ; Koiffmann, Celia Priszkulnik ; Passos-Bueno, Maria Rita ; Mendes, Tiago Antonio de Oliveira; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Gene. Unidades: IB, BIOTECNOLOGIA, IQ
Subjects: GENÉTICA MÉDICA, DOENÇAS GENÉTICAS, PESSOAS COM DEFICIÊNCIA INTELECTUAL
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ABNT
CARVALHO, Laura Machado Lara et al. Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: models for Xia-Gibbs syndrome. Gene, v. 871, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147424. Acesso em: 10 maio 2024.
APA
Carvalho, L. M. L., Branco, E. V., Sarafian, R. D., Kobayashi, G. S., Araújo, F. T. de, Souza, L. S., et al. (2023). Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: models for Xia-Gibbs syndrome. Gene, 871. doi:10.1016/j.gene.2023.147424
NLM
Carvalho LML, Branco EV, Sarafian RD, Kobayashi GS, Araújo FT de, Souza LS, Moreira D de P, Hsia GSP, Bertollo EMG, Buck CB, Costa SS da, Fialho DM, Vasconcelos FTGR de, Brito LA, Machado LE de SF, Ramos IC, Pereira L da V, Koiffmann CP, Passos-Bueno MR, Mendes TA de O, Krepischi ACV, Rosenberg C. Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: models for Xia-Gibbs syndrome [Internet]. Gene. 2023 ; 871[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.gene.2023.147424
Vancouver
Carvalho LML, Branco EV, Sarafian RD, Kobayashi GS, Araújo FT de, Souza LS, Moreira D de P, Hsia GSP, Bertollo EMG, Buck CB, Costa SS da, Fialho DM, Vasconcelos FTGR de, Brito LA, Machado LE de SF, Ramos IC, Pereira L da V, Koiffmann CP, Passos-Bueno MR, Mendes TA de O, Krepischi ACV, Rosenberg C. Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: models for Xia-Gibbs syndrome [Internet]. Gene. 2023 ; 871[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.gene.2023.147424
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: 10 maio 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 maio 10 ] 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 maio 10 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair (2022)
Castro, Mateus V. de ; Santos, Keity S ; Apostolico, Juliana S; Fernandes, Edgar R; Almeida, Rafael R ; Levin, Gabriel ; Magawa, Jhosiene Y; Nunes, João Paulo S ; Bruni, Mirian; Yamamoto, Marcio M; Lima, Ariane C; Silva, Monize V. R; Matos, Larissa R. B; Coria, Vivian R; Castelli, Erick C; Scliar, Marilia O; Kuramoto, Andreia; Bruno, Fernanda R; Jacintho, Lucas C; Nunes, Kelly; Wang, Jaqueline Y. T; Coelho, Veronica P ; Mitne Neto, Miguel; Maciel, Rui M. B; Naslavsky, Michel ; Passos-Bueno, Maria Rita ; Boscardin, Silvia Beatriz ; Rosa, Daniela S ; Kalil, Jorge ; Zatz, Mayana ; Cunha-Neto, Edecio
Source: Open Biology. Unidades: FM, ICB, IB, BIOINFORMÁTICA
Subjects: COVID-19, GÊMEOS, INFECÇÕES POR CORONAVIRUS, DOENÇAS INFECCIOSAS, IMUNOGENÉTICA
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ABNT
CASTRO, Mateus V. de et al. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair. Open Biology, v. 12, n. 2, 2022Tradução . . Disponível em: https://doi.org/10.1098/rsob.210240. Acesso em: 10 maio 2024.
APA
Castro, M. V. de, Santos, K. S., Apostolico, J. S., Fernandes, E. R., Almeida, R. R., Levin, G., et al. (2022). Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair. Open Biology, 12( 2). doi:10.1098/rsob.210240
NLM
Castro MV de, Santos KS, Apostolico JS, Fernandes ER, Almeida RR, Levin G, Magawa JY, Nunes JPS, Bruni M, Yamamoto MM, Lima AC, Silva MVR, Matos LRB, Coria VR, Castelli EC, Scliar MO, Kuramoto A, Bruno FR, Jacintho LC, Nunes K, Wang JYT, Coelho VP, Mitne Neto M, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha-Neto E. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair [Internet]. Open Biology. 2022 ; 12( 2):[citado 2024 maio 10 ] Available from: https://doi.org/10.1098/rsob.210240
Vancouver
Castro MV de, Santos KS, Apostolico JS, Fernandes ER, Almeida RR, Levin G, Magawa JY, Nunes JPS, Bruni M, Yamamoto MM, Lima AC, Silva MVR, Matos LRB, Coria VR, Castelli EC, Scliar MO, Kuramoto A, Bruno FR, Jacintho LC, Nunes K, Wang JYT, Coelho VP, Mitne Neto M, Maciel RMB, Naslavsky M, Passos-Bueno MR, Boscardin SB, Rosa DS, Kalil J, Zatz M, Cunha-Neto E. Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair [Internet]. Open Biology. 2022 ; 12( 2):[citado 2024 maio 10 ] Available from: https://doi.org/10.1098/rsob.210240
Artigo de periodico
Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila (2022)
Palacios-Muñoz, Angelina ; Moreira, Danielle de Paula; Silva, Valeria ; García, Isaac E; Aboitiz, Francisco; Zarrei, Mehdi; Campos, Gabriele ; Rennie, Olivia ; Howe, Jennifer L; Anagnostou, Evdokia; Ambrozewic, Patricia; Scherer, Stephen W ; Passos-Bueno, Maria Rita ; Ewer, John
Source: Molecular Psychiatry. Unidade: IB
Subjects: TRANSTORNO DO ESPECTRO AUTISTA, NEUROBIOLOGIA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALACIOS-MUÑOZ, Angelina et al. Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila. Molecular Psychiatry, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41380-022-01555-1. Acesso em: 10 maio 2024.
APA
Palacios-Muñoz, A., Moreira, D. de P., Silva, V., García, I. E., Aboitiz, F., Zarrei, M., et al. (2022). Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila. Molecular Psychiatry. doi:10.1038/s41380-022-01555-1
NLM
Palacios-Muñoz A, Moreira D de P, Silva V, García IE, Aboitiz F, Zarrei M, Campos G, Rennie O, Howe JL, Anagnostou E, Ambrozewic P, Scherer SW, Passos-Bueno MR, Ewer J. Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila [Internet]. Molecular Psychiatry. 2022 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41380-022-01555-1
Vancouver
Palacios-Muñoz A, Moreira D de P, Silva V, García IE, Aboitiz F, Zarrei M, Campos G, Rennie O, Howe JL, Anagnostou E, Ambrozewic P, Scherer SW, Passos-Bueno MR, Ewer J. Mutations in trpγ, the homologue of TRPC6 autism candidate gene, causes autism-like behavioral deficits in Drosophila [Internet]. Molecular Psychiatry. 2022 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41380-022-01555-1
Artigo de periodico
Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature (2022)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Freire, Bruna Lucheze; Homma, Thais Kataoka; Honjo, Rachel Sayuri ; Yamamoto, Guilherme Lopes ; Passos-Bueno, Maria Rita ; Koiffmann, Celia Priszkulnik ; Kim, Chong Ae ; Vianna-Morgante, Angela M ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino
Source: Journal of Autism and Developmental Disorders. Unidades: IB, FM
Subjects: MICROCEFALIA, REVISÃO SISTEMÁTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEZANO, Giovanna Cantini et al. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10803-022-05853-z. Acesso em: 10 maio 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Freire, B. L., Homma, T. K., Honjo, R. S., et al. (2022). Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders. doi:10.1007/s10803-022-05853-z
NLM
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 maio 10 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Artigo de periodico-carta/editorial
Correction: the oldest unvaccinated Covid-19 survivors in South America (2022)
Castro, Mateus Vidigal de ; Silva, Moníze Valéria Ramos da ; Naslavsky, Michel ; Scliar, Marilia O ; Nunes, Kelly ; Passos-Bueno, Maria Rita ; Magawa, Jhosiene Yukari; Adami, Flávia L ; Moretti, Ana Iochabel Soares ; Oliveira, Vivian L. de; Boscardin, Silvia Beatriz ; Cunha Neto, Edecio ; Kalil Filho, Jorge Elias ; Santos, Keity Souza ; Zatz, Mayana ; Jouanguy, Emmanuelle ; Bastard, Paul ; Casanova, Jean-Laurent ; Vega, Maruricio Quiñones; Acosta, Patricia Sosa ; Guedes, Jessica S. de; Almeida, Natalia P. de; Nogueira, Fabio C. S. ; Domont, Gilberto B.
Source: Immunity & Ageing. Unidades: IB, ICB, FM
Subjects: PARASITOLOGIA, COVID-19, SOBREVIVÊNCIA LIVRE DE DOENÇA, IDOSOS, INFECÇÕES POR VÍRUS DE RNA, INFECÇÕES POR CORONAVIRUS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus Vidigal de et al. Correction: the oldest unvaccinated Covid-19 survivors in South America. Immunity & Ageing. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1186/s12979-022-00319-3. Acesso em: 10 maio 2024. , 2022
APA
Castro, M. V. de, Silva, M. V. R. da, Naslavsky, M., Scliar, M. O., Nunes, K., Passos-Bueno, M. R., et al. (2022). Correction: the oldest unvaccinated Covid-19 survivors in South America. Immunity & Ageing. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1186/s12979-022-00319-3
NLM
Castro MV de, Silva MVR da, Naslavsky M, Scliar MO, Nunes K, Passos-Bueno MR, Magawa JY, Adami FL, Moretti AIS, Oliveira VL de, Boscardin SB, Cunha Neto E, Kalil Filho JE, Santos KS, Zatz M, Jouanguy E, Bastard P, Casanova J-L, Vega MQ, Acosta PS, Guedes JS de, Almeida NP de, Nogueira FCS, Domont GB. Correction: the oldest unvaccinated Covid-19 survivors in South America [Internet]. Immunity & Ageing. 2022 ; 19 1 .[citado 2024 maio 10 ] Available from: https://doi.org/10.1186/s12979-022-00319-3
Vancouver
Castro MV de, Silva MVR da, Naslavsky M, Scliar MO, Nunes K, Passos-Bueno MR, Magawa JY, Adami FL, Moretti AIS, Oliveira VL de, Boscardin SB, Cunha Neto E, Kalil Filho JE, Santos KS, Zatz M, Jouanguy E, Bastard P, Casanova J-L, Vega MQ, Acosta PS, Guedes JS de, Almeida NP de, Nogueira FCS, Domont GB. Correction: the oldest unvaccinated Covid-19 survivors in South America [Internet]. Immunity & Ageing. 2022 ; 19 1 .[citado 2024 maio 10 ] Available from: https://doi.org/10.1186/s12979-022-00319-3
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
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 Brazil. Nature, v. 13, n. 1004, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-28648-3. Acesso em: 10 maio 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 maio 10 ] 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 maio 10 ] Available from: https://doi.org/10.1038/s41467-022-28648-3
Artigo de periodico-carta/editorial
FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? (2022)
Girardi, Ana Cristina De Sanctis ; Takahashi, Vanessa Naomi Van Opstal ; Vadasz, Estêvão ; Costa, Claudia Ismania Samogi ; Zachi, Elaine Cristina; Vianna-Morgante, Angela M ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidades: IB, IP
Subjects: TRANSTORNO AUTÍSTICO, CRIANÇAS AUTISTAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIRARDI, Ana Cristina De Sanctis et al. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed?. American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/ajmg.a.62624. Acesso em: 10 maio 2024. , 2022
APA
Girardi, A. C. D. S., Takahashi, V. N. V. O., Vadasz, E., Costa, C. I. S., Zachi, E. C., Vianna-Morgante, A. M., & Passos-Bueno, M. R. (2022). FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/ajmg.a.62624
NLM
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Vancouver
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Artigo de periodico
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022)
Fu, Jack M; Satterstrom, F. Kyle; Peng, Minshi; Passos-Bueno, Maria Rita
Source: Nature Genetics. Unidade: IB
Subjects: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FU, Jack M et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, v. 54, p. 1320–1331, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41588-022-01104-0. Acesso em: 10 maio 2024.
APA
Fu, J. M., Satterstrom, F. K., Peng, M., & Passos-Bueno, M. R. (2022). Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics, 54, 1320–1331. doi:10.1038/s41588-022-01104-0
NLM
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Vancouver
Fu JM, Satterstrom FK, Peng M, Passos-Bueno MR. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism [Internet]. Nature Genetics. 2022 ; 54 1320–1331.[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41588-022-01104-0
Artigo de periodico
Neuroprogenitor cells from patients with TBCK encephalopathy suggest deregulation of early secretory vesicle transport (2022)
Moreira, Danielle de Paula; Suzuki, Angela May; Silva, André Luiz Teles e; Varella-Branco, Elisa; Meneghetti, Maria Cecília Zorél; Kobayashi, Gerson Shigeru ; Fogo, Mariana; Ferrari, Merari de Fátima Ramires ; Cardoso, Rafaela Regina; Lourenço, Naila Cristina Vilaça ; Griesi-Oliveira, Karina; Zachi, Elaine Cristina; Bertola, Débora Romeo; Weinmann, Karina de Souza; Lima, Marcelo Andrade de; Nader, Helena Bonciani; Sertié, Andrea Laurato; Passos-Bueno, Maria Rita
Source: Frontiers in Plant Science. Unidades: IB, IP
Subjects: NEUROBIOLOGIA, GENÉTICA MÉDICA, DOENÇAS CEREBRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, Danielle de Paula et al. Neuroprogenitor cells from patients with TBCK encephalopathy suggest deregulation of early secretory vesicle transport. Frontiers in Plant Science, v. 12, 2022Tradução . . Disponível em: https://doi.org/10.3389/fncel.2021.803302. Acesso em: 10 maio 2024.
APA
Moreira, D. de P., Suzuki, A. M., Silva, A. L. T. e, Varella-Branco, E., Meneghetti, M. C. Z., Kobayashi, G. S., et al. (2022). Neuroprogenitor cells from patients with TBCK encephalopathy suggest deregulation of early secretory vesicle transport. Frontiers in Plant Science, 12. doi:10.3389/fncel.2021.803302
NLM
Moreira D de P, Suzuki AM, Silva ALT e, Varella-Branco E, Meneghetti MCZ, Kobayashi GS, Fogo M, Ferrari M de FR, Cardoso RR, Lourenço NCV, Griesi-Oliveira K, Zachi EC, Bertola DR, Weinmann K de S, Lima MA de, Nader HB, Sertié AL, Passos-Bueno MR. Neuroprogenitor cells from patients with TBCK encephalopathy suggest deregulation of early secretory vesicle transport [Internet]. Frontiers in Plant Science. 2022 ; 12[citado 2024 maio 10 ] Available from: https://doi.org/10.3389/fncel.2021.803302
Vancouver
Moreira D de P, Suzuki AM, Silva ALT e, Varella-Branco E, Meneghetti MCZ, Kobayashi GS, Fogo M, Ferrari M de FR, Cardoso RR, Lourenço NCV, Griesi-Oliveira K, Zachi EC, Bertola DR, Weinmann K de S, Lima MA de, Nader HB, Sertié AL, Passos-Bueno MR. Neuroprogenitor cells from patients with TBCK encephalopathy suggest deregulation of early secretory vesicle transport [Internet]. Frontiers in Plant Science. 2022 ; 12[citado 2024 maio 10 ] Available from: https://doi.org/10.3389/fncel.2021.803302
Artigo de periodico
Interleukin-17a induces neuronal differentiation of induced-pluripotent stem cell-derived neural progenitors from autistic and control subjects (2022)
Gomes, Ana Karolyne Santos; Dantas, Rafaelly Mayara; Yokota, Bruno Yukio; Silva, André Luiz Teles e; Griesi-Oliveira, Karina; Passos-Bueno, Maria Rita ; Sertié, Andréa Laurato
Source: Frontiers in Plant Science. Unidade: IB
Subjects: TRANSTORNO AUTÍSTICO, DOENÇAS GENÉTICAS, DOENÇAS DO SISTEMA NERVOSO, NEUROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Ana Karolyne Santos et al. Interleukin-17a induces neuronal differentiation of induced-pluripotent stem cell-derived neural progenitors from autistic and control subjects. Frontiers in Plant Science, v. 16, 2022Tradução . . Disponível em: https://doi.org/10.3389/fnins.2022.828646. Acesso em: 10 maio 2024.
APA
Gomes, A. K. S., Dantas, R. M., Yokota, B. Y., Silva, A. L. T. e, Griesi-Oliveira, K., Passos-Bueno, M. R., & Sertié, A. L. (2022). Interleukin-17a induces neuronal differentiation of induced-pluripotent stem cell-derived neural progenitors from autistic and control subjects. Frontiers in Plant Science, 16. doi:10.3389/fnins.2022.828646
NLM
Gomes AKS, Dantas RM, Yokota BY, Silva ALT e, Griesi-Oliveira K, Passos-Bueno MR, Sertié AL. Interleukin-17a induces neuronal differentiation of induced-pluripotent stem cell-derived neural progenitors from autistic and control subjects [Internet]. Frontiers in Plant Science. 2022 ; 16[citado 2024 maio 10 ] Available from: https://doi.org/10.3389/fnins.2022.828646
Vancouver
Gomes AKS, Dantas RM, Yokota BY, Silva ALT e, Griesi-Oliveira K, Passos-Bueno MR, Sertié AL. Interleukin-17a induces neuronal differentiation of induced-pluripotent stem cell-derived neural progenitors from autistic and control subjects [Internet]. Frontiers in Plant Science. 2022 ; 16[citado 2024 maio 10 ] Available from: https://doi.org/10.3389/fnins.2022.828646
Artigo de periodico
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder (2022)
Silva, André Luíz Teles e ; Glaser, Talita ; Oliveira, Karina Griesi ; Velloso, Juliana da Cruz Corrêa ; Wang, Jaqueline Yu Ting; Campos, Gabriele da Silva ; Ulrich, Henning ; Balan, Andrea ; Zarrei, Mehdi; Higginbotham, Edward J.; Scherer, Stephen W. ; Passos-Bueno, Maria Rita ; Sertié, Andrea Laurato
Source: Translational Psychiatry. Unidades: IQ, ICB, IB
Subjects: MICROBIOLOGIA, FÁRMACOS IMUNOSSUPRESSORES, TRANSTORNO DO ESPECTRO AUTISTA, CANAIS DE CÁLCIO, DISTÚRBIOS PSICOLÓGICOS, HERANÇA GENÉTICA, VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, André Luíz Teles e et al. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder. Translational Psychiatry, v. 12, p. 1-11, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41398-022-01997-9. Acesso em: 10 maio 2024.
APA
Silva, A. L. T. e, Glaser, T., Oliveira, K. G., Velloso, J. da C. C., Wang, J. Y. T., Campos, G. da S., et al. (2022). Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder. Translational Psychiatry, 12, 1-11. doi:10.1038/s41398-022-01997-9
NLM
Silva ALT e, Glaser T, Oliveira KG, Velloso J da CC, Wang JYT, Campos G da S, Ulrich H, Balan A, Zarrei M, Higginbotham EJ, Scherer SW, Passos-Bueno MR, Sertié AL. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder [Internet]. Translational Psychiatry. 2022 ; 12 1-11.[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41398-022-01997-9
Vancouver
Silva ALT e, Glaser T, Oliveira KG, Velloso J da CC, Wang JYT, Campos G da S, Ulrich H, Balan A, Zarrei M, Higginbotham EJ, Scherer SW, Passos-Bueno MR, Sertié AL. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder [Internet]. Translational Psychiatry. 2022 ; 12 1-11.[citado 2024 maio 10 ] Available from: https://doi.org/10.1038/s41398-022-01997-9
Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 10 maio 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 maio 10 ] Available from: https://doi.org/10.1002/humu.24349

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