Resultados da busca - Rodrigo Bertollo de Alexandre
- Mostrando 1 - 12 resultados de 12
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MASP2 gene polymorphism is associated with susceptibility to hepatitis C virus infection por Siumara Túlio, Fábio R. Faucz, Renata Iani Werneck, Márcia Olandoski, Rodrigo Bertollo de Alexandre, Angelica Beate Winter Boldt, Maria Lúcia Alves Pedroso, Iara Messias-Reason
Publicado em 2011Artigo -
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Clinical and Molecular Genetics of the Phosphodiesterases (PDEs) por Monalisa Ferreira Azevedo, Fábio R. Faucz, Eirini I. Bimpaki, Anélia Horvath, Isaac Lévy, Rodrigo Bertollo de Alexandre, Faiyaz Ahmad, Vincent C. Manganiello, Constantine A. Stratakis
Publicado em 2013Revisão -
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Familiar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects por Elen Dias Accordi, Paraskevi Xekouki, Bruna Azevedo, Rodrigo Bertollo de Alexandre, Carla Frasson, Siliane Marie Gantzel, Georgios Z. Papadakis, Anna Angelousi, Constantine A. Stratakis, Vanessa Santos Sotomaior, Fábio R. Faucz
Publicado em 2016Artigo -
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Phosphodiesterase sequence variants may predispose to prostate cancer por Rodrigo Bertollo de Alexandre, Anélia Horvath, Eva Szarek, Allison Manning, Letícia Ferro Leal, Fabio Kardauke, Jonathan A. Epstein, Dirce Maria Carraro, Fernando Augusto Soares, Tatiyana V. Apanasovich, Constantine A. Stratakis, Fábio R. Faucz
Publicado em 2015Artigo -
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The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients por Jarbas Maciel de Oliveira, Nuria Bengala Zurro, Antônio Victor Campos Coelho, Marcel Pinheiro Caraciolo, Rodrigo Bertollo de Alexandre, Murilo Castro Cervato, Renata Moldenhauer Minillo, George de Vasconcelos Carvalho Neto, Ivana Grivicich, João Bosco Oliveira
Publicado em 2021Pré-impressão -
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The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients por Jarbas Maciel de Oliveira, Nuria Bengala Zurro, Antônio Victor Campos Coelho, Marcel Pinheiro Caraciolo, Rodrigo Bertollo de Alexandre, Murilo Castro Cervato, Renata Moldenhauer Minillo, George de Vasconcelos Carvalho Neto, Ivana Grivicich, João Bosco Oliveira
Publicado em 2022Artigo -
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The Brazilian Rare Genomes Project: Validation of Whole Genome Sequencing for Rare Diseases Diagnosis por Antônio Victor Campos Coelho, Bruna Mascaro-Cordeiro, Danielle Ribeiro Lucon, Maria Soares Nóbrega, Rodrigo de Souza Reis, Rodrigo Bertollo de Alexandre, Livia Maria Silva Moura, Gustavo Santos de Oliveira, Rafael Lucas Muniz Guedes, Marcel Pinheiro Caraciolo, Nuria Bengala Zurro, Murilo Castro Cervato, João Bosco Oliveira
Publicado em 2022Artigo -
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Phosphodiesterase 11A (<i>PDE11A</i>) Genetic Variants May Increase Susceptibility to Prostatic Cancer por Fábio R. Faucz, Anélia Horvath, Anya Rothenbühler, Madson Q. Almeida, Rossella Libé, Marie-Laure Raffin-Sanson, Jérôme Bertherat, Dirce Maria Carraro, Fernando Augusto Soares, Gustavo de Campos Molina, Antônio Hugo José Fróes Marques Campos, Rodrigo Bertollo de Alexandre, Marcelo L. Bendhack, Maria Nesterova, Constantine A. Stratakis
Publicado em 2010Artigo -
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The Brazilian Rare Genomes Project: validation of whole genome sequencing for rare diseases diagnosis por Antônio Victor Campos Coelho, Bruna Mascaro Cordeiro de Azevedo, Danielle Ribeiro Lucon, Maria Soares Nóbrega, Rodrigo de Souza Reis, Rodrigo Bertollo de Alexandre, Livia Maria Silva Moura, Gustavo Santos de Oliveira, Rafael Lucas Muniz Guedes, Marcel Pinheiro Caraciolo, Nuria Bengala Zurro, Murilo Castro Cervato, João Bosco Oliveira
Publicado em 2021Pré-impressão -
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Is IGSF1 involved in human pituitary tumor formation? por Fábio R. Faucz, Anélia Horvath, Monalisa Ferreira Azevedo, Isaac Lévy, Beata Bąk, Ying Wang, Paraskevi Xekouki, Eva Szarek, Evgenia Gourgari, Allison Manning, Rodrigo Bertollo de Alexandre, Emmanouil Saloustros, Giampaolo Trivellin, Maya Lodish, Paul L. Hofman, Yvonne C. Anderson, I. M. Holdaway, Edward H. Oldfield, Prashant Chittiboina, Maria Nesterova, Nienke R. Biermasz, Jan M. Wit, Daniel J. Bernard, Constantine A. Stratakis
Publicado em 2014Artigo -
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Gigantism and Acromegaly Due to Xq26 Microduplications and <i>GPR101</i> Mutation por Giampaolo Trivellin, Adrian Daly, Fábio R. Faucz, Bo Yuan, Liliya Rostomyan, Darwin O. Larco, Marie Helene Schernthaner-Reiter, Eva Szarek, Letícia Ferro Leal, Jean‐Hubert Caberg, Emilie Castermans, Chiara Villa, Aggeliki Dimopoulos, Prashant Chittiboina, Paraskevi Xekouki, Nalini S. Shah, Daniel L. Metzger, Philippe A. Lysy, Emanuele Ferrante, Natalia Strebkova, Nadezhda Mazerkina, Maria Chiara Zatelli, Maya Lodish, Anélia Horvath, Rodrigo Bertollo de Alexandre, Allison Manning, Isaac Lévy, Margaret F. Keil, Maria De La Luz Sierra, Léonor Palmeira, Wouter Coppieters, Michel Georges, Luciana Ansaneli Naves, Mauricette Jamar, Vincent Bours, T. John Wu, Catherine S. Choong, Jérôme Bertherat, Philippe Chanson, Peter Kamenický, William E. Farrell, Anne Barlier, Martha Quezado, Ivana Bjelobaba, Stanko S. Stojilković, Jürgen Wess, Stefano Costanzi, Pengfei Liu, James R. Lupski, Albert Beckers, Constantine A. Stratakis
Publicado em 2014Artigo
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Biology
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