Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Ana Elizabete Silva"'
Autor:
Fernanda S. Manoel-Caetano, Ana Flávia T. Rossi, Gabriela Calvet de Morais, Fábio Eduardo Severino, Ana Elizabete Silva
Publikováno v:
Genes and Diseases, Vol 6, Iss 2, Pp 176-184 (2019)
Gastric cancer remains one of the leading causes of cancer-related death worldwide, and most of the cases are associated with Helicobacter pylori infection. This bacterium promotes the production of reactive oxygen species (ROS), which cause DNA dama
Externí odkaz:
https://doaj.org/article/37e3350c9b1443a99883551e53f46a85
Autor:
Evelyn Pedroso Toscano, Fernanda Fernandez Madeira, Mayra Pinheiro Dutra-Rulli, Luiz Otavio Maia Gonçalves, Marcela Alcântara Proença, Viviane Silva Borghi, Aline Cristina Targa Cadamuro, Giselda Warick Mazzale, Ricardo Acayaba, Ana Elizabete Silva
Publikováno v:
Gastroenterology Research and Practice, Vol 2019 (2019)
Externí odkaz:
https://doaj.org/article/5d3a27259b96494288de9262ec6840fc
Autor:
Evelyn Pedroso Toscano, Fernanda Fernandes Madeira, Mayra Pinheiro Dutra-Rulli, Luiz Otavio Maia Gonçalves, Marcela Alcântara Proença, Viviane Silva Borghi, Aline Cristina Targa Cadamuro, Giselda Warick Mazzale, Ricardo Acayaba, Ana Elizabete Silva
Publikováno v:
Gastroenterology Research and Practice, Vol 2018 (2018)
Aim. To evaluate the prevalence and risk factors of H. pylori infection in the pediatric and adult population seen at a public hospital in São José do Rio Preto, SP, Brazil. Methods. This is a retrospective study that evaluated 2406 medical records
Externí odkaz:
https://doaj.org/article/d8ecf53e64f140cb8f389ee7acd7f742
Publikováno v:
Genetics and Molecular Biology, Vol 33, Iss 2, Pp 205-213 (2010)
This review summarizes the chromosomal changes detected by molecular cytogenetic approaches in esophageal squamous cell carcinoma (ESCC), the ninth most common malignancy in the world. Whole genome analyses of ESCC cell lines and tumors indicated tha
Externí odkaz:
https://doaj.org/article/dbc44dcce9c4486aae63d8af279245dc
Publikováno v:
Genetics and Molecular Biology, Vol 32, Iss 2, Pp 242-250 (2009)
Interphase chromosomes have been shown to occupy discrete regions of the nucleus denominated chromosome territories (CTs), their active genes being preferentially positioned on the surfaces of these CTs, where they are accessible to transcriptional m
Externí odkaz:
https://doaj.org/article/eb6322216c1c479e82a7372875a53241
Publikováno v:
Cadernos de Saúde Pública, Vol 23, Iss 10, Pp 2263-2274 (2007)
Trypanosoma cruzi, the etiological agent of Chagas disease, presents a high degree of intraspecific genetic variability, with possible implications for the clinical forms of the disease, like the development of cardiopathy, megaesophagus, and megacol
Externí odkaz:
https://doaj.org/article/84fadc3f6ecb4b91ae8a1bf00eb99b82
Autor:
Aline Cristina Targa Cadamuro, Ana Flávia Teixeira Rossi, Joice Matos Biselli-Périco, Patrícia Fucuta Pereira, Edla Polsinelli Bedin Mascarin Do Vale, Ricardo Acayaba, Kátia Ramos Moreira Leite, Eny Maria Goloni-Bertollo, Ana Elizabete Silva
Publikováno v:
Mediators of Inflammation, Vol 2015 (2015)
Objective. Helicobacter pylori (Hp) is recognized by TLR4 and TLR2 receptors, which trigger the activation of genes involved in the host immune response. Thus, we evaluated the effect of eradication therapy on TLR2 and TLR4 mRNA and protein expressio
Externí odkaz:
https://doaj.org/article/5fe9464cab3b43109d232c639dd868c7
Publikováno v:
Genetics and Molecular Biology, Vol 29, Iss 1, Pp 1-7 (2006)
Gene amplification increases the number of genes in a genome and can give rise to karyotype abnormalities called double minutes (DM) and homogeneously staining regions (HSR), both of which have been widely observed in human tumors but are also known
Externí odkaz:
https://doaj.org/article/72fd3f9ac96040f3a34b4b3d5097524b
Publikováno v:
Genetics and Molecular Biology, Vol 28, Iss 3, Pp 397-401 (2005)
In several DNA repair genes, polymorphisms may result in reduced repair capacity, which has been implicated as a risk factor for various types of cancer. The frequency of the polymorphic alleles varies among populations, suggesting an ethnic distribu
Externí odkaz:
https://doaj.org/article/8f943786e0c94c298ec79365c438db8e
Autor:
Ana Elizabete Silva, Sheila Adami Vayego-Lourenço, Agnes Cristina Fett-Conte, Eny Maria Goloni-Bertollo, Marileila Varella-Garcia
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 60, Iss 2A, Pp 290-294 (2002)
We report a female child with tetrasomy of the 15q11-q13 chromosomal region, and autistic disorder associated with mental retardation, developmental problems and behavioral disorders. Combining classical and molecular cytogenetic approaches by fluore
Externí odkaz:
https://doaj.org/article/d17ff220f3ff4aa1b55a85a315af25e9