Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Fernando Lopes Alberto"'
Autor:
DANILO SOARES-SILVA, LUIZ CARLOS DI SERIO, FERNANDO LOPES ALBERTO, RODOLFO MODRIGAIS STRAUSS NUNES
Publikováno v:
Cadernos EBAPE.BR. 20:561-579
This teaching case reflects the strategic choices of the Fleury Group in the face of the Brazilian economic scenario and the particularities of the private health services sector in Brazil. The teaching case invites the reader to reflect on challenge
Autor:
Ubirajara Rocha Ferreira, Fabricio J. Pontes, Fernando Lopes Alberto, Cinthia B. Moyses, Messias Borges Silva, Helder Jose Celani de Souza, Roberto N. Duarte, Carlos Eduardo Sanches da Silva
Publikováno v:
Molecular and Cellular Probes. 25:231-237
Two mutations - Factor V Leiden (1691G > A) and the 20210G > A on the Prothrombin gene - are key risk factors for a frequent and potentially fatal disorder called Venous Thromboembolism. These molecular alterations can be investigated using real-time
Autor:
Carla Adriana Loureiro de Matos, Fernando Lopes Alberto, Lara B. Lemos, Renata M. Perez, Eloisa de Sá Moreira, Antonio Eduardo Benedito Silva, Maria Lucia Gomes Ferraz, Jose O. Medina-Pestana, Valéria P. Lanzoni
Publikováno v:
European Journal of Gastroenterology & Hepatology. 19:653-657
Hepatitis B may show a more aggressive course after kidney transplantation, but the factors associated with the progression of fibrosis in this group have not been identified.To determine the influence of hepatitis B virus (HBV) viral load and host-r
Autor:
Denise P. Cavalcanti, Luis Garcia Alonso, Ethylin Wang Jabs, E de Sá Moreira, Chong Ae Kim, Simeon A. Boyadjiev, David W. Johnson, Maria Rita Passos-Bueno, Fernanda Sarquis Jehee, Steven A. Wall, Andrew O.M. Wilkie, Fernando Lopes Alberto, Fernando Kok
Publikováno v:
Clinical Genetics. 67:503-510
Trigonocephaly is a rare form of craniosynostosis characterized by the premature closure of the metopic suture. To contribute to a better understanding of the genetic basis of metopic synostosis and in an attempt to restrict the candidate regions rel
Autor:
Joyce M. Annichino-Bizzacchi, Fernando Ferreira Costa, Vagner Castro, Sara T.O. Saad, Maria Stella Figueiredo, Fernando Lopes Alberto, Sandra Fátima Menosi Gualandro, J. Lepikson-Neto, R. N. P. Costa
Publikováno v:
Vox Sanguinis. 87:118-123
Background Polymorphisms of platelet membrane glycoproteins such as human platelet antigen (HPA)-1b, HPA-2b, the -5T/C Kozak sequence and C807T have been described as risk factors for vascular disease. Vaso-occlusion episodes are a common feature of
Autor:
Valder R. Arruda, Carmen Silvia Passos Lima, Sara T.O. Saad, Fernando Ferreira Costa, Fernando Lopes Alberto, Erich Vinicius De Paula
Publikováno v:
European Journal of Haematology. 70:151-155
Objective: The study aimed to investigate the use of hydroxyurea (HU) for the treatment of beta-thalassaemia (β-thal) patients. Methods: We examined the haematological effects of orally administered HU (10–20 mg/kg/d) in 11 patients, including fou
Autor:
Daniel F. Simão, Luis F.L. Reis, Vanderlei Rodrigues, Dirce Maria Carraro, Marco Antônio Zago, Ismael Dale Cotrim Guerreiro da Silva, Rui M. B. Maciel, Heloisa Zalcberg, Alex F. Carvalho, Maria Lucia C. Corrêa, Daniela C. Miranda, Paula Rahal, Ari J. S. Ferreira, E. C. Miracca, Silvia Regina Rogatto, Ana L. T. O. Nascimento, Simone Cristina Sant'anna, Andrew J. G. Simpson, Nancy da Rós, Wilson A. Silva, Maria E. R. de Camargo, Christine Hackel, Gilberto K. Furuzawa, Fernando Lopes Alberto, Gustavo H. Goldman, Vanessa Bombonato, Elida B. Ojopi, Aline Maria Da Silva, Cláudia Aparecida Rainho, Angela Maria de Assis, Maria de Fátima Sonati, Maria Aparecida Nagai, Rosana F. R. Corrêa, Hamza El-Dorry, Maria Luísa Paço-Larson, Sergio Verjovski-Almeida, Nádia Aparecida Bérgamo, Fernando Augusto Soares, Mari Cleide Sogayar, Valeria Valente, Maria Inês de Moura Campos Pardini, Aline C. Prevedel, Arthur Gruber, Analy Salles de Azevedo Melo, Anamaria A. Camargo, Mozart Marins, Sandro Roberto Valentini, Janete M. Cerutti, Mariana Lopes dos Santos, Marina P. Nobrega, Francisco G. Nobrega, Eloiza H. Tajara, M. E. J. Amaral, Edna Teruko Kimura, Italo A. Migotto, Marcelo Lima Ribeiro, Daniel Giannella-Neto, Josane F. Sousa, M B Melo, Paula de Oliveira Montandon Hokama, José Rodrigo C. Pandolfi, Ricardo R. Brentani, Diana N. Nunes, Renata de Azevedo Canevari, Fernando Tsukumo, Liliane A. T. Arnaldi, Renata G. de Sá, Ivy Aneas, Elizabeth A. L. Martins, Mario H. Bengtson, Elza Kimura, Emmanuel Dias-Neto, Eduardo M. Reis, Daniella Stecconi, Suely Kazue Nagahashi Marie, Paromita Majumder, Rosana A Silveira, Carlos Alberto Mestriner, Enilza Maria Espreáfico, M. C. R. Costa, João Bosco Pesquero, Luciana C. C. Leite, José Eduardo Krieger, Sandro J. de Souza, Helena B. Samaia, Gonçalo A.G. Pereira, Helaine Carrer, Magaly M. Sales, Paulo L. Ho, Everaldo dos Reis Marques, Fernando Ferreira Costa, Ricardo G. Correa, Neusa Pereira da Silva, Angelita Habr-Gama, Luciana Gilbert Pessoa, Eloisa de Sá Moreira, Tsieko Gushiken, Cyntia Curcio, Luis Eduardo Coelho Andrade, Marcelo R.S. Briones
Publikováno v:
Proceedings of the National Academy of Sciences. 98:12103-12108
Open reading frame expressed sequences tags (ORESTES) differ from conventional ESTs by providing sequence data from the central protein coding portion of transcripts. We generated a total of 696,745 ORESTES sequences from 24 human tissues and used a
Autor:
Carmen Silvia Passos Lima, Fernando Ferreira Costa, Sara T.O. Saad, Valder R. Arruda, Irene Lorand-Metze, Fernando Lopes Alberto, M B Melo, C.R.E. Grignoli
Publikováno v:
European Journal of Haematology. 66:383-388
Objectives: Glutathione S-transferases (GST) modulate the effects of exposure to various cytotoxic and genotoxic agents, including those associated with increased risks of the myelodysplastic syndrome (MDS), acute myeloid leukaemia (AML) and aplastic
Autor:
Sandro J. de Souza, Analy Salles de Azevedo Melo, Eloiza H. Tajara, Andrew J. G. Simpson, Fernando Ferreira Costa, Elida B. Ojopi, Luis Eduardo Coelho Andrade, Edna Teruko Kimura, Luciana C. C. Leite, Marco Antônio Zago, Helaine Carrer, Sandro Roberto Valentini, Magaly M. Sales, Fernando Lopes Alberto, Marcelo R.S. Briones, Ricardo R. Brentani, Gustavo H. Goldman, Lúcia Helena Carvalho, Paromita Majumder, Francisco G. Nobrega, Paulo L. Ho, Alex F. Carvalho, Maria Luísa Paço-Larson, José Rodrigo C. Pandolfi, M. E. J. Amaral, Daniel F. Simão, Gustavo Maia, Silvia Regina Rogatto, E. C. Miracca, Elizabeth A. L. Martins, Elza Kimura, Carlos Alberto Mestriner, Janete M. Cerutti, M. C. R. Costa, Hamza El-Dorry, Enilza Maria Espreáfico, Christine Hackel, Luis F.L. Reis, Dirce Maria Carraro, João Bosco Pesquero, Mario H. Bengtson, Ismael Dale Cotrim Guerreiro da Silva, Rui M. B. Maciel, Sergio Verjovski-Almeida, Maria Inês de Moura Campos Pardini, Daniella Stecconi, Tereza Cristina Lima Silva, Renata G. de Sá, Mozart Marins, Arthur Gruber, Mari Cleide Sogayar, Valeria Valente, I. Anéas, Suely Kazue Nagahashi Marie, Maria de Fátima Sonati, Wilson da Silva, Gonçalo A.G. Pereira, Vanderlei Rodrigues, Heloisa Zalcberg, Maria Aparecida Nagai, Fernando Tsukumo, Daniela C. Miranda, Paula Rahal, Emmanuel Dias-Neto, Adriana Yamaguti Matsukuma, Cláudia Aparecida Rainho, Josane F. Sousa, Tsieko Gushiken, Cyntia Curcio, Maria Lucia C. Corrêa, Daniel Giannella-Neto, Ana L. T. O. Nascimento, Nancy da Rós, Neusa Pereira da Silva, Angelita Habr-Gama, Marcio Luis Acencio, Anamaria A. Camargo, Marina P. Nobrega, Luciana Gilbert Pessoa
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Transcribed sequences in the human genome can be identified with confidence only by alignment with sequences derived from cDNAs synthesized from naturally occurring mRNAs. We constructed a set of 250,000 cDNAs that represent partial expressed gene se
Autor:
Eloisa de Sá Moreira, Daniela Borri, Fernando Lopes Alberto, Maria de Lourdes Lopes Ferrari Chauffaille, Rodrigo Proto-Siqueira
Publikováno v:
Leukemia & Lymphoma. 49:2387-2389
Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia (AML) characterised by t(15;17)(q22;q21), a balanced reciprocal translocation involving PML and RARA genes. Rarely...