Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Luciano Abreu Brito"'
Autor:
Lucas Alvizi, Diogo Nani, Luciano Abreu Brito, Gerson Shigeru Kobayashi, Maria Rita Passos-Bueno, Roberto Mayor
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Gene–environment interactions are believed to play a role in multifactorial phenotypes, although poorly described mechanistically. Cleft lip/palate (CLP), the most common craniofacial malformation, has been associated with both genetic and
Externí odkaz:
https://doaj.org/article/36cad45c8b4c480c9d01f3a2abc79137
Autor:
Lucas Alvizi, Luciano Abreu Brito, Gerson Shigeru Kobayashi, Bárbara Bischain, Camila Bassi Fernandes da Silva, Sofia Ligia Guimaraes Ramos, Jaqueline Wang, Maria Rita Passos-Bueno
Publikováno v:
Epigenetics, Vol 17, Iss 13, Pp 2278-2295 (2022)
Non-syndromic cleft lip with or without cleft palate (NSCLP), the most common human craniofacial malformation, is a complex disorder given its genetic heterogeneity and multifactorial component revealed by genetic, epidemiological, and epigenetic fin
Externí odkaz:
https://doaj.org/article/373da2f176254d3ca92182598dfd9fe0
Autor:
Gerson Shigeru Kobayashi, Luciano Abreu Brito, Danielle de Paula Moreira, Angela May Suzuki, Gabriella Shih Ping Hsia, Lylyan Fragoso Pimentel, Ana Paula Barreto de Paiva, Carolina Regoli Dias, Naila Cristina Vilaça Lourenço, Beatriz Araujo Oliveira, Erika Regina Manuli, Marcelo Andreetta Corral, Natale Cavaçana, Miguel Mitne-Neto, Maria Mirtes Sales, Luiz Phellipe Dell’ Aquila, Alvaro Razuk Filho, Eduardo Fagundes Parrillo, Maria Cássia Mendes-Corrêa, Ester Cerdeira Sabino, Silvia Figueiredo Costa, Fabio Eudes Leal, Germán Gustavo Sgro, Chuck Shaker Farah, Mayana Zatz, Maria Rita Passos-Bueno
Publikováno v:
Diagnostics, Vol 11, Iss 8, p 1400 (2021)
Rapid diagnostics is pivotal to curb SARS-CoV-2 transmission, and saliva has emerged as a practical alternative to naso/oropharyngeal (NOP) specimens. We aimed to develop a direct RT-LAMP (reverse transcription loop-mediated isothermal amplification)
Externí odkaz:
https://doaj.org/article/3789d85647b349c2bcc5995fe8e2699c
Autor:
Lucas Alvizi, Xiayi Ke, Luciano Abreu Brito, Rimante Seselgyte, Gudrun E. Moore, Philip Stanier, Maria Rita Passos-Bueno
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Non-syndromic cleft lip and/or palate (NSCLP) is a common congenital malformation with a multifactorial model of inheritance. Although several at-risk alleles have been identified, they do not completely explain the high heritability. We pos
Externí odkaz:
https://doaj.org/article/e5bb70625e764a11be2c07ab251f41fb
Autor:
Maria Rita Passos‐Bueno, Debora Bertola, Dafne Dain Gandelman Horovitz, Victor Evangelista deFaria Ferraz, Luciano Abreu Brito
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 280-291 (2014)
Externí odkaz:
https://doaj.org/article/d568d10d2c9b478aaf73a11147cdd028
Autor:
Luciano Abreu Brito
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
As fissuras orofaciais, ou fissuras labiopalatinas, são malformações prevalentes na população mundial, presente em cerca de um a cada 700 nascimentos. Dentro das fissuras orofaciais, um grupo etiologicamente distinto é composto pelas fissuras d
Autor:
Luciano Abreu Brito
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
Fissura labial com ou sem fissura de palato não sindrômica (FL±P NS) é uma doença complexa que afeta 1:700 indivíduos no mundo. A busca das causas genéticas dessa malformação é dificultada pelo padrão multifatorial de herança e pela heter
Autor:
Lucas, Alvizi, Luciano Abreu, Brito, Gerson Shigeru, Kobayashi, Bárbara, Bischain, Camila Bassi Fernandes, da Silva, Sofia Ligia Guimaraes, Ramos, Jaqueline, Wang, Maria Rita, Passos-Bueno
Publikováno v:
Epigenetics. 17(13)
Non-syndromic cleft lip with or without cleft palate (NSCLP), the most common human craniofacial malformation, is a complex disorder given its genetic heterogeneity and multifactorial component revealed by genetic, epidemiological, and epigenetic fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63592e9b3a4a1e5a0899ebe95891dde3
https://pubmed.ncbi.nlm.nih.gov/36047706
https://pubmed.ncbi.nlm.nih.gov/36047706
Autor:
Michel Satya Naslavsky, Claudia K. Suemoto, Luciano Abreu Brito, Marília Oliveira Scliar, Renata Eloah Ferretti-Rebustini, Roberta Diehl Rodriguez, Renata E. P. Leite, Nathalia Matta Araujo, Victor Borda, Eduardo Tarazona-Santos, Wilson Jacob-Filho, Carlos Pasqualucci, Ricardo Nitrini, Kristine Yaffe, Mayana Zatz, Lea T. Grinberg
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Molecular psychiatry, vol 27, iss 11
Universidade de São Paulo (USP)
instacron:USP
Molecular psychiatry, vol 27, iss 11
Dementia is more prevalent in Blacks than in Whites, likely due to a combination of environmental and biological factors. Paradoxically, clinical studies suggest an attenuation of APOE ε4 risk of dementia in African ancestry (AFR), but a dearth of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969bb65be42d033508e8803ea1d387fb
https://doi.org/10.1002/alz.067651
https://doi.org/10.1002/alz.067651
Autor:
Laura Machado Lara Carvalho, Elisa Varella Branco, Raquel Delgado Sarafian, Gerson Shigeru Kobayashi, Fabiano Tófoli de Araújo, Lucas Santos Souza, Danielle de Paula Moreira, Gabriella Shih Ping Hsia, Eny Maria Goloni Bertollo, Cecília Barbosa Buck, Silvia Souza da Costa, Davi Mendes Fialho, Felipe Tadeu Galante Rocha de Vasconcelos, Luciano Abreu Brito, Luciana Elena de Souza Fraga Machado, Igor Cabreira Ramos, Lygia da Veiga Pereira, Celia Priszkulnik Koiffmann, Maria Rita dos Santos e Passos-Bueno, Tiago Antonio de Oliveira Mendes, Ana Cristina Victorino Krepischi, Carla Rosenberg
Publikováno v:
Gene. 871:147424
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f440891d43738380bd49640682e4ab98
https://doi.org/10.1016/j.gene.2023.147424
https://doi.org/10.1016/j.gene.2023.147424