Search Results - Varella Branco, Elisa

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  1. 1
    Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and mice

    Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and mice by Nair, Divya, Diaz-Rosado, Abdias, Varella-Branco, Elisa, Ramos, Igor, Black, Aaron, Angireddy, Rajesh, Park, Joseph, Murali, Svathi, Yoon, Andrew, Ciesielski, Brianna, O'Brien, W Timothy, Passos-Bueno, Maria Rita, Bhoj, Elizabeth

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  2. 2
    Generation and characterization of cortical organoids from iPSC-derived dental pulp stem cells using traditional and innovative approaches

    Generation and characterization of cortical organoids from iPSC-derived dental pulp stem cells using traditional and innovative approaches by Teles e Silva, André Luíz, Yokota-Moreno, Bruno Yukio, Branquinho, Mariana Silva, Salles, Geisa Rodrigues, de Souza, Thiago Cattuzo, de Carvalho, Ronald Almeida, Batista, Gabriel, Varella Branco, Elisa, Griesi-Oliveira, Karina, Passos Bueno, Maria Rita, Porcionatto, Marimélia Aparecida, Herai, Roberto Hirochi, Gamarra, Lionel Fernel, Sertié, Andrea Laurato

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  3. 3
    Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes

    Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes by Costa, Claudia Ismania Samogy, Silva Montenegro, Eduarda Morgana, Zarrei, Mehdi, Sá Moreira, Eloísa, Silva, Isabela Maya Wahys, Oliveira Scliar, Marília, Wang, Jaqueline Yu Ting, Zachi, Elaine Cristina, Branco, Elisa Varella, Costa, Silvia Souza, Lourenço, Naila Cristina Vilaça, Vianna‐Morgante, Angela Maria, Rosenberg, Carla, Krepischi, Ana Cristina Victorino, Scherer, Stephen W., Passos‐Bueno, Maria Rita

    Published in Clinical genetics
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  4. 4
    A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case

    A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case by Samogy-Costa, Claudia Ismania, Varella-Branco, Elisa, Monfardini, Frederico, Ferraz, Helen, Fock, Rodrigo Ambrósio, Barbosa, Ricardo Henrique Almeida, Pessoa, André Luiz Santos, Perez, Ana Beatriz Alvarez, Lourenço, Naila, Vibranovski, Maria, Krepischi, Ana, Rosenberg, Carla, Passos-Bueno, Maria Rita

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  5. 5
    Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A)

    Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hea... by Kobayashi, Gerson S., Vieira-Silva, Gleiciele A., Varella-Branco, Elisa, Moreira, Danielle P., Kitajima, João Paulo F.W., Hemza, Claudia R.M.L., Mingroni-Netto, Regina C., Lojudice, Fernando H., Oiticica, Jeanne, Bento, Ricardo F., Batissoco, Ana C., Lezirovitz, Karina

    Published in Stem cell research
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  6. 6
    Neuroprogenitor Cells From Patients With TBCK Encephalopathy Suggest Deregulation of Early Secretory Vesicle Transport

    Neuroprogenitor Cells From Patients With TBCK Encephalopathy Suggest Deregulation of Early Secretory Vesicle Transport by 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, de Lima, Marcelo Andrade, Nader, Helena Bonciani, Sertié, Andrea Laurato, Passos-Bueno, Maria Rita

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  7. 7
    Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome

    Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome by Carvalho, Laura Machado Lara, Branco, Elisa Varella, Sarafian, Raquel Delgado, Kobayashi, Gerson Shigeru, de Araújo, Fabiano Tófoli, Santos Souza, Lucas, Moreira, Danielle de Paula, Hsia, Gabriella Shih Ping, Bertollo, Eny Maria Goloni, Buck, Cecília Barbosa, da Costa, Silvia Souza, Fialho, Davi Mendes, de Vasconcelos, Felipe Tadeu Galante Rocha, Brito, Luciano Abreu, de Souza Fraga Machado, Luciana Elena, Ramos, Igor Cabreira, Pereira, Lygia da Veiga, Koiffmann, Celia Priszkulnik, e Passos-Bueno, Maria Rita dos Santos, Oliveira Mendes, Tiago Antonio de, Krepischi, Ana Cristina Victorino, Rosenberg, Carla

    Published in Gene
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  8. 8
    DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ

    DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKMζ by Pramio, Dimitrius Tansini, Vieceli, Felipe Monteleone, Varella-Branco, Elisa, Goes, Carolina Purcell, Kobayashi, Gerson Shigeru, da Silva Pelegrina, Diogo Vieira, de Moraes, Beatriz Caroline, El Allam, Aicha, De Kumar, Bony, Jara, Gabriel, Farfel, José Marcelo, Bennett, David Alan, Kundu, Somanath, Viapiano, Mariano S., Reis, Eduardo Moraes, de Oliveira, Paulo Sergio Lopes, dos Santos e Passos-Bueno, Maria Rita, Rothlin, Carla V., Ghosh, Sourav, Schechtman, Deborah

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  9. 9
    EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome

    EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome by Carvalho, Laura Machado Lara, Rzasa, Jessica, Kerkhof, Jennifer, McConkey, Haley, Fishman, Veniamin, Koksharova, Galina, de Lima Jorge, Alexander Augusto, Branco, Elisa Varella, de Oliveira, Danyllo Felipe, Martinez-Delgado, Beatriz, Barrero, Maria J, Kleefstra, Tjitske, Sadikovic, Bekim, Haddad, Luciana Amaral, Bertola, Débora Romeo, Rosenberg, Carla, Krepischi, Ana Cristina Victorino

    Published in Molecular neurobiology
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