A Mutation in the KCNE3 Potassium Channel Gene Is Associated with Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis von Dias Da Silva, Magnus R., Cerutti, Janete M., Arnaldi, Liliane A. T., Maciel, Rui M. B.

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Antithrombin Deficiency in Brazilian Patients with Venous Thrombosis: Molecular Characterization of a Single Splice Site Mutation, an Insertion and a De Novo Point Mutation von Arnaldi, Liliane A.T, Pretti, Fernando A, Zampieri, Jose P, Ramos, Clarisa F, Arruda, Valder R, Annichino-Bizzacchi, Joyce M

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The Generation and Utilization of a Cancer-Oriented Representation of the Human Transcriptome by Using Expressed Sequence Tags von Brentani, Helena, Caballero, Otávia L., Camargo, Anamaria A., da Silva, Aline M., da Silva, Wilson Araújo, Neto, Emmanuel Dias, Grivet, Marco, Gruber, Arthur, Pedro Edson Moreira Guimaraes, Hide, Winston, Iseli, Christian, Jongeneel, C. Victor, Kelso, Janet, Nagai, Maria Aparecida, Elida Paula Benquique Ojopi, Osorio, Elisson C., Eduardo M. R. Reis, Riggins, Gregory J., Andrew John George Simpson, de Souza, Sandro, Stevenson, Brian J., Strausberg, Robert L., Tajara, Eloiza H., Verjovski-Almeida, Sergio, The Human Cancer Genome Project/Cancer Genome Anatomy Project Annotation Consortium, The Human Cancer Genome Project Sequencing Consortium

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The Contribution of 700,000 ORF Sequence Tags to the Definition of the Human Transcriptome von Camargo, Anamaria A., Helena P. B. Samaia, Dias-Neto, Emmanuel, Simão, Daniel F., Migotto, Italo A., Marcelo R. S. Briones, Costa, Fernando F., Nagai, Maria Aparecida, Verjovski-Almeida, Sergio, Zago, Marco A., Luis Eduardo C. Andrade, Carrer, Helaine, Hamza F. A. El-Dorry, Espreafico, Enilza M., Habr-Gama, Angelita, Giannella-Neto, Daniel, Goldman, Gustavo H., Gruber, Arthur, Hackel, Christine, Kimura, Edna T., Rui M. B. Maciel, Suely K. N. Marie, Elizabeth A. L. Martins, Nóbrega, Marina P., Paçó-Larson, Maria Luisa, Maria Inês M. C. Pardini, Pereira, Gonçalo G., Pesquero, João Bosco, Rodrigues, Vanderlei, Rogatto, Silvia R., Ismael D. C. G. da Silva, Sogayar, Mari C., Maria de Fátima Sonati, Tajara, Eloiza H., Valentini, Sandro R., Alberto, Fernando L., Maria Elisabete J. Amaral, Aneas, Ivy, Liliane A. T. Arnaldi, de Assis, Angela M., Bengtso, Mário Henrique, Bergamo, Nadia Aparecida, Bombonato, Vanessa, Maria E. R. de Camargo, Canevari, Renata A., Carraro, Dirce M., Cerutti, Janete M., Maria Lucia C. Corrêa, Rosana F. R. Corrêa, Maria Cristina R. Costa, Curcio, Cyntia, Paula O. M. Hokama, Ari J. S. Ferreira, Furuzawa, Gilberto K., Gushiken, Tsieko, Ho, Paulo L., Kimura, Elza, Krieger, José E., Luciana C. C. Leite, Majumder, Paromita, Marins, Mozart, Marques, Everaldo R., Analy S. A. Melo, Melo, Monica, Mestriner, Carlos Alberto, Miracca, Elisabete C., Miranda, Daniela C., Ana Lucia T. O. Nascimento, Nóbrega, Francisco G., Élida P. B. Ojopi, José Rodrigo C. Pandolfi, Pessoa, Luciana G., Prevedel, Aline C., Rahal, Paula, Rainho, Claudia A., Eduardo M. R. Reis, Ribeiro, Marcelo L., da Rós, Nancy, de Sá, Renata G., Sales, Magaly M., Simone Cristina Sant'anna, Mariana L. dos Santos, da Silva, Aline M., da Silva, Neusa P., Silva, Wilson A., da Silveira, Rosana A., Sousa, Josane F., Stecconi, Daniella, Tsukumo, Fernando, Valente, Valéria, Soares, Fernando, Moreira, Eloisa S., Nunes, Diana N., Correa, Ricardo G., Zalcberg, Heloisa, Carvalho, Alex F., Luis F. L. Reis, Brentani, Ricardo R., Andrew J. G. Simpson, de Souza, Sandro J.

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A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I von Arnaldi, Liliane A.T., Polimeno, Newton C., Arruda, Valder R., Annichino-Bizzacchi, Joyce M.

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Antithrombin Deficiency in Brazilian Patients with Venous Thrombosis von Arnaldi, Liliane A.T, Pretti, Fernando A, Zampieri, Jose P, Ramos, Clarisa F, Arruda, Valder R, Annichino-Bizzacchi, Joyce M

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