Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Camila M. Egidio"'
Autor:
C. Charles Wang, C. Ted Rigl, Eric T. Wang, Moraima Pagan, Ed Tom, Richard B. Lanman, Juan Rosai, Virginia A. LiVolsi, Jessica D. Reynolds, Jonathan I. Wilde, Hui Wang, Giulia C. Kennedy, Martha A. Zeiger, Lyssa Friedman, Giovanni Fellegara, Electron Kebebew, Nusrat Rabbee, Darya Chudova, Camila M. Egidio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 95:5296-5304
We set out to develop a molecular test that distinguishes benign and malignant thyroid nodules using fine-needle aspirates (FNA).We used mRNA expression analysis to measure more than 247,186 transcripts in 315 thyroid nodules, comprising multiple sub
Autor:
Katia R. M. Leite, Flavio C. Canavez, Etel Rodrigues Pereira Gimba, Rodrigo Louro, Franz S. Campos, Eduardo M. Reis, Giulliana T. Almeida, Fernanda Festa, Carlos Alberto Moreira-Filho, Renato Alvarenga, Helder I. Nakaya, Camila M. Egidio, Giselle M. Vignal, Aline Maria Da Silva, Sergio Daniel Simon, Marcello A. Barcinski, Sergio Verjovski-Almeida, Camille C. Caldeira da Silva, Mari Cleide Sogayar, Apuã C.M. Paquola, Aurea Valadares Folgueras Flatschart, Abimael A. Machado, Hamza El-Dorry, Luiz H. Camara-Lopes, Glauber Costa Brito, Denise Yamamoto
Publikováno v:
Oncogene. 23:6684-6692
A large fraction of transcripts are expressed antisense to introns of known genes in the human genome. Here we show the construction and use of a cDNA microarray platform enriched in intronic transcripts to assess their biological relevance in pathol
Autor:
Ricardo Z. N. Vêncio, Eduardo M. Reis, B. R. Peixoto, Sergio Verjovski-Almeida, Luisa Mota-Vieira, Camila M. Egidio
Publikováno v:
BMC Genomics, Vol 7, Iss 1, p 35 (2006)
BMC Genomics
BMC Genomics
Background Spotted cDNA microarrays generally employ co-hybridization of fluorescently-labeled RNA targets to produce gene expression ratios for subsequent analysis. Direct comparison of two RNA samples in the same microarray provides the highest lev
Autor:
Johanna M. Andreas, Ilona Holcomb, Ramesh Ramakrishnan, Alexander Schmidt, Vinzenz Lange, Kathrin Lang, Brian Fowler, Camila M. Egidio, Irina Boehme
Publikováno v:
Human Immunology. 75:488
Aim The most widely used platform for HLA typing, capillary electrophoresis-based Sanger sequencing technology, does not scale with the number of regions and samples required in complex study designs when compared to next-generation sequencing (NGS)