S
Silvia Regina Rogatto
Researcher at University of Southern Denmark
Publications - 205
Citations - 3773
Silvia Regina Rogatto is an academic researcher from University of Southern Denmark. The author has contributed to research in topics: Cancer & Gene. The author has an hindex of 30, co-authored 189 publications receiving 3135 citations. Previous affiliations of Silvia Regina Rogatto include National Institute of Standards and Technology & AC Camargo Hospital.
Papers
More filters
Journal ArticleDOI
CDH1 promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer.
José Roberto Fígaro Caldeira,Érika da Costa Prando,Francisco Carlos Quevedo,Francisco A. Moraes Neto,Cláudia Aparecida Rainho,Silvia Regina Rogatto +5 more
TL;DR: The preliminary findings suggested that abnormal CDH1 methylation occurs in high frequencies in infiltrating breast cancers associated with a decrease in E-cadherin expression in a subgroup of cases characterized by loss of expression of other important genes to the mammary carcinogenesis process, probably due to the disruption of the mechanism of maintenance of DNA methylation in tumoral cells.
Journal ArticleDOI
The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome
Anamaria A. Camargo,Helena B. Samaia,Emmanuel Dias-Neto,Daniel F. Simão,Italo A. Migotto,Marcelo R.S. Briones,Fernando Ferreira Costa,Maria Aparecida Nagai,Sergio Verjovski-Almeida,Marco Antônio Zago,Luis Eduardo Coelho Andrade,Helaine Carrer,Hamza El-Dorry,Enilza Maria Espreáfico,Angelita Habr-Gama,Daniel Giannella-Neto,Gustavo H. Goldman,Arthur Gruber,Christine Hackel,Edna Teruko Kimura,Rui M. B. Maciel,Suely Kazue Nagahashi Marie,Elizabeth A. L. Martins,Marina P. Nobrega,Maria Luísa Paço-Larson,Maria Inês de Moura Campos Pardini,Gonçalo A.G. Pereira,João Bosco Pesquero,Vanderlei Rodrigues,Silvia Regina Rogatto,Ismael Dale Cotrim Guerreiro da Silva,Mari Cleide Sogayar,Maria de Fátima Sonati,Eloiza H. Tajara,Sandro Roberto Valentini,Fernando Lopes Alberto,M. E. J. Amaral,Ivy Aneas,Liliane A. T. Arnaldi,Angela Maria de Assis,Mario H. Bengtson,Nádia Aparecida Bérgamo,Vanessa Bombonato,Maria E. R. de Camargo,Renata de Azevedo Canevari,Dirce Maria Carraro,Janete M. Cerutti,Maria Lucia C. Corrêa,Rosana F. R. Corrêa,M. C. R. Costa,Cyntia Curcio,Paula de Oliveira Montandon Hokama,Ari J. S. Ferreira,Gilberto K. Furuzawa,Tsieko Gushiken,Paulo L. Ho,Elza Kimura,José Eduardo Krieger,Luciana C. C. Leite,Paromita Majumder,Mozart Marins,Everaldo dos Reis Marques,Analy Salles de Azevedo Melo,M B Melo,Carlos Alberto Mestriner,E. C. Miracca,Daniela C. Miranda,Ana L. T. O. Nascimento,Francisco G. Nobrega,Elida B. Ojopi,José Rodrigo C. Pandolfi,Luciana Gilbert Pessoa,Aline C. Prevedel,Paula Rahal,Cláudia Aparecida Rainho,Eduardo M. Reis,Marcelo Lima Ribeiro,Nancy da Rós,Renata G. de Sá,Magaly M. Sales,Simone Cristina Sant'anna,Mariana Lopes dos Santos,Aline Maria Da Silva,Neusa Pereira da Silva,Wilson A. Silva,Rosana A Silveira,Josane F. Sousa,Daniella Stecconi,Fernando Tsukumo,Valeria Valente,Fernando Augusto Soares,Eloisa de Sá Moreira,Diana N. Nunes,Ricardo G. Correa,Heloisa Zalcberg,Alex F. Carvalho,Luis F.L. Reis,Ricardo R. Brentani,Andrew J. G. Simpson,Sandro J. de Souza +99 more
TL;DR: Open reading frame expressed sequences tags (ORESTES) as discussed by the authors differ from conventional ESTs by providing sequence data from the central protein coding portion of transcripts, which can be used for gene discovery and shotgun transcript sequence generation.
Journal ArticleDOI
Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags
Sandro J. de Souza,Anamaria A. Camargo,Marcelo R.S. Briones,Fernando Ferreira Costa,Maria Aparecida Nagai,Sergio Verjovski-Almeida,Marco Antônio Zago,Luis Eduardo Coelho Andrade,Helaine Carrer,Hamza El-Dorry,Enilza Maria Espreáfico,Angelita Habr-Gama,Daniel Giannella-Neto,Gustavo H. Goldman,Arthur Gruber,Christine Hackel,Edna Teruko Kimura,Rui M. B. Maciel,Suely Kazue Nagahashi Marie,Elizabeth A. L. Martins,Marina P. Nobrega,Maria Luísa Paço-Larson,Maria Inês de Moura Campos Pardini,Gonçalo A.G. Pereira,João Bosco Pesquero,Vanderlei Rodrigues,Silvia Regina Rogatto,Ismael Dale Cotrim Guerreiro da Silva,Mari Cleide Sogayar,Maria de Fátima Sonati,Eloiza H. Tajara,Sandro Roberto Valentini,Marcio Luis Acencio,Fernando Lopes Alberto,M. E. J. Amaral,I. Anéas,Mario H. Bengtson,Dirce Maria Carraro,Alex F. Carvalho,Lúcia Helena Carvalho,Janete M. Cerutti,Maria Lucia C. Corrêa,M. C. R. Costa,Cyntia Curcio,Tsieko Gushiken,Paulo L. Ho,Elza Kimura,Luciana C. C. Leite,Gustavo Maia,Paromita Majumder,Mozart Marins,Adriana Yamaguti Matsukuma,Analy Salles de Azevedo Melo,Carlos Alberto Mestriner,E. C. Miracca,Daniela C. Miranda,Ana L. T. O. Nascimento,Francisco G. Nobrega,Elida B. Ojopi,José Rodrigo C. Pandolfi,Luciana Gilbert Pessoa,Paula Rahal,Cláudia Aparecida Rainho,Nancy da Rós,Renata G. de Sá,Magaly M. Sales,Neusa Pereira da Silva,Tereza Cristina Lima Silva,Wilson da Silva,Daniel F. Simão,Josane F. Sousa,Daniella Stecconi,Fernando Tsukumo,Valeria Valente,Heloisa Zalcberg,Ricardo R. Brentani,Luis F.L. Reis,Emmanuel Dias-Neto,Andrew J. G. Simpson +78 more
TL;DR: A set of 250,000 cDNAs that represent partial expressed gene sequences and that are biased toward the central coding regions of the resulting transcripts, termed ORF expressed sequence tags (ORESTES), defined 48 transcribed sequences on chromosome 22 not defined by other sequences.
Journal ArticleDOI
An Inherited Small Microdeletion at 15q13.3 in a Patient with Early- Onset Obsessive-Compulsive Disorder
Carolina Cappi,Ana Gabriela Hounie,Daniel B Mariani,Juliana Belo Diniz,Aderbal R. T. Silva,Viviane Neri de Souza Reis,Ariane Fidelis Busso,Amanda Gonçalves Silva,Felipe Fidalgo,Silvia Regina Rogatto,Euripedes Constantino Miguel,Ana Cristina Victorino Krepischi,Helena Brentani +12 more
TL;DR: A pilot genome-wide screen for CNVs in a cohort of patients with early-onset obsessive-compulsive disorder and 12 mentally healthy individuals found a small rare paternal inherited microdeletion in one male patient with very early onset OCD, which supports the hypothesis of a complex network of several genes expressed in the brain contributing for the genetic risk of OCD.
Journal ArticleDOI
Circulating mRNAs and miRNAs as candidate markers for the diagnosis and prognosis of prostate cancer
Marilesia Ferreira de Souza,Hellen Kuasne,Mateus Camargo Barros-Filho,Heloísa Lizotti Cilião,Fabio Albuquerque Marchi,Paulo Emilio Fuganti,Alexandre Rossi Paschoal,Silvia Regina Rogatto,Ilce Mara de Syllos Cólus +8 more
TL;DR: The combination of circulating mRNA and miRNA was useful for the diagnosis and prognosis of PCa.