Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Gerson Shigeru, Kobayashi"'
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:
Danielle de Paula Moreira, Angela May Suzuki, André Luiz Teles e Silva, Elisa Varella-Branco, Maria Cecília Zorél Meneghetti, Gerson Shigeru Kobayashi, Mariana Fogo, Merari de Fátima Ramires Ferrari, Rafaela Regina Cardoso, Naila Cristina Vilaça Lourenço, Karina Griesi-Oliveira, Elaine Cristina Zachi, Débora Romeo Bertola, Karina de Souza Weinmann, Marcelo Andrade de Lima, Helena Bonciani Nader, Andrea Laurato Sertié, Maria Rita Passos-Bueno
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2022)
Biallelic pathogenic variants in TBCK cause encephaloneuropathy, infantile hypotonia with psychomotor retardation, and characteristic facies 3 (IHPRF3). The molecular mechanisms underlying its neuronal phenotype are largely unexplored. In this study,
Externí odkaz:
https://doaj.org/article/b6157e43dbaf43568d0bef65c5a89565
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:
Luiz Carlos Caires-Júnior, Ernesto Goulart, Uirá Souto Melo, Bruno Henrique Silva Araujo, Lucas Alvizi, Alessandra Soares-Schanoski, Danyllo Felipe de Oliveira, Gerson Shigeru Kobayashi, Karina Griesi-Oliveira, Camila Manso Musso, Murilo Sena Amaral, Lucas Ferreira daSilva, Renato Mancini Astray, Sandra Fernanda Suárez-Patiño, Daniella Cristina Ventini, Sérgio Gomes da Silva, Guilherme Lopes Yamamoto, Suzana Ezquina, Michel Satya Naslavsky, Kayque Alves Telles-Silva, Karina Weinmann, Vanessa van der Linden, Helio van der Linden, João Ricardo Mendes de Oliveira, Nivia Maria Rodrigues Arrais, Adriana Melo, Thalita Figueiredo, Silvana Santos, Joanna Goes Castro Meira, Saulo Duarte Passos, Roque Pacheco de Almeida, Ana Jovina Barreto Bispo, Esper Abrão Cavalheiro, Jorge Kalil, Edécio Cunha-Neto, Helder Nakaya, Robert Andreata-Santos, Luis Carlos de Souza Ferreira, Sergio Verjovski-Almeida, Paulo Lee Ho, Maria Rita Passos-Bueno, Mayana Zatz
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Zika virus (ZIKV) infection can cause congenital Zika syndrome (CZS), but the underlying mechanisms are poorly understood. Here, the authors generate neural progenitor cells from dizygotic twins with a discordant phenotype regarding CZS and study the
Externí odkaz:
https://doaj.org/article/2fae1218b8954f70ace6659a61a3d04f
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:
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
Autor:
Luiz Carlos Caires-Júnior, Ernesto Goulart, Uirá Souto Melo, Bruno Henrique Silva Araujo, Lucas Alvizi, Alessandra Soares-Schanoski, Danyllo Felipe de Oliveira, Gerson Shigeru Kobayashi, Karina Griesi-Oliveira, Camila Manso Musso, Murilo Sena Amaral, Lucas Ferreira daSilva, Renato Mancini Astray, Sandra Fernanda Suárez-Patiño, Daniella Cristina Ventini, Sérgio Gomes da Silva, Guilherme Lopes Yamamoto, Suzana Ezquina, Michel Satya Naslavsky, Kayque Alves Telles-Silva, Karina Weinmann, Vanessa van der Linden, Helio van der Linden, João Ricardo Mendes de Oliveira, Nivia Maria Rodrigues Arrais, Adriana Melo, Thalita Figueiredo, Silvana Santos, Joanna Goes Castro Meira, Saulo Duarte Passos, Roque Pacheco de Almeida, Ana Jovina Barreto Bispo, Esper Abrão Cavalheiro, Jorge Kalil, Edécio Cunha-Neto, Helder Nakaya, Robert Andreata-Santos, Luis Carlos de Souza Ferreira, Sergio Verjovski-Almeida, Paulo Lee Ho, Maria Rita Passos-Bueno, Mayana Zatz
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-2 (2018)
The original PDF version of this Article contained errors in the spelling of Luiz Carlos Caires-Júnior, Uirá Souto Melo, Bruno Henrique Silva Araujo, Alessandra Soares-Schanoski, Murilo Sena Amaral, Kayque Alves Telles-Silva, Vanessa van der Linden
Externí odkaz:
https://doaj.org/article/9203f91a5d55493495ac4983488712a1
Autor:
Dimitrius Tansini Pramio, Felipe Monteleone Vieceli, Elisa Varella-Branco, Carolina Purcell Goes, Gerson Shigeru Kobayashi, Diogo Vieira da Silva Pelegrina, Beatriz Caroline de Moraes, Aicha El Allam, Bony De Kumar, Gabriel Jara, José Marcelo Farfel, David Alan Bennett, Somanath Kundu, Mariano S. Viapiano, Eduardo Moraes Reis, Paulo Sergio Lopes de Oliveira, Maria Rita dos Santos e Passos-Bueno, Carla V. Rothlin, Sourav Ghosh, Deborah Schechtman
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1866:194909
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bbbbacbcaf728172cf860509e921e2c
https://doi.org/10.1016/j.bbagrm.2023.194909
https://doi.org/10.1016/j.bbagrm.2023.194909
Autor:
Dione Fernandes Tavares, Bruna Souza Magalhães, Emília Katiane Embiruçu de Araújo Leão, Joanna Goes Castro Meira, Gerson Shigeru Kobayashi, Isabella Brige Bonifácio Ferreira
Publikováno v:
American Journal of Medical Genetics Part A. 185:1569-1574
Heterozygous variants in USP9X are associated with female-restricted X-linked mental retardation (MRXS99F), a rare syndrome characterized by neurodevelopmental delay, intellectual disability (ID), and a wide variety of additional congenital anomalies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4d9261f4af501c19ff50bcfc3362289
https://doi.org/10.1002/ajmg.a.62141
https://doi.org/10.1002/ajmg.a.62141