Now showing items 1-6 of 6

    • Cytogenetic characterization and evaluation of c-MYC gene amplification in PG100, a new Brazilian gastric cancer cell line 

      Ribeiro, Hercules Ferreira [UNIFESP]; Alcântara, D.f.a.; Matos, L.a.; Sousa, J.m.c.; Leal, Mariana Ferreira [UNIFESP]; Smith, Marilia de Arruda Cardoso [UNIFESP]; Burbano, Rommel Rodríguez [UNIFESP]; Bahia, Marcelo de Oliveira (Associação Brasileira de Divulgação Científica, 2010-08-01)
      Gastric cancer is the fourth most frequent type of cancer and the second cause of cancer mortality worldwide. The genetic alterations described so far for gastric carcinomas include amplifications and mutations of the ...

    • Cytogenetic instability of dental pulp stem cell lines 

      Duailibi, Monica Talarico [UNIFESP]; Kulikowski, Leslie Domenici; Duailibi, Silvio Eduardo [UNIFESP]; Nunes Lipay, Monica Vannucci [UNIFESP]; Melaragno, Maria Isabel; Ferreira, Lydia Masako [UNIFESP]; Vacanti, Joseph Phillip; Yelick, Pamela Crotty (Springer, 2012-02-01)
      Human adult stem cells (hASCs) offer a potentially renewable source of cell types that are easily isolated and rapidly expanded for use in regenerative medicine and cell therapies without the complicating ethical problems ...

    • Dopplervelocimetria no Rastreamento de Aneuploidias no Primeiro Trimestre da Gestação 

      Murta, Carlos Geraldo Viana [UNIFESP]; Moron, Antonio Fernandes [UNIFESP]; Ávila, Márcio Augusto Pinto de (Federação Brasileira das Sociedades de Ginecologia e Obstetrícia, 2001-06-01)
      Objective: to study the value of Doppler velocimetry of the ductus venosus and of the umbilical artery and vein, in the screening for chromosomal abnormalities at 10-14 weeks of gestation. Patients and Methods: a total of ...

    • Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence 

      Assumpcao, Juliana Godoy; Berkofsky-Fessler, Windy; Campos, Nilma Viguetti; Maciel-Guerra, Andrea Trevas; Li, Shu Lan; Melaragno, Maria Isabel [UNIFESP]; Mello, Maricilda Palandi de; Warburton, Peter E. (Wiley-Blackwell, 2002-12-01)
      An 18‐year‐old woman was evaluated because of primary amenorrhea and hypogonadism. Chromosome analysis from peripheral blood lymphocytes revealed a nonmosaic 46,X,+mar constitution. The marker was shown to be a rearranged ...

    • Trissomia do cromossomo 9 associada com aumento da translucência nucal: correlação ultra-sonográfica e anatomopatológica ¾ relato de um caso 

      Murta, Carlos Geraldo Viana [UNIFESP]; Merçon-de-vargas, Paulo Roberto (Colégio Brasileiro de Radiologia e Diagnóstico por Imagem, 2001-04-01)
      We report a case of prenatal diagnosis of trisomy 9 in a fetus presenting increased translucency thickness (9.1 mm) observed on an ultrasound scan performed at 12 weeks pregnancy and confirmed by cariotype analysis of ...

    • Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries 

      Jehee, Fernanda Sarquis; Takamori, Jean Tetsuo; Vasconcelos Medeiros, Paula F.; Pordeus, Ana Carolina B.; Latini, Flavia Roche Moreira [UNIFESP]; Bertola, Debora Romeo; Kim, Chong Ae; Passos-Bueno, Maria Rita (Elsevier B.V., 2011-07-01)
      Conventional karyotyping detects anomalies in 3-15% of patients with multiple congenital anomalies and mental retardation (MCA/MR). Whole-genome array screening (WGAS) has been consistently suggested as the first choice ...